| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A rare G6PD variant (c.383T>G; p.128Leu>Arg) with a molecular pathophysiological mechanism similar to that of G6PD A− (68Val>Met, 126Asn>Asp)
|
Moradkhani, Kamran
|
|
2009
|
43 |
3 |
p. 226-229
4 p.
|
artikel
|
| 2 |
Editorial Board
|
|
|
2009
|
43 |
3 |
p. IFC-
1 p.
|
artikel
|
| 3 |
Genetic adaptation to extreme hypoxia:
|
Lorenzo V, Felipe
|
|
2009
|
43 |
3 |
p. 221-225
5 p.
|
artikel
|
| 4 |
Hb M Dothan [β 25/26 (B7/B8)/(GGT/GAG→GAG//Gly/Glu→Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics
|
Kutlar, F.
|
|
2009
|
43 |
3 |
p. 235-238
4 p.
|
artikel
|
| 5 |
Human blood mononuclear cell in vitro cytokine response before and after two different strenuous exercise bouts in the presence of bloodroot and Echinacea extracts
|
Senchina, David S.
|
|
2009
|
43 |
3 |
p. 298-303
6 p.
|
artikel
|
| 6 |
Human CD34+ cells are capable of generating normal and JAK2V617F positive endothelial like cells in vivo
|
Sozer, Selcuk
|
|
2009
|
43 |
3 |
p. 304-312
9 p.
|
artikel
|
| 7 |
Interethnic differences of CYP2C9 alleles in healthy Hungarian and Roma population samples: Relationship to worldwide allelic frequencies
|
Sipeky, Csilla
|
|
2009
|
43 |
3 |
p. 239-242
4 p.
|
artikel
|
| 8 |
Nature of frequent deletions in CEBPA
|
Fuchs, Ota
|
|
2009
|
43 |
3 |
p. 260-263
4 p.
|
artikel
|
| 9 |
Postoperative bypass bleeding: A bypass-associated dilutional (BAD) coagulopathy?
|
Bull, Brian S.
|
|
2009
|
43 |
3 |
p. 256-259
4 p.
|
artikel
|
| 10 |
Soluble endothelial adhesion molecules and inflammation markers in patients with β-thalassemia intermedia
|
Kanavaki, Ino
|
|
2009
|
43 |
3 |
p. 230-234
5 p.
|
artikel
|
| 11 |
Statistical clues to postoperative blood loss: Moving averages applied to medical data
|
Hay, Karen L.
|
|
2009
|
43 |
3 |
p. 250-255
6 p.
|
artikel
|
| 12 |
TfR2 expression in human colon carcinomas
|
Calzolari, Alessia
|
|
2009
|
43 |
3 |
p. 243-249
7 p.
|
artikel
|
| 13 |
The clinical course of untreated Gaucher disease in 22 patients over 10 years: Hematological and skeletal manifestations
|
Piran, Siavash
|
|
2009
|
43 |
3 |
p. 289-293
5 p.
|
artikel
|
| 14 |
The female Gaucher patient: The impact of enzyme replacement therapy around key reproductive events (menstruation, pregnancy and menopause)
|
Zimran, Ari
|
|
2009
|
43 |
3 |
p. 264-288
25 p.
|
artikel
|
| 15 |
Type 2 Gaucher disease occurs in Ashkenazi Jews but is surprisingly rare
|
Aviner, Shraga
|
|
2009
|
43 |
3 |
p. 294-297
4 p.
|
artikel
|
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