21. XCA - X-Linked Congenital Ataxia (genetics) Acronym Finder XCA stands for XLinked Congenital Ataxia (genetics) http://www.acronymfinder.com/X_Linked-Congenital-Ataxia-(genetics)-(XCA).html

22. CiteULike: Gthorisson's Friedreich-ataxia-genetics [1 Article] Recent papers added to gthorisson's library classified by the tag friedreichataxia-genetics. You can also see everyone's friedreich-ataxia-genetics. http://www.citeulike.org/user/gthorisson/tag/friedreich-ataxia-genetics

23. Spinocerebellar Ataxia InfantileOnset Spinocerebellar Ataxia Genetics Home Reference; Machado-Joseph Disease Information Page National Institute of Neurological Disorders and Stroke http://www.noah-health.org/en/bns/disorders/other/spinoataxia.html

Skip navigation About NOAH Help English Spanish Both Advanced NOAH Brain and Nervous System Change text size: Spinocerebellar Ataxia Updated: October 14, 2010 About MJD International Joseph Disease Foundation Ataxias and Cerebellar/Spinocerebellar Degeneration Information Page National Institute of Neurological Disorders and Stroke Infantile-Onset Spinocerebellar Ataxia Genetics Home Reference Machado-Joseph Disease Information Page National Institute of Neurological Disorders and Stroke Olivopontocerebellar Atrophy Information Page National Institute of Neurological Disorders and Stroke Spinocerebellar Ataxia: Making an Informed Choice about Genetic Testing University of Washington Spinocerebellar Ataxia Type 1 (SCA1) National Ataxia Foundation Spinocerebellar Ataxia Type 2 (SCA2) National Ataxia Foundation Spinocerebellar Ataxia Type 3 (SCA3)/ Machado-Joseph Disease (MJD) National Ataxia Foundation Symptoms and Diagnosis International Joseph Disease Foundation Cerebellar Ataxia Autosomal Recessive Cerebellar Ataxia Type 1 Genetics Home Reference Researched by NOAH Contributing Editor: NOAH Team NOAH Brain and Nervous System Specific Nervous System Disorders Other Neurological Problems > Spinocerebellar Ataxia Health Topics Index A to Z Page of the Month Advanced Search ... Feedback

24. Ataxia - Causes - NHS Choices If you have autosomal dominant ataxia, any children that you have will have a one in two chance of developing ataxia. Genetics and pregnancy http://www.nhs.uk/Conditions/Ataxia/Pages/Causes.aspx

25. Scientists Identify Gene For Spinocerebellar Ataxia 2: National Institute Of Neu The National Institute of Neurological Disorders and Stroke (NINDS) is the leading supporter of biomedical research on disorders of the brain and nervous system. http://www.ninds.nih.gov/news_and_events/news_articles/press_release_spinocerebe

Skip Navigation Search this site: Search You are here: Home News From NINDS News Articles Scientists Identify Gene for Spinocerebellar Ataxia 2 Skip secondary menu Home Disorders A - Z News From NINDS ... Funding News Events Calendar of Events Proceedings Congressional Testimony ... Microsoft Word Viewer For release: Thursday, October 31, 1996 Scientists have identified the gene altered in one of the most common hereditary ataxias, spinocerebellar ataxia 2 (SCA2). The discovery allows improved genetic testing and provides new clues about how genetic mutations cause several neurological disorders, including Huntington's disease. The findings are reported by three different groups in the November issue of Nature Genetics.* The gene, found on chromosome 12, normally contains a string of 15 to 29 repeats of a three-base (trinucleotide) sequence in the genetic code cytosine, adenine, and guanine, or CAG. In people with SCA2, however, the gene contains from 36 to 59 CAG repeats. Each CAG trinucleotide codes for a single amino acid called glutamine, so these CAG repeats result in a long string of glutamines (also known as a polyglutamine) that interrupts the sequence of a normal protein. CAG repeat mutations have previously been linked to Huntington's and four other diseases. The discovery of the SCA2 gene will allow more specific genetic testing for people with hereditary ataxias, says Stefan Pulst, MD, of Cedars-Sinai Medical Center at the University of California, Los Angeles. Pulst, a grantee of the National Institute of Neurological Disorders and Stroke (NINDS), is lead author on one report. Hereditary and sporadic ataxias combined affect an estimated 150,000 Americans. Scientists previously identified the genes for two other spinocerebellar ataxias (SCA 1 and 3), and recent genetic linkage studies suggest that there may be four more. The symptoms of these diseases often overlap, as do the ages of onset. One family with SCA2 might develop ataxia, for example, while another might show dementia and chorea (involuntary movements) resembling Huntington's disease.

