This document summarizes key points from Chapter 10 of the textbook "Neuroscience: Exploring the Brain, 3e" regarding the central visual system. It describes the retinofugal projection from the retina to the lateral geniculate nucleus and striate cortex. It discusses topics like retinal ganglion cell types, organization of the LGN, retinotopy and laminar organization in V1, and receptive field properties in the LGN and V1. It also summarizes the dorsal and ventral visual pathways beyond V1 and how parallel processing across areas underlies visual perception.
The document summarizes the central visual pathways and visual field deficits resulting from lesions in these pathways. It describes how ganglion cell axons from the nasal and temporal retina project either contralaterally or ipsilaterally. The lateral geniculate nucleus and optic radiations are involved in visual processing before projections reach the primary visual cortex. Lesions in different areas can cause anopsia, hemianopsia, quadrantanopsia or scotomas.
Physiology of the visual pathway & cerebral integrationHenok Samuel
The document summarizes the physiology of the visual pathway and cerebral integration. It discusses how light is converted to electrochemical signals in the retina which are then relayed by retinal ganglion cells whose axons form the optic nerve. It describes the retinotopic organization and different types of ganglion cells that project to various areas in the lateral geniculate nucleus and superior colliculus. It also discusses how information is transmitted from the LGN via the optic radiations to the primary visual cortex and then onto dorsal and ventral visual processing streams in the brain.
This document provides an overview of the visual pathway, which transmits visual impulses from the retina to the visual cortex of the brain. It describes the main components of the visual pathway, including rods and cones, bipolar cells, ganglionic cells that form the optic nerve, the lateral geniculate body, optic radiation and visual cortex. It also discusses lesions that can occur at different points along the visual pathway and the visual field defects they may cause, such as homonymous hemianopia.
The visual pathway/visual system is the part of central nervous system which gives organisms the ability to process visual detail , as well as enabling the formation of several non-image photo response functions.
It detects interprets information from visible light to build a representation of the surrounding environment .
The visual system carries out a number of complex tasks , including the reception of light and the formation of monocular representations; the buildup of a nuclear binocular perception from a pair of two dimensional projections ; the identification and categorization of visual objects ; assessing distances to and between objects and guiding body movements in relation to the objects seen.
The document discusses the history and types of microscopes. It describes the key parts of a microscope including the support system (base, pillars, body tube, stage), focusing system (coarse and fine adjustments), optical system (eyepiece, nosepiece, objective lenses), and illumination system (light source, mirror, condenser, diaphragm, filter). Different types of microscopes are listed along with the magnification and numerical aperture of objective lenses. Rules for using different objective lenses with the condenser and iris diaphragm are provided. In closing, the author provides their contact information.
The visual cortex is organized into a primary visual cortex and secondary visual areas. The primary visual cortex is located in the occipital lobe and receives direct input from the retina via the lateral geniculate nucleus. It is composed of six layers and contains vertical columns that process visual information like color, orientation, and motion. The secondary visual areas surround the primary cortex and further analyze and interpret visual information through two pathways - a fast pathway for position and motion, and an accurate pathway for color and detail. Removing the primary visual cortex causes blindness while removing secondary areas causes difficulties recognizing objects and reading words.
Design a EEG transmission and receving system using infrared waves for states...Viraj Shah
This document describes a student project to design an EEG transmission and receiving system using infrared waves. It aims to transmit EEG signals wirelessly during sleep studies. The document includes an introduction, table of contents, and chapters on brain anatomy, EEG signals, EEG diagnosis principles, system instrumentation, and results. It was submitted by 4 students for their Bachelor's degree and aims to demonstrate the equipment and describe the system block diagram.
The document summarizes the central visual pathways and visual field deficits resulting from lesions in these pathways. It describes how ganglion cell axons from the nasal and temporal retina project either contralaterally or ipsilaterally. The lateral geniculate nucleus and optic radiations are involved in visual processing before projections reach the primary visual cortex. Lesions in different areas can cause anopsia, hemianopsia, quadrantanopsia or scotomas.
Physiology of the visual pathway & cerebral integrationHenok Samuel
The document summarizes the physiology of the visual pathway and cerebral integration. It discusses how light is converted to electrochemical signals in the retina which are then relayed by retinal ganglion cells whose axons form the optic nerve. It describes the retinotopic organization and different types of ganglion cells that project to various areas in the lateral geniculate nucleus and superior colliculus. It also discusses how information is transmitted from the LGN via the optic radiations to the primary visual cortex and then onto dorsal and ventral visual processing streams in the brain.
This document provides an overview of the visual pathway, which transmits visual impulses from the retina to the visual cortex of the brain. It describes the main components of the visual pathway, including rods and cones, bipolar cells, ganglionic cells that form the optic nerve, the lateral geniculate body, optic radiation and visual cortex. It also discusses lesions that can occur at different points along the visual pathway and the visual field defects they may cause, such as homonymous hemianopia.
The visual pathway/visual system is the part of central nervous system which gives organisms the ability to process visual detail , as well as enabling the formation of several non-image photo response functions.
It detects interprets information from visible light to build a representation of the surrounding environment .
The visual system carries out a number of complex tasks , including the reception of light and the formation of monocular representations; the buildup of a nuclear binocular perception from a pair of two dimensional projections ; the identification and categorization of visual objects ; assessing distances to and between objects and guiding body movements in relation to the objects seen.
The document discusses the history and types of microscopes. It describes the key parts of a microscope including the support system (base, pillars, body tube, stage), focusing system (coarse and fine adjustments), optical system (eyepiece, nosepiece, objective lenses), and illumination system (light source, mirror, condenser, diaphragm, filter). Different types of microscopes are listed along with the magnification and numerical aperture of objective lenses. Rules for using different objective lenses with the condenser and iris diaphragm are provided. In closing, the author provides their contact information.
The visual cortex is organized into a primary visual cortex and secondary visual areas. The primary visual cortex is located in the occipital lobe and receives direct input from the retina via the lateral geniculate nucleus. It is composed of six layers and contains vertical columns that process visual information like color, orientation, and motion. The secondary visual areas surround the primary cortex and further analyze and interpret visual information through two pathways - a fast pathway for position and motion, and an accurate pathway for color and detail. Removing the primary visual cortex causes blindness while removing secondary areas causes difficulties recognizing objects and reading words.
