Phenotype, genotype, and outcome of 25 Palestinian patients with hereditary tyrosinemia type 1-Reference-Cited by-同舟云学术

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Phenotype, genotype, and outcome of 25 Palestinian patients with hereditary tyrosinemia type 1

Published:2021-03 Issue: Volume:9 Page:100083
ISSN:2589-9368
Container-title:Metabolism Open
language:en
Short-container-title:Metabolism Open

Author:

Dweikat Imad^ORCID,Qawasmi Nada,Najeeb Aysha,Radwan Mohammad

Publisher

Elsevier BV

Subject

General Medicine

Reference13 articles.

1. Hereditary tyrosinemia type 1 in Turkey: twenty year single-center experience;Zeybek;Pediatr Int,2015

2. Tyrosinemia type 1 in Spain: mutational analysis, treatment and long-term outcome;Couce;Pediatr Int,2011

3. Diagnosis and treatment of tyrosinemia type 1: a US and Canadian consensus group review and recommendations;Chinsky;Genet Med,2017

4. Cardiomyopathy in tyrosinemia type I is common but usually benign;Arora;J Inherit Metab Dis,2006

5. Silent tyrosinemia type I without elevated tyrosine or succinylacetone associated with liver cirrhosis and hepatocellular carcinoma;Blackburn;Hum Mutat,2016

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical Spectrum of Hereditary Tyrosinemia Type 1 in a Cohort of Pakistani Children;Clinical Medicine Insights: Pediatrics;2024-01

2. Diagnostic tardif de la tyrosinémie héréditaire de type I, le cas de deux faux jumeaux;Revue Francophone des Laboratoires;2022-09

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