| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel germ-line mutation of c-mpl gene in a sporadic case of essential thrombocythemia
|
Lombardi, Anna Maria
|
|
2017
|
64 |
C |
p. 51-52
2 p.
|
artikel
|
| 2 |
A retrospective study of paroxysmal nocturnal hemoglobinuria in pediatric and adolescent patients
|
Mercuri, Angela
|
|
2017
|
64 |
C |
p. 45-50
6 p.
|
artikel
|
| 3 |
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation
|
Satta, Stefania
|
|
2017
|
64 |
C |
p. 30-32
3 p.
|
artikel
|
| 4 |
Creatine kinase in human erythrocytes: A genetic anomaly reveals presence of soluble brain-type isoform
|
Kay, Laurence
|
|
2017
|
64 |
C |
p. 33-37
5 p.
|
artikel
|
| 5 |
Drug-induced endovesiculation of erythrocytes is modulated by the dynamics in the cytoskeleton/membrane interaction
|
Oberwagner, Walter
|
|
2017
|
64 |
C |
p. 15-22
8 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2017
|
64 |
C |
p. IFC-
1 p.
|
artikel
|
| 7 |
Enhancer deletion generates cellular phenotypic diversity due to bimodal gene expression
|
De Gobbi, Marco
|
|
2017
|
64 |
C |
p. 10-12
3 p.
|
artikel
|
| 8 |
Erythropoietin administration increases splenic erythroferrone protein content and liver TMPRSS6 protein content in rats
|
Gurieva, Iuliia
|
|
2017
|
64 |
C |
p. 1-7
7 p.
|
artikel
|
| 9 |
Increased peripheral leukemia blasts leading to false-positive blood culture
|
Khan, Maliha
|
|
2017
|
64 |
C |
p. 8-9
2 p.
|
artikel
|
| 10 |
Letter to the Editor on Pastores et al. Development of anti-velaglucerase alfa antibodies in clinical trial-treated patients with Gaucher disease
|
Keutzer, Joan
|
|
2017
|
64 |
C |
p. 13-14
2 p.
|
artikel
|
| 11 |
Micro- and macrovascular function in children with sickle cell anaemia and sickle cell haemoglobin C disease
|
Möckesch, Berenike
|
|
2017
|
64 |
C |
p. 23-29
7 p.
|
artikel
|
| 12 |
Recent advances in diagnostic and therapeutic guidelines for primary and secondary hemophagocytic lymphohistiocytosis
|
Ramachandran, Smita
|
|
2017
|
64 |
C |
p. 53-57
5 p.
|
artikel
|
| 13 |
Whole exome sequencing in the differential diagnosis of Diamond-Blackfan anemia: Clinical and molecular study of three patients with novel RPL5 and mosaic RPS19 mutations
|
Errichiello, Edoardo
|
|
2017
|
64 |
C |
p. 38-44
7 p.
|
artikel
|
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