Design a EEG transmission and receving system using infrared waves for states...Viraj Shah
This document describes a student project to design an EEG transmission and receiving system using infrared waves. It aims to transmit EEG signals wirelessly during sleep studies. The document includes an introduction, table of contents, and chapters on brain anatomy, EEG signals, EEG diagnosis principles, system instrumentation, and results. It was submitted by 4 students for their Bachelor's degree and aims to demonstrate the equipment and describe the system block diagram.
1. The visual pathway begins with light being absorbed by photoreceptors in the retina and transmitted via ganglion cells to the lateral geniculate body and optic radiation to the visual cortex.
2. Information crosses at the optic chiasm, with the nasal retina of each eye projecting to the opposite hemisphere.
3. The retina, optic nerve, optic chiasm, optic tract, lateral geniculate body, optic radiation, and visual cortex are organized retinotopically to preserve the point-to-point mapping of the visual field.
The visual pathway includes the optic nerve, optic chiasm, optic tracts, and lateral geniculate bodies that transmit visual information from the eyes to the brain. A 28-year old woman presented with progressive vision loss in both eyes, and CT scan revealed a high density lesion compressing the optic chiasm, producing bitemporal hemianopia. Cutting the right optic tract causes blindness in the left eye's temporal field and right eye's nasal field. A 72-year old man with a pituitary adenoma presented with bitemporal hemianopia.
The lateral geniculate nucleus is an oval-shaped structure in the thalamus that relays visual information from the retina to the visual cortex. It contains six layers of neurons that receive input from either the crossed or uncrossed retinal fibers in an organized retinotopic map. The lateral geniculate nucleus acts as a relay station, transmitting visual signals to the visual cortex while also gating the transmission under the control of feedback from the cortex and inhibitory signals from the midbrain.
The visual pathway consists of the retina, optic nerve, optic chiasm, optic tract, lateral geniculate body, optic radiations, and visual cortex. The retina contains photoreceptors and bipolar and ganglion cells. Ganglion cell axons form the optic nerve, which crosses at the optic chiasm. The optic tract relays signals to the lateral geniculate body before projecting to the primary visual cortex via the optic radiations. Lesions in different parts of the pathway cause specific visual field defects, such as homonymous hemianopia from damage to the optic radiation. The pupillary light reflex and accommodation reflex are mediated by subcortical structures.
It is also called as Visual system & is a part of Central nervous system.
Anatomy & Physiology of Visual pathway.
The References are given in the presentation itself.
1) The document is an orientation for a class on brain structure and origins taught at MIT in 2005.
2) It introduces the goals of learning vertebrate neuroanatomy through studies of development, evolution, and function.
3) The first topics to be covered are neural terminology, the evolution and study of neurons, and an overview of the central nervous system.
Anatomy of the visual pathways and visual cortexneurophq8
The document provides an overview of the anatomy and physiology of the visual pathways, beginning with the retina and optic nerve, then describing the optic chiasm, optic tracts, lateral geniculate bodies, optic radiations, visual cortex, and visual association areas. Key structures and functions are defined, including the types of retinal ganglion cells, pathways in the optic chiasm and lateral geniculate bodies, layers of the visual cortex, and the "what" and "where" pathways in visual processing.
This document provides an overview of neuronal migration disorders. It discusses the normal development of the cerebral cortex and process of neuronal migration. It then describes several types of neuronal migration disorders including lissencephaly, schizencephaly, polymicrogyrias, and neuronal heterotopias. For each type, it provides details on pathology, imaging findings, clinical features, and genetics when relevant. The document aims to educate on the anatomy, definitions, classification, and treatment of neuronal migration disorders.
The visual pathway begins in the retina and passes through the optic nerve, optic chiasm, optic tract, lateral geniculate nucleus, optic radiation, and visual cortex before terminating in the occipital lobe. Lesions in different parts of the visual pathway can cause different visual field defects, such as hemianopia or quadrantanopia. The more posterior the lesion, the more likely the visual field defects will be congruous between the two eyes.
The document describes the anatomy and blood supply of the visual pathway, which extends from the retina to the visual cortex. It discusses the key structures including the optic nerve, optic chiasm, optic tracts, lateral geniculate body, optic radiations, and visual cortex. Lesions in different parts of the visual pathway can cause various visual field defects, such as complete blindness from optic nerve lesions, quadrantic hemianopia from chiasmal lesions, and bitemporal hemianopia from central chiasmal lesions. The blood supply is also outlined for each structure, originating from branches of the internal carotid and vertebral arteries.
Anatomy of visual pathway and its lesions.Ruchi Pherwani
1) The visual pathway begins with photoreceptors in the retina which transmit visual information via the optic nerve and optic chiasm to the lateral geniculate nucleus. It then continues via the optic radiations to the primary visual cortex.
2) Lesions along the visual pathway can cause different types of visual field defects, including complete blindness from optic nerve lesions, bitemporal hemianopia from chiasmal lesions, and homonymous hemianopia from lesions of the optic tract or beyond.
3) The document discusses the anatomy and blood supply of structures in the visual pathway like the optic nerve, chiasm, tract, lateral geniculate nucleus and visual cortex. It also describes various causes and characteristics
Dr. Rahul Jain presented information on surgically treatable dementias with an emphasis on Normal Pressure Hydrocephalus (NPH). NPH is characterized by enlarged ventricles and a normal cerebrospinal fluid pressure. It commonly causes a triad of gait impairment, cognitive decline, and urinary incontinence. Imaging shows ventriculomegaly disproportionate to cortical atrophy. The presence of Disproportionately Enlarged Subarachnoid Space Hydrocephalus (DESH) on imaging predicts better response to CSF shunting surgery in NPH patients. Differential diagnosis includes neurodegenerative disorders, but NPH can be distinguished by its prominent gait dysfunction and lack of
This document provides an overview of the anatomy and physiology of the visual system for postgraduate students. It describes the main parts of the eye including the retina, rods and cones, lens, iris, and other structures. It explains how light is focused on the retina through refraction and the process of accommodation. Common vision conditions like myopia, hyperopia and presbyopia are also discussed. The document concludes with descriptions of the photoreceptor mechanism and how light triggers electrical responses in rods and cones that are transmitted to the brain.
