Risk Minimization of Hemolytic Disease of the Fetus and Newborn Using Droplet Digital PCR Method for Accurate Fetal Genotype Assessment of RHD, KEL, and RHCE from Cell-Free Fetal D...

por Vodicka, Radek, Bohmova, Jana, Holuskova, Iva, Krejcirikova, Eva, Prochazka, Martin, Vrtel, Radek
Publicado 2021

Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development

por Kolarikova, Kristyna, Vodicka, Radek, Vrtel, Radek, Stellmachova, Julia, Prochazka, Martin, Mensikova, Katerina, Kanovsky, Petr
Publicado 2022

High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic

por Kolarikova, Kristyna, Vodicka, Radek, Vrtel, Radek, Stellmachova, Julia, Prochazka, Martin, Mensikova, Katerina, Bartonikova, Tereza, Furst, Tomas, Kanovsky, Petr, Geryk, Jan
Publicado 2022

Two Reliable Methodical Approaches for Non-Invasive RHD Genotyping of a Fetus from Maternal Plasma

por Bohmova, Jana, Lubusky, Marek, Holuskova, Iva, Studnickova, Martina, Kratochvilova, Romana, Krejcirikova, Eva, Durdova, Veronika, Kratochvilova, Tereza, Dusek, Ladislav, Prochazka, Martin, Vodicka, Radek
Publicado 2020

Familial atypical parkinsonism with rare variant in VPS35 and FBXO7 genes: A case report

por Bartonikova, Tereza, Mensikova, Katerina, Mikulicova, Lenka, Vodicka, Radek, Vrtel, Radek, Godava, Marek, Vastik, Miroslav, Kaiserova, Michaela, Otruba, Pavel, Dolinova, Iva, Nevrly, Martin, Kanovsky, Petr
Publicado 2016

Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing

por Vrtel, Petr, Slavik, Ludek, Vodicka, Radek, Stellmachova, Julia, Prochazka, Martin, Prochazkova, Jana, Ulehlova, Jana, Rohon, Peter, Simurda, Tomas, Stasko, Jan, Martinkova, Ivana, Vrtel, Radek
Publicado 2022

Mutational analysis of TSC1 and TSC2 genes in Tuberous Sclerosis Complex patients from Greece

por Avgeris, Socratis, Fostira, Florentia, Vagena, Andromachi, Ninios, Yiannis, Delimitsou, Angeliki, Vodicka, Radek, Vrtel, Radek, Youroukos, Sotirios, Stravopodis, Dimitrios J., Vlassi, Metaxia, Astrinidis, Aristotelis, Yannoukakos, Drakoulis, Voutsinas, Gerassimos E.
Publicado 2017

Lewy body disease or diseases with Lewy bodies?

por Menšíková, Kateřina, Matěj, Radoslav, Colosimo, Carlo, Rosales, Raymond, Tučková, Lucie, Ehrmann, Jiří, Hraboš, Dominik, Kolaříková, Kristýna, Vodička, Radek, Vrtěl, Radek, Procházka, Martin, Nevrlý, Martin, Kaiserová, Michaela, Kurčová, Sandra, Otruba, Pavel, Kaňovský, Petr
Publicado 2022

Reply: Matters Arising ‘Lewy body disease or diseases with Lewy bodies?’

por Menšíková, Kateřina, Matěj, Radoslav, Colosimo, Carlo, Rosales, Raymond, Tučková, Lucie, Ehrmann, Jiří, Hraboš, Dominik, Kolaříková, Kristýna, Vodička, Radek, Vrtěl, Radek, Procházka, Martin, Nevrlý, Martin, Kaiserová, Michaela, Kurčová, Sandra, Otruba, Pavel, Kaňovský, Petr
Publicado 2022

New endemic familial parkinsonism in south Moravia, Czech Republic and its genetical background

por Bartoníková, Tereza, Menšíková, Kateřina, Kolaříková, Kristýna, Vodička, Radek, Vrtěl, Radek, Otruba, Pavel, Kaiserová, Michaela, Vaštík, Miroslav, Mikulicová, Lenka, Ovečka, Josef, Šáchová, Ludmila, Dvorský, František, Krša, Jiří, Jugas, Petr, Godava, Marek, Bareš, Martin, Janout, Vladimír, Hluštík, Petr, Procházka, Martin, Kaňovský, Petr
Publicado 2018