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2. 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 [Abstract] [Full Text] [Related]
3. 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]
4. Low proline diet in type I hyperprolinaemia. Harries JT, Piesowicz AT, Seakins JW, Francis DE, Wolff OH. Arch Dis Child; 1971 Feb; 46(245):72-81. PubMed ID: 5555491 [Abstract] [Full Text] [Related]
12. A patient with hypophosphatasia and hyperprolinaemia. De Vries HR, Duran M, De Bree PK, Wadman SK. Neth J Med; 1978 Dec; 21(1):28-34. PubMed ID: 634414 [No Abstract] [Full Text] [Related]
13. 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]
14. Intravenous proline tolerance in a patient with hyperprolinaemia type II and his relatives. Similä S. Helv Paediatr Acta; 1970 Jul; 25(3):287-92. PubMed ID: 5518053 [No Abstract] [Full Text] [Related]
15. [Renal clearance of amino acid in a hyperprolinemic child]. Dodinval P, Willems C, Heusden AM, Hainaut H, Gottschalk C. J Genet Hum; 1969 Oct; 17(3):297-315. PubMed ID: 5387412 [No Abstract] [Full Text] [Related]
16. Non-ketotic hyperglycinaemia in a family with an unusual phenotype. Ando T, Nyhan WL, Bicknell J, Harris R, Stern J. J Inherit Metab Dis; 1978 Oct; 1(3):79-83. PubMed ID: 116082 [Abstract] [Full Text] [Related]