1. Friedreich's Ataxia Information Page National Institute Of An information sheet the National Institute of Neurological Disorders and Stroke . http://tmsyn.an.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

2. THE MERCK MANUAL, Sec. 14, Ch. 179, Disorders Of Movement spinocerebellar degenerations. A group of disorders characterized by progressiveataxia due spinocerebellar degenerations can be broadly categorized as http://www.merck.com/mrkshared/mmanual/section14/chapter179/179g.jsp

3. Marinesco-Sjogren Syndrome Information and a support group for families affected with this syndrome, a rare genetic disorder characterized by ataxia, cataracts, very small http://tmsyn.an.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

4. THE MERCK MANUAL, Sec. 14, Ch. 179, Disorders Of Movement and degenerative disorders, including striatonigral degeneration and multiplesystems atrophy (see spinocerebellar degenerations, below). http://www.merck.com/mrkshared/mmanual/section14/chapter179/179e.jsp

5. CajunHeart's HomePage - Life With Ataxia An informative site about living a positive life in spite of having a progressive hereditary neurological disease called Friedreich's Ataxia. http://tmsyn.an.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

6. Spinocerebellar Degenerations This resource contains a summary and bibliographical references of the review.Last revised in April 2005. spinocerebellar degenerations / genetics; http://omni.ac.uk/browse/mesh/D013132.html

low graphics Spinocerebellar Degenerations other: Canavan Disease Cockayne Syndrome Hepatolenticular Degeneration Hereditary Central Nervous System Demyelinating Diseases ... Tuberous Sclerosis narrower: Friedreich Ataxia GeneReviews : hereditary ataxia overview Notes for physicians on hereditary ataxia. This document includes diagnosis, a clinical description, differential diagnosis, management, genetic counselling, and molecular genetics. Posted in September 1998 (revised September 2001), this resource forms part of GeneReviews (formerly GeneClinics profile), a peer-reviewed clinical genetic information resource that is funded by the US National Institutes of Health (NIH) and produced by the University of Washington, Seattle. This resource contains a summary and bibliographical references of the review. Last revised in April 2005. Spinocerebellar Degenerations / genetics Last modified: 09 Sep 2005

7. GeneReviews Friedreich Ataxia An in depth look at this disorder. Includes a summary, diagnosing, molecular genetic testing, clinical description and management. http://tmsyn.an.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

8. Spinocerebellar Degenerations (from Nervous System Disease) --  Encyclopædia B spinocerebellar degenerations (from nervous system disease) Spinocerebellardegenerations are genetically determined conditions characterized by dysfunction http://www.britannica.com/eb/article-75737

Home Browse Newsletters Store ... Subscribe Already a member? Log in Content Related to this Topic This Article's Table of Contents Expand all Collapse all Introduction The neurological examination Medical history Altered consciousness Headache Cognitive changes ... Localization of neurological disease Lower-level sites Muscle Motor end plate Peripheral nerves Spinal nerve roots ... Spinal cord Higher-level sites Brainstem Cerebellum Basal ganglia and thalamus Cerebral hemispheres ... Autoimmune disorders Diseases and disorders The skull and spine Neural tube defects Cephalic disorders Fractures Tumours ... Vertebral disorders The meninges and cerebrospinal fluid Raised or decreased intracranial pressure Blood clots Meningitis Tumours The peripheral system Neuropathies Neuronal neuropathies Poliomyelitis Hereditary motor neuropathies Motor neuron disease ... Disease of the neuromuscular junction Diseases of muscle Genetic dystrophies Other inherited muscle diseases Acquired diseases of muscle The spinal cord changeTocNode('toc75736','img75736'); Spinocerebellar degenerations Inflammation Trauma Tumours ... Myoclonus Cranial nerves Olfactory nerve Optic nerve Oculomotor, trochlear, and abducens nerves

9. Neurogenic Bladder In Parkinson's, Multiple Sclerosis And Clinical findings of Neurogenic Bladder in Parkinson's, Multiple Sclerosis and SpinoCerebellar Degeneration http://tmsyn.an.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

10. Power, Balance Of --  Encyclopædia Britannica spinocerebellar degenerations from the nervous system disease article Spinocerebellardegenerations are genetically determined conditions characterized by http://www.britannica.com/eb/article?tocId=9061128

11. Spinocerebellar Degenerations spinocerebellar degenerations information http://tmsyn.an.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

12. Penn State Faculty Research Expertise Database (FRED) Early Onset Cerebellar Ataxia, Familial spinocerebellar degenerations. Hereditaryspinocerebellar degenerations, Inherited spinocerebellar degenerations http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D013132

13. Penn State Faculty Research Expertise Database (FRED) Degenerations, CorticostriatalSpinal. Degenerations, Familial spinocerebellar degenerations, Hereditary Spinocerebellar. Degenerations, Inherited http://tmsyn.an.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

14. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Neurological_Disor More news about spinocerebellar degenerations Volume 7 December 15, 2000. More books about spinocerebellar degenerations http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Neurologica

