| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A forgotten or minimized head trauma, rather than a mild FVII deficiency, is the most likely cause of a subdural hematoma
|
Girolami, A.
|
|
2016
|
60 |
C |
p. 73-
1 p.
|
artikel
|
| 2 |
Bengal macrothrombocytopenia is not totally an innocuous condition
|
Ali, Shahnaz
|
|
2016
|
60 |
C |
p. 3-6
4 p.
|
artikel
|
| 3 |
Clinical features of JAK2V617F- or CALR-mutated essential thrombocythemia and primary myelofibrosis
|
Monte-Mor, Bárbara da Costa Reis
|
|
2016
|
60 |
C |
p. 74-77
4 p.
|
artikel
|
| 4 |
Concurrent MPL W515L and Y591D mutations in a patient with myelofibrosis
|
Rashidi, Armin
|
|
2016
|
60 |
C |
p. 1-2
2 p.
|
artikel
|
| 5 |
Cryoglobulinemia in a patient with chronic lymphocytic leukemia — A case report and review of literature of renal involvement in CLL
|
Arora, Swaty
|
|
2016
|
60 |
C |
p. 7-11
5 p.
|
artikel
|
| 6 |
Dietary supplementation with ipriflavone decreases hepatic iron stores in wild type mice
|
Patchen, Bonnie
|
|
2016
|
60 |
C |
p. 36-43
8 p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
2016
|
60 |
C |
p. IFC-
1 p.
|
artikel
|
| 8 |
Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community
|
Reading, N. Scott
|
|
2016
|
60 |
C |
p. 58-64
7 p.
|
artikel
|
| 9 |
Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study
|
Manco, Licínio
|
|
2016
|
60 |
C |
p. 18-23
6 p.
|
artikel
|
| 10 |
High abundance of circulating megakaryocytic cells in chronic myeloid leukemia in Indian patients. Revisiting George Minot to re-interpret megakaryocytic maturation
|
Anand, Mona
|
|
2016
|
60 |
C |
p. 28-32
5 p.
|
artikel
|
| 11 |
Imaging characteristics of focal splenic and hepatic lesions in type 1 Gaucher disease
|
Regenboog, Martine
|
|
2016
|
60 |
C |
p. 49-57
9 p.
|
artikel
|
| 12 |
Lectin-like oxidized low-density lipoprotein receptor (LOX-1) in sickle cell disease vasculopathy
|
Chen, Mingyi
|
|
2016
|
60 |
C |
p. 44-48
5 p.
|
artikel
|
| 13 |
Mott cells
|
Rashidi, Armin
|
|
2016
|
60 |
C |
p. 16-17
2 p.
|
artikel
|
| 14 |
Novel interactions between erythroblast macrophage protein and cell migration
|
Javan, Gulnaz T.
|
|
2016
|
60 |
C |
p. 24-27
4 p.
|
artikel
|
| 15 |
Re-evaluation of bone pain in patients with type 1 Gaucher disease suggests that bone crises occur in small bones as well as long bones
|
Baris, Hagit N.
|
|
2016
|
60 |
C |
p. 65-72
8 p.
|
artikel
|
| 16 |
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients
|
Minelli, Antonella
|
|
2016
|
60 |
C |
p. 33-35
3 p.
|
artikel
|
| 17 |
The World Health Organization revisits the classification of the myelodysplastic syndromes: Improvement and insufficiencies
|
Lichtman, Marshall A.
|
|
2016
|
60 |
C |
p. 12-15
4 p.
|
artikel
|
Tijdschrift beschrijving