258 related articles for article (PubMed ID: 25564536)
1. Outcome of children with hereditary tyrosinaemia following newborn screening.
McKiernan PJ; Preece MA; Chakrapani A
Arch Dis Child; 2015 Aug; 100(8):738-41. PubMed ID: 25564536
[TBL] [Abstract][Full Text] [Related]
2. Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in Québec.
Larochelle J; Alvarez F; Bussières JF; Chevalier I; Dallaire L; Dubois J; Faucher F; Fenyves D; Goodyer P; Grenier A; Holme E; Laframboise R; Lambert M; Lindstedt S; Maranda B; Melançon S; Merouani A; Mitchell J; Parizeault G; Pelletier L; Phan V; Rinaldo P; Scott CR; Scriver C; Mitchell GA
Mol Genet Metab; 2012 Sep; 107(1-2):49-54. PubMed ID: 22885033
[TBL] [Abstract][Full Text] [Related]
3. Long-term safety and outcomes in hereditary tyrosinaemia type 1 with nitisinone treatment: a 15-year non-interventional, multicentre study.
Spiekerkoetter U; Couce ML; Das AM; de Laet C; Dionisi-Vici C; Lund AM; Schiff M; Spada M; Sparve E; Szamosi J; Vara R; Rudebeck M
Lancet Diabetes Endocrinol; 2021 Jul; 9(7):427-435. PubMed ID: 34023005
[TBL] [Abstract][Full Text] [Related]
4. Nitisinone in the treatment of hereditary tyrosinaemia type 1.
McKiernan PJ
Drugs; 2006; 66(6):743-50. PubMed ID: 16706549
[TBL] [Abstract][Full Text] [Related]
5. Tyrosinemia type 1 in Spain: mutational analysis, treatment and long-term outcome.
Couce ML; Dalmau J; del Toro M; Pintos-Morell G; Aldámiz-Echevarría L;
Pediatr Int; 2011 Dec; 53(6):985-9. PubMed ID: 21752152
[TBL] [Abstract][Full Text] [Related]
6. Experience of nitisinone for the pharmacological treatment of hereditary tyrosinaemia type 1.
Santra S; Baumann U
Expert Opin Pharmacother; 2008 May; 9(7):1229-36. PubMed ID: 18422479
[TBL] [Abstract][Full Text] [Related]
7. Early nitisinone treatment reduces the need for liver transplantation in children with tyrosinaemia type 1 and improves post-transplant renal function.
Bartlett DC; Lloyd C; McKiernan PJ; Newsome PN
J Inherit Metab Dis; 2014 Sep; 37(5):745-52. PubMed ID: 24515874
[TBL] [Abstract][Full Text] [Related]
8. Evolution of tyrosinemia type 1 disease in patients treated with nitisinone in Spain.
Couce ML; Sánchez-Pintos P; Aldámiz-Echevarría L; Vitoria I; Navas V; Martín-Hernández E; García-Volpe C; Pintos G; Peña-Quintana L; Hernández T; Gil D; Sánchez-Valverde F; Bueno M; Roca I; López-Ruzafa E; Díaz-Fernández C
Medicine (Baltimore); 2019 Sep; 98(39):e17303. PubMed ID: 31574857
[TBL] [Abstract][Full Text] [Related]
9. Hereditary tyrosinemia type 1 in Turkey: twenty year single-center experience.
Zeybek AC; Kiykim E; Soyucen E; Cansever S; Altay S; Zubarioglu T; Erkan T; Aydin A
Pediatr Int; 2015 Apr; 57(2):281-9. PubMed ID: 25223216
[TBL] [Abstract][Full Text] [Related]
10. Neonatal screening for hereditary tyrosinaemia: are we there yet?
Hadžić N; Vara R
Arch Dis Child; 2015 Aug; 100(8):720-1. PubMed ID: 25957320
[No Abstract] [Full Text] [Related]
11. The Québec NTBC Study.
; Alvarez F; Atkinson S; Bouchard M; Brunel-Guitton C; Buhas D; Bussières JF; Dubois J; Fenyves D; Goodyer P; Gosselin M; Halac U; Labbé P; Laframboise R; Maranda B; Melançon S; Merouani A; Mitchell GA; Mitchell J; Parizeault G; Pelletier L; Phan V; Turcotte JF
Adv Exp Med Biol; 2017; 959():187-195. PubMed ID: 28755196
[TBL] [Abstract][Full Text] [Related]
12. The outcome of seven patients with hereditary tyrosinemia type 1.
Gokay S; Ustkoyuncu PS; Kardas F; Kendirci M
J Pediatr Endocrinol Metab; 2016 Oct; 29(10):1151-1157. PubMed ID: 27682708
[TBL] [Abstract][Full Text] [Related]
13. Type 1 tyrosinemia in Finland: a nationwide study.
Äärelä L; Hiltunen P; Soini T; Vuorela N; Huhtala H; Nevalainen PI; Heikinheimo M; Kivelä L; Kurppa K
Orphanet J Rare Dis; 2020 Oct; 15(1):281. PubMed ID: 33046095
[TBL] [Abstract][Full Text] [Related]
14. Experience with NTBC therapy in hereditary tyrosinaemia type I: an alternative to liver transplantation.
Joshi SN; Venugopalan P
Ann Trop Paediatr; 2004 Sep; 24(3):259-65. PubMed ID: 15479577
[TBL] [Abstract][Full Text] [Related]
15. Nitisinone: new drug. Type 1 tyrosinemia: an effective drug.
Prescrire Int; 2007 Apr; 16(88):56-8. PubMed ID: 17458044
[TBL] [Abstract][Full Text] [Related]
16. Recommendations for the management of tyrosinaemia type 1.
de Laet C; Dionisi-Vici C; Leonard JV; McKiernan P; Mitchell G; Monti L; de Baulny HO; Pintos-Morell G; Spiekerkötter U
Orphanet J Rare Dis; 2013 Jan; 8():8. PubMed ID: 23311542
[TBL] [Abstract][Full Text] [Related]
17. Plasma succinylacetone is persistently raised after liver transplantation in tyrosinaemia type 1.
Bartlett DC; Preece MA; Holme E; Lloyd C; Newsome PN; McKiernan PJ
J Inherit Metab Dis; 2013 Jan; 36(1):15-20. PubMed ID: 22456946
[TBL] [Abstract][Full Text] [Related]
18. In brief: Nitisinone (Orfadin) for hereditary tyrosinemia.
Med Lett Drugs Ther; 2016 Oct; 58(1505):e132. PubMed ID: 27701365
[No Abstract] [Full Text] [Related]
19. [New drugs; nitisinone].
Cohen AF; van Bronswijk H
Ned Tijdschr Geneeskd; 2006 Nov; 150(46):2541-2. PubMed ID: 17152330
[TBL] [Abstract][Full Text] [Related]
20. The fate of tyrosinaemic Hungarian patients before the NTBC aera.
László A; Rózsa M; Sallay E; Tiszlavicz L; Janovszky A; Várkonyi A; Karg E; Wittmann G; Túri S; Ugarte M
Ideggyogy Sz; 2013 Nov; 66(11-12):415-9. PubMed ID: 24555242
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
