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Lewy body disease or diseases with Lewy bodies?
Menšíková K, Matěj R, Colosimo C, Rosales R, Tučková L, Ehrmann J, Hraboš D, Kolaříková K, Vodička R, Vrtěl R, Procházka M, Nevrlý M, Kaiserová M, Kurčová S, Otruba P, Kaňovský P. Menšíková K, et al. Among authors: prochazka m. NPJ Parkinsons Dis. 2022 Jan 10;8(1):3. doi: 10.1038/s41531-021-00273-9. NPJ Parkinsons Dis. 2022. PMID: 35013341 Free PMC article. Review.
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: prochazka m. Fetal Diagn Ther. 2016;40(1):48-53. doi: 10.1159/000441296. Epub 2015 Oct 23. Fetal Diagn Ther. 2016. PMID: 26492079
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: prochazka m. 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: prochazka m. 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.
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
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.
Risk Minimization of Hemolytic Disease of the Fetus and Newborn Using Droplet Digital PCR Method for Accurate Fetal Genotype Assessment of RHD, KEL, and RHCE from Cell-Free Fetal DNA of Maternal Plasma.
Vodicka R, Bohmova J, Holuskova I, Krejcirikova E, Prochazka M, Vrtel R. Vodicka R, et al. Among authors: prochazka m. Diagnostics (Basel). 2021 Apr 28;11(5):803. doi: 10.3390/diagnostics11050803. Diagnostics (Basel). 2021. PMID: 33925253 Free PMC article.
390 results