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5. [Suspected congenital lactic acidosis in an infant with arthrogryposis multiplex congenita. Description of a case]. Loiodice G; Bellicini G; Bergamo F Minerva Pediatr; 1971 Mar; 23(10):437-41. PubMed ID: 5574951 [No Abstract] [Full Text] [Related]
6. [Encephalopathy and congenital lactic acidosis (apropos of an anatomo-clinical case)]. Peytel J; Salle B; Tommasi M; Mathieu M; Antener I; Rosenberg D; Monnet P Arch Fr Pediatr; 1969 Mar; 26(3):321-36. PubMed ID: 5797344 [No Abstract] [Full Text] [Related]
7. A defect in branched-chain amino acid metabolism in a patient with congenital lactic acidosis due to dihydrolipoyl dehydrogenase deficiency. Taylor J; Robinson BH; Sherwood WG Pediatr Res; 1978 Jan; 12(1):60-2. PubMed ID: 643378 [TBL] [Abstract][Full Text] [Related]
8. Fatal congenital lactic acidosis in two siblings. II. Biochemical studies in vivo and in vitro. Skrede S; Strömme JH; Stokke O; Lie SO; Eldjarn L Acta Paediatr Scand; 1971 Mar; 60(2):138-45. PubMed ID: 5548118 [No Abstract] [Full Text] [Related]
9. [Organic acidemias: current diagnostic practical possibilities]. Vecchio F; Carnevale F; Di Bitonto G Pediatria (Napoli); 1983; 91(1):3-13. PubMed ID: 6577403 [No Abstract] [Full Text] [Related]