Cytoplasmic Transfer Improves Human Egg Fertilization and Embryo Quality: an Evaluation of Sibling Oocytes in Women with Low Oocyte Quality

por Sobek, Ales, Tkadlec, Emil, Klaskova, Eva, Prochazka, Martin
Publicado 2020

Duplication of 9p24.3 in three unrelated patients and their phenotypes, considering affected genes, and similar recurrent variants

por Capkova, Zuzana, Capkova, Pavlina, Srovnal, Josef, Adamova, Katerina, Prochazka, Martin, Hajduch, Marian
Publicado 2021

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

Desire for Parenthood and Associated Trends in Czech Lesbian Women

por Turcan, Pavel, Prochazka, Martin, Pokorny, Pavel, Kvintova, Jana, Sigmund, Martin, Juraskova, Eva Sedlata
Publicado 2020

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

MLPA is a practical and complementary alternative to CMA for diagnostic testing in patients with autism spectrum disorders and identifying new candidate CNVs associated with autism

por Capkova, Pavlina, Srovnal, Josef, Capkova, Zuzana, Staffova, Katerina, Becvarova, Vera, Trkova, Marie, Adamova, Katerina, Santava, Alena, Curtisova, Vaclava, Hajduch, Marian, Prochazka, Martin
Publicado 2019

Differences in the importance of microcephaly, dysmorphism, and epilepsy in the detection of pathogenic CNVs in ID and ASD patients

por Capkova, Zuzana, Capkova, Pavlina, Srovnal, Josef, Staffova, Katerina, Becvarova, Vera, Trkova, Marie, Adamova, Katerina, Santava, Alena, Curtisova, Vaclava, Hajduch, Marian, Prochazka, Martin
Publicado 2019

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

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

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

The Role of miR-126 in Critical Limb Ischemia Treatment Using Adipose-Derived Stem Cell Therapeutic Factor Concentrate and Extracellular Matrix Microparticles

por Procházka, Václav, Jurčíková, Jana, Vítková, Kateřina, Pavliska, Lubomír, Porubová, Ludmila, Lassák, Ondrej, Buszman, Piotr, Fernandez, Carlos A., Jalůvka, František, Špačková, Iveta, Lochman, Ivo, Procházka, Martin, Janíková, Mária, Tauber, Zdeněk, Franková, Jana, Lachnit, Martin, Hiles, Michael C., Johnstone, Brian H.
Publicado 2018

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