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Page 1
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: zapletalova j. 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: zapletalova j. J Pediatr Endocrinol Metab. 2017 Mar 1;30(3):319-325. doi: 10.1515/jpem-2016-0301. J Pediatr Endocrinol Metab. 2017. PMID: 28236629
Primary School Performance of Girls with Turner Syndrome: A Transcultural Assessment.
Lebl J, Hamza RT, Stoklasova J, Zapletalova J, Kolouskova S, Soucek O, Obermannova B, Snajderova M, Amaratunga SA, Sumnik Z, Pavlikova M, Pruhova S. Lebl J, et al. Among authors: zapletalova j. Pediatr Endocrinol Rev. 2019 Dec;17(2):117-124. doi: 10.17458/per.vol17.2019.lhs.gilrsturnersyndrome. Pediatr Endocrinol Rev. 2019. PMID: 31763804
Prospective study of hypothalamo-hypophyseal dysfunction in children and adolescents following traumatic brain injury.
Krahulik D, Aleksijevic D, Smolka V, Klaskova E, Venhacova P, Vaverka M, Mihal V, Zapletalova J. Krahulik D, et al. Among authors: zapletalova j. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2017 Mar;161(1):80-85. doi: 10.5507/bp.2016.047. Epub 2016 Sep 19. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2017. PMID: 27646495 Free article.
Acute lymphoblastic leukemia in a child with Leri-Weill syndrome and complete SHOX gene deletion: A Case Report.
Volejnikova J, Zapletalova J, Jarosova M, Urbankova H, Petr V, Klaskova E, Horwitz MS, Hajduch M, Mihal V. Volejnikova J, et al. Among authors: zapletalova j. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2018 Mar;162(1):65-70. doi: 10.5507/bp.2018.002. Epub 2018 Feb 21. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2018. PMID: 29469136 Free article.
IGF-I resistance and Turner's syndrome.
Lebl J, Průhová S, Zapletalová J, Pechová M. Lebl J, et al. Among authors: zapletalova j. J Pediatr Endocrinol Metab. 2001 Jan;14(1):37-41. doi: 10.1515/jpem.2001.14.1.37. J Pediatr Endocrinol Metab. 2001. PMID: 11220703
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: zapletalova j. Horm Res Paediatr. 2022;95(5):465-475. doi: 10.1159/000525823. Epub 2022 Jul 1. Horm Res Paediatr. 2022. PMID: 35970147
310 results