291 related articles for article (PubMed ID: 6712098)
1. [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]
2. 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]
3. 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]
4. [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]
5. [Hereditary tyrosinemia and vitamin-dependent rickets in Saguenay. A genetic and demographic approach].
Bouchard G; Laberge C; Scriver CR
Union Med Can; 1985 Aug; 114(8):633-6. PubMed ID: 4060342
[No Abstract] [Full Text] [Related]
6. [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]
7. [Hereditary tyrosinemia].
Rubecz I; Gombos A; Klujber L; Kádas I; Sipos J
Orv Hetil; 1985 Dec; 126(51):3141-5. PubMed ID: 4080375
[No Abstract] [Full Text] [Related]
8. [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]
9. [Tyrosinemia].
Salo MK
Duodecim; 1992; 108(9):841-3. PubMed ID: 1366298
[No Abstract] [Full Text] [Related]
10. [Existence of alpha-1-fetoprotein in 8 patients with hereditary tyrosinemia. Preliminary report].
Bélanger L; Bélanger M; Larochelle J
Union Med Can; 1972 May; 101(5):877-8. PubMed ID: 4666892
[No Abstract] [Full Text] [Related]
11. 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]
12. [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]
13. Hereditary tyrosinemia and tyrosyluria: clinical report of four patients.
Scriver CR; Silverberg M; Clow CL
Can Med Assoc J; 1967 Oct; 97(18):1047-50. PubMed ID: 6050903
[No Abstract] [Full Text] [Related]
14. [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]
15. Tyrosinemia without liver or renal damage with plantar and palmar keratosis and keratitis (hypertyrosinemia type II).
Pelet B; Antener I; Faggioni R; Spahr A; Gautier E
Helv Paediatr Acta; 1979 May; 34(2):177-83. PubMed ID: 156708
[TBL] [Abstract][Full Text] [Related]
16. [Tyrosinemia II].
Kalimo K; Ivaska K; Koistinen T; Havu VK
Duodecim; 1985; 101(16):1585-9. PubMed ID: 2865123
[No Abstract] [Full Text] [Related]
17. 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]
18. Hereditary tyrosinemia.
Mardesić D; Crnojević-Ivanusić R; Lipovac K; Simunić I; Katona G
Acta Med Iugosl; 1979 Dec; 33(5):471-88. PubMed ID: 543455
[No Abstract] [Full Text] [Related]
19. Phenylalanine-tyrosine deficiency syndrome as a complication of the management of hereditary tyrosinemia.
Cohn RM; Yudkoff M; Yost B; Segal S
Am J Clin Nutr; 1977 Feb; 30(2):209-14. PubMed ID: 835507
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]