Divoký Vladimír
E-mail: vladimir.divoky@upol.cz
Groups: AFFILIATED STAFF, BIOLOGY
Journals
Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin. Blood cells, molecules & diseases. 2017, 69, 23-29, ISSN: 1079-9796, PMID: 28803808,
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency. Haematologica. 2014, 99(7), e118-121, ISSN: 0390-6078, PMID: 24727814,
Iron status in patients with pyruvate kinase deficiency: neonatal hyperferritinaemia associated with a novel frameshift deletion in the PKLR gene (p.Arg518fs), and low hepcidin to ferritin ratios. British Journal of Haematology. 2014, 165(4), 556-563, ISSN: 0007-1048, PMID: 24533562,