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45. Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family. Mollica F, Pavone L, Antener I. Pediatrics; 1971 Aug; 48(2):225-31. PubMed ID: 5560617 [No Abstract] [Full Text] [Related]
49. [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]
50. 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]
52. Dietary treatment in hyperprolinaemia type II. Similä S. Acta Paediatr Scand; 1974 Mar; 63(2):249-56. PubMed ID: 4820590 [No Abstract] [Full Text] [Related]
53. Isovaleric acidemia: results of family study and dietary treatment. Levy HL, Erickson AM, Lott IT, Kurtz DJ. Pediatrics; 1973 Jul; 52(1):83-94. PubMed ID: 4125080 [No Abstract] [Full Text] [Related]
54. Rapid short-column chromatography of amino acids. A method for blood and urine specimens in the diagnosis and treatment of metabolic disease. Shih VE, Efron ML, Mechanic GL. Anal Biochem; 1967 Aug; 20(2):299-311. PubMed ID: 6048171 [No Abstract] [Full Text] [Related]
55. Biochemical, morphological and hybrid studies in hyperprolinemic mice. Kanwar YS, Krakower CA, Manaligod JR, Justice P, Wong PW. Biomedicine; 1975 May; 22(3):209-16. PubMed ID: 240452 [Abstract] [Full Text] [Related]
56. A familial spinal cord disorder with hyperglycinemia. Bank WJ, Morrow G. Arch Neurol; 1972 Aug; 27(2):136-44. PubMed ID: 4402738 [No Abstract] [Full Text] [Related]