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                             11 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A novel pathogenic mutation in RPL11 identified in a patient diagnosed with diamond Blackfan anemia as a young adult Narla, Anupama
2016
61 C p. 46-47
2 p.
artikel
2 Association between a combination of single nucleotide polymorphisms and large vessel cerebral vasculopathy in African children with sickle cell disease Martella, Maddalena
2016
61 C p. 1-3
3 p.
artikel
3 Characterization of hepcidin response to holotransferrin in novel recombinant TfR1 HepG2 cells Mehta, Kosha
2016
61 C p. 37-45
9 p.
artikel
4 Conditioned medium from human umbilical vein endothelial cells markedly improves the proliferation and differentiation of circulating endothelial progenitors Castelli, Germana
2016
61 C p. 58-65
8 p.
artikel
5 Differences in frequency and regulation of T follicular helper cells between newly diagnosed and chronic pediatric immune thrombocytopenia Yao, Xin
2016
61 C p. 26-36
11 p.
artikel
6 Editorial Board 2016
61 C p. IFC-
1 p.
artikel
7 Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis Niss, Omar
2016
61 C p. 4-9
6 p.
artikel
8 Inflammation-induced up-regulation of hepcidin and down-regulation of ferroportin transcription are dependent on macrophage polarization Agoro, Rafiou
2016
61 C p. 16-25
10 p.
artikel
9 Next-generation sequencing of hereditary hemochromatosis-related genes: Novel likely pathogenic variants found in the Portuguese population Faria, Ricardo
2016
61 C p. 10-15
6 p.
artikel
10 The assessment of noncoding variant of PPOX gene in variegate porphyria reveals post-transcriptional role of the 5′ untranslated exon 1 Fiorentino, Valeria
2016
61 C p. 48-53
6 p.
artikel
11 The disappearance of acute erythroid leukemia: An act of legerdemain at the World Health Organization Lichtman, Marshall A.
2016
61 C p. 54-57
4 p.
artikel
                             11 gevonden resultaten
 
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