Multiple system atrophy, or MSA, is a rare, degenerative neurologic condition that affects both men and women, usually starting in the 50’s or early 60’s1. MSA is considered a type of parkinsonism but with more widespread effects on the brain and body. Get all the latest news & updates about multiple system atrophy at MSA Coalition. For more information visit https://www.multiplesystematrophy.org or call (866)737-5999
Disorders of the neuromuscular junction include Myasthenia gravis, Lambert-Eaton myasthenic syndrome, Botulism, Tetanus, Strychnine intoxication, Organophosphates poisoning and neuromyotonia. Pharmacology of the NMJ is also reviewed in brief.
Motor neuron disease is a rare disease it doesn't have any cure here in this video I have tried playing what is mnd its types causes how to diagnose and its management plan
Dystonia
Dystonia is a movement disorder in which your muscles contract involuntarily, causing repetitive or twisting movements.
The condition can affect one part of your body (focal dystonia), two or more adjacent parts (segmental dystonia) or all parts of your body (general dystonia). The muscle spasms can range from mild to severe. They may be painful, and they can interfere with your performance of day-to-day tasks.
Dystonia: Causes, Types, Symptoms, and Treatments
این ارائه در کارگاه تخصصی تقلید و آپراکسی سرنخ هایی برای مداخلات مبتنی بر شواهد توسط دکتر هاشم فرهنگ دوست تدریس شده است.
برای مطالعه مطالب بیشتر در این زمینه به وب سایت فروردین مراجعه کنید.
www.farvardin-group.com
Disorders of the neuromuscular junction include Myasthenia gravis, Lambert-Eaton myasthenic syndrome, Botulism, Tetanus, Strychnine intoxication, Organophosphates poisoning and neuromyotonia. Pharmacology of the NMJ is also reviewed in brief.
Motor neuron disease is a rare disease it doesn't have any cure here in this video I have tried playing what is mnd its types causes how to diagnose and its management plan
Dystonia
Dystonia is a movement disorder in which your muscles contract involuntarily, causing repetitive or twisting movements.
The condition can affect one part of your body (focal dystonia), two or more adjacent parts (segmental dystonia) or all parts of your body (general dystonia). The muscle spasms can range from mild to severe. They may be painful, and they can interfere with your performance of day-to-day tasks.
Dystonia: Causes, Types, Symptoms, and Treatments
این ارائه در کارگاه تخصصی تقلید و آپراکسی سرنخ هایی برای مداخلات مبتنی بر شواهد توسط دکتر هاشم فرهنگ دوست تدریس شده است.
برای مطالعه مطالب بیشتر در این زمینه به وب سایت فروردین مراجعه کنید.
www.farvardin-group.com
Parkinson’s: What Do We Know About the Disease and What Can Be Done About It?asclepiuspdfs
ABSTRACT
In this article, I aim to answer important questions regarding Parkinson’s disease and the associated dementia. While the
disease was identified and described over a century ago, we still have not as yet been able to ferret out its root cause,
notwithstanding the tremendous progress made in recent years. Like for many other diseases, it is believed to involve three
main causal components (inherited genetics, environmental influences, and, to a much lesser extent, lifestyle choices),
which collectively determine if someone will develop the disease. I will survey its signs, symptoms (motor and non-motor),
risks, and stages, distinguishing between the disease’s early- and late-onset. While discriminating between the disease and
its associated dementia, I will localize the latter within the broad spectrum of dementias. I will also describe what happens
to the brain as the disease takes hold and evolves. A number of medical conditions called Parkinsonisms may have one or
more of their signs and symptoms mimicking Parkinson’s. I will discuss them in some detail, including their five proposed
mechanisms (protein aggregation in Lewy bodies, disruption of autophagy, mitophagy, neuroinflammation, and breakdown
of the blood–brain barrier). I will further describe the approach to diagnosis, prediction, prevention, and prognosis. While
there is no cure and treatment for each affected person, motor symptoms are managed with several medications (Levodopa
always combined with a dopa decarboxylase inhibitor and sometimes also with a catechol-O-methyltransferase [COMT]
inhibitor, dopamine agonists, and monoamine oxidase-B [MAOB]-inhibitors) and eventually surgical therapy. Numerous
pharmaceutical agents are also available for individual non-motor symptoms (L-Dopa emulsions, non-ergot dopamine
agonists, cholinesterase inhibitors for dementia, modafinil for daytime sleepiness, and quetiapine for psychosis). Fortunately,
we can track the drug effectiveness with exosomes. Keeping in mind patients and their caregivers/partners, I will outline
available complementary therapies, palliative care, and rehabilitation, measures they can take beyond seeking standard
treatments, and supporting and advocating organizations at their disposal. Finally, I will survey promising new research
vistas in the field.
