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14. Hyperglycinemia and propionyl coA carboxylase deficiency and episodic severe illness without consistent ketosis. Wadlington WB; Kilroy A; Ando T; Sweetman L; Nyhan WL J Pediatr; 1975 May; 86(5):707-12. PubMed ID: 1133651 [TBL] [Abstract][Full Text] [Related]
15. Hyperglycinemia with ketoacidosis and leukopenia. Metabolic studies on the nature of the defect. Soriano JR; Taitz LS; Finberg L; Edelmann CM Pediatrics; 1967 Jun; 39(6):818-28. PubMed ID: 6026548 [No Abstract] [Full Text] [Related]
16. [Methylmalonic aciduria - diagnosis and therapy using as example 2 cases of this genetic metabolic disorder]. Lubs H; Seidlitz G; Pfau E Padiatr Grenzgeb; 1982; 21(4):319-26. PubMed ID: 7177670 [No Abstract] [Full Text] [Related]
17. [Methylmalonic aciduria. A case report]. van Dyk JC; Meiring JL; Prinsloo JG S Afr Med J; 1982 Oct; 62(19):700-2. PubMed ID: 7135128 [TBL] [Abstract][Full Text] [Related]
19. Hyperglycinemia with ketosis due to a defect in isoleucine metabolism: a preliminary report. Keating JP; Feigin RD; Tenenbaum SM; Hillman RE Pediatrics; 1972 Dec; 50(6):890-5. PubMed ID: 4636454 [No Abstract] [Full Text] [Related]