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Page 1
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: buckova h. 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.
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: buckova h. Pediatrics. 2012 Feb;129(2):e523-8. doi: 10.1542/peds.2011-0870. Epub 2012 Jan 23. Pediatrics. 2012. PMID: 22271700
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. 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.
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. Among authors: buckova h. 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.
Types of congenital nonsyndromic ichthyoses.
Pinkova B, Buckova H, Borska R, Fajkusova L. Pinkova B, et al. Among authors: buckova h. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2020 Dec;164(4):357-365. doi: 10.5507/bp.2020.050. Epub 2020 Oct 21. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2020. PMID: 33087941 Free article. Review.
21 results