This document discusses ocular movements and their neural control pathways. It describes four types of ocular movements - versions, ductions, vergences, and supranuclear eye movements. Supranuclear eye movements include saccades, smooth pursuit, vestibulo-ocular, and optokinetic movements. The document outlines the cortical and brainstem control centers that generate each type of eye movement, including pathways like the medial longitudinal fasciculus. It also discusses various disorders that can occur with abnormalities in horizontal and vertical gaze, vergence, and other types of supranuclear eye movements.
1. Visual pathway lesions can occur prechiasmally in the optic nerve or retrochiasmally in the optic tract, lateral geniculate nucleus, optic radiations, and occipital cortex.
2. Optic neuropathy manifestations include visual field defects such as arcuate scotomas. Optic tract lesions cause incongruous homonymous hemianopsia.
3. Lateral geniculate nucleus lesions result in an incongruous wedge defect pointing toward fixation. Occipital cortex lesions cause homonymous field defects that can be paracentral or peripheral.
Phototransduction & Visual Pathway Mmp March 10Anan
This document summarizes the visual pathway from phototransduction in the retina through processing in the brain. Light stimulation is converted to nerve impulses by photoreceptors in the retina through a process called phototransduction. These impulses are carried by the optic nerve to the lateral geniculate body and primary visual cortex for further processing to perceive images. The visual cortex associates visual inputs from both eyes to construct a single image and enable recognition of objects and patterns.
1. The visual pathway begins in the retina and transmits visual information to the brain.
2. It consists of the optic nerves, optic chiasm, optic tracts, lateral geniculate bodies, optic radiations, and visual cortex.
3. The optic nerves carry axons from retinal ganglion cells and transmit information from the eyes to the optic chiasm where fibers from the nasal retina cross to the opposite side.
The visual pathway begins in the retina and passes through the optic nerves, optic chiasm, optic tracts, lateral geniculate nucleus, optic radiations, and terminates in the occipital lobe. Lesions along this pathway can cause various visual field defects including hemianopias and quadrantanopias depending on the location of the lesion. Lesions in the optic nerve cause blindness on the affected side while lesions in the optic chiasm or tracts cause incongruous homonymous hemianopias. Lesions of the optic radiations or visual cortex cause congruous homonymous defects.
The visual pathway comprises the retina, optic nerve, optic chiasm, optic tracts, lateral geniculate bodies, optic radiations, and visual cortex. The optic nerve has four parts - intraocular, intraorbital, intracanalicular, and intracranial. It carries axons from retinal ganglion cells and does not regenerate when cut due to the lack of a neurilemma sheath. Lesions in different parts of the visual pathway cause characteristic visual field defects, such as complete blindness from optic nerve lesions, bitemporal hemianopia from central chiasmal lesions, and binasal hemianopia from lateral chiasmal lesions.
A synapse is a gap that is present between two neurones. Action potentials are propagated across the synapse by synaptic transmission, also known as neurotransmission. The neurone that sends the signal is the presynaptic neurone, whilst the postsynaptic neurone receives the signal.Neurotransmission starts with the release of a readily available neurotransmitter from the presynaptic neurone, followed by its diffusion and binding to the postsynaptic receptors. Then the postsynaptic cell responds according to the neurotransmitter. Following this, the neurotransmitter is removed or deactivated, allowing the entire cycle to occur again.Synthesis and Storage of Neurotransmitters
This is the first step of synaptic transmission. Some neurotransmitters (eg acetylcholine, ACh) are synthesised in the axon, while others (eg neuropeptides) are made in the cell body.Acetylcholine – This is synthesised within the synaptic terminal of the axon. Its precursors (choline, acetate) are taken into the cell by membrane channels or created as byproducts of other processes. Enzymes (such as choline acetyltransferase) convert precursors into the neurotransmitter.
Endogenous opioids (eg. enkephalins) – These are an example of neuropeptides. These large neurotransmitters are produced within the cell body via transcription in the nucleus and translation in the endoplasmic reticulum. Synthesised precursors are then packaged into secretory granules and sent to the axonal terminal. Importantly, proteases present in the granules cleave the precursors into their mature neuropeptide form during this journey.Once synthesised, neurotransmitters are stored in vesicles within the synaptic terminal until an action potential arrives, causing their release. Neurotransmitters such as acetylcholine are stored within the small synaptic vesicles, whereas neuropeptides reside within large dense-core vesicles.Once the post-synaptic membrane has responded to the neurotransmitter in the synaptic cleft; it is either inactivated or removed. This can be done in several ways:
Re-uptake – serotonin is taken back into the pre-synaptic neurone by the transporter proteins in the neuronal membrane. These neurotransmitters are subsequently either recycled by re-packaging into vesicles or broken down by enzymes.
Breakdown – acetylcholine is broken down by acetylcholinesterase present in the synaptic cleft, inactivating the neurotransmitter.
Diffusion – into surrounding areasAction potentials depolarising the synaptic terminal lead to the opening of voltage-gated calcium channels. This allows an influx of calcium in the terminal and fusion of the synaptic vesicles with the cell membrane (exocytosis). Consequently, the neurotransmitter is released into the synaptic cleft.The neurotransmitter in the synaptic cleft diffuses across the gap to the post-synaptic membrane. Here, they can bind to two types of post-synaptic receptors.Acetylcholinesterase inhibitors are a class of drug that inhibits the activity of
- Visual signals are processed through multiple stages in the retina, visual pathway and visual cortex before visual perception.
- In the retina, photoreceptors transmit signals to bipolar and ganglion cells which transmit to the lateral geniculate nucleus.
- The LGN relays signals to the primary visual cortex which contains columns for processing features like orientation, ocular dominance and color.
- Extrastriate visual areas further analyze signals for motion, depth and color perception before perception in the visual cortex.
1. The visual pathway begins with light being absorbed by photoreceptors in the retina and transmitted via ganglion cells to the lateral geniculate body and optic radiation to the visual cortex.
2. Information crosses at the optic chiasm, with the nasal retina of each eye projecting to the opposite hemisphere.
3. The retina, optic nerve, optic chiasm, optic tract, lateral geniculate body, optic radiation, and visual cortex are organized retinotopically to preserve the point-to-point mapping of the visual field.
