The Aicardi-Goutières syndrome: Variable clinical expression in two siblings-Reference-Cited by-同舟云学术

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The Aicardi-Goutières syndrome: Variable clinical expression in two siblings

Published:1997-05 Issue:4 Volume:16 Page:323-325
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Verrips Aad,Hiel Johan A.P.,Gabreëls Fons J.M.,Wesseling Pieter,Rotteveel Jan J.

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference9 articles.

1. A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis;Aicardi;Ann Neurol,1984

2. Encephalopathy of infancy with intracerebral calcification and chronic spinal fluid lymphocytosis—another case of the Aicardi-Goutières syndrome;Bönnemann;Neuropediatrics,1992

3. A case of progressive familial encephalopathy in infancy with calcification of the basal ganglia and chronic cerebrospinal fluid lymphocytosis;Giroud;Childs Nerv Syst,1986

4. Familial calcification of the basal ganglia with cerebrospinal fluid pleocytosis;Mehta;J Med Genet,1986

5. A syndrome of basal ganglia calcifications, leucodystrophy and a chronic cerebrospinal fluid lymphomonocytic pleiocytosis. Report of a case;Diament;Arq Neuropsiquiatr,1986

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