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Documents Communication orale SENP/BRESCIA 2013 Lésions bi-pallidales, dystonie progressive et tâches rouges...

Page 1 Communication orale SENP/BRESCIA 2013 Lésions bi-pallidales, dystonie progressive et tâches rouges sur la peau : un diagnostic inattendu J. Fluss (1), L.Merlini…

Documents KINS 7338 Micronutrient Metabolism in Sports Nutrition Pantothenic Acid Alaine Mills.

Slide 1 KINS 7338 Micronutrient Metabolism in Sports Nutrition Pantothenic Acid Alaine Mills Slide 2 History Pantothenic Acid was first isolated in 1931 by R.J. Williams…

Documents Pantothenate kinase-associated neurodegeneration

Pantothenate kinase-associated neurodegenerationPantothenate kinase-associated neurodegeneration Pantothenate kinase-associated neurodegeneration (formerly called Hallervorden-Spatz

Documents Hallervorden Spatz disease: MR and pathological findings of a rare case

NI_Jan-Mar_05.pmdCase Report Chitra Sarkar Department of Pathology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110029, India. E-mail: [email protected]

Documents Hallervorden-Spatz Disease: Case Report based on Radiological and Genetic Analytical Findings

Microsoft Word - Hallervorden-Spatz Disease - (M-III) - Case Report -- Aijaz Ahmed - Language check done - Ready for Online firstJ Liaquat Uni Med Health Sci November 23,

Documents Pantothenate kinase associated neurodegeneration (PKAN) presenting as a seizure disorder

12 Pantothenate.inddPantothenate kinase associated neurodegeneration (PKAN) presenting as a seizure disorder Human P Sinha DM, Manish Modi MD DM, Sudesh Prabhakar MD DM,

Documents A Novel PANK2 Mutation in a Patient with Atypical Pantothenate-Kinase-Associated Neurodegeneration.....

Microsoft Word - 54-6.docPrint ISSN 1738-6586 / On-line ISSN 2005-5013 10.3988/jcn.2009.5.4.192J Clin Neurol 2009;5:192-194 A Novel PANK2 Mutation in a Patient with Atypical

Documents Consensus Clinical Management Guidelines for Pantothenate Kinase-Associated Neurodegeneration (PKAN)

Pantothenate Kinase-Associated Neurodegeneration (PKAN) Penelope Hogarth1,2, Manju A. Kurian3, Allison Gregory1, Barbara Csányi3, Tamara Zagustin4, Tomasz Kmiec5,

Documents Novel Compound Heterozygous Mutations in the Pantothenate Kinase 2 Gene in a Korean Patient with...

Microsoft Word - 21-12.docJournal of Movement Disorders 2009;2:45-47 ISSN 2005-940X CASE REPORT Novel Compound Heterozygous Mutations in the Pantothenate Kinase 2 Gene in

Documents Psychotic Disorder in Neurodegeneration with Brain Iron Accumulation

1Bakirkoy Research and Training Hospital for Psychiatry, Neurology and Neurosurgery—Psychiatry Department, Istanbul, Turkey Address for correspondence: Nurhan Fistikci,