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Sbornik Lekarsky|April 12, 2003
[Molecular genetic diagnosis of autosomal dominant polycystic kidney disease]J Reiterová, M Merta, J Stekrová, et al.Casopis Lekaru Ceskych|July 17, 2008
[Single nucleotide c.645+32c>T substitution in the APC gene is a non-pathogenic polymorphism appearing in about 16% of the Czech population]P Plevová, L Drobcinská, J Stekrová, et al.Human Mutation|March 17, 2004
Molecular analysis of the APC and MYH genes in Czech families affected by FAP or multiple adenomas: 13 novel mutationsJ Vandrovcová, J Stekrová, V Kebrdlová, et al.Casopis Lekaru Ceskych|August 23, 1995
[Autosomal dominant hereditary polycystic kidney disease]J Kapras, J Stekrová, J Zidovská, et al.Prague Medical Report|June 7, 2006
Genetic basis of nephrotic syndrome--reviewH Obeidová, M Merta, J Reiterová, et al.Prague Medical Report|October 28, 2006
The pathogenetic aspects and gene polymorphisms of IgA nephropathyD Maixnerová, M Merta, J Reiterová, et al.Folia Biologica|October 8, 2011
The influence of vascular endothelial growth factor (VEGF) polymorphism on the progression of chronic glomerulonephritidesH Safránková, M Merta, J Reiterová, et al.Folia Biologica|August 21, 2007
The influence of endothelin-A receptor gene polymorphism on the progression of autosomal dominant polycystic kidney disease and IgA nephropathyJ Reiterová, M Merta, J Stekrová, et al.Folia Biologica|July 30, 2013
Mutational analysis of ACTN4, encoding α-actinin 4, in patients with focal segmental glomerulosclerosis using HRM methodM Safaříková, J Reiterová, H Safránková, et al.Folia Biologica|May 24, 2008
The influence of two megsin polymorphisms on the progression of IgA nephropathyD Maixnerová, M Merta, J Reiterová, et al.Pageof 2