Results 181 to 190 of about 5,194 (193)

Increased nitric oxide release by neutrophils of a patient with tyrosinemia type III

Biomedicine and Pharmacotherapy, 2009
Mauro Celli
exaly  

Tyrosinemia Type 1 and symptoms of ADHD: Biochemical mechanisms and implications for treatment and prognosis

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2020
Helene Barone, Peter Daniel Szigetvari, Rune Kleppe   +2 more
exaly  

Altered gene expression in tyrosinemia type 1

Gastroenterology, 1995
openaire   +1 more source

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 III in an asymptomatic girl

Molecular Genetics and Metabolism Reports, 2015
Edyta Szymanska, Elżbieta Ciara, Dorota Piekutowska-Abramczuk   +2 more
exaly  

Re: Comment on pancreatitis in type 1 tyrosinemia

2019
[No abstract available]
openaire   +1 more source

Molecular changes associated with chronic liver damage and neoplastic lesions in a murine model of hereditary tyrosinemia type 1

Biochimica Et Biophysica Acta - Molecular Basis of Disease, 2015
Francesca Angileri, Robert M Tanguay
exaly  

Improved method to determine succinylacetone in dried blood spots for diagnosis of tyrosinemia type 1 using UPLC‐MS/MS

Biomedical Chromatography, 2008
Zuhair Rahbeeni
exaly  

Evidence for Liver Disease Preceding Amino Acid Abnormalities in Hereditary Tyrosinemia

New England Journal of Medicine, 1983
exaly  

Mutations in the 4-hydroxyphenylpyruvate dioxygenase gene (HPD) in patients with tyrosinemia type III

Human Genetics, 2000
Ulla Rüetschi
exaly