26. Sideroblastic Anemia Sideroblastic Anemias Merck Manual; Xlinked Sideroblastic Anemia Genetics Home Reference; X-Linked Sideroblastic Anemia and Ataxia Genetics Home Reference http://www.noah-health.org/en/blood/anemia/types/sideroblastic.html

Skip navigation About NOAH Help English Spanish Both Advanced NOAH Heart, Blood and Bone Marrow Change text size: Sideroblastic Anemia Updated: November 12, 2009 Anemias, Sideroblastic WebMD Iron Overload Iron Disorders Institute Sideroblastic Anemias Harvard University Sideroblastic Anemias Merck Manual X-linked Sideroblastic Anemia Genetics Home Reference X-Linked Sideroblastic Anemia and Ataxia Genetics Home Reference Researched by NOAH Contributing Editor: NOAH Team NOAH Heart, Blood and Bone Marrow Anemia Types of Anemia > Sideroblastic Anemia Health Topics Index A to Z Page of the Month Advanced Search ... Feedback

27. GAA Repeat Expansions And Frataxin. - Free Online Library Free Online Library GAA Repeat Expansions and Frataxin.(ataxia genetics) by Generations ; Seniors Health, general Ataxia Genetic aspects Disease susceptibility Genetic http://www.thefreelibrary.com/GAA Repeat Expansions and Frataxin.(ataxia genetic

CacheBuster('') Printer Friendly 18,416,712 articles and books Periodicals Literature Keyword Title Author Topic Member login User name Password Remember me Join us Forgot password? Submit articles free The Free Library ... Generations artId=63690635;usrSelf=false; GAA Repeat Expansions and Frataxin. I will talk a little about genetics and move onto Friedreich ataxia ataxia , lack of coordination of the voluntary muscles resulting in irregular movements of the body. Ataxia can be brought on by an injury, infection, or degenerative disease of the central nervous system, e.g. (FA), in particular the GAA GAA Goals Against Average (Hockey) GAA Gaelic Athletic Association GAA Gravure Association of America (Rochester, NY) GAA German Agro Action GAA Global Aquaculture Alliance GAA Gay Activists Alliance repeat, and Frataxin. The human genome The human genome is the genome of Homo sapiens refers to all of the genetic material that is in the nucleus of most of our cells. We estimate that there are 80,000 to 120,000 genes. But we don't know Don't know (DK, DKed)

28. Ataxia (The 5-Minute Pediatric Consult) - WrongDiagnosis.com Ataxia genetics. Hereditary causes of chronic ataxia include the recessively inherited Friedreich ataxia, ataxia telangiectasia, and late-infantile/juvenile-onset forms of some http://www.wrongdiagnosis.com/r/retts_syndrome/book-diseases-20a.htm

29. CiteULike: Wardle's Ataxiageneticsphysiopathology [5 Articles] Recent papers added to wardle's library classified by the tag ataxiageneticsphysiopathology. You can also see everyone's ataxiageneticsphysiopathology. http://www.citeulike.org/user/wardle/tag/ataxiageneticsphysiopathology

30. Progressive Cerebellar Ataxia With Variable Episod... [Eur Neurol. 2008] - PubMe Ataxia/genetics; Ataxia/physiopathology; Calcium Channels/genetics* Cerebellar Ataxia/genetics* Cerebellar Ataxia/physiopathology; Disease Progression http://www.ncbi.nlm.nih.gov/pubmed/18437043

31. FreeMD® Friedreich's Ataxia Underlying Cause Friedreich's ataxia is an inherited disorder. Friedreich's ataxia causes Continue to Friedreich's Ataxia Genetics http://www.freemd.com/friedreichs-ataxia/underlying-cause.htm

32. The Fragile X Tremor Ataxia Syndrome In The Differ... [Brain. 2005] - PubMed Res Ataxia/genetics* Cerebellar Ataxia/complications; Cerebellar Ataxia/diagnosis; Cerebellar Ataxia/genetics; Cohort Studies; Diagnosis, Differential; Female http://www.ncbi.nlm.nih.gov/pubmed/15947063

33. Movement Disorders: MedlinePlus Genetics Home Reference Xlinked sideroblastic anemia and ataxia Genetics Home Reference X-linked sideroblastic anemia and ataxia http//ghr.nlm.nih.gov/condition/x-linked http://www.nlm.nih.gov/medlineplus/movementdisorders.html

pttitle = ""; Skip navigation A service of the U.S. National Library of Medicine National Institutes of Health Home About MedlinePlus ... Contact Us Search MedlinePlus Health Topics ESPAƑOL Other Topics: A B C D ... All Topics Movement Disorders URL of this page: http://www.nlm.nih.gov/medlineplus/movementdisorders.html Imagine if you couldn't walk normally or get up from a chair, or if parts of your body moved when you didn't want them to. If you have a movement disorder, you experience these kinds of impaired movement. Dyskinesia is a common symptom of many movement disorders. Dyskinesia results in broken or jerky motions. Tremors are a type of dyskinesia. Nerve diseases cause many movement disorders, such as Parkinson's disease . Other causes include injuries, autoimmune diseases, infections and certain medicines. Many movement disorders are inherited, which means they run in families. Treatment varies by disorder. Medicine can cure some disorders. Others get better when an underlying disease is treated. Often, however, there is no cure. In that case, the goal of treatment is to improve symptoms and relieve pain. Imagine if you couldn't walk normally or get up from a chair, or if parts of your body moved when you didn't want them to. If you have a movement disorder, you experience these kinds of impaired movement. Dyskinesia is a common symptom of many movement disorders. Dyskinesia results in broken or jerky motions. Tremors are a type of dyskinesia.