@import "/styles/navbar.css"; @import "/styles/tabStyles.css"; Set home page Bookmark site Add search Latest News ... Email to friend Text Size A A A Front Page ... Spinal Cord : Spinocerebellar Degenerations Subtopics Ataxia Friedreich's Ataxia Machado-Joseph Olivopontocerebellar Atrophy Search Google: Spinocerebellar Degenerations News Books Links ... Pinpointing The Cause Of A Neurodegenerative Disorder (August 30, 2005) full story Solving The Mystery Of Mutated Proteins And The Brain (August 26, 2005) Cell . Dr. Huda Zoghbi and her colleagues have determined that a genetic mutation actually enhances the normal activity of a protein, and in the case of ataxin-1, the disease spinocerebellar ataxia type 1 results. full story UCI Eye Doctors Invent Laser-assisted Cornea-transplant Surgery (May 3, 2005) full story From Gene Discovery To Preventing Eye Disease (April 7, 2005) full story Livermore Scientists Join DOE Consortium In Partnering With Private Company To Develop Artificial Retina (October 20, 2004) full story Combination Of Gene Therapy And Gene Silencing Prevents Neurodegenerative Disease (July 5, 2004) full story Researchers Selectively Silence Disease-causing Gene (May 28, 2003)

15. THE MERCK MANUAL, Sec. 14, Ch. 179, Disorders Of Movement spinocerebellar degenerations A group of disorders characterized by progressive ataxia due to degeneration of the cerebellum, brain stem, spinal cord http://tmsyn.an.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

16. THE MERCK MANUAL, Sec. 14, Ch. 179, Disorders Of Movement and degenerative disorders, including striatonigral degeneration and multiple systems atrophy (see spinocerebellar degenerations, below). http://tmsyn.an.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

17. Pyruvate Dehydrogenase Deficiency In Spinocerebellar Degenerations -- Kark And R Pyruvate dehydrogenase deficiency in spinocerebellar degenerations. RA Kark andM RodriguezBudelli. To study the incidence of abnormalities of the pyruvate http://www.neurology.org/cgi/content/abstract/29/1/126

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Correspondence: Submit a response Alert me when this article is cited Alert me when Correspondence are posted ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Kark, R. A. Articles by Rodriguez-Budelli, M. ARTICLES Pyruvate dehydrogenase deficiency in spinocerebellar degenerations RA Kark and M Rodriguez-Budelli To study the incidence of abnormalities of the pyruvate (PDH) or ketoglutarate (KGDH) dehydrogenase complexes in patients with spinocerebellar degenerations, we measured the activities of PDH and KGDH in platelet-enriched preparations from the blood of 14 patients. Low PDH was found in 6 of the 14 patients; low KGDH was found in 2 of the 6. PDH-normal and PDH-abnormal patients could not be distinguished by clinical criteria. These results extend previous studies, which suggested

18. Spinocerebellar Ataxia Type 3 (Machado-Joseph Disease) Severe Spinocerebellar ataxia type 3 (Machado Joseph disease) severe destruction of the lateral reticular nucleus U. R b1 , R. A. I. de Vos2 http://tmsyn.an.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

19. Bedside And Electro-oculographic Analysis Of Abnormal Ocular Movements In Spinoc in spinocerebellar degenerations effects of thyrotropinreleasing hormone ocular movements in 130 patients with spinocerebellar degenerations. http://www.neurology.org/cgi/content/abstract/38/1/110

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Correspondence: Submit a response Alert me when this article is cited Alert me when Correspondence are posted ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Yamamoto, H. Articles by Sobue, I. JOURNAL ARTICLE Bedside and electro-oculographic analysis of abnormal ocular movements in spinocerebellar degenerations: effects of thyrotropin-releasing hormone H Yamamoto, S Saito and I Sobue Department of Neurology, Fujita-Gakuen Health University, School of Medicine, Toyoake Aichi, Japan. We studied ocular movements in 130 patients with spinocerebellar degenerations. Patients had blurred vision (33.3%), diplopia (40.2%), oscillopsia (18.6%), ocular flutter (22.3%), rebound nystagmus (25.4%), square-wave jerks, (29.2%), macro square-wave jerks (6.2%), and macro

20. Spinocerebellar Degenerations Topic - Unified Search Environment spinocerebellar degenerations Topic Tree spinocerebellar degenerationsMSH/MH/D013132 MSH/PM/D013132 COSTAR/PT/NOCODE MSH/EP/D013132 MSH/PM/ http://www.use.hcn.com.au/portals/shared/subject.`Spinocerebellar Degenerations`

Spinocerebellar Degenerations Topic Tree Definition: A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. Synonyms and Source Vocabularies: Spinocerebellar Degenerations Spinocerebellar Diseases Spino-Cerebellar Degenerations Spinocerebellar disease, unspecified spinocerebellar disorder Cerebellar Diseases Ataxia Telangiectasia Cerebellar Neoplasms Dandy-Walker Syndrome Spinocerebellar Degenerations Myoclonic Cerebellar Dyssynergia Friedreich Ataxia Olivopontocerebellar Atrophies Spinocerebellar Ataxias ... Spinal Cord Neoplasms Spinocerebellar Degenerations Myoclonic Cerebellar Dyssynergia Friedreich Ataxia Olivopontocerebellar Atrophies Spinocerebellar Ataxias ... Rett Syndrome Spinocerebellar Degenerations Myoclonic Cerebellar Dyssynergia Friedreich Ataxia Olivopontocerebellar Atrophies Spinocerebellar Ataxias ... Mental Retardation, X-Linked

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