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3. 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]
4. [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]
6. [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]
7. [Hyperprolinemia and hydroxyprolinemia]. Berger R; Broyer M Presse Med (1893); 1969 May; 77(26):957-8. PubMed ID: 5795142 [No Abstract] [Full Text] [Related]
8. [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]
9. 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]
10. [Hyperprolinemia type I]. Thomsen B; Vetner M; Rosleff F; Reske-Nielsen E Ugeskr Laeger; 1974 Oct; 136(44):2460-1. PubMed ID: 4420280 [No Abstract] [Full Text] [Related]
11. Hydroxyprolinemia: an apparently harmless familial metabolic disorder. Pelkonen R; Kivirikko KI N Engl J Med; 1970 Aug; 283(9):451-6. PubMed ID: 4393577 [No Abstract] [Full Text] [Related]
12. [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]
13. [Hyperprolinemia type II]. Thomsen B; Vetner M; Rosleff F; Reske-Nielsen E Ugeskr Laeger; 1974 Nov; 136(45):2530. PubMed ID: 4420281 [No Abstract] [Full Text] [Related]
15. Hyperprolinaemia type II. Similä S Fla Dent J; 1970 Aug; 2(2):143-50. PubMed ID: 5271041 [No Abstract] [Full Text] [Related]
16. Ocular manifestations of familial hyperlysinemia. Smith TH; Holland MG; Woody NC Trans Am Acad Ophthalmol Otolaryngol; 1971; 75(2):355-60. PubMed ID: 5557172 [No Abstract] [Full Text] [Related]
17. Familial nephropathy and deafness: first observation of a family and close relatives in Switzerland. Dubach UC; Minder FC; Antener I Helv Med Acta; 1966 Apr; 33(1):36-43. PubMed ID: 5927986 [No Abstract] [Full Text] [Related]
18. 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]
19. Hyperprolinaemia in two successive generations of a North American Indian family. Perry TL; Hardwick DF; Lowry RB; Hansen S Ann Hum Genet; 1968 May; 31(4):401-7. PubMed ID: 4299764 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]