about
Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosisMutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosisA novel immunological assay for hepcidin quantification in human serumHepcidin in iron overload disordersOsteoporosis in HFE2 juvenile hemochromatosis. A case report and review of the literature.Mineral intake.Familial Mediterranean fever and E148Q pyrin gene mutation in Greece.Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity.Conditional disruption of mouse HFE2 gene: maintenance of systemic iron homeostasis requires hepatic but not skeletal muscle hemojuvelin.Linkage to chromosome 1q in Greek families with juvenile hemochromatosisGenetic heterogeneity underlies juvenile hemochromatosis phenotype: analysis of three families of northern Greek originArthropathy in juvenile hemochromatosisHereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IREExpression of three different ATP-binding cassette transporters and correlation to chemoresistance in acute myeloid leukemia
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
George Papanikolaou
@ast
George Papanikolaou
@en
George Papanikolaou
@es
George Papanikolaou
@nl
George Papanikolaou
@sl
type
label
George Papanikolaou
@ast
George Papanikolaou
@en
George Papanikolaou
@es
George Papanikolaou
@nl
George Papanikolaou
@sl
prefLabel
George Papanikolaou
@ast
George Papanikolaou
@en
George Papanikolaou
@es
George Papanikolaou
@nl
George Papanikolaou
@sl
P106
P21
P31
P496
0000-0002-6755-3633