Feature story from the Garvan Institute of Medical Research's August 2012 issue of Breakthrough newsletter. More at https://www.garvan.org.au/news-events/newsletters
20180202 3 j. lombard genomind milan relazione part 2 to pub.pptxRoberto Scarafia
https://www.linkedin.com/pulse/simposio-toma-implementazione-della-farmacogenetica-nel-scarafia/
https://www.linkedin.com/pulse/malattie-psichiatriche-e-neurologiche-arriva-toma-il-test-scarafia/
2 febbraio 2018, Sala Congressi Laboratorio TOMA
Relatori: Dr. J. Lombard, Dr.ssa F.R. Grati, Dr.ssa S. De Toffol
BREVE PREMESSA
La farmacogenetica studia l’influenza dei fattori genetici sull’attività di un farmaco, la sua assimilazione e il suo metabolismo allo scopo di massimizzarne l’efficacia terapeutica e minimizzare gli effetti avversi. I fattori genetici possono giustificare fino al 95% della variabilità interpersonale nella risposta e nelle reazioni avverse a determinati trattamenti farmacologici. Finora la diagnosi ed il trattamento farmacologico in psichiatria si sono basati principalmente sul un protocollo ‘trial and error’ tramite colloquio, osservazione clinica e analisi di laboratorio costituivano esclusivamente un complemento per valutare possibili effetti collaterali o i livelli plasmatici di alcuni farmaci. L’introduzione di test di farmacogenetica consente di fornire al clinico informazioni costitutive dell’individuo relativamente al metabolismo di molti farmaci e la potenziale risposta in determinati contesti clinici al fine di ridurre i tempi ottenimento del trattamento efficace personalizzato e arricchire con le più recenti informazioni genetiche la gestione terapeutica dei pazienti.
OBIETTIVI FORMATIVI
Introdurre i principi scientifici alla base del test genetico che si presenterà durante il corso, il significato, la funzione e la rilevanza clinica per la salute mentale di ciascun gene indagato dal test;
L’utilità clinica del test Genecept: presentare come vengono riportati i risultati del test e come meglio interpretarli;
Presentare alcuni casi clinici reali per discutere circa l’utilità di un trattamento farmacologico guidato dai risultati del test genetico rispetto all’approccio tradizionale ‘trial and error’
Neurogenic orthostatic hypotension (NOH) is a very rare syndrome where low blood pressure occurs upon standing. The Multiple System Atrophy Coalition is dedicated to funding MSA research that will lead to the discovery of a cure for NOH. Call now @ (866)737-5999 to donate to the MSA Coalition.
Start the MSA fundraising campaign with the help of Multiple System Atrophy Coalition. We are partnered with FirstGiving & CrowdRise that helps the fundraiser in donations. For more information visit: https://goo.gl/LIuCwp
Have a look at the list of clinics and doctors & get MSA diagnosed. They will help you in treating Multiple System Atrophy disease. The list contains doctors from world wide. Find a neurologist near you. https://goo.gl/LIuCwp
History of MSA-Multiple System Atrophy is very rarely known to people. MSA was discovered by by Dr. Milton Shy and Dr. Glen Drager and thus named as Shy Drager Syndrome. MSA disease is a neurological disease occurs due to degeneration of certain nerve cells in the brain and spinal cord. For Support call us at 866-737-4999 or visit http://www.multiplesystematrophy.org/.
Have a look at this guide which addresses the problems you may face if you care for someone suffering from multiple system atrophy (MSA). Visit https://www.multiplesystematrophy.org/ or call us @ (866)737-5999
Here is the list of MSA parkinson's disease center and movement disorder clinics in USA and Canada. Call Multiple System Atrophy Coalition at (866)737-5999 or visit https://www.multiplesystematrophy.org/
Have a look at the list of clinics and doctors treating multiple system atrophy. The list contains doctors from world wide. For more information, visit http://www.multiplesystematrophy.org/ and find a neurologist near you.
Multiple System Atrophy or SDS is a neurodegenerative disorder in which individuals complain of dizziness, unsteady gait, slurring of speech. Join us in our efforts & make a donation to The MSA Coalition either with a chec or credit card. Donate now & provide funding for MSA research, education & advocacy. For more information visit https://www.multiplesystematrophy.org or call (866)737-5999
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