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32. Familial hyperprolinemia and mental retardation. A second metabolic type. Selkoe DJ Neurology; 1969 May; 19(5):494-502. PubMed ID: 5815222 [No Abstract] [Full Text] [Related]
33. From the Clinical Conference St. Louis Children's Hospital. Phenylketonuria. Diagnostic and therapeutic dilemma. Kahn LI Clin Pediatr (Phila); 1970 May; 9(5):263-71. PubMed ID: 5445064 [No Abstract] [Full Text] [Related]
34. Medical research council unit for metabolic studies in psychiatry, Sheffield. Jenner FA Psychol Med; 1973 Aug; 3(3):379-84. PubMed ID: 4729197 [No Abstract] [Full Text] [Related]
35. Argininosuccinic aciduria: antenatal investigations in an affected family. Burgess EA; Oberholzer VG; Palmer T; Wagstaff TI Am J Obstet Gynecol; 1974 Oct; 120(4):560-2. PubMed ID: 4412079 [No Abstract] [Full Text] [Related]
36. Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels. Przyrembel H; Bremer HJ; Duran M; Bruinvis L; Ketting D; Wadman SK; Baumgartner R; Irle U; Bachmann C Eur J Pediatr; 1979 Jan; 130(1):1-14. PubMed ID: 759179 [TBL] [Abstract][Full Text] [Related]
37. Studies in cystathioninemia. Berlow S Am J Dis Child; 1966 Aug; 112(2):135-42. PubMed ID: 5947491 [No Abstract] [Full Text] [Related]
38. Hyperglycinuria and hyperglycinemia in two siblings with mild developmental delays. Frazier DM; Summer GK; Chamberlin HR Am J Dis Child; 1978 Aug; 132(8):777-81. PubMed ID: 80128 [TBL] [Abstract][Full Text] [Related]
39. [Case of aminoaciduria in mental deficiency and obesity]. Fujiwara M; Ida S; Takahashi K; Tanaka M; Kawashima M Horumon To Rinsho; 1966 Jun; 14(6):493-5. PubMed ID: 6007024 [No Abstract] [Full Text] [Related]