Search Results - Prochazka, Martin

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  1. 1
    Cytoplasmic Transfer Improves Human Egg Fertilization and Embryo Quality: an Evaluation of Sibling Oocytes in Women with Low Oocyte Quality

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

    Published 2020
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  2. 2
    Duplication of 9p24.3 in three unrelated patients and their phenotypes, considering affected genes, and similar recurrent variants

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

    Published 2021
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  3. 3
    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 DNA of Maternal Plasma

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

    Published 2021
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  4. 4
    Desire for Parenthood and Associated Trends in Czech Lesbian Women

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

    Published 2020
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  5. 5
    Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development

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

    Published 2022
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  6. 6
    High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic

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

    Published 2022
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  7. 7
    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

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

    Published 2019
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  8. 8
    Differences in the importance of microcephaly, dysmorphism, and epilepsy in the detection of pathogenic CNVs in ID and ASD patients

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

    Published 2019
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  9. 9
    Two Reliable Methodical Approaches for Non-Invasive RHD Genotyping of a Fetus from Maternal Plasma

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

    Published 2020
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  10. 10
    Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing

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

    Published 2022
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  11. 11
    Lewy body disease or diseases with Lewy bodies?

    Lewy body disease or diseases with Lewy bodies? by 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

    Published 2022
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  12. 12
    Reply: Matters Arising ‘Lewy body disease or diseases with Lewy bodies?’

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

    Published 2022
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  13. 13
    The Role of miR-126 in Critical Limb Ischemia Treatment Using Adipose-Derived Stem Cell Therapeutic Factor Concentrate and Extracellular Matrix Microparticles

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

    Published 2018
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  14. 14
    New endemic familial parkinsonism in south Moravia, Czech Republic and its genetical background

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

    Published 2018
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