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2. [A system of early screening for inborn errors of metabolism: methods and results for hereditary tyrosinemia]. Bélanger M; Saint-Hilaire B; Bélanger L Union Med Can; 1973 Feb; 102(2):294-302. PubMed ID: 4709460 [No Abstract] [Full Text] [Related]
3. Diagnosis and treatment of tyrosinosis. Fairney A; Francis D; Ersser RS; Seakins JW; Cottom D Arch Dis Child; 1968 Oct; 43(231):540-7. PubMed ID: 5696464 [No Abstract] [Full Text] [Related]
4. Dietary treatment in tyrosinemia (tyrosinosis). With a note on the possible recognition of the carrier state. Gentz J; Lindblad B; Lindstedt S; Levy L; Shasteen W; Zetterstrom R Am J Dis Child; 1967 Jan; 113(1):31-7. PubMed ID: 6015903 [No Abstract] [Full Text] [Related]
5. Hereditary tyrosinemia: metabolic studies in a patient with partial p-hydroxyphenylpyruvate hydroxylase activity. Jagenburg R; Landblad B; De Maré JM; Rödjer S J Pediatr; 1972 Jun; 80(6):994-1004. PubMed ID: 5026040 [No Abstract] [Full Text] [Related]
6. Clinical significance of tyrosinemia of prematurity. Light IJ; Sutherland JM; Berry HK Am J Dis Child; 1973 Feb; 125(2):243-7. PubMed ID: 4685839 [No Abstract] [Full Text] [Related]
8. Hereditary tyrosinemia. 3. On the differential diagnosis and the lack of effect of early dietary treatment. Bodegård G; Gentz J; Lindblad B; Lindstedt S; Zetterström R Acta Paediatr Scand; 1969 Jan; 58(1):37-48. PubMed ID: 5789740 [No Abstract] [Full Text] [Related]
9. Recovery after dietary treatment of an infant with features of tyrosinosis. Harries JT; Seakins JW; Ersser RS; Lloyd JK Arch Dis Child; 1969 Apr; 44(234):258-67. PubMed ID: 5779435 [No Abstract] [Full Text] [Related]
10. 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]
11. Dietary treatment in hyperprolinaemia type II. Similä S Acta Paediatr Scand; 1974 Mar; 63(2):249-56. PubMed ID: 4820590 [No Abstract] [Full Text] [Related]
12. Recent advances in the early detection and treatment of inborn errors with brain damage. Bickel H Neuropadiatrie; 1969; 1(1):1-11. PubMed ID: 4942066 [No Abstract] [Full Text] [Related]
18. 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]
19. [Hereditary tyrosinemia. II. Presentation of a system of detection]. Bélanger M; Saint-Hilaire B Pediatrie; 1973; 28(1):19-22. PubMed ID: 4715464 [No Abstract] [Full Text] [Related]
20. Tyrosinosis: a new variant. Zaleski WA; Hill A Can Med Assoc J; 1973 Feb; 108(4):477 passim. PubMed ID: 4687372 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]