Extractions: Program Nr: 2511 Linkage of a Large Family with Hereditary Spastic Paraplegia to Chromosome 2p. D.R. Rosen , N.H. Chapman , C. He , T.F. Thurmon , E.M. Wijsman 1) Div Genetic Disorders, Wadsworth Ctr, Albany, NY; 2) Dept. of Biostatistics, University of Washington Seattle, WA; 3) Louisiana State University Medical Center, Shreveport, LA; 4) Division of Medical Genetics, University of Washington Seattle, WA.
Hereditary Spastic Paraplegia Home Up . Click Here! hereditary spastic paraplegia. Click Here!Musice.net Just-recipes.net EnvyMag.com Scholarships-4u.com http://www.health-server.com/hereditary_spastic_paraplegia.htm
Hereditary Spastic Paraplegia From Linkspider UK Health Directory hereditary spastic paraplegia by Linkspider UK, hereditary spastic paraplegialinks and hereditary spastic paraplegia topics from our Health directory. http://linkspider.co.uk/Health/ConditionsandDiseases/GeneticDisorders/Hereditary
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Hereditary Spastic Paraplegia hereditary spastic paraplegia Directory Guide to Hereditary SpasticParaplegia sites on the internet. hereditary spastic paraplegia. http://www.directory.net/Health/Conditions_and_Diseases/Genetic_Disorders/Heredi
Extractions: Hereditary Spastic Paraplegia Directory: Guide to Hereditary Spastic Paraplegia sites on the internet. Search Engines: Google Yahoo MSN FindWhat ... City Guides Health Conditions and Diseases Genetic Disorders Hereditary Spastic Paraplegia Websites Hereditary Spastic Paraplegia http://www.med.umich.edu/hsp/
Entrez PubMed hereditary spastic paraplegia. Dennis SC, Green NE. hereditary spastic paraplegiais a genetically transmitted disease that is usually autosomal dominant. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=3
Seminar Details of Pennsylvania School of Medicine NIPA 1 mutations in hereditary spastic paraplegia(SPG6) define a putative membrane transporter superfamily Friday, May 21 http://www.genomics.upenn.edu/events/seminars/files/525.html
The First International Symposium For Hereditary Spastic Paraplegia NINDS is part of the National Institutes of Health. Contact us Content for thispage. The First International Symposium for hereditary spastic paraplegia. http://accessible.ninds.nih.gov/news_and_events/proceedings/spastic_paraplegia.h
Extractions: News and Events - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus Home About NINDS Disorders ... Find People The nation's leading supporter of biomedical research on disorders of the brain and nervous system. Select Topic Disorder Quick Links Alzheimer's Autism Cerebral Palsy Chronic Pain Epilepsy Headache Multiple Sclerosis Parkinson's Stroke Traumatic Brain Injury Current Archived Events Proceedings ... NINDS Notes Current Archived Upcoming Archived Labs at NINDS NINDS Search (search help) Contact us My privacy NINDS is part of the National Institutes of Health Contact us Get Web page suited for printing
Extractions: ATAXIA What is ataxia? Ataxia is a symptom, not a specific disease or diagnosis. Ataxia means clumsiness, or loss of coordination. Ataxia may affect the fingers and hands, the arms or legs, the body, speech or eye movements. This loss of coordination may be caused by a number of different medical or neurologic conditions; for this reason, it is important that a person with ataxia seek medical attention to determine the underlying cause of the symptom and to get the appropriate treatment. What causes ataxia?
Dictionary Definition Of SPASTIC PARAPLEGIA, HEREDITARY Dictionary definition of spastic paraplegia, hereditary. Medical dictionary.Browse Dictionary by alphabet. 0 1 2 3 4 5 6 7 8 9 A B http://www.dictionarybarn.com/SPASTIC-PARAPLEGIA-HEREDITARY.php
Neurology -- Collected Resources : Spastic Paraplegia ARTICLES Further evidence of dementia in SPG4linked autosomal dominant hereditaryspastic paraplegia Paul McMonagle, Paula Byrne, and Michael Hutchinson http://www.neurology.org/cgi/collection/spastic_paraplegia
Extractions: Program Nr: 2476 Silver syndrome, a distinct form of hereditary spastic paraplegia (HSP), is not linked to any of the known HSP loci. V.A. Murday , H. Patel , P. Hart , T. Warner , I. Allen , H. Phillimore , M. Patton , A.H. Crosby 1) Dept Medical Genetics, St Georges Hosp Medical Sch, London, England; 2) Dept Neurology, Royal Free Hospital, London, England. The hereditary spastic paraplegias are a clinically and genetically diverse group of disorders which share the primary feature of a progressive and severe lower extremity spasticity. The HSPs have been divided into 'pure' and 'complicated' forms depending upon the absence or presence of secondary neurological abnormalities. Silver syndrome is a particularly disabling autosomal dominant form of complicated HSP in which the leg spasticity is associated with wasting of the hand muscles. In view of the fact that genes for hereditary spastic paraplegia can produce highly variable phenotypes, the five known autosomal dominant loci were investigated for linkage to Silver syndrome. However, genotyping of these loci in 2 large multigeneration families was incompatible with linkage to any of these regions, suggesting that an additional locus is responsible for this syndrome.
UMHS News Release may also help research on spinal cord injury and ALS Childhood form of hereditaryspastic paraplegia stems from mutated gene for key nerve cell protein. http://www.med.umich.edu/opm/newspage/2001/hspgene.htm
Extractions: Childhood form of hereditary spastic paraplegia stems from mutated gene for key nerve cell protein ANN ARBOR, MI - Scientists report today that they have found a gene for a rare leg-weakening nerve disease that slowly robs children of their ability to walk - a finding that opens the door to better diagnosis and treatment of the disorder, and to insights into other spinal cord problems. Led by researchers from the University of Michigan Health System who have focused for years on both the childhood and adult forms of the mysterious group of disorders known as hereditary spastic paraplegia , the team publishes its results in the November issue of Nature Genetics "This is a major step forward in our understanding of HSP's causes, and has already allowed us to provide diagnostic testing to a few patients," says U-M neurologist and senior author John K. Fink, M.D. "We've been looking for HSP genes since 1993, and we're happy to have found, at last, the first one for a childhood form of the disease. Now, the search continues for the rest."
Vanderbilt Brain Institute . . . Publications. Brewer Fax Lab Address 6140 MRB III. Research Specialty. hereditary SpasticParaplegia/Epilepsy. Research http://medschool1.mc.vanderbilt.edu/brain_institute/php_files/faculty_desc.php?I