| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An age dependent response to hydroxyurea in pediatric sickle cell anemia patients with alpha thalassemia trait
|
Figueiredo, Lisa
|
|
2017
|
66 |
C |
p. 19-23
5 p.
|
artikel
|
| 2 |
Association of genetic polymorphisms with plasma TFPI level: Boon or curse for DVT patients – Study from India
|
Kamal, Kishor
|
|
2017
|
66 |
C |
p. 31-36
6 p.
|
artikel
|
| 3 |
Coexistence of aberrant hematopoietic and stromal elements in myelodysplastic syndromes
|
Abbas, Salar
|
|
2017
|
66 |
C |
p. 37-46
10 p.
|
artikel
|
| 4 |
Combination of hemostatic therapies for treatment of patients with hemophilia A and inhibitors
|
Livnat, Tami
|
|
2017
|
66 |
C |
p. 1-5
5 p.
|
artikel
|
| 5 |
Does novel P5′N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?
|
Warang, Prashant
|
|
2017
|
66 |
C |
p. 8-10
3 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2017
|
66 |
C |
p. IFC-
1 p.
|
artikel
|
| 7 |
Hypocoagulability as assessed by thrombin generation test in newly-diagnosed patients with multiple myeloma
|
Legendre, Pauline
|
|
2017
|
66 |
C |
p. 47-49
3 p.
|
artikel
|
| 8 |
Isolated erythrocytosis associated with a CALR mutation
|
Langabeer, Stephen E.
|
|
2017
|
66 |
C |
p. 6-7
2 p.
|
artikel
|
| 9 |
Mutation in an exonic splicing enhancer site causing chronic granulomatous disease
|
de Boer, Martin
|
|
2017
|
66 |
C |
p. 50-57
8 p.
|
artikel
|
| 10 |
Non syndromic childhood onset congenital sideroblastic anemia: A report of 13 patients identified with an ALAS2 or SLC25A38 mutation
|
Le Rouzic, Marie-Amelyne
|
|
2017
|
66 |
C |
p. 11-18
8 p.
|
artikel
|
| 11 |
Prevalence and predictors of cardiac and liver iron overload in patients with thalassemia: A multicenter study based on real-world data
|
Krittayaphong, Rungroj
|
|
2017
|
66 |
C |
p. 24-30
7 p.
|
artikel
|
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