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Hallervorden-spatz Syndrome: more detail |
1. Pantothenate Kinase-associated Neurodegeneration - Wikipedia, The Pantothenate kinaseassociated neurodegeneration (PKAN), also known as neurodegeneration with brain iron accumulation 1 (NBIA1) and formerly called Hallervorden-Spatz syndrome (use of http://en.wikipedia.org/wiki/Hallervorden-Spatz_syndrome |
2. Hallervorden-spatz Syndrome Lose Weight on Pasta! 'THE CARBLOVERS DIET Eat What You Love, Get Slim For Life', by Health magazine, introduces a clinically proven weight loss diet plan for carb lovers! http://health.kosmix.com/topic/Hallervorden-spatz_syndrome |
3. Hallervorden-Spatz Syndrome - WikiGenetics This page was last modified 1836, 30 October 2007. This page has been accessed 353 times. Privacy policy; About WikiGenetics; Disclaimers http://wikigenetics.org/index.php/Hallervorden-Spatz_Syndrome |
4. Hallervorden-Spatz Syndrome Article Radiopaedia.org The HallervordenSpatz syndrome is an autosomal recessive disorder causing involuntary spasticity and progressive dementia. It is also known as pantothenate kinase-associated http://radiopaedia.org/articles/hallervorden-spatz_syndrome |
5. Hallervorden-spatz Syndrome - Kosmix Reference, Videos, Images Pantothenate kinaseassociated neurodegeneration (PKAN), also known as neurodegeneration with brain iron accumulation 1 (NBIA1) and formerly called Hallervorden-Spatz syndrome (use http://www.kosmix.com/topic/Hallervorden-spatz_syndrome |
6. Hallervorden-Spatz Disease EMedicine Neurology Taylor TD, Litt M, Kramer P, et al. Homozygosity mapping of HallervordenSpatz syndrome to chromosome 20p12.3-p13. Nat Genet. Dec 1996;14(4)479-81. http://emedicine.medscape.com/article/1150519-overview |
7. 010203 Genetic, Clinical, And Radiographic Delineation Of n engl j med 348;1 www.nejm.orgjanuary 2, 2003 The new england journal of medicine 33 original article Genetic, Clinical, and Radiographic Delineation of HallervordenSpatz Syndrome Susan J http://www.ohsu.edu/xd/research/clinical-research/hgi/consortium/disorders/uploa |
8. Hallervorden-Spatz Syndrome (www.whonamedit.com) HallervordenSpatz syndrome A very rare disease with degeneration of the globus pallidus, red nucleus, and substantia nigra of the brain. It is characterized by progressive http://www.whonamedit.com/synd.cfm/1082.html |
9. Mineralization Of The Basal Ganglia Detected By CT In Hallervorden The most widely read and highly cited peerreviewed Neurology journal http://neurology.org/cgi/content/abstract/38/1/154 |
10. Hallervorden-Spatz Syndrome - Definition Of Hallervorden-Spatz Hal ler vor denSpatz syndrome (h l l r-v r dn-shp tz, h l r-) or Hallervorden syndrome. n. An inherited syndrome in which the nerve fibers connecting the striatum and globus pallidus http://medical-dictionary.thefreedictionary.com/Hallervorden-Spatz syndrome |
11. The EyePathologist - Hallervorden-Spatz Syndrome - Duke University The EyePathologist is a webbased, instructional environment on the anatomy and pathology of the eye designed to emulate one-to-one interaction with an expert eye pathologist. http://eyepathologist.com/disease.asp?IDNUM=313110 |
12. Hallervorden-Spatz Syndrome Symptoms, Diagnosis, Treatments And HallervordenSpatz Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis. http://www.wrongdiagnosis.com/h/hallervorden_spatz_syndrome/intro.htm |
13. Br Br Font Size=3 Hallervorden-Spatz Syndrome Haemophilus Aegyptius to Hysteria HallervordenSpatz Syndrome Haemophilus Aegyptius Haemophilus Influenzae Hajdu-Cheney Syndrome Hallermann-Streiff Syndrome Hallervorden http://telemedicine.orbis.org/bins/content_page.asp?cid=1-2896-5637-5789 |
14. Hallervorden-Spatz Syndrome. [Pediatr Neurol. 2001] - PubMed Result 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/11551740 |
15. Homozygosity Mapping Of Hallervorden−Spatz Syndrome To Letter Nature Genetics 14, 479 481 (1996) doi10.1038/ng1296-479 Homozygosity mapping of Hallervorden−Spatz syndrome to chromosome 20p12.3−p13 http://www.nature.com/ng/journal/v14/n4/abs/ng1296-479.html |
16. Hallervorden-Spatz Syndrome Links to information and resources for HallervordenSpatz syndrome, an inherited neurological movement disorder. http://rarediseases.about.com/cs/hallervordenspatz/ |
17. Pantothenate Kinase-associated Neurodegeneration - Definition Of HallervordenSpatz syndrome. Hallervorden-Spatz disease Neurology An AR condition first seen in childhood or adolescence Clinical Progressive neurologic degeneration with defects in http://medical-dictionary.thefreedictionary.com/Pantothenate kinase-associated n |
18. Hallervorden-Spatz Syndrome - WrongDiagnosis.com HallervordenSpatz syndrome symptoms, causes, diagnosis, and treatment information for Hallervorden-Spatz syndrome (Hallervorden-Spatz Syndrome) with alternative diagnoses, full http://www.wrongdiagnosis.com/medical/hallervorden_spatz_syndrome.htm |
19. Hallervorden-Spatz Syndrome - Pigmentary Pallidal Degeneration A rare autosomal recessive degenerative disorder which usually presents in late http://www.hon.ch/HONselect/RareDiseases/EN/C10.228.140.079.493.html |
20. Hugo Spatz (www.whonamedit.com) Hugo Spatz German neuropathologist, born September 2, 1888, Munich; died January 27, 1969. Associated with HallervordenSpatz syndrome,Spatz-Stiefler reaction http://www.whonamedit.com/doctor.cfm/1063.html |
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