I型酪氨酸血症：治疗策略的考量以及风险评估、饮食和移植方面的经验 - Suppr

Suppr

超能文献

Tyrosinaemia type I: considerations of treatment strategy and experiences with risk assessment, diet and transplantation.

作者信息

van Spronsen F J, Smit G P, Wijburg F A, Thomasse Y, Visser G, Heymans H S

机构信息

Beatrix Children's University Hospital, Groningen, The Netherlands.

出版信息

J Inherit Metab Dis. 1995;18(2):111-4. doi: 10.1007/BF00711742.

DOI:10.1007/BF00711742

PMID:7564222

Abstract

摘要

相似文献

Tyrosinaemia type I: considerations of treatment strategy and experiences with risk assessment, diet and transplantation.

J Inherit Metab Dis. 1995;18(2):111-4. doi: 10.1007/BF00711742.

Liver transplantation in tyrosinaemia type I: the Groningen experience.

J Inherit Metab Dis. 1995;18(2):115-8. doi: 10.1007/BF00711743.

Liver transplantation in nine Spanish patients with tyrosinaemia type I.

J Inherit Metab Dis. 1995;18(2):119-22. doi: 10.1007/BF00711744.

Outcome in tyrosinaemia type II.

Arch Dis Child. 1991 Oct;66(10):1249-50. doi: 10.1136/adc.66.10.1249.

Outcome of therapy of hereditary tyrosinemia.

Acta Paediatr Jpn. 1988 Aug;30(4):425-8. doi: 10.1111/j.1442-200x.1988.tb02532.x.

Hepatic imaging with computed tomography of chronic tyrosinaemia type 1.

Br J Radiol. 1990 Aug;63(752):605-8. doi: 10.1259/0007-1285-63-752-605.

Hepatic tyrosine aminotransferase in tyrosinaemia type II.

J Inherit Metab Dis. 1982;5(4):229-30. doi: 10.1007/BF02179149.

Neurological crisis in hereditary tyrosinaemia and complete reversal after liver transplantation.

Arch Dis Child. 1994 Jun;70(6):544-5. doi: 10.1136/adc.70.6.544.

Tyrosinaemia type I and hypertrophic obstructive cardiomyopathy.

Lancet. 1987 Jun 20;1(8547):1437-8. doi: 10.1016/s0140-6736(87)90631-3.

Plasma amino acid disturbance in infancy. I: Hypermethioninaemia and transient tyrosinaemia.

Arch Dis Child. 1969 Jun;44(235):418-21. doi: 10.1136/adc.44.235.418.

引用本文的文献

Decoding hepatorenal tyrosinemia type 1: Unraveling the impact of early detection, NTBC, and the role of liver transplantation.

Can Liver J. 2024 Feb 26;7(1):54-63. doi: 10.3138/canlivj-2023-0018. eCollection 2024 Feb.

Long-Term Outcomes and Practical Considerations in the Pharmacological Management of Tyrosinemia Type 1.

Paediatr Drugs. 2019 Dec;21(6):413-426. doi: 10.1007/s40272-019-00364-4.

Experience of a Single Center in NTBC Use in Management of Hereditary Tyrosinemia Type I in Libya.

Iran J Pediatr. 2015 Oct;25(5):e3608. doi: 10.5812/ijp.3608. Epub 2015 Oct 6.

Single amino acid supplementation in aminoacidopathies: a systematic review.

Orphanet J Rare Dis. 2014 Jan 13;9:7. doi: 10.1186/1750-1172-9-7.

Mutation spectrum of fumarylacetoacetase gene and clinical aspects of tyrosinemia type I disease.

JIMD Rep. 2011;1:17-21. doi: 10.1007/8904_2011_10. Epub 2011 Jun 22.

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

J Inherit Metab Dis. 2012 Mar;35(2):263-8. doi: 10.1007/s10545-011-9394-5. Epub 2011 Nov 9.

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

J Inherit Metab Dis. 2008 Feb;31(1):81-7. doi: 10.1007/s10545-008-0793-1. Epub 2008 Jan 25.

Nitisinone in the treatment of hereditary tyrosinaemia type 1.

Drugs. 2006;66(6):743-50. doi: 10.2165/00003495-200666060-00002.

Renal function in tyrosinaemia type I after liver transplantation: a long-term follow-up.

J Inherit Metab Dis. 2005;28(6):871-6. doi: 10.1007/s10545-005-0059-0.

Therapeutic trials in the murine model of hereditary tyrosinaemia type I: a progress report.

J Inherit Metab Dis. 1998 Aug;21(5):518-31. doi: 10.1023/a:1005462804271.

本文引用的文献

Hereditary tyrosinemia type I: a new clinical classification with difference in prognosis on dietary treatment.

Hepatology. 1994 Nov;20(5):1187-91.

Liver transplantation in tyrosinaemia type I: the Groningen experience.

J Inherit Metab Dis. 1995;18(2):115-8. doi: 10.1007/BF00711743.

Pediatric liver transplantation.

Transplant Proc. 1987 Aug;19(4):3230-5.

Tyrosinaemia type I: orthotopic liver transplantation as the only definitive answer to a metabolic as well as an oncological problem.

J Inherit Metab Dis. 1989;12 Suppl 2:339-42. doi: 10.1007/BF03335416.

Liver transplantation for hereditary tyrosinemia in the presence of hepatocellular carcinoma.

Transplant Proc. 1989 Feb;21(1 Pt 2):2445-6.

Hereditary tyrosinemia type I (chronic form): pathologic findings in the liver.

Hum Pathol. 1989 Feb;20(2):149-58. doi: 10.1016/0046-8177(89)90179-2.

The effects of early treatment of hereditary tyrosinemia type I in infancy by orthotopic liver transplantation.

Transplantation. 1990 May;49(5):916-21. doi: 10.1097/00007890-199005000-00017.

Neurologic crises in hereditary tyrosinemia.

N Engl J Med. 1990 Feb 15;322(7):432-7. doi: 10.1056/NEJM199002153220704.

Liver transplantation for tyrosinemia. A review of 10 cases from the University of Pittsburgh.

Dig Dis Sci. 1990 Jan;35(1):153-7. doi: 10.1007/BF01537237.

Early liver transplantation is indicated for tyrosinemia type I.

J Pediatr Gastroenterol Nutr. 1991 Jul;13(1):10-5. doi: 10.1097/00005176-199107000-00002.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验