The inherited leukodystrophies: A clinical overview
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF00711905
Reference38 articles.
1. Adams RD, Lyon G (1982)Neurology of Hereditary Metabolic Diseases of Children. New York: McGraw-Hill.
2. Aicardi J (1989) Progrediente Enzephalopathie-Syndrome unbekannter Ursache. In Hanefeld F, ed.Aktuelle Neuropädiatrie. Heidelberg: Springer Verlag, 3?15.
3. Aicardi J (1992)Diseases of the Nervous System in Childhood. London: MacKeith Press.
4. Aicardi J, Coutières F (1984) A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis.Ann Neurol 16: 60?65.
5. Aubourg PR, Sellier N, Chaussain JL, Kalifa G (1989) MRI detects cerebral involvement in neurologically asymptomatic patients with adrenoleukodystrophy.Neurology 39: 1619?1621.
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