nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Creutzfeldt-Jakob disease: reflections on the risk from blood product therapy
|
BROWN, P. |
|
2007 |
13 |
s5 |
p. 33-40 |
artikel |
2 |
Diagnosis and treatment of von Willebrand disease: new perspectives and nuances
|
KESSLER, C. M. |
|
2007 |
13 |
s5 |
p. 3-14 |
artikel |
3 |
Factor VIII inhibitors: role of von Willebrand factor on the uptake of factor VIII by dendritic cells
|
KAVERI, S. V. |
|
2007 |
13 |
s5 |
p. 61-64 |
artikel |
4 |
Factor VIII products and inhibitor development: the SIPPET study (survey of inhibitors in plasma-product exposed toddlers)
|
MANNUCCI, P. M. |
|
2007 |
13 |
s5 |
p. 65-68 |
artikel |
5 |
Fanhdi®, efficacy and safety in von Willebrand’s disease: prospective international study results
|
BELLO, I. F. |
|
2007 |
13 |
s5 |
p. 25-32 |
artikel |
6 |
Highly purified VWF/FVIII concentrates in the treatment and prophylaxis of von Willebrand disease: the PRO.WILL Study
|
FEDERICI, A. B. |
|
2007 |
13 |
s5 |
p. 15-24 |
artikel |
7 |
History of haemophilia
|
ALEDORT, L. M. |
|
2007 |
13 |
s5 |
p. 1-2 |
artikel |
8 |
Inhibitor development in haemophilia A: the role of von Willebrand factor/factor VIII concentrates
|
GOUDEMAND, J. |
|
2007 |
13 |
s5 |
p. 47-51 |
artikel |
9 |
Inhibitors in haemophilia A: current management and open issues
|
HAYA, S. |
|
2007 |
13 |
s5 |
p. 52-60 |
artikel |
10 |
Safety procedures of coagulation factors
|
JORQUERA, J. I. |
|
2007 |
13 |
s5 |
p. 41-46 |
artikel |
11 |
VWF/FVIII complex and the management of patient with inhibitors: from laboratory to clinical practice
|
BERNTORP, E. |
|
2007 |
13 |
s5 |
p. 69-72 |
artikel |
12 |
VWF/FVIII concentrates in high-risk immunotolerance: the RESIST study
|
GRINGERI, A. |
|
2007 |
13 |
s5 |
p. 73-77 |
artikel |