Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets: Studies in patients with identical mutations

Neurology

Volumn 49, Issue 6, 1997, Pages 1655-1661

  Wexler, I D ^a   Hemalatha, S G ^a   McConnell, J ^a   Buist, N R M ^b   Dahl, H H M ^c   Berry, S A ^d   Cederbaum, S D ^e   Patel, M S ^a,f   Kerr, Douglas S ^a,g  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c ROYAL CHILDREN'S HOSPITAL   (Australia)

^d UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

^f UNIVERSITY AT BUFFALO   (United States)

^g CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PYRUVATE DEHYDROGENASE;

ARTICLE; CARBOHYDRATE INTAKE; CLINICAL ARTICLE; ENZYME ACTIVATION; ENZYME ACTIVITY; GENE MUTATION; HUMAN; INFANT; KETOGENESIS; LACTIC ACIDOSIS; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; PYRUVATE DEHYDROGENASE COMPLEX DEFICIENCY; X CHROMOSOME LINKAGE;

EID: 0031456509     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.49.6.1655     Document Type: Article

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