The visual pathway includes the optic nerve, optic chiasm, optic tracts, and lateral geniculate bodies that transmit visual information from the eyes to the brain. A 28-year old woman presented with progressive vision loss in both eyes, and CT scan revealed a high density lesion compressing the optic chiasm, producing bitemporal hemianopia. Cutting the right optic tract causes blindness in the left eye's temporal field and right eye's nasal field. A 72-year old man with a pituitary adenoma presented with bitemporal hemianopia.
The lateral geniculate nucleus is an oval-shaped structure in the thalamus that relays visual information from the retina to the visual cortex. It contains six layers of neurons that receive input from either the crossed or uncrossed retinal fibers in an organized retinotopic map. The lateral geniculate nucleus acts as a relay station, transmitting visual signals to the visual cortex while also gating the transmission under the control of feedback from the cortex and inhibitory signals from the midbrain.
The visual pathway consists of the retina, optic nerve, optic chiasm, optic tract, lateral geniculate body, optic radiations, and visual cortex. The retina contains photoreceptors and bipolar and ganglion cells. Ganglion cell axons form the optic nerve, which crosses at the optic chiasm. The optic tract relays signals to the lateral geniculate body before projecting to the primary visual cortex via the optic radiations. Lesions in different parts of the pathway cause specific visual field defects, such as homonymous hemianopia from damage to the optic radiation. The pupillary light reflex and accommodation reflex are mediated by subcortical structures.
It is also called as Visual system & is a part of Central nervous system.
Anatomy & Physiology of Visual pathway.
The References are given in the presentation itself.
1) The document is an orientation for a class on brain structure and origins taught at MIT in 2005.
2) It introduces the goals of learning vertebrate neuroanatomy through studies of development, evolution, and function.
3) The first topics to be covered are neural terminology, the evolution and study of neurons, and an overview of the central nervous system.
Anatomy of the visual pathways and visual cortexneurophq8
The document provides an overview of the anatomy and physiology of the visual pathways, beginning with the retina and optic nerve, then describing the optic chiasm, optic tracts, lateral geniculate bodies, optic radiations, visual cortex, and visual association areas. Key structures and functions are defined, including the types of retinal ganglion cells, pathways in the optic chiasm and lateral geniculate bodies, layers of the visual cortex, and the "what" and "where" pathways in visual processing.
This document provides an overview of neuronal migration disorders. It discusses the normal development of the cerebral cortex and process of neuronal migration. It then describes several types of neuronal migration disorders including lissencephaly, schizencephaly, polymicrogyrias, and neuronal heterotopias. For each type, it provides details on pathology, imaging findings, clinical features, and genetics when relevant. The document aims to educate on the anatomy, definitions, classification, and treatment of neuronal migration disorders.
The visual pathway begins in the retina and passes through the optic nerve, optic chiasm, optic tract, lateral geniculate nucleus, optic radiation, and visual cortex before terminating in the occipital lobe. Lesions in different parts of the visual pathway can cause different visual field defects, such as hemianopia or quadrantanopia. The more posterior the lesion, the more likely the visual field defects will be congruous between the two eyes.
The document describes the anatomy and blood supply of the visual pathway, which extends from the retina to the visual cortex. It discusses the key structures including the optic nerve, optic chiasm, optic tracts, lateral geniculate body, optic radiations, and visual cortex. Lesions in different parts of the visual pathway can cause various visual field defects, such as complete blindness from optic nerve lesions, quadrantic hemianopia from chiasmal lesions, and bitemporal hemianopia from central chiasmal lesions. The blood supply is also outlined for each structure, originating from branches of the internal carotid and vertebral arteries.
Anatomy of visual pathway and its lesions.Ruchi Pherwani
1) The visual pathway begins with photoreceptors in the retina which transmit visual information via the optic nerve and optic chiasm to the lateral geniculate nucleus. It then continues via the optic radiations to the primary visual cortex.
2) Lesions along the visual pathway can cause different types of visual field defects, including complete blindness from optic nerve lesions, bitemporal hemianopia from chiasmal lesions, and homonymous hemianopia from lesions of the optic tract or beyond.
3) The document discusses the anatomy and blood supply of structures in the visual pathway like the optic nerve, chiasm, tract, lateral geniculate nucleus and visual cortex. It also describes various causes and characteristics
Dr. Rahul Jain presented information on surgically treatable dementias with an emphasis on Normal Pressure Hydrocephalus (NPH). NPH is characterized by enlarged ventricles and a normal cerebrospinal fluid pressure. It commonly causes a triad of gait impairment, cognitive decline, and urinary incontinence. Imaging shows ventriculomegaly disproportionate to cortical atrophy. The presence of Disproportionately Enlarged Subarachnoid Space Hydrocephalus (DESH) on imaging predicts better response to CSF shunting surgery in NPH patients. Differential diagnosis includes neurodegenerative disorders, but NPH can be distinguished by its prominent gait dysfunction and lack of
This document provides an overview of the anatomy and physiology of the visual system for postgraduate students. It describes the main parts of the eye including the retina, rods and cones, lens, iris, and other structures. It explains how light is focused on the retina through refraction and the process of accommodation. Common vision conditions like myopia, hyperopia and presbyopia are also discussed. The document concludes with descriptions of the photoreceptor mechanism and how light triggers electrical responses in rods and cones that are transmitted to the brain.
This document discusses ocular movements and their neural control pathways. It describes four types of ocular movements - versions, ductions, vergences, and supranuclear eye movements. Supranuclear eye movements include saccades, smooth pursuit, vestibulo-ocular, and optokinetic movements. The document outlines the cortical and brainstem control centers that generate each type of eye movement, including pathways like the medial longitudinal fasciculus. It also discusses various disorders that can occur with abnormalities in horizontal and vertical gaze, vergence, and other types of supranuclear eye movements.
1. Visual pathway lesions can occur prechiasmally in the optic nerve or retrochiasmally in the optic tract, lateral geniculate nucleus, optic radiations, and occipital cortex.
2. Optic neuropathy manifestations include visual field defects such as arcuate scotomas. Optic tract lesions cause incongruous homonymous hemianopsia.
3. Lateral geniculate nucleus lesions result in an incongruous wedge defect pointing toward fixation. Occipital cortex lesions cause homonymous field defects that can be paracentral or peripheral.
