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                             23 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A chemical screen identifies small molecules that regulate hepcidin expression Gaun, Vera
2014
53 4 p. 231-240
10 p.
artikel
2 A novel HBA2 gene conversion in cis or trans: “α12 allele” in a Saudi population Borgio, J. Francis
2014
53 4 p. 199-203
5 p.
artikel
3 A novel mutation in Wiskott–Aldrich syndrome and successfully treated with umbilical cord blood transplantation Zhu, Xiaoyu
2014
53 4 p. 283-285
3 p.
artikel
4 A novel variant mutation for congenital dyserythropoietic anemia, type II Song, Joo Y.
2014
53 4 p. 272-273
2 p.
artikel
5 A Phase 3, multicenter, open-label, switchover trial to assess the safety and efficacy of taliglucerase alfa, a plant cell-expressed recombinant human glucocerebrosidase, in adult and pediatric patients with Gaucher disease previously treated with imiglucerase Pastores, Gregory M.
2014
53 4 p. 253-260
8 p.
artikel
6 A prospective randomized wait list control trial of intravenous iron sucrose in older adults with unexplained anemia and serum ferritin 20–200ng/mL Price, Elizabeth
2014
53 4 p. 221-230
10 p.
artikel
7 BMI1 gene expression in myeloid leukemias and its impact on prognosis Saudy, Niveen S.
2014
53 4 p. 194-198
5 p.
artikel
8 Cbl negatively regulates erythropoietin-induced growth and survival signaling through the proteasomal degradation of Src kinase Shintani, Takamichi
2014
53 4 p. 211-218
8 p.
artikel
9 CD18 deficiency evolving to megakaryocytic (M7) acute myeloid leukemia: Case report de Moraes Vasconcelos, Dewton
2014
53 4 p. 180-184
5 p.
artikel
10 Circulating factors are involved in hypoxia-induced hepcidin suppression Ravasi, Giulia
2014
53 4 p. 204-210
7 p.
artikel
11 Deferiprone versus Deferoxamine in Sickle Cell Disease: Results from a 5-year long-term Italian multi-center randomized clinical trial Calvaruso, Giusi
2014
53 4 p. 265-271
7 p.
artikel
12 Delineation of the molecular basis of borderline hemoglobin A2 in Chinese individuals Lou, Ji-Wu
2014
53 4 p. 261-264
4 p.
artikel
13 DNA hypermethylation and X chromosome inactivation are major determinants of phenotypic variation in women heterozygous for G6PD mutations Wang, Jin
2014
53 4 p. 241-245
5 p.
artikel
14 DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil Cardoso, Greice Lemos
2014
53 4 p. 176-179
4 p.
artikel
15 Editorial Board 2014
53 4 p. IFC-
1 p.
artikel
16 Eliglustat, an investigational oral therapy for Gaucher disease type 1: Phase 2 trial results after 4years of treatment Lukina, Elena
2014
53 4 p. 274-276
3 p.
artikel
17 Flow cytometric assessment of lymphocyte subsets in Gaucher type 1 patients Rodic, Predrag
2014
53 4 p. 169-170
2 p.
artikel
18 Growth differentiation factor-15 in young sickle cell disease patients: Relation to hemolysis, iron overload and vascular complications Tantawy, Azza Abdel Gawad
2014
53 4 p. 189-193
5 p.
artikel
19 High expression of GTPase regulator associated with the focal adhesion kinase (GRAF) is a favorable prognostic factor in acute myeloid leukemia Aly, Rabab M.
2014
53 4 p. 185-188
4 p.
artikel
20 Hypothesis: Concordance of Gaucher disease and large granular lymphocytic leukemia has biological plausibility Ruchlemer, Rosa
2014
53 4 p. 219-220
2 p.
artikel
21 Iron homeostasis and infIammatory biomarker analysis in patients with type 1 Gaucher disease Medrano-Engay, B.
2014
53 4 p. 171-175
5 p.
artikel
22 Pyrimidine-5′-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5′-nucleotidase type I deficiency and influence of Gilbert's Syndrome on clinical expression dos Santos, Andrey
2014
53 4 p. 246-252
7 p.
artikel
23 Serial assessment of laser Doppler flow during acute pain crises in sickle cell disease Shi, Patricia Ann
2014
53 4 p. 277-282
6 p.
artikel
                             23 gevonden resultaten
 
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