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Inherited ichthyoses: molecular causes of the disease in Czech patients.
Borská R, Pinková B, Réblová K, Bučková H, Kopečková L, Němečková J, Puchmajerová A, Malíková M, Hermanová M, Fajkusová L. Borská R, et al. Among authors: kopeckova l. Orphanet J Rare Dis. 2019 May 2;14(1):92. doi: 10.1186/s13023-019-1076-7. Orphanet J Rare Dis. 2019. PMID: 31046801 Free PMC article.
Ten years of DNA diagnostics of epidermolysis bullosa in the Czech Republic.
Kopečková L, Bučková H, Kýrová J, Gaillyová R, Němečková J, Jeřábková B, Veselý K, Stehlíková K, Fajkusová L. Kopečková L, et al. Br J Dermatol. 2016 Jun;174(6):1388-91. doi: 10.1111/bjd.14370. Epub 2016 Mar 1. Br J Dermatol. 2016. PMID: 26707537 No abstract available.
Autosomal recessive congenital ichthyoses in the Czech Republic.
Bučková H, Nosková H, Borská R, Réblová K, Pinková B, Zapletalová E, Kopečková L, Horký O, Němečková J, Gaillyová R, Nagy Z, Veselý K, Hermanová M, Stehlíková K, Fajkusová L. Bučková H, et al. Among authors: kopeckova l. Br J Dermatol. 2016 Feb;174(2):405-7. doi: 10.1111/bjd.13918. Epub 2015 Nov 14. Br J Dermatol. 2016. PMID: 25998749 No abstract available.
Skin lesions in a boy with X-linked lymphoproliferative disorder: comparison of 5 SH2D1A deletion cases.
Mejstríková E, Janda A, Hrusák O, Bucková H, Vlcková M, Hancárová M, Freiberger T, Ravcuková B, Vesely K, Fajkusová L, Kopecková L, Sumerauer D, Kabícková E, Sedivá A, Stary J, Sedlácek Z. Mejstríková E, et al. Among authors: kopeckova l. Pediatrics. 2012 Feb;129(2):e523-8. doi: 10.1542/peds.2011-0870. Epub 2012 Jan 23. Pediatrics. 2012. PMID: 22271700
The Age Dependent Progression of Hajdu-Cheney Syndrome in Two Families.
Jirečková J, Magner M, Lambert L, Baxová A, Leiská A, Kopečková L, Fajkusová L, Zeman J. Jirečková J, et al. Among authors: kopeckova l. Prague Med Rep. 2018;119(4):156-164. doi: 10.14712/23362936.2019.3. Prague Med Rep. 2018. PMID: 30779700 Free article.
11 results