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Increased prevalence of bicuspid aortic valve in Turner syndrome links with karyotype: the crucial importance of detailed cardiovascular screening.
Klásková E, Zapletalová J, Kaprálová S, Šnajderová M, Lebl J, Tüdös Z, Pavlíček J, Černá J, Mihál V, Stará V, Procházka M. Klásková E, et al. Among authors: prochazka m. J Pediatr Endocrinol Metab. 2017 Mar 1;30(3):319-325. doi: 10.1515/jpem-2016-0301. J Pediatr Endocrinol Metab. 2017. PMID: 28236629
Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms.
Vrtel P, Vrtel R, Klaskova E, Vrbicka D, Adamova K, Pavlicek J, Hana V, Hana V, Soucek O, Stara V, Lebl J, Snajdrova M, Zapletalova J, Furst T, Kapralova S, Tauber Z, Krejcirikova E, Routilova M, Stellmachova J, Vodicka R, Prochazka M. Vrtel P, et al. Among authors: prochazka m. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022 Mar;166(1):63-67. doi: 10.5507/bp.2020.060. Epub 2021 Jan 12. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022. PMID: 33463629 Free article.
Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features.
Pavlicek J, Soucek O, Vrtel R, Klaskova E, Hana V, Stara V, Adamova K, Fürst T, Hana V Jr, Kapralova S, Prochazka M, Snajderova M, Tomaskova H, Tüdös Z, Vrbicka D, Vrtel P, Zapletalova J, Tauber Z, Lebl J. Pavlicek J, et al. Among authors: prochazka m. Horm Res Paediatr. 2022;95(5):465-475. doi: 10.1159/000525823. Epub 2022 Jul 1. Horm Res Paediatr. 2022. PMID: 35970147
Low-level 45,X/46,XX mosaicism is not associated with congenital heart disease and thoracic aorta dilatation:prospective magnetic resonance imaging and ultrasound study.
Klásková E, Tüdös Z, Sobek A, Zapletalová J, Dostál J, Zbořilová B, Sobek A Jr, Adamová K, Lattová V, Dostálová Z, Procházka M. Klásková E, et al. Among authors: prochazka m. Ultrasound Obstet Gynecol. 2015 Jun;45(6):722-7. doi: 10.1002/uog.14627. Epub 2015 May 11. Ultrasound Obstet Gynecol. 2015. PMID: 25042300 Free article.
Associations between congenital heart defects and genetic and morphological anomalies. The importance of prenatal screening.
Pavlicek J, Gruszka T, Kapralova S, Prochazka M, Silhanova E, Kaniova R, Polanska S, Cernickova R, Klaskova E. Pavlicek J, et al. Among authors: prochazka m. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2019 Feb;163(1):67-74. doi: 10.5507/bp.2018.049. Epub 2018 Sep 6. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2019. PMID: 30198518 Free article.
Fetal heart rhabdomyomatosis: a single-center experience.
Pavlicek J, Klaskova E, Kapralova S, Prochazka M, Vrtel R, Gruszka T, Kacerovsky M. Pavlicek J, et al. Among authors: prochazka m. J Matern Fetal Neonatal Med. 2021 Mar;34(5):701-707. doi: 10.1080/14767058.2019.1613365. Epub 2019 May 15. J Matern Fetal Neonatal Med. 2021. PMID: 31032681
Congenital fetal heart defect - an agreement between fetal echocardiography and autopsy findings.
Pavlicek J, Tauber Z, Klaskova E, Cizkova K, Prochazka M, Delongova P, Stefunko B, Szotkovska I, Dvorackova J, Gruszka T. Pavlicek J, et al. Among authors: prochazka m. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2020 Mar;164(1):92-99. doi: 10.5507/bp.2019.042. Epub 2019 Sep 23. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2020. PMID: 31548732 Free article.
391 results