Defects in energy metabolism: Coming of age, slowly

Journal of Pediatrics

Volumn 136, Issue 2, 2000, Pages 147-148

  Cederbaum, S ^a   Vilain, E ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EDITORIAL; ENERGY METABOLISM; GENETIC DISORDER; HUMAN; METABOLIC DISORDER; PRIORITY JOURNAL;

EID: 0033912980     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(00)70093-X     Document Type: Editorial

References (4)

1. R Luft D Ikkos G Palmieri L Ernster B. Afzelius A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical and morphological study J Clin Invest 41 1962 1776 1804
2. JM Shoffner DC. Wallace Oxidative phosphorylation diseases CR Scriver AL Beaudet WS Sly D Valle The metabolic and molecular bases of inherited disease. 1995 : McGraw-Hill New York 1535 1609
3. P de Lonlay-Debeney J-C von Kleist-Retzow L Hertz-Pannier S Peudenier V Cormier-Daire P Berquin Cerebral white matter disease in children may be caused by mitochondrial respiratory chain deficiency J Pediatr 136 2000 209 214
4. GM Enns MJ Bennett CL Hoppel SI Goodman K Weisiger C Ohnstad Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency J Pediatr 136 2000 251 254