176 related articles for article (PubMed ID: 4060342)
21. [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]
22. A novel missense mutation (C84R) in a patient with type II vitamin d-dependent rickets.
Asunis I; Marini MG; Porcu L; Meloni A; Cabriolu AL; Cao A; Moi P
Exp Clin Endocrinol Diabetes; 2010 Mar; 118(3):177-9. PubMed ID: 20146166
[TBL] [Abstract][Full Text] [Related]
23. Frequency of the IVS12 + 5G-->A splice mutation of the fumarylacetoacetate hydrolase gene in carriers of hereditary tyrosinaemia in the French Canadian population of Saguenay-Lac-St-Jean.
Poudrier J; St-Louis M; Lettre F; Gibson K; Prévost C; Larochelle J; Tanguay RM
Prenat Diagn; 1996 Jan; 16(1):59-64. PubMed ID: 8821854
[TBL] [Abstract][Full Text] [Related]
24. [Biochemical, clinical and genetic analysis of various aminoacidopathies (non-ketotic hyperglycemia, maple syrup urine disease, histidinemia, tyrosinemia)].
László A; Nagy I; Szücs L; Havass Z; Sztriha L; Svékus A; Veres E
Orv Hetil; 1992 Nov; 133(48):3075-80. PubMed ID: 1448273
[TBL] [Abstract][Full Text] [Related]
25. [Sepsis, as the presenting form of hereditary tyrosinemia type I].
Iglesias Niubo J; Riudor Taravilla E; Goma Brufau AR; Civit Colas MA; Suñé Gracia JM; Bertrán Sanges JM; Gallart Catalá A
An Esp Pediatr; 1988 Sep; 29(3):235-8. PubMed ID: 3057981
[TBL] [Abstract][Full Text] [Related]
26. Hereditary tyrosinemia type I. Self-induced correction of the fumarylacetoacetase defect.
Kvittingen EA; Rootwelt H; Brandtzaeg P; Bergan A; Berger R
J Clin Invest; 1993 Apr; 91(4):1816-21. PubMed ID: 8473520
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. [Hereditary acute tyrosinemia. a case report (author's trnasl)].
Sanjurjo P; Rodríguez Soriano J; Vallo A; Bilbao F; Loridán L
An Esp Pediatr; 1976; 9(5):547-52. PubMed ID: 999104
[TBL] [Abstract][Full Text] [Related]
29. [A hereditary disorder of vitamin D metabolism in swine. Pseudo- vitamin D deficiency rickets, type I].
Kaune R; Harmeyer J
Berl Munch Tierarztl Wochenschr; 1987 Jan; 100(1):6-13. PubMed ID: 3827809
[No Abstract] [Full Text] [Related]
30. [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]
31. [Hereditary tyrosinemia. I. Clinical and biological study of 62 cases].
Larochelle J; Privé L; Bélanger M; Bélanger L; Tremblay M; Claveau JC; Aubin G; Paradis D
Pediatrie; 1973; 28(1):5-18. PubMed ID: 4715467
[No Abstract] [Full Text] [Related]
32. [Neonatal transitory tyrosinemia and other types of tyrosinemia].
Lanza I
Minerva Pediatr; 1976 Mar; 28(11):637-43. PubMed ID: 995075
[No Abstract] [Full Text] [Related]
33. Biochemical observations on so-called hereditary tyrosinemia.
Gaull GE; Rassin DK; Solomon GE; Harris RC; Sturman JA
Pediatr Res; 1970 Jul; 4(4):337-44. PubMed ID: 4393588
[No Abstract] [Full Text] [Related]
34. [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]
35. The management of transient tyrosinemia of the newborn.
Chase HP; O'Brien D
Pediatrics; 1967 Aug; 40(2):308-9. PubMed ID: 5006599
[No Abstract] [Full Text] [Related]
36. A mouse model for human hereditary tyrosinemia I.
Holdener BC; Magnuson T
Bioessays; 1994 Feb; 16(2):85-7. PubMed ID: 8147847
[No Abstract] [Full Text] [Related]
37. [Hereditary tyrosinemia].
Halvorsen S
Ugeskr Laeger; 1979 Sep; 141(37):2540-1. PubMed ID: 483445
[No Abstract] [Full Text] [Related]
38. Genetic aspects of tyrosinemia.
Dallaire L
Can Med Assoc J; 1967 Oct; 97(18):1098-9. PubMed ID: 6050913
[No Abstract] [Full Text] [Related]
39. The enzymatic deficiency in tyrosinemia.
Du BN
Can Med Assoc J; 1967 Oct; 97(18):1076-8. PubMed ID: 6050909
[No Abstract] [Full Text] [Related]
40. [Hereditary tyrosinemia with tyrosiluria. Study of 44 cases in infants].
Larochelle J; Privé L; Saidi M; Bélanger M; Tremblay M; Claveau JC; Aubin G
Union Med Can; 1968 Jun; 97(6):762-72. PubMed ID: 5758623
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
