New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease

Por Stekrova, Jitka, Reiterova, Jana, Svobodova, Stanislava, Kebrdlova, Vera, Lnenicka, Petr, Merta, Miroslav, Viklicky, Ondrej, Kohoutova, Milada
Publicado em 2009

Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease

Por Obeidova, Lena, Elisakova, Veronika, Stekrova, Jitka, Reiterova, Jana, Merta, Miroslav, Tesar, Vladimir, Losan, Frantisek, Kohoutova, Milada
Publicado em 2014

Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele

Por Reiterová, Jana, Štekrová, Jitka, Merta, Miroslav, Kotlas, Jaroslav, Elišáková, Veronika, Lněnička, Petr, Korabečná, Marie, Kohoutová, Milada, Tesař, Vladimír
Publicado em 2013

The coincidence of IgA nephropathy and Fabry disease

Por Maixnerová Dita, Tesař Vladimír, Ryšavá Romana, Reiterová Jana, Poupětová Helena, Dvořáková Lenka, Goláň Lubor, Neprašová Michaela, Kidorová Jana, Merta Miroslav, Honsová Eva
Publicado em 2013-01-01

The coincidence of IgA nephropathy and Fabry disease

Por Maixnerová, Dita, Tesař, Vladimír, Ryšavá, Romana, Reiterová, Jana, Poupětová, Helena, Dvořáková, Lenka, Goláň, Lubor, Neprašová, Michaela, Kidorová, Jana, Merta, Miroslav, Honsová, Eva
Publicado em 2013