Hallervorden-spatz Syndrome Define Hallervorden-spatz Syndrome Medical Dictionary HallervordenSpatz syndrome Hal ler vor den-Spatz syndrome (hāl'lər-v r'dn-shp tz', h 'lər-) or Hallervorden syndrome n. An inherited syndrome in http://dictionary.reference.com/browse/Hallervorden-Spatz syndrome
Arch Neurol Abstract Hallervorden-Spatz Syndrome, December Archives of Neurology, a monthly professional medical journal published by the American Medical Association, publishes original, peerreviewed scientific research on the http://archneur.ama-assn.org/cgi/content/abstract/34/12/729
Hallervorden-Spatz Syndrome - What Does HSS Stand For? Acronyms Acronym Definition; HSS Health, Safety and Security (US Department of Energy) HSS Humanities and Social Sciences HSS High Speed Steel HSS Hospital for Special Surgery http://acronyms.thefreedictionary.com/Hallervorden-Spatz syndrome
The First Scientific Workshop Of Hallervorden-Spatz Syndrome The First Scientific Workshop of HallervordenSpatz Syndrome Grant Number NS40452-01 May 19 - 20, 2000 National Institute of Neurological Disorders Stroke, Bethesda, Maryland http://www.ninds.nih.gov/news_and_events/proceedings/Hallervorden-Spatz.htm
Hallervorden-Spatz Syndrome Definition From Answers.com or Hallervorden syndrome n. An inherited syndrome in which the nerve fibers connecting the striatum and globus pallidus are completely demyelinated. http://www.answers.com/topic/hallervorden-spatz-syndrome
Hallervorden-Spatz Syndrome Definition Drugs.com Definition of HallervordenSpatz syndrome. Provided by Stedman's medical dictionary and Drugs.com. Includes medical terms and definitions. http://www.drugs.com/dict/hallervorden-spatz-syndrome.html
Welcome To The Hallervorden-Spatz Syndrome Support Group Welcome to the HallervordenSpatz Syndrome Support Group Hello, Welcome to the Hallervorden-Spatz Syndrome Support Group. This Support Group is a comfort place for family members http://www.mdjunction.com/forums/hallervorden-spatz-syndrome-discussions/general
Hallervorden-Spatz Syndrome Articles HallervordenSpatz Syndrome Articles. Information and resources about PKAN shared by the members of the Hallervorden-Spatz Syndrome community. http://www.mdjunction.com/hallervorden-spatz-syndrome/articles/
Hallervorden-Spatz Syndrome (Journal Contents) Subject HallervordenSpatz Syndrome (Journal Contents) Date 10/20/2001. The journal Pediatric Neurology has devoted a recent issue to an overview of Hallervorden-Spatz syndrome. http://www.mdvu.org/emove/article.asp?ID=397
PANK2 (gene) - Wikipedia, The Free Encyclopedia Mutations in this gene are associated with HARP syndrome and pantothenate kinaseassociated neurodegeneration (PKAN), formerly Hallervorden-Spatz syndrome. http://en.wikipedia.org/wiki/PANK2_(gene)
Homozygosity Mapping Of Hallervorden-Spatz Syndrome To Chromosome PubMed is a service of the U.S. National Library of Medicine that includes over 19 million citations from MEDLINE and other life science journals for biomedical articles back to http://www.ncbi.nlm.nih.gov/pubmed/8944032
Hallervorden-Spatz Syndrome - Definition HallervordenSpatz syndrome definition from the mondofacto online medical dictionary http://www.mondofacto.com/facts/dictionary?Hallervorden-Spatz syndrome
About Hallervorden-Spatz Syndrome And Its Underlying Genetic Causes HallervordenSpatz Syndrome is a genetic disorder that arises early in life and almost always causes premature death in those who suffer from it. This article describes the http://www.brighthub.com/science/genetics/articles/92036.aspx
Genetic, Clinical, And Radiographic Delineation Of Hallervorden BACKGROUND HallervordenSpatz syndrome is an autosomal recessive disorder characterized by dystonia, parkinsonism, and iron accumulation in the brain. http://www.medscape.com/medline/abstract/12510040
Arch Neurol Abstract Hallervorden-Spatz Syndrome And Brain Archives of Neurology, a monthly professional medical journal published by the American Medical Association, publishes original, peerreviewed scientific research on the nervous http://archneur.ama-assn.org/cgi/content/abstract/48/12/1285
