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                             21 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Acute lymphoblastic leukemia presenting with hypereosinophilia: Case report and review of the literature Ali, Alaa M.
2017
65 C p. 97-100
4 p.
artikel
2 A systematic review of the literature for severity predictors in children with sickle cell anemia Meier, Emily Riehm
2017
65 C p. 86-94
9 p.
artikel
3 Cerebral and muscle microvascular oxygenation in children with sickle cell disease: Influence of hematology, hemorheology and vasomotion Charlot, Keyne
2017
65 C p. 23-28
6 p.
artikel
4 Clinical and molecular characterization of 6 children with glutamate-cysteine ligase deficiency causing hemolytic anemia Almusafri, Fatima
2017
65 C p. 73-77
5 p.
artikel
5 Clinical course and disease burden in patients with paroxysmal nocturnal hemoglobinuria by hemolytic status Yenerel, Mustafa N.
2017
65 C p. 29-34
6 p.
artikel
6 Cytoskeletal connectivity may guide erythrocyte membrane ex- and invagination – A discussion point how biophysical principles might be exploited by a parasite invading erythrocytes Gov, Nir
2017
65 C p. 78-80
3 p.
artikel
7 Dysfunctional fibrinolysis and cerebral venous thrombosis Prabhudesai, Aniket
2017
65 C p. 51-55
5 p.
artikel
8 Editorial Board 2017
65 C p. IFC-
1 p.
artikel
9 Exacerbated in vivo metabolic changes suggestive of a spontaneous muscular vaso-occlusive crisis in exercising muscle of a sickle cell mouse Chatel, Benjamin
2017
65 C p. 56-59
4 p.
artikel
10 Flow cytometry analysis reveals different activation profiles of thrombin- or TRAP-stimulated platelets in db/db mice. The regulatory role of PAR-3 Kassassir, Hassan
2017
65 C p. 16-22
7 p.
artikel
11 Functional MRI BOLD response in sickle mice with hyperalgesia Wang, Ying
2017
65 C p. 81-85
5 p.
artikel
12 Gaucher disease and β-thalassemia: A rare coinheritance Makis, Alexandros
2017
65 C p. 35-37
3 p.
artikel
13 Genome-wide association study of erythrocyte density in sickle cell disease patients Ilboudo, Yann
2017
65 C p. 60-65
6 p.
artikel
14 Low T cell receptor excision circles (TRECs) in a case of ZAP 70 deficient severe combined immunodeficiency (SCID) with a novel mutation from India Aluri, Jahnavi
2017
65 C p. 95-96
2 p.
artikel
15 Measurements of red cell deformability and hydration reflect HbF and HbA2 in blood from patients with sickle cell anemia Parrow, Nermi L.
2017
65 C p. 41-50
10 p.
artikel
16 Response to request by journal editorship from Blood Cells, Molecules and Diseases in reference to a “Dear Editor” letter to the Pastores et al. paper, 2016 Pastores, Gregory M.
2017
65 C p. 71-72
2 p.
artikel
17 RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients Dezan, Marcia R.
2017
65 C p. 8-15
8 p.
artikel
18 The first report of chronic myelogenous leukemia with e19a2 micro-BCR/ABL1 presenting with massive myelofibrosis Kim, Hyun-Young
2017
65 C p. 68-70
3 p.
artikel
19 The mutant CALR allele burden in essential thrombocythemia at transformation to acute myeloid leukemia Langabeer, Stephen E.
2017
65 C p. 66-67
2 p.
artikel
20 Thrombin generation as a predictor of thromboembolic events in multiple myeloma patients Leiba, Merav
2017
65 C p. 1-7
7 p.
artikel
21 Two novel mutations in TMPRSS6 associated with iron-refractory iron deficiency anemia in a mother and child Yaish, Hassan M.
2017
65 C p. 38-40
3 p.
artikel
                             21 gevonden resultaten
 
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