Phototransduction & Visual Pathway Mmp March 10Anan
This document summarizes the visual pathway from phototransduction in the retina through processing in the brain. Light stimulation is converted to nerve impulses by photoreceptors in the retina through a process called phototransduction. These impulses are carried by the optic nerve to the lateral geniculate body and primary visual cortex for further processing to perceive images. The visual cortex associates visual inputs from both eyes to construct a single image and enable recognition of objects and patterns.
1. The visual pathway begins in the retina and transmits visual information to the brain.
2. It consists of the optic nerves, optic chiasm, optic tracts, lateral geniculate bodies, optic radiations, and visual cortex.
3. The optic nerves carry axons from retinal ganglion cells and transmit information from the eyes to the optic chiasm where fibers from the nasal retina cross to the opposite side.
The visual pathway begins in the retina and passes through the optic nerves, optic chiasm, optic tracts, lateral geniculate nucleus, optic radiations, and terminates in the occipital lobe. Lesions along this pathway can cause various visual field defects including hemianopias and quadrantanopias depending on the location of the lesion. Lesions in the optic nerve cause blindness on the affected side while lesions in the optic chiasm or tracts cause incongruous homonymous hemianopias. Lesions of the optic radiations or visual cortex cause congruous homonymous defects.
The visual pathway comprises the retina, optic nerve, optic chiasm, optic tracts, lateral geniculate bodies, optic radiations, and visual cortex. The optic nerve has four parts - intraocular, intraorbital, intracanalicular, and intracranial. It carries axons from retinal ganglion cells and does not regenerate when cut due to the lack of a neurilemma sheath. Lesions in different parts of the visual pathway cause characteristic visual field defects, such as complete blindness from optic nerve lesions, bitemporal hemianopia from central chiasmal lesions, and binasal hemianopia from lateral chiasmal lesions.
A synapse is a gap that is present between two neurones. Action potentials are propagated across the synapse by synaptic transmission, also known as neurotransmission. The neurone that sends the signal is the presynaptic neurone, whilst the postsynaptic neurone receives the signal.Neurotransmission starts with the release of a readily available neurotransmitter from the presynaptic neurone, followed by its diffusion and binding to the postsynaptic receptors. Then the postsynaptic cell responds according to the neurotransmitter. Following this, the neurotransmitter is removed or deactivated, allowing the entire cycle to occur again.Synthesis and Storage of Neurotransmitters
This is the first step of synaptic transmission. Some neurotransmitters (eg acetylcholine, ACh) are synthesised in the axon, while others (eg neuropeptides) are made in the cell body.Acetylcholine – This is synthesised within the synaptic terminal of the axon. Its precursors (choline, acetate) are taken into the cell by membrane channels or created as byproducts of other processes. Enzymes (such as choline acetyltransferase) convert precursors into the neurotransmitter.
Endogenous opioids (eg. enkephalins) – These are an example of neuropeptides. These large neurotransmitters are produced within the cell body via transcription in the nucleus and translation in the endoplasmic reticulum. Synthesised precursors are then packaged into secretory granules and sent to the axonal terminal. Importantly, proteases present in the granules cleave the precursors into their mature neuropeptide form during this journey.Once synthesised, neurotransmitters are stored in vesicles within the synaptic terminal until an action potential arrives, causing their release. Neurotransmitters such as acetylcholine are stored within the small synaptic vesicles, whereas neuropeptides reside within large dense-core vesicles.Once the post-synaptic membrane has responded to the neurotransmitter in the synaptic cleft; it is either inactivated or removed. This can be done in several ways:
Re-uptake – serotonin is taken back into the pre-synaptic neurone by the transporter proteins in the neuronal membrane. These neurotransmitters are subsequently either recycled by re-packaging into vesicles or broken down by enzymes.
Breakdown – acetylcholine is broken down by acetylcholinesterase present in the synaptic cleft, inactivating the neurotransmitter.
Diffusion – into surrounding areasAction potentials depolarising the synaptic terminal lead to the opening of voltage-gated calcium channels. This allows an influx of calcium in the terminal and fusion of the synaptic vesicles with the cell membrane (exocytosis). Consequently, the neurotransmitter is released into the synaptic cleft.The neurotransmitter in the synaptic cleft diffuses across the gap to the post-synaptic membrane. Here, they can bind to two types of post-synaptic receptors.Acetylcholinesterase inhibitors are a class of drug that inhibits the activity of
- Visual signals are processed through multiple stages in the retina, visual pathway and visual cortex before visual perception.
- In the retina, photoreceptors transmit signals to bipolar and ganglion cells which transmit to the lateral geniculate nucleus.
- The LGN relays signals to the primary visual cortex which contains columns for processing features like orientation, ocular dominance and color.
- Extrastriate visual areas further analyze signals for motion, depth and color perception before perception in the visual cortex.
This document summarizes the physiology of vision. It discusses:
1) How visual impulses are processed and transmitted from photoreceptors in the retina through the visual pathway to the visual cortex.
2) The types of cells involved in retinal processing and their functions, including rods, cones, horizontal cells, bipolar cells, amacrine cells and ganglion cells.
3) How visual signals are transmitted from the retina through the optic nerve, lateral geniculate body, and optic radiations to the primary visual cortex.
4) The layers and connections of the primary visual cortex and properties of simple, complex and hypercomplex cells in the visual cortex.
1. Visual Evoked Potentials (VEPs) provide an objective assessment of visual function, especially of the retina and optic nerve.
2. VEPs measure the electrical response of the visual cortex to visual stimuli, such as flashing lights or patterns.
3. The major components of the VEP response are the N75, P100, and N145 waves. Abnormalities in the latency and amplitude of these waves can help localize lesions along the visual pathway.
The document summarizes key aspects of the nervous system, including definitions of the central and peripheral nervous systems. It describes the main regions and components of the brain and spinal cord that make up the central nervous system. It also outlines the 12 pairs of cranial nerves and peripheral nerves that are part of the peripheral nervous system. Finally, it provides guidance on examining various aspects of the nervous system, such as cranial nerves, motor and sensory function, coordination, and reflexes.
