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Page 1
Ovarian tumors and genetic predisposition.
Štellmachová Júlia, Vrtěl Petr, Vrtěl Radek, Janíková Mária, Kolaříková Kristýna, Procházka Martin, Vodička Radek. Štellmachová Júlia, et al. Among authors: vodicka radek. Ceska Gynekol. 2022;87(3):211-216. doi: 10.48095/cccg2022211. Ceska Gynekol. 2022. PMID: 35896402 English.
STAT6 - polymorphisms, haplotypes and epistasis in relation to atopy and asthma.
Godava M, Vrtel R, Vodicka R. Godava M, et al. Among authors: vodicka r. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2013 Jun;157(2):172-80. doi: 10.5507/bp.2013.043. Epub 2013 Jun 6. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2013. PMID: 23752766 Free 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: vodicka r. Fetal Diagn Ther. 2016;40(1):48-53. doi: 10.1159/000441296. Epub 2015 Oct 23. Fetal Diagn Ther. 2016. PMID: 26492079
Familial atypical parkinsonism with rare variant in VPS35 and FBXO7 genes: A case report.
Bartonikova T, Mensikova K, Mikulicova L, Vodicka R, Vrtel R, Godava M, Vastik M, Kaiserova M, Otruba P, Dolinova I, Nevrly M, Kanovsky P. Bartonikova T, et al. Among authors: vodicka r. Medicine (Baltimore). 2016 Nov;95(46):e5398. doi: 10.1097/MD.0000000000005398. Medicine (Baltimore). 2016. PMID: 27861377 Free PMC 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: vodicka 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: vodicka 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.
42 results