Results 131 to 140 of about 3,205 (146)

Prenatal Diagnosis of Tyrosinemia Type 1 Using Next Generation Sequencing

Fetal and Pediatric Pathology, 2016
Maryam Rafati, Saeed Reza Ghaffari
exaly  

In vivo quantitative photoacoustic evaluation of the liver and kidney pathology in tyrosinemia

Photoacoustics, 2022
exaly  

Simple detection of a (Finnish) hereditary tyrosinemia type 1 mutation

Human Mutation, 1996
M, St-Louis, J, Poudrier, R M, Tanguay
openaire   +2 more sources

Tyrosinemia type I treated by NTBC: How does AFP predict liver cancer?

Molecular Genetics and Metabolism, 2006
Marry M Van Den Heuvel-Eibrink
exaly  

Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin

Molecular Genetics and Metabolism, 2011
Faiqa Imtiaz, Bashayer R Al-Mubarak, Hanaa El-Karaksy   +2 more
exaly  

Tissue-specific FAH deficiency alters sleep–wake patterns and results in chronic tyrosinemia in mice

Proceedings of the National Academy of Sciences of the United States of America, 2019
Kimberly H Cox, Vivek Kumar, Benjamin P Tu   +2 more
exaly  

Chromosomal Instability in Hereditary Tyrosinemia Type I

Pediatric Pathology, 1990
exaly  

Tyrosinemia type 1 and irreversible neurologic crisis after one month discontinuation of nitisone

Metabolic Brain Disease, 2016
Halise Neslihan Önenli Mungan, Deniz Kor, Ozden Ozgur Horoz   +2 more
exaly  

Neurologic Crises in Hereditary Tyrosinemia

New England Journal of Medicine, 1990
Grant A Mitchell, Serge Melancon
exaly  

Renal proximal tubular cells acquire resistance to cell death stimuli in mice with hereditary tyrosinemia type 1

Kidney International, 2004
Markus Grompe
exaly