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Kidney & Blood Pressure Research|November 27, 2010
Uromodulin biology and pathophysiology--an updatePetr Vyletal, Anthony J Bleyer, Stanislav KmochClinica Chimica Acta; International Journal of Clinical Chemistry|October 4, 2011
Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecular genetic analysis in two Czech families with xanthinuria type IBlanka Stiburkova, Jakub Krijt, Petr Vyletal, et al.Kidney International|September 17, 2005
Mapping of a new candidate locus for uromodulin-associated kidney disease (UAKD) to chromosome 1q41Katerina Hodanová, Jacek Majewski, Martina Kublová, et al.Human Mutation|October 31, 2006
Diversity of cystathionine beta-synthase haplotypes bearing the most common homocystinuria mutation c.833T>C: a possible role for gene conversionPetr Vyletal, Jitka Sokolová, David N Cooper, et al.Pageof 1