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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: vrtel r. 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
Clinical Potential of Effective Noninvasive Exclusion of KEL1-Positive Fetuses in KEL1-Negative Pregnant Women.
Böhmova J, Vodicka R, Lubusky M, Holuskova I, Studnickova M, Kratochvilova R, Krejcirikova E, Janikova M, Durdová V, Dolezalová T, Filipová H, Dusek L, Dhaifalah I, Vomackova K, Kacerovsky M, Prochazka M, Vrtel R. Böhmova J, et al. Among authors: vrtel r. Fetal Diagn Ther. 2016;40(1):48-53. doi: 10.1159/000441296. Epub 2015 Oct 23. Fetal Diagn Ther. 2016. PMID: 26492079
Single giant mediastinal rhabdomyoma as a sole manifestation of TSC in foetus.
Godava M, Filipova H, Dubrava L, Vrtel R, Michalkova K, Janikova M, Bakaj-Zbrozkova L, Navratil J. Godava M, et al. Among authors: vrtel r. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2017 Sep;161(3):326-329. doi: 10.5507/bp.2017.023. Epub 2017 Jun 12. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2017. PMID: 28659645 Free article.
New endemic familial parkinsonism in south Moravia, Czech Republic and its genetical background.
Bartoníková T, Menšíková K, Kolaříková K, Vodička R, Vrtěl R, Otruba P, Kaiserová M, Vaštík M, Mikulicová L, Ovečka J, Šáchová L, Dvorský F, Krša J, Jugas P, Godava M, Bareš M, Janout V, Hluštík P, Procházka M, Kaňovský P. Bartoníková T, et al. Among authors: vrtel r. Medicine (Baltimore). 2018 Sep;97(38):e12313. doi: 10.1097/MD.0000000000012313. Medicine (Baltimore). 2018. PMID: 30235682 Free PMC article.
Atypical parkinsonism of progressive supranuclear palsy-parkinsonism (PSP-P) phenotype with rare variants in FBXO7 and VPS35 genes associated with Lewy body pathology.
Menšíková K, Tučková L, Kolařiková K, Bartoníková T, Vodička R, Ehrmann J, Vrtěl R, Procházka M, Kaňovský P, Kovacs GG. Menšíková K, et al. Among authors: vrtel r. Acta Neuropathol. 2019 Jan;137(1):171-173. doi: 10.1007/s00401-018-1923-y. Epub 2018 Oct 29. Acta Neuropathol. 2019. PMID: 30374525 No abstract available.
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: vrtel r. 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.
65 results