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4. 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 24; 48(2):225-31. PubMed ID: 5560617 [No Abstract] [Full Text] [Related]
5. [Familial hyperprolinemia with nephropathy]. Ortuño Mirete J, Guardiola Vicente JM, Botella García J. Rev Clin Esp; 1970 Jul 31; 118(2):141-50. PubMed ID: 5486371 [No Abstract] [Full Text] [Related]
9. [Acute leucinosis, normal psychomotor development at one year of age]. Costil J, Aymard P, Repesse G, Richardet JM, Brissaud HE. Ann Med Interne (Paris); 1971 Dec 31; 122(12):1273-8. PubMed ID: 5170224 [No Abstract] [Full Text] [Related]
17. [Hyperprolinemia type II]. Thomsen B, Vetner M, Rosleff F, Reske-Nielsen E. Ugeskr Laeger; 1974 Nov 04; 136(45):2530. PubMed ID: 4420281 [No Abstract] [Full Text] [Related]
18. Evidence for delayed histidine transamination in neonates with histidinemia. Levy HL, Madigan PM, Peneva P. Pediatrics; 1971 Jan 04; 47(1):128-32. PubMed ID: 5547620 [No Abstract] [Full Text] [Related]
19. [A case of type I hyperprolinemia associated with photogenic epilepsy]. Ishikawa Y, Kameda K, Okabe M, Imai T, Nagaoka M, Minami R. No To Hattatsu; 1991 Jan 04; 23(1):81-6. PubMed ID: 1994998 [Abstract] [Full Text] [Related]