234 related articles for article (PubMed ID: 3057981)
1. [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]
2. Hereditary tyrosinemia type I--an overview.
Kvittingen EA
Scand J Clin Lab Invest Suppl; 1986; 184():27-34. PubMed ID: 3296130
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. Effect of dietary treatment on the renal tubular function in a patient with hereditary tyrosinemia.
Suzuki Y; Konda M; Imai I; Imamura H; Shimao S; Okaka T
Int J Pediatr Nephrol; 1987; 8(3):171-6. PubMed ID: 3429140
[TBL] [Abstract][Full Text] [Related]
5. Evidence for liver disease preceding amino acid abnormalities in hereditary tyrosinemia.
Hostetter MK; Levy HL; Winter HS; Knight GJ; Haddow JE
N Engl J Med; 1983 May; 308(21):1265-7. PubMed ID: 6188953
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. [Hereditary tyrosinemia and alpha-1-fetoprotein. I. Clinical value of alpha-fetoprotein in hereditary tyrosinemia].
Bélanger L; Bélanger M; Prive L; Larochelle J; Tremblay M; Aubin G
Pathol Biol (Paris); 1973 May; 21(5):449-55. PubMed ID: 4125220
[No Abstract] [Full Text] [Related]
8. 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]
9. Dietary treatment of tyrosinemia type I: importance of methionine restriction.
Michals K; Matolon R; Wong PW
J Am Diet Assoc; 1978 Nov; 73(5):507-14. PubMed ID: 701680
[TBL] [Abstract][Full Text] [Related]
10. [Incurable keratitis and chronic palmoplantar hyperkeratosis with hypertyrosinemia. Cure using a tyrosine-restricted diet. Type II tyrosinemia].
Hervé F; Moreno JL; Ogier H; Saudubray JM; De Prost Y; Duffier JL; Charpentier C; Lemonnier F; Frézal J
Arch Fr Pediatr; 1986 Jan; 43(1):19-22. PubMed ID: 2939812
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A single mutation of the fumarylacetoacetate hydrolase gene in French Canadians with hereditary tyrosinemia type I.
Grompe M; St-Louis M; Demers SI; al-Dhalimy M; Leclerc B; Tanguay RM
N Engl J Med; 1994 Aug; 331(6):353-7. PubMed ID: 8028615
[TBL] [Abstract][Full Text] [Related]
13. The nephropathy of type I tyrosinemia after liver transplantation.
Laine J; Salo MK; Krogerus L; Kärkkäinen J; Wahlroos O; Holmberg C
Pediatr Res; 1995 May; 37(5):640-5. PubMed ID: 7603784
[TBL] [Abstract][Full Text] [Related]
14. [Juvenile form of tyrosinemia type I].
Nothjunge J; Rosendahl W
Klin Padiatr; 1989; 201(6):458-63. PubMed ID: 2601281
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of hereditary tyrosinemia.
Steinmann B; Gitzelmann R; Kvittingen EA; Stokke O
N Engl J Med; 1984 Mar; 310(13):855-6. PubMed ID: 6700679
[No Abstract] [Full Text] [Related]
16. [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]
17. 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]
18. [Palmoplantar keratosis associated with keratitis: hereditary hypertyrosinemia treated by diet].
Ogier H; Hervé F; Saudubray JM; Dufier JL; Charpentier C; Lemonnier F; Moreno JL; Frezal J
Ann Med Interne (Paris); 1986; 137(2):129-32. PubMed ID: 2940955
[TBL] [Abstract][Full Text] [Related]
19. [A case of Richner-Hanhart syndrome (tyrosinosis with ocular, cutaneous and mental manifestations].
Goddé-Jolly D; Larregue M; Roussat B; Van Effenterre G
J Fr Ophtalmol; 1979 Jan; 2(1):23-8. PubMed ID: 34642
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
