Umbra is a stealth technology company that develops augmented reality systems to help soldiers and first responders. Their flagship product is the Umbra Tactical Augmented Reality System (UTARS) which projects holograms onto a soldier's visor to provide situational awareness and mission critical data without revealing their position or exposing them to danger. UTARS aims to enhance situational awareness and decision making while keeping users safe in hazardous environments.
El documento parece estar escrito en un idioma que no reconozco. No puedo generar un resumen útil de solo 3 oraciones debido a que no entiendo el contenido o significado del texto original.
The document discusses summarizing information concisely in a single word. Providing concise yet informative summaries allows for efficiently conveying key details and concepts from a document in as few words as possible. Summarizing skills are useful for effectively communicating complex ideas or large amounts of information in a clear and straightforward manner.
This document lists various domestic animals including dogs, sheep, pigs, goats, cows, cats, chickens, roosters, ducks, geese, turkeys, rabbits, water buffalo, and other farm animals.
Umbra is a stealth technology company that develops augmented reality systems to help soldiers and first responders. Their flagship product is the Umbra Tactical Augmented Reality System (UTARS) which projects holograms onto a soldier's visor to provide situational awareness and mission critical data without revealing their position or exposing them to danger. UTARS aims to enhance situational awareness and decision making while keeping users safe in hazardous environments.
El documento parece estar escrito en un idioma que no reconozco. No puedo generar un resumen útil de solo 3 oraciones debido a que no entiendo el contenido o significado del texto original.
The document discusses summarizing information concisely in a single word. Providing concise yet informative summaries allows for efficiently conveying key details and concepts from a document in as few words as possible. Summarizing skills are useful for effectively communicating complex ideas or large amounts of information in a clear and straightforward manner.
This document lists various domestic animals including dogs, sheep, pigs, goats, cows, cats, chickens, roosters, ducks, geese, turkeys, rabbits, water buffalo, and other farm animals.
Revista Frunza a Asociației Medisprof a luat naștere ca urmare a nevoii de comunicare intre specialiștii clinicii Medisprof și pacienți. In revista veți regăsi articole legate de activitățile Asociației si partenerilor ei și articole din domeniul radioterapiei, nutriției, psihologiei.
Partenerii oficiali ai Revistei Frunza:
Roche Romania
Oncompass GMBH
Farmacia Vinca
Revista Frunza a Asociației Medisprof a luat naștere ca urmare a nevoii de comunicare intre specialiștii clinicii Medisprof și pacienți. In revista veți regăsi articole legate de activitățile Asociației si partenerilor ei și articole din domeniul radioterapiei, nutriției, psihologiei.
Partenerii oficiali ai Revistei Frunza:
Roche Romania
Oncompass GMBH
Farmacia Vinca
The document discusses the sensory systems and processing, providing information on the different sensory systems (tactile, vestibular, proprioception, auditory, visual, olfactory, and gustatory), how they function, possible problems with sensory processing, and strategies to address behaviors related to sensory needs.
The document discusses the sensory systems and how they work together to give us information about the world. It describes the main sensory systems - tactile, vestibular, proprioception, auditory, visual, olfactory, and gustatory. It explains how sensory processing occurs and potential problems with sensory processing. The roles of different neurotransmitters are outlined. Sensory behaviors and strategies to address them are provided, along with calming and alerting activities.
The document outlines the daily routine and schedule for a classroom. It includes purposes and descriptions for different parts of the day like entrance routine, sensory activities, reviewing the schedule, morning dialogue, independent work, calendar/circle time, rotations between activities, you choose time, peer buddies, academics/small groups, relaxation, art/music/gym, and reviewing the day's activities. The schedule is designed to promote independence, reduce anxiety, and provide a variety of learning experiences including sensory, social, and academic activities.
Introduction To Structured Teaching For TranslationMihaiela Fazacas
The document provides an introduction to structured teaching for students with autism. Structured teaching is based on the Heartland Model and incorporates elements from TEACCH. Its primary goal is to develop independence and communication skills through visual structure, schedules, and work systems. These tools make the environment more predictable and help students understand expectations and complete tasks independently.
This document describes a study conducted at the Medical Genetics Center in Iasi, Romania to diagnose the genetic causes of mental retardation in patients. Researchers developed a clinical protocol involving tests like karyotyping, fragile X testing, and MLPA to efficiently screen 200 patients. Results identified numerous chromosomal abnormalities, four specific monogenic disorders, and subtelomeric rearrangements in some patients. The De Vries score was found useful for case selection. MLPA was reliable for subtelomeric screening and identifying complex chromosomal changes. The protocol provides an effective approach but could be optimized further.
