Results 231 to 236 of about 1,520,545 (236)

[One case of hereditary tyrosinemia type I].

Zhonghua er ke za zhi = Chinese journal of pediatrics, 2004
Yong-lan, Huang, Xiao-jing, Li, Xiao-ping, Luo, Hong, Wei, Yan-yan, Song   +4 more
openaire   +1 more source

Mutations in the 4-Hydroxyphenylpyruvic Acid Dioxygenase Gene Are Responsible for Tyrosinemia Type III and Hawkinsinuria

Molecular Genetics and Metabolism, 2000
exaly  

Spectrum of mutations in the fumarylacetoacetate hydrolase gene of tyrosinemia type 1 patients in northwestern Europe and Mediterranean countries

Human Mutation, 1998
exaly  

An engineered Escherichia coli Nissle strain prevents lethal liver injury in a mouse model of tyrosinemia type 1

Journal of Hepatology

exaly  

Long-term cognitive functioning in individuals with tyrosinemia type 1 treated with nitisinone and protein-restricted diet

Molecular Genetics and Metabolism Reports, 2017
exaly  

Promising new treatment for type I tyrosinemia.

Journal of pediatric gastroenterology and nutrition, 1994
openaire   +1 more source