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11. [Physiopathological considerations on the limits of detection of certain metabolic syndromes of the cystinuria-cystinosis type. Possibilities of rapid diagnosis]. Pâtea P; Tănase-Mogos I; Ciortoloman H; Petrescu L; Ciucă C; Orăşeanu D; Jemna M; Meila P Physiologie; 1980; 17(2):113-20. PubMed ID: 6770383 [No Abstract] [Full Text] [Related]
12. [Histidinemia--with special reference to screening and treatment]. Matsuda I; Shinozuka S; Hayashida T Nihon Rinsho; 1978 May; Suppl():1344-5. PubMed ID: 691347 [No Abstract] [Full Text] [Related]
15. Amino acid excretion in infancy and early childhood. A survey of 200,000 infants. Turner B; Brown DA Med J Aust; 1972 Jan; 1(2):62-5. PubMed ID: 5025157 [No Abstract] [Full Text] [Related]
16. Screening for inherited metabolic disease in Wales using urine-impregnated filter paper. Bradley DM Arch Dis Child; 1975 Apr; 50(4):264-8. PubMed ID: 1147666 [TBL] [Abstract][Full Text] [Related]
17. [Clinical and biochemical study of a case of histidinemia]. Beauvais P; Klein F; Humbel R; Dreyfus J; Gast Arch Fr Pediatr; 1971 Feb; 28(2):191-203. PubMed ID: 5574024 [No Abstract] [Full Text] [Related]
18. Sibship with histidinemia and an unrelated encephalopathy. Clinical and biochemical studies. Brown ES; Waisman HA; Geison RL; Gerritsen T Helv Paediatr Acta; 1977 Nov; 32(4-5):401-11. PubMed ID: 617985 [TBL] [Abstract][Full Text] [Related]
19. Variations in clinical and laboratory findings in histidinemia. Waisman HA Am J Dis Child; 1967 Jan; 113(1):93-4. PubMed ID: 6015914 [No Abstract] [Full Text] [Related]