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2. Letter: Nonketotic hyperglycinemia with increased propionic acid excretion and hyperammonemia. Farriaux JP; Morel P; Hommes FA N Engl J Med; 1976 Mar; 294(10):558. PubMed ID: 1250266 [No Abstract] [Full Text] [Related]
3. Identification of the insertion/deletion mutation in Spanish beta-propionyl-CoA carboxylase-deficient patients. Pérez-Cerdá C; Rodríguez-Pombo P; Ugarte M J Inherit Metab Dis; 1994; 17(6):661-3. PubMed ID: 7707688 [No Abstract] [Full Text] [Related]
4. An 84 bp insertion found in a propionic acidaemia patient is not a disease-causing mutation but a product of cryptic mRNA. Ohura T; Narisawa K; Tada K; Iinuma K J Inherit Metab Dis; 1999 Jun; 22(5):676-7. PubMed ID: 10399105 [No Abstract] [Full Text] [Related]
7. Treatment of a neonate with propionic acidaemia and severe hyperammonaemia by peritoneal dialysis. Robert MF; Schultz DJ; Wolf B; Cochran WD; Schwartz AL Arch Dis Child; 1979 Dec; 54(12):962-5. PubMed ID: 533302 [TBL] [Abstract][Full Text] [Related]
8. Biotinidase deficiency in juvenile multiple carboxylase deficiency. Thoene J; Wolf B Lancet; 1983 Aug; 2(8346):398. PubMed ID: 6135890 [No Abstract] [Full Text] [Related]