Хайлтын үр дүнгүүд - Prochazka, Martin

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