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Molecular characterization of six new cases of red blood cell hexokinase deficiency yields four novel mutations in HK1.
Blood Cells Mol Dis. 2016 Jul;59:71-6. doi: 10.1016/j.bcmd.2016.04.002. Epub 2016 Apr 22.
Blood Cells Mol Dis. 2016.
PMID: 27282571
Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome.
Nováková M, Žaliová M, Suková M, Wlodarski M, Janda A, Froňková E, Campr V, Lejhancová K, Zapletal O, Pospíšilová D, Černá Z, Kuhn T, Švec P, Pelková V, Zemanová Z, Kerndrup G, van den Heuvel-Eibrink M, van der Velden V, Niemeyer C, Kalina T, Trka J, Starý J, Hrušák O, Mejstříková E.
Nováková M, et al. Among authors: lejhancova k.
Haematologica. 2016 Jun;101(6):707-16. doi: 10.3324/haematol.2015.137711. Epub 2016 Mar 24.
Haematologica. 2016.
PMID: 27013649
Free PMC article.
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Venous thromboembolism in adolescents.
Samková A, Lejhancová K, Hak J, Lukes A.
Samková A, et al. Among authors: lejhancova k.
Acta Medica (Hradec Kralove). 2012;55(2):78-82. doi: 10.14712/18059694.2015.59.
Acta Medica (Hradec Kralove). 2012.
PMID: 23101270
Free article.
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