This document discusses supranuclear pathways and lesions that can affect eye movements. It begins with the fundamentals of extraocular movements and anatomy of cortical and brainstem centers that control eye movements. It then covers the basic types of eye movements like saccades, smooth pursuit, vestibular-ocular reflex, and vergence movements. It provides a step-wise approach to evaluating eye movement disorders and localizing lesions based on the type of eye movement affected. Supranuclear lesions can cause bilateral eye movement involvement, while specific brainstem lesions impact horizontal or vertical eye movements or specific eye movement types like saccades or vestibular-ocular reflex.
This document provides information about examining the 12 cranial nerves. It discusses approaches to testing each nerve including optimal positioning of the patient, specific maneuvers to assess nerve function, and potential causes of abnormalities. For each nerve, it describes the anatomical course and key structures innervated. The summary focuses on testing methodology:
Cranial nerve examination involves positioning and comforting the patient, then testing individual nerves using specialized maneuvers like visual acuity tests, eye movement assessments, facial expression checks, and sensory evaluations to identify potential lesions. Proper lighting and explanation of procedures is important. Each nerve is analyzed for motor, sensory and reflex functions to localize neurological disorders.
The document describes the structure and function of the nervous system. It defines the central nervous system as the brain and spinal cord, and the peripheral nervous system as cranial nerves, spinal nerves, and peripheral nerves. It then provides details on the four main regions of the brain, the structure and segments of the spinal cord, and the 12 pairs of cranial nerves. Finally, it outlines techniques for examining the cranial nerves, motor system, sensory system, coordination, and mental status during a neurological exam.
Visual evoked potentials (VEPs) record electrical signals from the scalp in response to visual stimuli. VEPs are useful for objectively assessing visual function, especially of the retina and optic nerve. The VEP involves presenting a visual stimulus such as a flashing light or alternating checkerboard pattern. Electrodes placed on the scalp record the P100 waveform generated in the striate and peristriate cortex in response to the stimulus. Analysis of the P100 latency, amplitude, and interocular latency difference can help detect and localize abnormalities in the retina, optic nerve, optic tract, and visual cortex.
Mechanism of balance & vestibular function test Dr Utkal MishraDr Utkal Mishra
This powerpoint elaborates the mechanism of balance & anatomy of vestibular apparutus. It also depicts the anatomy & physiology of haircells in detail. I also explained the vestibular function tests used for diagnosis of various vestibular disorders.
The occipital lobe is the visual processing center of the brain containing most of the visual cortex. It contains the primary visual cortex (V1) and several extrastriate areas involved in more complex visual tasks. Lesions can cause visual field defects, cortical blindness, visual agnosias or hallucinations depending on the location and extent of damage. Balint's syndrome and simultanagnosia involve bilateral lesions disrupting global visual perception while preserving local details.
1. The supranuclear control centers for eye movements include the brainstem, cerebellum, basal ganglia, and cerebral cortex. The brainstem centers determine how the eyes move while the cortex determines when and where the eyes move.
2. Important brainstem centers include the PPRF, MLF, NPH, riMLF, and INC which control horizontal, vertical, and torsional eye movements through connections to the cranial nerve nuclei. Lesions can cause gaze palsies, nystagmus, and impaired gaze holding.
3. Other centers control smooth pursuit, vergence, and the vestibulo-ocular reflex. Supranuclear disorders can impair sacc
The vestibulocochlear nerve, also known as Cranial Nerve VIII, has two components - the vestibular nerve and the auditory nerve. The auditory nerve receives input from the cochlea and is responsible for hearing. The vestibular nerve receives input from structures in the inner ear involved in balance and equilibrium. Clinical examination of the vestibular system includes tests of the vestibulo-ocular reflex like dolls-eye test and head thrust test. It also includes tests of the vestibulospinal reflex like Romberg test and past pointing. Caloric testing and positional maneuvers help differentiate peripheral and central causes of vertigo and dizziness.
1. The document describes the visual pathway from the eye to the visual cortex. It begins with the retina and optic nerve, followed by the optic chiasm, optic tract, lateral geniculate nucleus, optic radiations including Meyer's loop, and primary visual cortex (V1).
2. V1 contains two main types of cells - simple cells that respond to oriented edges in specific positions, and complex cells that are position invariant but retain orientation tuning.
3. Cells in V1 are organized into orientation columns where neurons within a column prefer the same stimulus orientation.
The document provides an overview of the sensory system, including:
- The sensory system provides awareness of external and internal environments through sensory receptors that detect stimuli and transmit nerve impulses to the brain.
- Sensory receptors are classified based on their structure as free dendrites, end organs, or specialized cells, and based on the stimulus detected as chemoreceptors, photoreceptors, thermoreceptors, or mechanoreceptors.
- The special senses of vision, hearing, taste, and smell have specific sense organs and are located in the head, while the general senses of touch, pain, temperature, and proprioception are located throughout the body.
This document discusses central visual processing and the pathways from the retina to the primary visual cortex. It notes that ganglion cell axons from the nasal retina cross the midline while those from the temporal retina remain ipsilateral. These axons synapse in the lateral geniculate nucleus and then travel via the optic radiations to the primary visual cortex. There are parallel magnocellular and parvocellular pathways that are involved in motion detection and shape/color processing respectively. Damage to the fusiform gyrus can cause prosopagnosia or the inability to recognize faces.
This document summarizes research on the visual system from the retina to primary visual cortex (V1). Key points include:
- The retina contains two types of ganglion cells (midget and parasol) that project to different layers in the lateral geniculate nucleus (LGN).
- Hubel and Wiesel discovered that V1 neurons have receptive fields tuned to stimulus orientation, forming the basis of the hierarchical model of visual processing.
- V1 contains two main cell types, simple cells with discrete receptive fields and complex cells without. Retinotopic maps and ocular dominance columns organize V1 architecture.
Visual System - the visual pathway basicRituYadav112
It consists of a brief description of the visual system. The different types of cells present in the retina and their connections among each other. Signal transmission in the retina. Some basic description about the visual field , receptive field and some basic terminologies. The brief description about the visual pathway. The visual cortex and the primary and extrastriate Visual Cortex.
این پاورپوینت در اولین کارگاه از سیر تا پیاز اوتیسم توسط دکتر هاشم فرهنگ دوست ارائه شده است.
