| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An acquired, calcium-dependent, factor X inhibitor
|
Broze Jr., George J.
|
|
2014
|
|
2-3 |
p. 116-120
5 p.
|
artikel
|
| 2 |
Editorial Board
|
|
|
2014
|
|
2-3 |
p. IFC-
1 p.
|
artikel
|
| 3 |
Expression of LYN and PTEN genes in chronic myeloid leukemia and their importance in therapeutic strategy
|
Ferri, Cristian
|
|
2014
|
|
2-3 |
p. 121-125
5 p.
|
artikel
|
| 4 |
Expression profile of shelterin components in plasma cell disorders. Clinical significance of POT1 overexpression
|
Panero, Julieta
|
|
2014
|
|
2-3 |
p. 134-139
6 p.
|
artikel
|
| 5 |
Haptoglobin and myeloperoxidase (−G463A) gene polymorphisms in Brazilian sickle cell patients with and without secondary iron overload
|
Barbosa, Lilian Carla Pereira
|
|
2014
|
|
2-3 |
p. 95-107
13 p.
|
artikel
|
| 6 |
High-resolution melting analyses for genetic variants in ARID5B and IKZF1 with childhood acute lymphoblastic leukemia susceptibility loci in Taiwan
|
Lin, Chien-Yu
|
|
2014
|
|
2-3 |
p. 140-145
6 p.
|
artikel
|
| 7 |
Interleukin-6 directly impairs the erythroid development of human TF-1 erythroleukemic cells
|
McCranor, Bryan J.
|
|
2014
|
|
2-3 |
p. 126-133
8 p.
|
artikel
|
| 8 |
Iron chelation therapy for non-transfusion-dependent thalassemia (NTDT): A status quo
|
Taher, Ali T.
|
|
2014
|
|
2-3 |
p. 88-90
3 p.
|
artikel
|
| 9 |
TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy
|
Radio, Francesca Clementina
|
|
2014
|
|
2-3 |
p. 83-87
5 p.
|
artikel
|
| 10 |
Thalassemic osteopathy: A new marker of bone deposition
|
Baldini, M.
|
|
2014
|
|
2-3 |
p. 91-94
4 p.
|
artikel
|
| 11 |
The canonical transient receptor potential 6 (TRPC6) channel is sensitive to extracellular pH in mouse platelets
|
Berna-Erro, Alejandro
|
|
2014
|
|
2-3 |
p. 108-115
8 p.
|
artikel
|
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