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26. Enzyme defect in a case of tyrosinemia type I, acute form. Furukawa N; Kinugasa A; Seo T; Ishii T; Ota T; Machida Y; Inoue F; Imashuku S; Kusunoki T; Takamatsu T Pediatr Res; 1984 May; 18(5):463-6. PubMed ID: 6145143 [TBL] [Abstract][Full Text] [Related]
27. New forms of hereditary tyrosinemia type II in mink: hepatic tyrosine aminotransferase defect. Christensen K; Henriksen P; Sørensen H Hereditas; 1986; 104(2):215-22. PubMed ID: 2876972 [No Abstract] [Full Text] [Related]
28. Novel and recurrent tyrosine aminotransferase gene mutations in tyrosinemia type II. Hühn R; Stoermer H; Klingele B; Bausch E; Fois A; Farnetani M; Di Rocco M; Boué J; Kirk JM; Coleman R; Scherer G Hum Genet; 1998 Mar; 102(3):305-13. PubMed ID: 9544843 [TBL] [Abstract][Full Text] [Related]
30. Tyrosinaemia type II (Richner-Hanhart syndrome)--report of two cases treated with etretinate. Fraser NG; MacDonald J; Griffiths WA; McPhie JL Clin Exp Dermatol; 1987 Nov; 12(6):440-3. PubMed ID: 2974325 [No Abstract] [Full Text] [Related]
31. Richner-Hanhart syndrome (tyrosinemia type II): a case report of delayed diagnosis with pseudodendritic corneal lesion. Iskeleli G; Bilgeç MD; Arici C; Atalay E; Oğreden T; Aydin A Turk J Pediatr; 2011; 53(6):692-4. PubMed ID: 22389994 [TBL] [Abstract][Full Text] [Related]
32. [Oculocutaneous type II tyrosinosis]. Podglajen-Wecxsteen O; Delaporte E; Piette F; le Flohic X; Bergoend H Ann Dermatol Venereol; 1993; 120(2):139-42. PubMed ID: 8363306 [TBL] [Abstract][Full Text] [Related]
33. Tyrosine aminotransferase deficiency in mink (Mustela vision): a model for human tyrosinemia II. Goldsmith LA; Thorpe JM; Marsh RF Biochem Genet; 1981 Aug; 19(7-8):687-93. PubMed ID: 6117279 [TBL] [Abstract][Full Text] [Related]
34. The Richner-Hanhart syndrome: report of a case with associated tyrosinemia. Bienfang DC; Kuwabara T; Pueschel SM Arch Ophthalmol; 1976 Jul; 94(7):1133-7. PubMed ID: 180943 [TBL] [Abstract][Full Text] [Related]
35. Richner-Hanhart syndrome (tyrosinaemia-II) (report of four cases without ocular involvement). Rehák A; Selim MM; Yadav G Br J Dermatol; 1981 Apr; 104(4):469-75. PubMed ID: 6453606 [TBL] [Abstract][Full Text] [Related]
36. Richner-Hanhart syndrome: importance of early diagnosis and early intervention. Tallab TM J Am Acad Dermatol; 1996 Nov; 35(5 Pt 2):857-9. PubMed ID: 8912606 [TBL] [Abstract][Full Text] [Related]
37. Defect in soluble tyrosine aminotransferase in skin fibroblasts of a patient with tyrosinemia. deGroot GW; Dakshinamurti K; Allan L; Haworth JC Pediatr Res; 1980 Jul; 14(7):896-8. PubMed ID: 6106182 [No Abstract] [Full Text] [Related]
38. Enzymatic studies in a case of hereditary tyrosinemia with hepatoma. Gentz J; Heinrich J; Lindblad B; Lindstedt S; Zetterström R Acta Paediatr Scand; 1969 Jul; 58(4):393-6. PubMed ID: 4390478 [No Abstract] [Full Text] [Related]