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این پاورپوینت در کارگاه توانبخشی هوش دکتر میثم محمدی ارائه شده است. برای مشاهده فایلهای بیشتر در این زمینه، به وب سایت فروردین مراجعه کنید.
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این پاورپوینت در کارگاه توانبخشی هوش دکتر محمدی ارائه شده است.
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این پاورپوینت در کارگاه توانبخشی هوش توسط دکتر میثم محمدی ارائه شده است. برای مطالعه مطالب بیشتر در این زمینه به وب سایت فروردین مراجعه کنید.
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این پاورپوینت در کارگاه رویکرد ادراکی حرکتی در کودکان مبتلا به فلج مغزی توسط دکتر ابراهیم پیشیاره ارائه شده است.
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این پاورپوینت در کارگاه رویکرد ادراکی حرکتی در کودکان مبتلا به فلج مغزی توسط دکتر پیشیاره ارائه شده است. برای مشاهده مطالب بیشتر در این زمینه به وب سایت فروردین مراجعه نمایید.
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این پاورپوینت در کارگاه ارزیابی و توانبخشی مشکلات راه رفتن در کودکان فلج مغزی توسط دکتر محمد خیاط زاده ارائه شده است.
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این پاورپوینت در کارگاه ارزیابی و توانبخشی مشکلات راه رفتن در کودکان مبتلا به فلج مغزی توسط دکتر محمد خیاط زاده ارائه شده است.
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این پاورپوینت توسط دکتر محمد خیاط زاده در کارگاه ارزیابی و توانبخشی مشکلات راه رفتن در کودکان مبتلا به فلج مغزی ارائه شده است.
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This document summarizes gait abnormalities in children with cerebral palsy. It begins by defining cerebral palsy and describing the three main types: spastic, dyskinetic, and ataxic. For each type, it outlines the characteristic neuromuscular deficits that affect gait. It then describes normal gait cycle and determinants. Key factors that influence gait in CP are weaknesses, shortened muscles, spasticity, and bone deformities from altered forces. Gait abnormalities range from mild toe-walking to severe crouched gait. Prognosis for walking depends on CP type, severity, and age of independent walking. Over time, walking ability tends to decline in adolescents and adults with CP
این پاورپوینت در کارگاه مداخلات ادراکی حرکتی در کودکان با فلج مغزی توسط دکتر جانمحمدی ارائه شده است.
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این پاورپوینت در کارگاه معاینات عصبی در توانبخشی کودکان توسط دکتر محمدی ارائه شده است.
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این پاورپوینت در کارگاه معاینات عصبی در توانبخشی کودکان توسط دکتر میثم محمدی ارائه شده است.
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این ارائه در کارگاه تخصصی تقلید و آپراکسی سرنخ هایی برای مداخلات مبتنی بر شواهد توسط دکتر هاشم فرهنگ دوست تدریس شده است.
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این پاورپوینت در کارگاه ارزیابی و توانبخشی کودکان مبتلا به فلج مغزی توسط کاردرمانگر مهدی بیغم ارائه شده است.
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این فایل متنی توسط دکتر میثم محمدی در کارگاه تخصصی آگاهی، توجه، عصب شناسی و توانبخشی ارائه شده است.
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این پاورپوینت در کارگاه تخصصی توانبخشی شناختی در اختلالات یادگیری توسط دکتر هاشم فرهنگ دوست ارائه شده است.
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این پاورپوینت در کارگاه تخصصی رویکرد جدید بوبات در توانبخشی کودکان مبتلا به فلج مغزی ارائه شده است.
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این پاورپوینت در کارگاه تخصصی آگاهی، توجه، عصب شناسی و توانبخشی توسط دکتر میثم محمدی، دکترای کاردرمانی تدریس شده است. برای مشاهده مطالب بیشتر در این زمینه به وب سایت فروردین مراجعه نمایید.
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این پاورپوینت توسط دکتر محمدی در کارگاه آگاهی، توجه، عصب شناسی و توانبخشی ارائه شده است.
برای دریافت مطالب بیشتر در این زمینه به وب سایت فروردین مراجعه نمایید.
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More from Farvardin Neuro-Cognitive Training Group (20)
Discover the benefits of homeopathic medicine for irregular periods with our guide on 5 common remedies. Learn how these natural treatments can help regulate menstrual cycles and improve overall menstrual health.
Visit Us: https://drdeepikashomeopathy.com/service/irregular-periods-treatment/
Giloy in Ayurveda - Classical Categorization and SynonymsPlanet Ayurveda
Giloy, also known as Guduchi or Amrita in classical Ayurvedic texts, is a revered herb renowned for its myriad health benefits. It is categorized as a Rasayana, meaning it has rejuvenating properties that enhance vitality and longevity. Giloy is celebrated for its ability to boost the immune system, detoxify the body, and promote overall wellness. Its anti-inflammatory, antipyretic, and antioxidant properties make it a staple in managing conditions like fever, diabetes, and stress. The versatility and efficacy of Giloy in supporting health naturally highlight its importance in Ayurveda. At Planet Ayurveda, we provide a comprehensive range of health services and 100% herbal supplements that harness the power of natural ingredients like Giloy. Our products are globally available and affordable, ensuring that everyone can benefit from the ancient wisdom of Ayurveda. If you or your loved ones are dealing with health issues, contact Planet Ayurveda at 01725214040 to book an online video consultation with our professional doctors. Let us help you achieve optimal health and wellness naturally.
Computer in pharmaceutical research and development-Mpharm(Pharmaceutics)MuskanShingari
Statistics- Statistics is the science of collecting, organizing, presenting, analyzing and interpreting numerical data to assist in making more effective decisions.
A statistics is a measure which is used to estimate the population parameter
Parameters-It is used to describe the properties of an entire population.
Examples-Measures of central tendency Dispersion, Variance, Standard Deviation (SD), Absolute Error, Mean Absolute Error (MAE), Eigen Value
Nano-gold for Cancer Therapy chemistry investigatory projectSIVAVINAYAKPK
chemistry investigatory project
The development of nanogold-based cancer therapy could revolutionize oncology by providing a more targeted, less invasive treatment option. This project contributes to the growing body of research aimed at harnessing nanotechnology for medical applications, paving the way for future clinical trials and potential commercial applications.
