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Nucleosides, Nucleotides & Nucleic Acids|May 4, 2018
Hereditary xanthinuria is not so rare disorder of purine metabolismI Sebesta, B Stiburkova, J KrijtCasopis Lekaru Ceskych|September 16, 2005
[Diagnostic aspects of familial juvenile hyperuriceamic nephropathy]B Stibůrková, I Sebesta, S KmochSbornik Lekarsky|January 1, 1994
The importance of uric acid examinationI Sebesta, J Krijt, P SchneiderkaNucleosides, Nucleotides & Nucleic Acids|October 27, 2006
Analysis of excretion fraction of uric acidB Stibůrková, E Pospísilová, S Kmoch, et al.Nucleosides, Nucleotides & Nucleic Acids|October 27, 2006
Purine and pyrimidine metabolism: a firm basis for a transformed societyG J Peters, E A Carrey, I SebestaJournal of Chromatography. B, Biomedical Sciences and Applications|May 29, 1999
Identification and determination of succinyladenosine in human cerebrospinal fluidJ Krijt, S Kmoch, H Hartmannová, et al.Casopis Lekaru Ceskych|October 23, 1996
[Familial juvenile gouty nephropathy]K Pavelka, I Sebesta, J Blovská, et al.Human Molecular Genetics|July 11, 2000
Human adenylosuccinate lyase (ADSL), cloning and characterization of full-length cDNA and its isoform, gene structure and molecular basis for ADSL deficiency in six patientsS Kmoch, H Hartmannová, B Stibůrková, et al.American Journal of Human Genetics|April 26, 2000
Familial juvenile hyperuricemic nephropathy: localization of the gene on chromosome 16p11.2-and evidence for genetic heterogeneityB Stibůrková, J Majewski, I Sebesta, et al.Nucleosides, Nucleotides & Nucleic Acids|October 27, 2006
An unusual cause of renal amyloidosis secondary to gout: the first description of familial occurrenceZ Vernerová, I Rychlík, L Brunerová, et al.Pageof 2