This document discusses Alport Syndrome, a genetic disorder that affects the glomerular basement membrane (GBM) and can cause progressive kidney disease. It presents three cases of Alport Syndrome with different modes of inheritance: X-linked dominant, autosomal recessive, and autosomal dominant. For each case, it describes the patients' clinical features and pedigrees to demonstrate how inheritance patterns were determined. The conclusion emphasizes the importance of thoroughly examining probands, relatives, and renal biopsy ultrastructure to establish diagnoses and inheritance patterns in Alport Syndrome families.
The National Alliance of People with Rare Diseases - Bulgaria (NAPRD) was officially registered in June 2007. It was created to represent people living with rare diseases and encourage the development of programs and policies to help them. NAPRD now represents people with 24 rare diseases. It advocates for issues like ensuring access to treatment and raising public awareness. Major events organized by NAPRD include celebrating European Rare Disease Day and hosting charity concerts to raise funds.
The document discusses recent developments in European policy actions around rare diseases. It summarizes that in 1999 the EU adopted an orphan drug regulation, and since then there have been ongoing efforts to improve access to treatments. These include a 2009 EU Communication and Recommendation that call for national rare disease plans in all EU countries and proposals to improve access, newborn screening, and compassionate use at the EU level. It emphasizes the need for continued action both at the national level within countries and coordinated efforts between the EU, member states, and rare disease communities.
This document discusses services for rare disease patients in Europe. It summarizes that information on rare diseases is increasingly available through national centers and websites in many European countries. Orphanet is mentioned as a central portal providing information on rare diseases and orphan drugs in 38 languages, with over 20,000 daily users. The document outlines resources available through Orphanet including a database of rare diseases and clinical trials. It also discusses the availability of diagnostic testing, research activities, and the need to improve access to information, testing, and care across Europe.
This document describes a project in Romania to establish a multidisciplinary network approach for managing Prader-Willi syndrome and Angelman syndrome. The project involves 8 partner institutions and aims to implement new diagnostic methods, establish national expertise centers, collaborate with patient associations, and develop international partnerships. The goals are to create standardized clinical evaluation protocols, establish a national patient registry, and integrate a multidisciplinary care approach for patients.
The document summarizes the establishment of a national network for hereditary angioedema (HAE) in Romania. It discusses how HAE was previously misunderstood and untreated in Romania. It outlines the goals of building a national patient registry and improving care through education of clinicians. Key activities included workshops, articles, and establishing collaborations with international experts to advance diagnosis and management of HAE in Romania.
This document discusses the legal basis and priorities for developing EU policy on rare diseases and health surveillance. Key points include:
1) Article 152 of the EU Treaty provides the legal basis for EU action in public health, including programs on rare diseases.
2) Priorities have included exchanging information through networks, developing strategies for coordination, and supporting research collaborations.
3) The Commission Communication and Council Recommendation on rare diseases aim to establish an integrated EU approach through non-binding coordination rather than legislation.
This document discusses Prader-Willi syndrome, which is caused by a microdeletion on chromosome 15q11-q13 or lack of expression of paternally inherited genes in this region. The majority of cases involve a paternal deletion, while 2-4% involve a maternal uniparental disomy of chromosome 15. Clinically it is characterized by infantile central hypotonia, feeding problems in infancy leading to failure to thrive, rapid weight gain in childhood, distinctive facial features and developmental delays.
Living With Pompe Disease, Sharing Experience, Cluj, Romania 27 June 2009Mihaiela Fazacas
This document summarizes the experiences of living with Pompe disease from the perspective of Maryze Schoneveld van der Linde. It describes the history and discovery of Pompe disease by Dr. J.C. Pompe in 1932. It outlines the progression and symptoms of the disease, including how it affects muscles and can be fatal. It discusses the development of enzyme replacement therapy using recombinant DNA technology and the challenges faced by patients, researchers, and industry in making this treatment available.
12. Misiunea Dezvoltarea abilitatilor necesare pentru a face fata situatiilor curente sau extreme legata de patologia bolilor rare, în mediul social şi familial curent Sustinerea parintilor copiilor afectati de boli rare, severe, cronice şi invalidante in procesul: Intelegere Atitudine Ingrijire continua Dezvoltarea atitudinii eficiente în relatia cu sistemul de sanatate, asociatii medicale şi alte institutii. Mentinerea unui nivel nivel de sanatate fizica şi mentala prin abordare terapeutica avansata, alaturi de masuri simple.
13. probleme cotidiene Resurse: Reteaua multidisciplinara Alianta Nationala pentru Boli Rare Romania Pentru familii: prin ANBRaRo se pot organiza conditii de rezolvare pentru situatii complexe, care impun o abordare multidisciplinara Pentru profesionisti: prin ANBRaRo se pot organiza schimbul de know-how şi dezvoltarea abilitatilor Servicii sociale / educationale Copil / Pacient Pediatru Medic Specialist Ortoped MS / DSP Genetician Kinetoterapeut Familia Asistent