Results 111 to 120 of about 766 (123)

Xanthinuria and Pregnancy.

Lancet, The, 1977
R A Chalmers, R A Chalmers
exaly   +2 more sources

A Novel Mutation in Xanthine Dehydrogenase in a Case With Xanthinuria in Hunan Province of China

Clinica Chimica Acta, 2020
Ping Li
exaly  

Hereditary Xanthinuria Is Not so Rare Disorder of Purine Metabolism

Nucleosides, Nucleotides and Nucleic Acids, 2018
Ivan Sebesta, Jakub Krijt, Blanka Stibůrková   +2 more
exaly  

Mutation of Human Molybdenum Cofactor Sulfurase Gene Is Responsible for Classical Xanthinuria Type II

Biochemical and Biophysical Research Communications, 2001
Kimiyoshi Ichida, Takeshi Nishino, T Hosoya   +2 more
exaly  

A Case of Xanthinuria Type I With a Novel Mutation in Xanthine Dehydrogenase

CEN Case Reports, 2016
Ichiei Narita, Kimiyoshi Ichida, Hiroshi Hasegawa   +2 more
exaly  

Hypoxanthine and Xanthine Concentrations Determined by High Performance Liquid Chromatography in Biological Fluids From Patients With Xanthinuria

Clinica Chimica Acta, 1984
R Boulieu, P Divry, C Bory
exaly  

A Case of Hereditary Xanthinuria Type 1 Accompanied by Bilateral Renal Calculi

Internal Medicine, 2012
Kimiyoshi Ichida, Yoshihiko Shinohara, Yoshikazu Kawakami   +2 more
exaly  

Identification and Characterization of the First Mutation (Arg776Cys) in the C-Terminal Domain of the Human Molybdenum Cofactor Sulfurase (HMCS) Associated With Type II Classical Xanthinuria

Molecular Genetics and Metabolism, 2007
Daniel Landau, Hava Peretz
exaly  

Decreased Xanthine Oxidase Activities and Increased Urinary Oxypurines in Heterozygotes for Hereditary Xanthinuria

Clinica Chimica Acta, 1990
Norio Kôno, Masanori Kawachi, Yuya Yamada   +2 more
exaly  

Xanthinuria and Hemochromatosis

New England Journal of Medicine, 1964
exaly