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22. [Disorders in the tyrosine metabolism. II. Tyrosinemia - a congenital metabolic disorder]. Vulović D; Hajduković R; Sindjić M; FilipovićD ; Dozić S Srp Arh Celok Lek; 1974 Jan; 102(1):9-20. PubMed ID: 4368107 [No Abstract] [Full Text] [Related]
23. Serum type III procollagen in children with type I hereditary tyrosinemia. Pitkänen S; Salo MK; Vettenranta K; Näntö-Salonen K; Heikinheimo M J Pediatr Gastroenterol Nutr; 1999 Jul; 29(1):38-41. PubMed ID: 10400101 [TBL] [Abstract][Full Text] [Related]
24. Special imaging casebook. Hereditary tyrosinemia, acute type I. Herman TE; McAlister WH; Siegel MJ J Perinatol; 1997; 17(1):87-90. PubMed ID: 9069074 [No Abstract] [Full Text] [Related]
25. [Hereditary tyrosinemia: examination of the liver by electron microscopy of hepatic biopsies: observation of 7 cases]. Tremblay M; Bélanger L; Larochelle J; Privé L; Gagnon PM Union Med Can; 1977 Jul; 106(7):1014-6. PubMed ID: 898402 [No Abstract] [Full Text] [Related]
26. [Tyrosinosis. A difficult diagnosis of late infancy]. Bertolani MF; Pellegrino AM; Summa C; Scalera E Minerva Pediatr; 1990; 42(1-2):1-7. PubMed ID: 2159592 [TBL] [Abstract][Full Text] [Related]
28. [Hereditary tyrosinemia. IV. Pathogenesis. New therapeutic perspectives]. Bélanger L; Larochelle J; Bélanger M; Privé L Pediatrie; 1973; 28(1):35-55. PubMed ID: 4715466 [No Abstract] [Full Text] [Related]
29. Neurologic crises in hereditary tyrosinemia. Mitchell G; Larochelle J; Lambert M; Michaud J; Grenier A; Ogier H; Gauthier M; Lacroix J; Vanasse M; Larbrisseau A N Engl J Med; 1990 Feb; 322(7):432-7. PubMed ID: 2153931 [TBL] [Abstract][Full Text] [Related]
30. [Renal involvement in type I tyrosinemia]. Cochat P; Guibaud P; Baverel G Arch Pediatr; 1994 Apr; 1(4):417-8. PubMed ID: 7842099 [No Abstract] [Full Text] [Related]
31. [Dietary management of hereditary tyrosinemia. Apropos of 7 cases]. Jehan P; Buchman M; Odièvre M Ann Pediatr (Paris); 1984 Jan; 31(1):33-40. PubMed ID: 6712098 [No Abstract] [Full Text] [Related]
32. [Hereditary tyrosinemia in an acute form: a case report (author's transl)]. Di Battista C; Rossi L; Marcelli P; Di Saverio P; Laudizi Z; Moretti P Pediatr Med Chir; 1981; 3(1):101-4. PubMed ID: 6975468 [No Abstract] [Full Text] [Related]
39. The phenotypic manifestations of hereditary tyrosinemia and tyrosyluria: a hypothesis. Scriver CR Can Med Assoc J; 1967 Oct; 97(18):1073-5. PubMed ID: 6050908 [No Abstract] [Full Text] [Related]
40. [Presentation of a case of chronic type 1 tyrosinemia. Diet therapy and clinical outcome]. Gabrielli O; Maiorana A; Paris D; Zanobini R; Renda B; Montali U; Coppa G Minerva Pediatr; 1978 Aug; 30(16):1329-34. PubMed ID: 692506 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]