Resultats de la cerca - Prochazka, Martin

Cytoplasmic Transfer Improves Human Egg Fertilization and Embryo Quality: an Evaluation of Sibling Oocytes in Women with Low Oocyte Quality per Sobek, Ales, Tkadlec, Emil, Klaskova, Eva, Prochazka, Martin

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Duplication of 9p24.3 in three unrelated patients and their phenotypes, considering affected genes, and similar recurrent variants per Capkova, Zuzana, Capkova, Pavlina, Srovnal, Josef, Adamova, Katerina, Prochazka, Martin, Hajduch, Marian

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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... per Vodicka, Radek, Bohmova, Jana, Holuskova, Iva, Krejcirikova, Eva, Prochazka, Martin, Vrtel, Radek

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Desire for Parenthood and Associated Trends in Czech Lesbian Women per Turcan, Pavel, Prochazka, Martin, Pokorny, Pavel, Kvintova, Jana, Sigmund, Martin, Juraskova, Eva Sedlata

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Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development per Kolarikova, Kristyna, Vodicka, Radek, Vrtel, Radek, Stellmachova, Julia, Prochazka, Martin, Mensikova, Katerina, Kanovsky, Petr

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High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic per Kolarikova, Kristyna, Vodicka, Radek, Vrtel, Radek, Stellmachova, Julia, Prochazka, Martin, Mensikova, Katerina, Bartonikova, Tereza, Furst, Tomas, Kanovsky, Petr, Geryk, Jan

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

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Differences in the importance of microcephaly, dysmorphism, and epilepsy in the detection of pathogenic CNVs in ID and ASD patients per Capkova, Zuzana, Capkova, Pavlina, Srovnal, Josef, Staffova, Katerina, Becvarova, Vera, Trkova, Marie, Adamova, Katerina, Santava, Alena, Curtisova, Vaclava, Hajduch, Marian, Prochazka, Martin

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Two Reliable Methodical Approaches for Non-Invasive RHD Genotyping of a Fetus from Maternal Plasma per Bohmova, Jana, Lubusky, Marek, Holuskova, Iva, Studnickova, Martina, Kratochvilova, Romana, Krejcirikova, Eva, Durdova, Veronika, Kratochvilova, Tereza, Dusek, Ladislav, Prochazka, Martin, Vodicka, Radek

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Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing per Vrtel, Petr, Slavik, Ludek, Vodicka, Radek, Stellmachova, Julia, Prochazka, Martin, Prochazkova, Jana, Ulehlova, Jana, Rohon, Peter, Simurda, Tomas, Stasko, Jan, Martinkova, Ivana, Vrtel, Radek

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Lewy body disease or diseases with Lewy bodies? per 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

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

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

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

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