Cerebral dysgenesis and lactic acidemia: An MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency-Reference-Cited by-同舟云学术

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Cerebral dysgenesis and lactic acidemia: An MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency

Published:1994-10 Issue:3 Volume:11 Page:224-229
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Shevell Michael I.,Matthews Paul M.,Scriver Charles R.,Brown Ruth M.,Otero Lucy J.,Legris Masha,Brown Garry K.,Arnold Douglas L.

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference46 articles.

1. Pyruvate dehydrogenase E1α deficiency;Brown;J Inherited Metab Dis,1992

2. Lactic acidemia;Robinson,1989

3. Molecular biology and biochemistry of pyruvate dehydrogenase complexes;Patel;FASEB J,1990

4. Lactic acidaemia;Robinson;J Inherited Metab Dis,1984

5. The clinical and biochemical spectrum of human pyruvate dehydrogenase complex deficiency;Brown;Ann NY Acad Sci,1989

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