Publications De 1987 à 1978 Translate this page M, Chaabouni H, Madani S, Boussen S, Samoud S, Letaief F, Mrabet A, Hentati F, MiladiN. Genetic study of spinocerebellar hereditary degenerations in Tunisia. http://www.neurotunisie.org/publications78.htm
Cerebellar Diseases - Information / Diagnosis / Treatment / Prevention Cerebellar Degeneration An article written by Timothy C. Hain, MD. ? The MerckManual Disorders Of Movement Information about cerebellar and spinocerebellar http://www.healthcyclopedia.com/neurological-disorders/brain-diseases/cerebellar
Extractions: Web Directory: International Paraneoplastic Association An article about paraneoplastic cerebellar degeneration with an explanation what it is, diagnosis, treatment, research and some notes to care givers and family members. Paraneoplastic Cerebellar Degeneration An article written by Timothy C. Hain, MD.
Spinocerebellar Ataxia spinocerebellar degeneration (SCA6) http//www3.ncbi.nlm.nih.gov/htbinpost/Omim/dispmim?601011.Ataxia society www.ataxia.org; MJD society www.ataxiamjd.org. http://www.tchain.com/otoneurology/disorders/central/cerebellar/sca.htm
Extractions: Return to Education Index Last update: Feb 20, 2000 The main goal of this page is to serve as a repository for recent information about inherited cerebellar degenerations. It is not comprehensive, but we hope that it might be of some use to individuals searching for information about these rare conditions on the web. We highly recommend also using the OMIM database , which can be accessed on the web. A large number of the genetic ataxias can be tested for using contemporary methodology. An example of a lab that does this is Athena Most of the information here concerns inherited conditions, as there is considerable new data derived from researchers using a nearly complete map of the human genome (your tax dollar is doing some good !), and improvements in the technology of molecular biology. It seems quite feasible that within the next decade, we may be able to determine the gene that is damaged in most inherited cerebellar degenerations. As these data become known, it may also be possible to target specific therapies, probably over the next 2 decades. In other words, stay tuned, but we aren't there yet. There are numerous non-genetic causes of cerebellar disease.
PharmGKB Browse Diseases By Name Spinal Osteophytosis. Spinal Stenosis. spinocerebellar Ataxias. spinocerebellarDegenerations. Spirochaetales Infections. Spirurida Infections. Splenic Diseases. http://www.pharmgkb.org/search/browse/diseases.jsp?r=S
Spinocerebellar Ataxia spinocerebellar degeneration (SCA6) http//www3.ncbi.nlm.nih.gov/htbinpost/Omim/dispmim?601011.Ataxia society www.ataxia.org; REFERENCES http://www.dizziness-and-balance.com/disorders/central/cerebellar/sca.htm
Extractions: Please read our Return to Index Search this site Page last modified: January 20, 2004 The main goal of this page is to serve as a repository for recent information about inherited cerebellar degenerations. It is not comprehensive, but we hope that it might be of some use to individuals searching for information about these rare conditions on the web. We highly recommend also using the OMIM database , which can be accessed on the web. A large number of the genetic ataxias can be tested for using contemporary methodology. An example of a lab that does this is Athena Most of the information here concerns inherited conditions, as there is considerable new data derived from researchers using a nearly complete map of the human genome (your tax dollar is doing some good !), and improvements in the technology of molecular biology. It seems quite feasible that within the next decade, we may be able to determine the gene that is damaged in most inherited cerebellar degenerations. As these data become known, it may also be possible to target specific therapies, probably over the next 2 decades. In other words, stay tuned, but we aren't there yet. There are numerous non-genetic causes of cerebellar disease.
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Extractions: The differential diagnosis of a progressive cerebellar syndrome includes vitamin E deficiency, lipoprotein disorders , neurocanthocytosis, Wilson disease MLD hexosaminidase deficiency , aminoacidurias including Hartnup disease , cerebrotendinous xanthomatosis, mitochondrial cytopathies, giant axonal neuropathy, hemochromatosis, adrenoleukodystrophy, Krabbe disease , Whipples disease, demyelinating disease, Behcets, progressive multifocal leukoencephalopathy, vasculitides, biotinidase deficiency, sphingomyelinase deficiency, neuroaxonal dystrophy, Hallevorden-Spatz, Marinesco Sjogren syndrome, Huntingtons disease, Creutzfeld-Jakob and GSS disease, inflammatory spinocerebellar degeneration, GAPN syndrome(antiMAG), thyroid disease, Chediak-Higashi , ataxia telangiectasia, superficial siderosis, heavy metal intoxications, drug (eg. Lithium and Dilantin) intoxication, nutritional, paraneoplastic and familial cerebellar degenerations (including Freidrichs, Joseph disease and other OPCAs including multiple system atrophy) and structural lesions including posterior fossa cysts, tumors, and vascular malformation; craniocervical junction anomalies, occasionally lesions in the frontal lobes or in the cervical spinal cord, and hydrocephalus.
Agnosia, Apraxia And Ataxia Related Books To See but Not to See A Case Study of Visual Agnosia by Glyn W. Humphreys, M.Jane Riddoch Trh and spinocerebellar Degeneration by Itsuro Sobue (Editor) http://www.wtmy.com/manasota/books/eabooks.html
Hepatolenticular Degeneration Hepatolenticular Degeneration. text version of the review requiresbrief registration. Hepatolenticular Degeneration / genetics;. http://omni.ac.uk/browse/mesh/C0019202L0019202.html
Extractions: low graphics broader: Basal Ganglia Diseases Liver Diseases Movement Disorders other: Angelman Syndrome Canavan Disease Cockayne Syndrome Fatty Liver ... GeneReviews : Wilson disease Notes for physicians on Wilson Disease (Hepatolenticular Degeneration) covering diagnosis, clinical description, differential diagnosis, management, molecular genetics and genetic counselling. Reviewed during October 1999, 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, free access to the full-text version of the review requires brief registration. Hepatolenticular Degeneration / genetics
WWW: Ataxia All about ataxia www from BigTome.com http://www.bigtome.com/big/page/ataxia
Penn State Faculty Research Expertise Database (FRED) systems. Related Terms, Degenerative Disease, Nervous System, Hereditary,Degenerative Hereditary Disorders, Nervous System. Hereditary http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D020271
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Jørgen E. Nielsen 30 April 2004. Jørgen E. Nielsen. Clinical and genetic aspects of spinocerebellardegenerations. Cerebellar ataxias and spastic paraplegias http://www.neuroseminars.ku.dk/apr_1.html