nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Ames hypopituitary dwarf mice demonstrate imbalanced myelopoiesis between bone marrow and spleen
|
Capitano, Maegan L. |
|
2015 |
55 |
1 |
p. 15-20 6 p. |
artikel |
2 |
Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients
|
Al-Nafie, Awatif N. |
|
2015 |
55 |
1 |
p. 27-29 3 p. |
artikel |
3 |
Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects
|
Lin, Li |
|
2015 |
55 |
1 |
p. 62-67 6 p. |
artikel |
4 |
Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP)
|
Barone, Angelica |
|
2015 |
55 |
1 |
p. 40-47 8 p. |
artikel |
5 |
Distinguishing clonal evolution from so-called secondary acute myelogenous leukemia: Adhering to unifying concepts of the genetic basis of leukemogenesis
|
Lichtman, Marshall A. |
|
2015 |
55 |
1 |
p. 1-2 2 p. |
artikel |
6 |
Editorial Board
|
|
|
2015 |
55 |
1 |
p. IFC- 1 p. |
artikel |
7 |
Effect of systemic heparan sulfate haploinsufficiency on steady state hematopoiesis and engraftment of hematopoietic stem cells
|
Shekels, Laurie L. |
|
2015 |
55 |
1 |
p. 3-9 7 p. |
artikel |
8 |
Genetics factors associated with myelodysplastic syndromes
|
Macedo, Luciana Conci |
|
2015 |
55 |
1 |
p. 76-81 6 p. |
artikel |
9 |
Genotype–phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients
|
Nagar, Rachana |
|
2015 |
55 |
1 |
p. 10-14 5 p. |
artikel |
10 |
Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes
|
Radio, Francesca Clementina |
|
2015 |
55 |
1 |
p. 71-75 5 p. |
artikel |
11 |
Mechanism of interleukin-13 production by granulocyte-macrophage colony-stimulating factor-dependent macrophages via protease-activated receptor-2
|
Yamaguchi, Rui |
|
2015 |
55 |
1 |
p. 21-26 6 p. |
artikel |
12 |
Mitochondrial uncoupling protein (UCP2) gene expression is regulated by miR-2909
|
Kaul, Deepak |
|
2015 |
55 |
1 |
p. 89-93 5 p. |
artikel |
13 |
No increase of JAK2 46/1 haplotype frequency in essential thrombocythemia with CALR mutations: Functional effect of the haplotype limited to allele with JAK2V617F mutation but not CALR mutation
|
Gau, Jyh-Pyng |
|
2015 |
55 |
1 |
p. 36-39 4 p. |
artikel |
14 |
Omega 3 (n−3) fatty acids down-regulate nuclear factor-kappa B (NF-κB) gene and blood cell adhesion molecule expression in patients with homozygous sickle cell disease
|
Daak, Ahmed A. |
|
2015 |
55 |
1 |
p. 48-55 8 p. |
artikel |
15 |
Plasmodium vivax: N-terminal diversity in the blood stage SERA genes from Indian isolates
|
Rahul, C.N. |
|
2015 |
55 |
1 |
p. 30-35 6 p. |
artikel |
16 |
Thalassemia major between liver and heart: Where we are now
|
Dessì, Carlo |
|
2015 |
55 |
1 |
p. 82-88 7 p. |
artikel |
17 |
The effects of hydroxyurea and bone marrow transplant on Anti-Müllerian hormone (AMH) levels in females with sickle cell anemia
|
Elchuri, Swati V. |
|
2015 |
55 |
1 |
p. 56-61 6 p. |
artikel |
18 |
The long-term effects of radioactive phosphorous synoviorthesis on hemophilic arthropathy
|
Eraghi, Amir Sobhani |
|
2015 |
55 |
1 |
p. 68-70 3 p. |
artikel |