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23. 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]
24. Type II hyperprolinaemia in a pedigree of Irish travellers (nomads). Flynn MP; Martin MC; Moore PT; Stafford JA; Fleming GA; Phang JM Arch Dis Child; 1989 Dec; 64(12):1699-707. PubMed ID: 2624476 [TBL] [Abstract][Full Text] [Related]
25. Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype". Statter M; Ben-Zvi A; Shina A; Schein R; Russell A Helv Paediatr Acta; 1976 Aug; 31(2):173-82. PubMed ID: 955941 [TBL] [Abstract][Full Text] [Related]
26. Type II hyperprolinemia. Delta1-pyrroline-5-carboxylic acid dehydrogenase deficiency in cultured skin fibroblasts and circulating lymphocytes. Valle D; Goodman SI; Applegarth DA; Shih VE; Phang JM J Clin Invest; 1976 Sep; 58(3):598-603. PubMed ID: 956388 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. Formation and excretion of pyrrole-2-carboxylic acid. Whole animal and enzyme studies in the rat. Heacock AM; Adams E J Biol Chem; 1975 Apr; 250(7):2599-608. PubMed ID: 235519 [TBL] [Abstract][Full Text] [Related]
29. Cystathioninuria and renal iminoglycinuria in a pedigree. Whelan DT; Scriver CR N Engl J Med; 1968 Apr; 278(17):924-7. PubMed ID: 5644557 [No Abstract] [Full Text] [Related]
30. The use of hydroxy-DL-proline-2-(14)C in the investigation of hydroxyproline metabolism in normal subjects and in patients with renal insufficiency. Hart W; van den Hamer CJ; van der Sluys Veer J Clin Nephrol; 1976 Sep; 6(3):379-87. PubMed ID: 991465 [TBL] [Abstract][Full Text] [Related]
31. The relationship between proline and hydroxyproline urinary excretion in human as an index of collagen catabolism. Nusgens B; Lapiere CM Clin Chim Acta; 1973 Oct; 48(2):203-11. PubMed ID: 4758883 [No Abstract] [Full Text] [Related]
33. Hyperprolinemia type II: evidence of the excretion of 3-hydroxy delta 1-pyrroline 5-carboxylic acid. Dooley KC; Applegarth DA Clin Biochem; 1979 Apr; 12(2):62-5. PubMed ID: 445797 [TBL] [Abstract][Full Text] [Related]
34. [Prolinuria]. Tada K Saishin Igaku; 1969 Jun; 24(6):1226-34. PubMed ID: 5805578 [No Abstract] [Full Text] [Related]
35. Hyperprolinemia: clinical and biochemical family study. Woody NC; Snyder CH; Harris JA Pediatrics; 1969 Oct; 44(4):554-63. PubMed ID: 5346634 [No Abstract] [Full Text] [Related]
36. Aminoacidurias due to inherited disorders of metabolism. 2. Frimpter GW N Engl J Med; 1973 Oct; 289(17):895-901. PubMed ID: 4598151 [No Abstract] [Full Text] [Related]
37. [Results of a period of research (1967-1974) in the field of disorders of transport amino acid and metabolism using chromatographic, electrophoretic and dosimetric methods]. Berio A; Allegranza A; Scapaticci E; Cadoni M; Camozzi C; Cavallo V; Di Stefano A; Santos JG Minerva Pediatr; 1975 Sep; 27(30):1609-23. PubMed ID: 1177852 [No Abstract] [Full Text] [Related]
38. 3-Hydroxyproline content of normal urine. Adams E; Ramaswamy S; Lamon M J Clin Invest; 1978 Jun; 61(6):1482-7. PubMed ID: 659611 [TBL] [Abstract][Full Text] [Related]
39. Metabolic studies in two families with hyperornithinemia and gyrate atrophy of choroid and retina. Yatziv S; Statter M; Merin S J Lab Clin Med; 1979 May; 93(5):749-57. PubMed ID: 429873 [TBL] [Abstract][Full Text] [Related]
40. Iminoacidopathy in renal failure. Simon NM; Bell NH; Del Greco F Arch Intern Med; 1970 Feb; 125(2):299-301. PubMed ID: 5412018 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]