Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Radek Vodicka"'
Autor:
Petr Vrtel, Radek Vrtel, Eva Klaskova, Dita Vrbicka, Katerina Adamova, Jan Pavlicek, Vaclav Hana, Ondrej Soucek, Veronika Stara, Jan Lebl, Marta Snajdrova, Jirina Zapletalova, Tomas Furst, Sabina Kapralova, Zdenek Tauber, Eva Krejcirikova, Marketa Routilova, Julia Stellmachova, Radek Vodicka, Martin Prochazka
Publikováno v:
Biomedical Papers, Vol 166, Iss 1, Pp 63-67 (2022)
Aims. Turner syndrome is the only chromosome monosomy that is postnatally compatible with life. The reported incidence of TS is 1 in 2500 liveborn girls. The phenotype of these girls is highly variable, with cardiac abnormalities being life-threateni
Externí odkaz:
https://doaj.org/article/25b523ce827d4ec6b9611619f2e11f93
Autor:
Kristyna Kolarikova, Radek Vodicka, Radek Vrtel, Julia Stellmachova, Martin Prochazka, Katerina Mensikova, Petr Kanovsky
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Parkinsonism belongs to the most common neurodegenerative disease. Genetic predisposition could be one of the significant risk factor for disease development. It has been described higher prevalence of parkinsonism in large pedigree from southeastern
Externí odkaz:
https://doaj.org/article/a5e6fb538a254f0fbace1761fcd93aec
Autor:
Petr Vrtel, Ludek Slavik, Radek Vodicka, Julia Stellmachova, Martin Prochazka, Jana Prochazkova, Jana Ulehlova, Peter Rohon, Tomas Simurda, Jan Stasko, Ivana Martinkova, Radek Vrtel
Publikováno v:
Diagnostics, Vol 12, Iss 5, p 1060 (2022)
The deficiency of natural anticoagulants—antithrombin (AT), protein C (PC), and protein S (PS)—is a highly predisposing factor for thrombosis, which is still underdiagnosed at the genetic level. We aimed to establish and evaluate an optimal diagn
Externí odkaz:
https://doaj.org/article/003c59edd04342368e96e880a89cfc57
Autor:
Kristyna Kolarikova, Radek Vodicka, Radek Vrtel, Julia Stellmachova, Martin Prochazka, Katerina Mensikova, Tereza Bartonikova, Tomas Furst, Petr Kanovsky, Jan Geryk
Publikováno v:
Life, Vol 12, Iss 1, p 121 (2022)
Parkinson’s disease and parkinsonism are relatively common neurodegenerative disorders. This study aimed to assess potential genetic risk factors of haplotypes in genes associated with parkinsonism in a population in which endemic parkinsonism and
Externí odkaz:
https://doaj.org/article/b5971695dbe7497280991f88cd222b47
Publikováno v:
Diagnostics, Vol 11, Iss 5, p 803 (2021)
The molecular pathology of hemolytic disease of the fetus and newborn (HDFN) is determined by different RHD, RHCE, and KEL genotypes and by blood group incompatibility between the mother and fetus that is caused by erythrocyte antigen presence/absenc
Externí odkaz:
https://doaj.org/article/05d362594be14feb86bf92203e135411
Autor:
Jana Bohmova, Marek Lubusky, Iva Holuskova, Martina Studnickova, Romana Kratochvilova, Eva Krejcirikova, Veronika Durdova, Tereza Kratochvilova, Ladislav Dusek, Martin Prochazka, Radek Vodicka
Publikováno v:
Diagnostics, Vol 10, Iss 8, p 564 (2020)
Noninvasive fetal RHD genotyping is an important tool for predicting RhD incompatibility between a pregnant woman and a fetus. This study aimed to assess a methodological approach other than the commonly used one for noninvasive fetal RHD genotyping
Externí odkaz:
https://doaj.org/article/606e908108164c52a748189d2dfdb6b9
Autor:
Katerina Mensikova, Marek Godava, Petr Kanovsky, Pavel Otruba, Michaela Kaiserova, Miroslav Vastik, Lenka Mikulicova, Tereza Bartonikova, Radek Vrtel, Radek Vodicka, Sandra Kurcova, Petr Jugas, Josef Ovecka, Ludmila Sachova, Frantisek Dvorsky
Publikováno v:
Biomedical Papers, Vol 160, Iss 1, Pp 158-160 (2016)
Background: An epidemiological study conducted over four years revealed increased prevalence of neurodegenerative parkinsonism in a small, isolated region (10 villages, with a combined population of 8664, with approx. 2927 over 50 years of age) of so
Externí odkaz:
https://doaj.org/article/18bc6b39476c45b2acc8b29d79471ca6
Autor:
Kristyna, Kolarikova, Radek, Vodicka, Radek, Vrtel, Julia, Stellmachova, Martin, Prochazka, Katerina, Mensikova, Tereza, Bartonikova, Tomas, Furst, Petr, Kanovsky, Jan, Geryk
Publikováno v:
Life
Parkinson’s disease and parkinsonism are relatively common neurodegenerative disorders. This study aimed to assess potential genetic risk factors of haplotypes in genes associated with parkinsonism in a population in which endemic parkinsonism and
Autor:
Petr Vrtel, Radek Vrtel, Eva Klaskova, Dita Vrbicka, Katerina Adamova, Jan Pavlicek, Vaclav Hana, Ondrej Soucek, Veronika Stara, Jan Lebl, Marta Snajdrova, Jirina Zapletalova, Tomas Furst, Sabina Kapralova, Zdenek Tauber, Eva Krejcirikova, Marketa Routilova, Julia Stellmachova, Radek Vodicka, Martin Prochazka
Publikováno v:
Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia. 166(1)
Aims Turner syndrome is the only chromosome monosomy that is postnatally compatible with life. The reported incidence of TS is 1 in 2500 liveborn girls. The phenotype of these girls is highly variable, with cardiac abnormalities being life-threatenin
Autor:
Marek Lubusky, Tereza Kratochvilova, Eva Krejcirikova, Martin Prochazka, Radek Vodicka, Romana Kratochvilova, M. Studnickova, V. Durdova, Jana Bohmova, I. Holuskova, Ladislav Dušek
Publikováno v:
Diagnostics
Volume 10
Issue 8
Diagnostics, Vol 10, Iss 564, p 564 (2020)
Volume 10
Issue 8
Diagnostics, Vol 10, Iss 564, p 564 (2020)
Noninvasive fetal RHD genotyping is an important tool for predicting RhD incompatibility between a pregnant woman and a fetus. This study aimed to assess a methodological approach other than the commonly used one for noninvasive fetal RHD genotyping