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Nationwide observational study of paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) in the Czech Republic.
David J, Stara V, Hradsky O, Tuckova J, Slaba K, Jabandziev P, Sasek L, Huml M, Zidkova I, Pavlicek J, Palatova A, Klaskova E, Banszka K, Terifajova E, Vyhnanek R, Bloomfield M, Fingerhutova S, Dolezalova P, Prochazkova L, Chramostova G, Fencl F, Lebl J. David J, et al. Among authors: stara v. Eur J Pediatr. 2022 Oct;181(10):3663-3672. doi: 10.1007/s00431-022-04593-7. Epub 2022 Aug 20. Eur J Pediatr. 2022. PMID: 35987943 Free PMC article.
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: stara v. 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.
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: stara v. J Pediatr Endocrinol Metab. 2017 Mar 1;30(3):319-325. doi: 10.1515/jpem-2016-0301. J Pediatr Endocrinol Metab. 2017. PMID: 28236629
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: stara v. Horm Res Paediatr. 2022;95(5):465-475. doi: 10.1159/000525823. Epub 2022 Jul 1. Horm Res Paediatr. 2022. PMID: 35970147
Pigmentary retinopathy can indicate the presence of pathogenic LAMP2 variants even in somatic mosaic carriers with no additional signs of Danon disease.
Kousal B, Majer F, Vlaskova H, Dvorakova L, Piherova L, Meliska M, Langrova H, Palecek T, Kubanek M, Krebsova A, Gurka J, Stara V, Michaelides M, Kalina T, Sikora J, Liskova P. Kousal B, et al. Among authors: stara v. Acta Ophthalmol. 2021 Feb;99(1):61-68. doi: 10.1111/aos.14478. Epub 2020 Jun 13. Acta Ophthalmol. 2021. PMID: 32533651 Free article.
53 results