Alexander Disease: A Case Report and Review of the Literature
Author:
Publisher
Informa UK Limited
Subject
Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.1080/15513819609169294
Reference69 articles.
1. PROGRESSIVE FIBRINOID DEGENERATION OF FIBRILLARY ASTROCYTES ASSOCIATED WITH MENTAL RETARDATION IN A HYDROCEPHALIC INFANT
2. ALEXANDER'S DISEASE
3. Alexander's Disease: Clues to Diagnosis
4. McKusick V A. Mendelian Inheritance in Man. 10th ed. Johns Hopkins University Press, Baltimore 1992; Vol. 2: 1207–8
5. Dysmyelinogenic Leukodystrophy
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1. Megalencephalic Leukoencephalopathy with Subcortical Cysts: A Third Confirmed Case with Literature Review;Pediatric and Developmental Pathology;2009-05
2. Alexander Disease: A Genetic Disorder of Astrocytes;Astrocytes in (Patho)Physiology of the Nervous System;2008-11-08
3. The Alexander Disease–Causing Glial Fibrillary Acidic Protein Mutant, R416W, Accumulates into Rosenthal Fibers by a Pathway That Involves Filament Aggregation and the Association of αB-Crystallin and HSP27;The American Journal of Human Genetics;2006-08
4. Alexander-disease mutation of GFAP causes filament disorganization and decreased solubility of GFAP;Journal of Cell Science;2005-05-01
5. Infantile Alexander Disease: Spectrum of GFAP Mutations and Genotype-Phenotype Correlation;The American Journal of Human Genetics;2001-11
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