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4. [Type I hyperprolinemia. Study of a familial case]. Fontaine G; Farriaux JP; Dautrevaux M Helv Paediatr Acta; 1970 Apr; 25(2):165-75. PubMed ID: 5419477 [No Abstract] [Full Text] [Related]
5. 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]
6. Type I hyperprolinemia: genotype/phenotype correlations. Guilmatre A; Legallic S; Steel G; Willis A; Di Rosa G; Goldenberg A; Drouin-Garraud V; Guet A; Mignot C; Des Portes V; Valayannopoulos V; Van Maldergem L; Hoffman JD; Izzi C; Espil-Taris C; Orcesi S; Bonafé L; Le Galloudec E; Maurey H; Ioos C; Afenjar A; Blanchet P; Echenne B; Roubertie A; Frebourg T; Valle D; Campion D Hum Mutat; 2010 Aug; 31(8):961-5. PubMed ID: 20524212 [TBL] [Abstract][Full Text] [Related]
10. [Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy]. Jeune M; Collombel C; Michel M; David M; Guibaud P; Guerrier G; Albert J Ann Pediatr (Paris); 1970 Feb; 17(2):349-63. PubMed ID: 5513158 [No Abstract] [Full Text] [Related]
11. 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]
12. Hyperprolinaemia type II. Similä S Fla Dent J; 1970 Aug; 2(2):143-50. PubMed ID: 5271041 [No Abstract] [Full Text] [Related]
13. [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]
14. [Hyperprolinemia and hydroxyprolinemia]. Berger R; Broyer M Presse Med (1893); 1969 May; 77(26):957-8. PubMed ID: 5795142 [No Abstract] [Full Text] [Related]
15. 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]
16. [Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland)]. Minder FC; Dubach UC; Antener I Z Klin Med; 1965 Dec; 158(7):601-32. PubMed ID: 5869106 [No Abstract] [Full Text] [Related]
17. [Diseases caused by altered intermediate metabolism of amino acids]. Bulgarelli R; Berio A Minerva Nipiol; 1969; 19(6):328-61 contd. PubMed ID: 4923874 [No Abstract] [Full Text] [Related]
18. [Familial hyperprolinemia--a case in a family]. Oknińska A; Grygalewicz J; Kowalewska-Kantecka B; Iwańska J Pol Arch Med Wewn; 1974 Feb; 51(2):189-97. PubMed ID: 4816363 [No Abstract] [Full Text] [Related]
19. Type 2 hyperprolinemia: absence of delta1-pyrroline-5-carboxylic acid dehydrogenase activity. Valle DL; Phang JM; Goodman SI Science; 1974 Sep; 185(4156):1053-4. PubMed ID: 4369405 [TBL] [Abstract][Full Text] [Related]
20. Hyperprolinemia. I. Study of a large family. Potter JL; Waickman FJ J Pediatr; 1973 Oct; 83(4):635-8. PubMed ID: 4729989 [No Abstract] [Full Text] [Related] [Next] [New Search]