Publications by authors named "Martin Prochazka"

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Surgical and/ or conservative treatment improves quality of life (EHP-30) in patients with endometriosis.
Kateřina Janoušková, Adéla Lemrová, Kateřina Ivanová, Martin Procházka, Martin Němec

Ceska Gynekol· July 2024

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Reply to: Questioning the cycad theory of Kii ALS-PDC causation.
Katerina Menšíková, Raymond Rosales, Carlo Colosimo, Peter Spencer, Annie Lannuzel, Martin Prochazka

Nat Rev Neurol· March 2024

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Endemic parkinsonism: clusters, biology and clinical features.
Katerina Menšíková, John C Steele, Raymond Rosales, Carlo Colosimo, Peter Spencer, Martin Prochazka

Nat Rev Neurol· October 2023

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Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and microarray analysis.
Andrea Štefeková, Pavlína Čapková, Václava Curtisová, Enghjargalan Mracká, Hana Filipová

Ceska Gynekol· June 2023

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Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features.
Jan Pavlicek, Ondrej Soucek, Radek Vrtel, Eva Klaskova, Vaclav Hana, Martin Prochazka

Horm Res Paediatr· November 2022

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Ovarian tumors and genetic predisposition.
Júlia Štellmachová, Petr Vrtěl, Radek Vrtěl, Mária Janíková, Kristýna Kolaříková

Ceska Gynekol· July 2022

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Reply: Matters Arising 'Lewy body disease or diseases with Lewy bodies?'.
Kateřina Menšíková, Radoslav Matěj, Carlo Colosimo, Raymond Rosales, Lucie Tučková

NPJ Parkinsons Dis· June 2022

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MLPA analysis of 32 foetuses with a congenital heart defect and 1 foetus with renal defects - pilot study. The significant frequency rate of presented pathological CNV.
Andrea Stefekova, Pavlina Capkova, Zuzana Capkova, Vaclava Curtisova, Josef Srovnal, Martin Prochazka

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub· May 2022

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Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing.
Petr Vrtel, Ludek Slavik, Radek Vodicka, Julia Stellmachova, Martin Prochazka

Diagnostics (Basel)· April 2022

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Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms.
Petr Vrtel, Radek Vrtel, Eva Klaskova, Dita Vrbicka, Katerina Adamova, Martin Prochazka

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub· March 2022

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

Front Neurosci· March 2022

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Lewy body disease or diseases with Lewy bodies?
Kateřina Menšíková, Radoslav Matěj, Carlo Colosimo, Raymond Rosales, Lucie Tučková

NPJ Parkinsons Dis· January 2022

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High-Throughput Sequencing Haplotype Analysis Indicates in Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic.
Kristyna Kolarikova, Radek Vodicka, Radek Vrtel, Julia Stellmachova, Martin Prochazka

Life (Basel)· January 2022

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

Reprod Sci· May 2021

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Quality of life and sexuality in women with urinary incontinence.
Petra Pičmanová, Martin Procházka

Ceska Gynekol· May 2021

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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 , , and from Cell-Free Fetal DNA of Maternal Plasma.
Radek Vodicka, Jana Bohmova, Iva Holuskova, Eva Krejcirikova, Martin Prochazka

Diagnostics (Basel)· April 2021

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Fetal heart rhabdomyomatosis: a single-center experience.
Jan Pavlicek, Eva Klaskova, Sabina Kapralova, Martin Prochazka, Radek Vrtel

J Matern Fetal Neonatal Med· March 2021

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

Mol Genet Genomic Med· March 2021

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Desire for Parenthood and Associated Trends in Czech Lesbian Women.
Pavel Turcan, Martin Prochazka, Pavel Pokorny, Jana Kvintova, Martin Sigmund

Sex Med· December 2020

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Two Reliable Methodical Approaches for Non-Invasive Genotyping of a Fetus from Maternal Plasma.
Jana Bohmova, Marek Lubusky, Iva Holuskova, Martina Studnickova, Romana Kratochvilova, Martin Prochazka

Diagnostics (Basel)· August 2020

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Congenital fetal heart defect - an agreement between fetal echocardiography and autopsy findings.
Jan Pavlicek, Zdenek Tauber, Eva Klaskova, Katerina Cizkova, Martin Prochazka

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub· March 2020

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Differences in the importance of microcephaly, dysmorphism, and epilepsy in the detection of pathogenic CNVs in ID and ASD patients.
Zuzana Capkova, Pavlina Capkova, Josef Srovnal, Katerina Staffova, Vera Becvarova, Martin Prochazka

PeerJ· November 2019

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Searching for genetic variants associated with thrombophilia.
Petr Vrtěl, Luděk Slavík, Radek Vodička, Martin Procházka, Jana Procházková

Cas Lek Cesk· June 2019

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The association between mode of birth delivery and attention-deficit/hyperactivity disorder: a systematic review protocol of epidemiological evidence.
Jitka Klugarová, Kateřina Janoušková, Martin Procházka, Jan Hálek, Věra Šibravová

Int J Evid Based Healthc· June 2019

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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.
Pavlina Capkova, Josef Srovnal, Zuzana Capkova, Katerina Staffova, Vera Becvarova, Martin Prochazka

PeerJ· January 2019

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