Cancer remains one of the leading causes of death worldwide, prompting the need for innovative treatment methods. Nanotechnology offers promising new approaches, including the use of gold nanoparticles (nanogold) for targeted cancer therapy. Nanogold particles possess unique physical and chemical properties that make them suitable for drug delivery, imaging, and photothermal therapy.
Pictorial and detailed description of patellar instability with sign and symptoms and how to diagnose , what investigations you should go with and how to approach with treatment options . I have presented this slide in my 2nd year junior residency in orthopedics at LLRM medical college Meerut and got good reviews for it
After getting it read you will definitely understand the topic.
PGx Analysis in VarSeq: A User’s PerspectiveGolden Helix
Since our release of the PGx capabilities in VarSeq, we’ve had a few months to gather some insights from various use cases. Some users approach PGx workflows by means of array genotyping or what seems to be a growing trend of adding the star allele calling to the existing NGS pipeline for whole genome data. Luckily, both approaches are supported with the VarSeq software platform. The genotyping method being used will also dictate what the scope of the tertiary analysis will be. For example, are your PGx reports a standalone pipeline or would your lab’s goal be to handle a dual-purpose workflow and report on PGx + Diagnostic findings.
The purpose of this webcast is to:
Discuss and demonstrate the approaches with array and NGS genotyping methods for star allele calling to prep for downstream analysis.
Following genotyping, explore alternative tertiary workflow concepts in VarSeq to handle PGx reporting.
Moreover, we will include insights users will need to consider when validating their PGx workflow for all possible star alleles and options you have for automating your PGx analysis for large number of samples. Please join us for a session dedicated to the application of star allele genotyping and subsequent PGx workflows in our VarSeq software.
These lecture slides, by Dr Sidra Arshad, offer a simplified look into the mechanisms involved in the regulation of respiration:
Learning objectives:
1. Describe the organisation of respiratory center
2. Describe the nervous control of inspiration and respiratory rhythm
3. Describe the functions of the dorsal and respiratory groups of neurons
4. Describe the influences of the Pneumotaxic and Apneustic centers
5. Explain the role of Hering-Breur inflation reflex in regulation of inspiration
6. Explain the role of central chemoreceptors in regulation of respiration
7. Explain the role of peripheral chemoreceptors in regulation of respiration
8. Explain the regulation of respiration during exercise
9. Integrate the respiratory regulatory mechanisms
10. Describe the Cheyne-Stokes breathing
Study Resources:
1. Chapter 42, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 36, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 13, Human Physiology by Lauralee Sherwood, 9th edition
Histololgy of Female Reproductive System.pptxAyeshaZaid1
Dive into an in-depth exploration of the histological structure of female reproductive system with this comprehensive lecture. Presented by Dr. Ayesha Irfan, Assistant Professor of Anatomy, this presentation covers the Gross anatomy and functional histology of the female reproductive organs. Ideal for students, educators, and anyone interested in medical science, this lecture provides clear explanations, detailed diagrams, and valuable insights into female reproductive system. Enhance your knowledge and understanding of this essential aspect of human biology.
Breast cancer: Post menopausal endocrine therapyDr. Sumit KUMAR
Breast cancer in postmenopausal women with hormone receptor-positive (HR+) status is a common and complex condition that necessitates a multifaceted approach to management. HR+ breast cancer means that the cancer cells grow in response to hormones such as estrogen and progesterone. This subtype is prevalent among postmenopausal women and typically exhibits a more indolent course compared to other forms of breast cancer, which allows for a variety of treatment options.
Diagnosis and Staging
The diagnosis of HR+ breast cancer begins with clinical evaluation, imaging, and biopsy. Imaging modalities such as mammography, ultrasound, and MRI help in assessing the extent of the disease. Histopathological examination and immunohistochemical staining of the biopsy sample confirm the diagnosis and hormone receptor status by identifying the presence of estrogen receptors (ER) and progesterone receptors (PR) on the tumor cells.
Staging involves determining the size of the tumor (T), the involvement of regional lymph nodes (N), and the presence of distant metastasis (M). The American Joint Committee on Cancer (AJCC) staging system is commonly used. Accurate staging is critical as it guides treatment decisions.
Treatment Options
Endocrine Therapy
Endocrine therapy is the cornerstone of treatment for HR+ breast cancer in postmenopausal women. The primary goal is to reduce the levels of estrogen or block its effects on cancer cells. Commonly used agents include:
Selective Estrogen Receptor Modulators (SERMs): Tamoxifen is a SERM that binds to estrogen receptors, blocking estrogen from stimulating breast cancer cells. It is effective but may have side effects such as increased risk of endometrial cancer and thromboembolic events.
Aromatase Inhibitors (AIs): These drugs, including anastrozole, letrozole, and exemestane, lower estrogen levels by inhibiting the aromatase enzyme, which converts androgens to estrogen in peripheral tissues. AIs are generally preferred in postmenopausal women due to their efficacy and safety profile compared to tamoxifen.
Selective Estrogen Receptor Downregulators (SERDs): Fulvestrant is a SERD that degrades estrogen receptors and is used in cases where resistance to other endocrine therapies develops.
Combination Therapies
Combining endocrine therapy with other treatments enhances efficacy. Examples include:
Endocrine Therapy with CDK4/6 Inhibitors: Palbociclib, ribociclib, and abemaciclib are CDK4/6 inhibitors that, when combined with endocrine therapy, significantly improve progression-free survival in advanced HR+ breast cancer.
Endocrine Therapy with mTOR Inhibitors: Everolimus, an mTOR inhibitor, can be added to endocrine therapy for patients who have developed resistance to aromatase inhibitors.
Chemotherapy
Chemotherapy is generally reserved for patients with high-risk features, such as large tumor size, high-grade histology, or extensive lymph node involvement. Regimens often include anthracyclines and taxanes.
Know the difference between Endodontics and Orthodontics.Gokuldas Hospital
Your smile is beautiful.
Let’s be honest. Maintaining that beautiful smile is not an easy task. It is more than brushing and flossing. Sometimes, you might encounter dental issues that need special dental care. These issues can range anywhere from misalignment of the jaw to pain in the root of teeth.
- Video recording of this lecture in English language: https://youtu.be/Pt1nA32sdHQ
- Video recording of this lecture in Arabic language: https://youtu.be/uFdc9F0rlP0
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html