Literature DB >> 11232358

Nontransplant treatment of tyrosinemia.

E Holme1, S Lindstedt.   

Abstract

NTBC treatment has greatly improved the survival of patients with acute tyrosinemia and has reduced the need for liver transplantation during early childhood. In patients in whom treatment with NTBC was started early in life, 2 cases (1%) of HCC have occurred during the first year of treatment, but no further cases have occurred among these patients, who have been followed for up to 9 years. In patients with late start of NTBC treatment, there is a considerable risk for liver malignancy. The risk for malignancy in this group of patients must be evaluated on an individual basis, taking into account the phenotype and clinical status of the patient. Porphyric crises are not seen in patients who comply with the medication regimen. NTBC is a well-tolerated drug with few adverse effects.

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Year:  2000        PMID: 11232358     DOI: 10.1016/s1089-3261(05)70142-2

Source DB:  PubMed          Journal:  Clin Liver Dis        ISSN: 1089-3261            Impact factor:   6.126


  36 in total

1.  Hereditary tyrosinemia type 1 from a single center in Egypt: clinical study of 22 cases.

Authors:  Hanaa El-Karaksy; Mona Fahmy; Mona El-Raziky; Nehal El-Koofy; Rokaya El-Sayed; Mohamed S Rashed; Hasan El-Kiki; Ahmad El-Hennawy; Nabil Mohsen
Journal:  World J Pediatr       Date:  2011-06-01       Impact factor: 2.764

2.  Single dose NTBC-treatment of hereditary tyrosinemia type I.

Authors:  A Schlune; E Thimm; D Herebian; U Spiekerkoetter
Journal:  J Inherit Metab Dis       Date:  2012-02-04       Impact factor: 4.982

3.  Neurocognitive outcome in patients with hypertyrosinemia type I after long-term treatment with NTBC.

Authors:  Eva Thimm; Renate Richter-Werkle; Gudrun Kamp; Bettina Molke; Diran Herebian; Dirk Klee; Ertan Mayatepek; Ute Spiekerkoetter
Journal:  J Inherit Metab Dis       Date:  2011-11-09       Impact factor: 4.982

4.  In vivo selection of transplanted hepatocytes by pharmacological inhibition of fumarylacetoacetate hydrolase in wild-type mice.

Authors:  Nicole K Paulk; Karsten Wursthorn; Annelise Haft; Carl Pelz; Gregory Clarke; Amy H Newell; Susan B Olson; Cary O Harding; Milton J Finegold; Raymond L Bateman; John F Witte; Ronald McClard; Markus Grompe
Journal:  Mol Ther       Date:  2012-08-07       Impact factor: 11.454

Review 5.  Treatment strategies for acute metabolic disorders in neonates.

Authors:  Sarar Mohamed
Journal:  Sudan J Paediatr       Date:  2011

Review 6.  CRISPR/Cas9: at the cutting edge of hepatology.

Authors:  Francis P Pankowicz; Kelsey E Jarrett; William R Lagor; Karl-Dimiter Bissig
Journal:  Gut       Date:  2017-05-09       Impact factor: 23.059

7.  Cost-Consequence Analysis of Nitisinone for Treatment of Tyrosinemia Type I.

Authors:  Mariève Simoncelli; Johanne Samson; Jean-François Bussières; Jacques Lacroix; Marc Dorais; Renaldo Battista; Sylvie Perreault
Journal:  Can J Hosp Pharm       Date:  2015 May-Jun

8.  Clinical practice. NTBC therapy for tyrosinemia type 1: how much is enough?

Authors:  Hanaa El-Karaksy; Mohmmad Rashed; Rokaya El-Sayed; Mona El-Raziky; Nehal El-Koofy; Manal El-Hawary; Osama Al-Dirbashi
Journal:  Eur J Pediatr       Date:  2009-10-31       Impact factor: 3.183

9.  NTBC treatment in tyrosinaemia type I: long-term outcome in French patients.

Authors:  A Masurel-Paulet; J Poggi-Bach; M-O Rolland; O Bernard; N Guffon; D Dobbelaere; J Sarles; H Ogier de Baulny; G Touati
Journal:  J Inherit Metab Dis       Date:  2008-01-25       Impact factor: 4.982

Review 10.  New management options for end-stage chronic liver disease and acute liver failure: potential for pediatric patients.

Authors:  Dominique Debray; Nadya Yousef; Philippe Durand
Journal:  Paediatr Drugs       Date:  2006       Impact factor: 3.022

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