Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Eva Krejcirikova"'
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
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:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::277256da8e215c60fecd5fcc470f67f5
https://pubmed.ncbi.nlm.nih.gov/33463629
https://pubmed.ncbi.nlm.nih.gov/33463629
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b20eed403894b7806d4d47784ebc58ff
Autor:
I. Holuskova, Radek Vrtel, Katherine Vomackova, Marian Kacerovsky, V. Durdova, Radek Vodicka, Maria Janikova, Hana Filipova, Martin Prochazka, Romana Kratochvilova, Ladislav Dušek, M. Studnickova, Ishraq Dhaifalah, Tereza Dolezalová, Eva Krejcirikova, Marek Lubusky, Jana Bohmova
Publikováno v:
Fetal Diagnosis and Therapy. 40:48-53
Background: The clinical importance of assessing the fetal KEL genotype is to exclude ‘K'-positive fetuses (genotype KEL1/KEL2) in ‘K'-alloimmunized pregnant women (genotype KEL2/KEL2). Noninvasive assessment of the fetal KEL genotype is not yet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7516b9d51b0974b1d92a2a8dfb2c44a
https://doi.org/10.1159/000441296
https://doi.org/10.1159/000441296
Autor:
Jana, Böhmova, Radek, Vodicka, Marek, Lubusky, Iva, Holuskova, Martina, Studnickova, Romana, Kratochvilova, Eva, Krejcirikova, Maria, Janikova, Veronika, Durdová, Tereza, Dolezalová, Hana, Filipová, Ladislav, Dusek, Ishraq, Dhaifalah, Katherine, Vomackova, Marian, Kacerovsky, Martin, Prochazka, Radek, Vrtel
Publikováno v:
Fetal diagnosis and therapy. 40(1)
The clinical importance of assessing the fetal KEL genotype is to exclude 'K'-positive fetuses (genotype KEL1/KEL2) in 'K'-alloimmunized pregnant women (genotype KEL2/KEL2). Noninvasive assessment of the fetal KEL genotype is not yet available in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7f7ef3701496f5f4f2e800ad72c667a7
https://pubmed.ncbi.nlm.nih.gov/26492079
https://pubmed.ncbi.nlm.nih.gov/26492079
Autor:
Eva Krejcirikova, Martin Prochazka, Ladislav Dušek, Ishraq Dhaifalah, Radek Vrtel, Eva Schneiderova, D Vrbická, Alena Santava, Radek Vodicka, Jiri Santavy
Publikováno v:
Prenatal diagnosis. 28(5)
Background Cell-free fetal (cff) DNA analysis by short tandem repeats (STR) has the advantage of better recognizing the different genotypes. However, quantitative examination by quantitative fluorescent (QF) polymerase chain reaction (PCR) by STRs is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65a862465973e5e16029dd6baf8e8045
https://pubmed.ncbi.nlm.nih.gov/18395872
https://pubmed.ncbi.nlm.nih.gov/18395872