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22. [Results of screening for aminoacidopathies in pregnant women]. Hyánek J; Trnka V; Homolka J; Vácha V; Srácek J; Cervenka J; Dolezal A; Seemanová E; Kapras J; Malá M; Wünschová N; Holub J; Hoza J; Losan F; Nevsímalová S; Kubík M; Viletová H; Ronová R; Kunová V; Matousová M Cesk Pediatr; 1977 Aug; 32(8):460-3. PubMed ID: 597929 [No Abstract] [Full Text] [Related]
23. Novel mutations of the glutaryl-CoA dehydrogenase gene in two Japanese patients with glutaric aciduria type I. Ikeda H; Kimura T; Ikegami T; Kato M; Matsunaga A; Yokoyama S; Yamaguchi S; Ohura T; Hayasaka K Am J Med Genet; 1998 Dec; 80(4):327-9. PubMed ID: 9856558 [TBL] [Abstract][Full Text] [Related]
24. Set of simple side-room urine tests for detection of inborn errors of metabolism. Buist NR Br Med J; 1968 Jun; 2(5607):745-9. PubMed ID: 4231911 [No Abstract] [Full Text] [Related]
25. Hyperprolinemia and prolinuria in a new inbred strain of mice, PRO-Re. Blake RL; Russell ES Science; 1972 May; 176(4036):809-11. PubMed ID: 5031477 [TBL] [Abstract][Full Text] [Related]
26. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies]. Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP Z Kinderheilkd; 1970; 107(4):313-23. PubMed ID: 5438972 [No Abstract] [Full Text] [Related]
27. A patient with hypophosphatasia and hyperprolinaemia. De Vries HR; Duran M; De Bree PK; Wadman SK Neth J Med; 1978; 21(1):28-34. PubMed ID: 634414 [No Abstract] [Full Text] [Related]
28. Familial hyperprolinemia without mental retardation and hereditary nephropathy. Mollica F; Pavone L; Antener I Monogr Hum Genet; 1972; 6():144-5. PubMed ID: 4663888 [No Abstract] [Full Text] [Related]
29. Iminoglycinuria in a child in Czechoslovakia. Blehová B; Păzoutová N; Hyánek J; Jirásek J Humangenetik; 1973 Jul; 19(2):207-10. PubMed ID: 4744406 [No Abstract] [Full Text] [Related]
30. [Stuttering in inborn defects of amino acid metabolism]. Raisová V Sb Lek; 1984 Sep; 86(8-9):277-81. PubMed ID: 6505611 [No Abstract] [Full Text] [Related]
32. High urinary excretion of N-(pyrrole-2-carboxyl) glycine in type II hyperprolinemia. Wajner M; Wannmacher CM; Purkiss P Clin Genet; 1990 Jun; 37(6):485-9. PubMed ID: 2383933 [TBL] [Abstract][Full Text] [Related]
33. Histidinemia: report of four new cases in one family and the effect of low-Histidine diets. Gatfield PD; Knights RM; Devereux M; Pozsonyi JP Can Med Assoc J; 1969 Oct; 101(8):71-5. PubMed ID: 5348485 [No Abstract] [Full Text] [Related]
34. [Hypersarcosinemia with sarcosinuria. Study of a new case]. Willems C; Heusden A; Hainaut A; Chapelle P J Genet Hum; 1971 Mar; 19(1):101-18. PubMed ID: 5158355 [No Abstract] [Full Text] [Related]
35. Carrier detection of urea cycle disorders. Ng WG; Oizumi J; Koch R; Shaw KN; McLaren J; Donnel GN; Carter M Pediatrics; 1981 Sep; 68(3):448-52. PubMed ID: 7279481 [No Abstract] [Full Text] [Related]
36. [Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies]. Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP Z Kinderheilkd; 1970; 107(4):298-312. PubMed ID: 5438971 [No Abstract] [Full Text] [Related]