نتایج جستجو برای: pick c

تعداد نتایج: 1066027  

2003
Marie T Vanier

Niemann-Pick disease type C (NPC) is an autosomal recessive neurovisceral lipid storage with a wide spectrum of clinical phenotypes. At the cellular level, the disorder is characterized by accumulation of unesterified cholesterol and glycolipids in the lysosomal/late endosomal system. Approximatively 95% of patients have mutations in the NPC1 gene (mapped at 18q11) which encodes a large membran...

Journal: :Indian pediatrics 1994
M K Jain V P Gharpure

Journal: :Indian pediatrics 2012
K N Vykuntaraju Hemalatha Lokanatha Shivananda

Niemann-Pick group of diseases are rare lysosomal storage disorders. The clinical phenotype is variable. We report a child who first time presented with tremors of tongue and tremors of one side of the body. On examination child had hemiparesis and hepatosplenomegaly. Bone marrow examination shows storage cells suggestive of Niemann-Pick cells and enzyme assay confirmed the diagnosis.

Journal: :iranian journal of child neurology 0
mohammad reza alaei pediatric endocrinology and metabolism department, mofid children hospital, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: alaei mr. preinatal types of niemann-pick disease type c. iran j child neurol. 2015 autumn;9:4(suppl.1): 12. pls see pdf.

Journal: :Movement Disorders Clinical Practice 2019

2016
A. V. Degtyareva S. V. Mikhailova E. Y. Zakharova E. L. Tumanova A. A. Puchkova

BACKGROUND Niemann-Pick disease type C is a rare metabolic disease characterized by progressive neurological deterioration with childhood onset, and often results in premature mortality. Niemann-Pick disease type C has an extremely heterogeneous clinical presentation with a wide range of visceral and neurological signs and symptoms that are not specific to the disease, and which progress over v...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1987
J D Butler M E Comly H S Kruth M Vanier M Filling-Katz J Fink N Barton H Weintroub J M Quirk T Tokoro

Fluorescence microscopic examination of filipin-stained cultured skin fibroblasts derived from two brothers with group D Niemann-Pick disease revealed abnormal storage of low density lipoprotein (LDL)-derived cholesterol. LDL stimulation of intracellular cholesteryl ester synthesis was severely compromised in the Niemann-Pick D fibroblasts, as it also was in fibroblasts obtained from Niemann-Pi...

Journal: :iranian journal of child neurology 0
bita shalbafan adult neurologist, social security organization, labafinejad hospital, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: shalbafan b. a family case report of niemman pick c with new mutation and different presentations. iran j child neurol. 2015 autumn;9:4(suppl.1): 20-21.   pls see pdf.

Journal: :iranian journal of child neurology 0
mohsen javadzadeh 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2.pediatric neurology center of excellence & pediatric neurology department sciences, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: javadzadeh m. prenatal diagnosis and genetic counseling for niemann-pick c disease. iran j child neurol. 2015 autumn;9:4(suppl.1): 22.   pls see pdf.

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