34. Log In Problems Friedreich Ataxia genetics metabolism physiopathology Genetic Predisposition to Disease genetics Hepatolenticular Degeneration genetics http://www.medscape.com/medline/abstract/17367269

35. Fragile X-associated Tremor/ataxia Syndrome Presenting In A Woman After Chemothe Medicine..Cerebellar Ataxia Genetics..Allele Related Articles. July 26 Highlights Neurology 2005 65 184185. The variable phenotype of http://www.neurology.org/cgi/content/citation/65/2/331

var callbackToken='427FDDCAE460D6D'; Skip to main page content Visit www.aan.com Home ... Correspondence Quick Search keyword author year volume page Search Advanced Search Login Help Feedback Clinical/Scientific Notes Clinical/Scientific Notes J. P. Oā€™Dwyer C. Clabby J. Crown D. E. Barton and M. Hutchinson Fragile X-associated tremor/ataxia syndrome presenting in a woman after chemotherapy Neurology July 26, 2005 Full Text Full Text (PDF) Figures Only Polish Data Supplement Related articles Editorials Christoph Kamm and Thomas Gasser The variable phenotype of FXTAS A common cause of ā€œidiopathicā€ disorders Neurology July 26, 2005 Full Text Full Text (PDF) Polish Data Supplement Brief Communications D. A. Hall E. Berry-Kravis S. Jacquemont C. D. Rice J. Cogswell L. Zhang R. J. Hagerman P. J. Hagerman and M. A. Leehey Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS) Neurology July 26, 2005 Abstract Full Text Full Text (PDF) Polish Data Supplement ... Table of Contents This Article doi: 10.1212/01.wnl.0000168865.36352.53

36. Find A Doctor - Beth Israel Deaconness Medical Center Clinical Interest(s) Movement Disorders; Parkinson's Disease; Tourette Syndrome; Tremors; Ataxia; Genetics; Mitochondrial Disorders http://services.bidmc.org/Find_a_doc/doc_detail.asp?sid=41414547454945

37. Friedreich's Ataxia: MedlinePlus Genetics Home Reference Friedreich ataxia Genetics Home Reference Friedreich ataxia http//ghr.nlm.nih.gov/condition/friedreichataxia (National Library of Medicine) http://www.nlm.nih.gov/medlineplus/friedreichsataxia.html

pttitle = ""; Skip navigation A service of the U.S. National Library of Medicine National Institutes of Health Home About MedlinePlus ... Contact Us Search MedlinePlus Health Topics ESPAƑOL Other Topics: A B C D ... All Topics Friedreich's Ataxia URL of this page: http://www.nlm.nih.gov/medlineplus/friedreichsataxia.html Friedreich's ataxia is an inherited disease that damages your nervous system. The damage affects your spinal cord and the nerves that control muscle movement in your arms and legs. Symptoms usually begin between the ages of 5 and 15. The main symptom is ataxia, which means trouble coordinating movements. Specific symptoms include Difficulty walking Muscle weakness Speech problems Involuntary eye movements Scoliosis Heart palpitations People with Friedreich's ataxia usually need a wheelchair 15 to 20 years after symptoms first appear. In severe cases, people become incapacitated. There is no cure. You can treat symptoms with medicines, braces, surgery and physical therapy. NIH: National Institute of Neurological Disorders and Stroke Friedreich's ataxia is an inherited disease that damages your nervous system. The damage affects your spinal cord and the nerves that control muscle movement in your arms and legs. Symptoms usually begin between the ages of 5 and 15. The main symptom is ataxia, which means trouble coordinating movements. Specific symptoms include

38. NIH - Rare Diseases Friedreich's Ataxia; Genetics Home Reference Harlequin Ichthyosis; Genetics Home Reference Methemoglobinemia, Betaglobin Type; Genetics Home Reference Tyrosinemia http://health.nih.gov/topic/RareDiseases/GeneticsBirthDefects

39. XCA - Definition By AcronymFinder Extracurricular Activity * XCA External Communications Adapter * XCA XLinked Congenital Ataxia (genetics) * XCA X-Ray Contrast Angiography (radiology) http://www.acronymfinder.com/XCA.html

40. Log In Problems Friedreich Ataxia genetics Humans; Mutation; Myotonic Dystrophy genetics Nervous System Diseases genetics Neurodegenerative Diseases genetics http://www.medscape.com/medline/abstract/16205714

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 2     21-40 of 45    Back | 1  | 2  | 3  | Next 20