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Journal Abstract Search
196 related items for PubMed ID: 8271141
1. Promising new treatment for type I tyrosinemia. Heubi JE. J Pediatr Gastroenterol Nutr; 1993 Oct; 17(3):340-1. PubMed ID: 8271141 [No Abstract] [Full Text] [Related]
3. NTBC as palliative treatment in chronic tyrosinaemia type I. Ros J, Vilaseca MA, Lambruschini N, Mas A, Lindstedt S, Holme E. J Inherit Metab Dis; 1999 Jun; 22(5):665-6. PubMed ID: 10399099 [No Abstract] [Full Text] [Related]
6. Plasma antioxidant capacity in two cases of tyrosinaemia type 1: one case treated with NTBC. Bird S, Miller NJ, Collins JE, Rice-Evans CA. J Inherit Metab Dis; 1995 Jun; 18(2):123-6. PubMed ID: 7564225 [No Abstract] [Full Text] [Related]
8. Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase. Lindstedt S, Holme E, Lock EA, Hjalmarson O, Strandvik B. Lancet; 1992 Oct 03; 340(8823):813-7. PubMed ID: 1383656 [Abstract] [Full Text] [Related]
9. Inhibition of 4-hydroxyphenylpyruvate dioxygenase by 2-(2-nitro-4-trifluoromethylbenzoyl)-cyclohexane-1,3-dione and 2-(2-chloro-4-methanesulfonylbenzoyl)-cyclohexane-1,3-dione. Mitchell GA. Hum Exp Toxicol; 1996 Feb 03; 15(2):179-81. PubMed ID: 8645506 [No Abstract] [Full Text] [Related]
13. [Late onset type I tyrosinemia]. Klujber V, Sallai A, Kálmánchey R, Szönyi L, Hosszú E. Orv Hetil; 1997 Jul 13; 138(28):1805-8. PubMed ID: 9280876 [Abstract] [Full Text] [Related]
14. Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenase. Gibbs TC, Payan J, Brett EM, Lindstedt S, Holme E, Clayton PT. J Neurol Neurosurg Psychiatry; 1993 Oct 13; 56(10):1129-32. PubMed ID: 8410015 [Abstract] [Full Text] [Related]
16. From toxicological problem to therapeutic use: the discovery of the mode of action of 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC), its toxicology and development as a drug. Lock EA, Ellis MK, Gaskin P, Robinson M, Auton TR, Provan WM, Smith LL, Prisbylla MP, Mutter LC, Lee DL. J Inherit Metab Dis; 1998 Aug 13; 21(5):498-506. PubMed ID: 9728330 [Abstract] [Full Text] [Related]
17. Diagnosis and management of tyrosinemia type I. Holme E, Lindstedt S. Curr Opin Pediatr; 1995 Dec 13; 7(6):726-32. PubMed ID: 8776026 [Abstract] [Full Text] [Related]
19. Therapeutic trials in the murine model of hereditary tyrosinaemia type I: a progress report. Grompe M, Overturf K, al-Dhalimy M, Finegold M. J Inherit Metab Dis; 1998 Aug 13; 21(5):518-31. PubMed ID: 9728332 [Abstract] [Full Text] [Related]
20. Experience of nitisinone for the pharmacological treatment of hereditary tyrosinaemia type 1. Santra S, Baumann U. Expert Opin Pharmacother; 2008 May 13; 9(7):1229-36. PubMed ID: 18422479 [Abstract] [Full Text] [Related] Page: [Next] [New Search]