| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acquired von Willebrand's syndrome resulting from untreated hypothyroidism in two prepubertal girls
|
GALLI-TSINOPOULOU, A.
|
|
2006
|
12 |
6 |
p. 687-689
|
artikel
|
| 2 |
Application of current knowledge to the management of bleeding events during immune tolerance induction
|
DI PAOLA, J.
|
|
2006
|
12 |
6 |
p. 591-597
|
artikel
|
| 3 |
Author index
|
|
|
2006
|
12 |
6 |
p. 694-696
|
artikel
|
| 4 |
Commentary: ‘Switching between full-length and B-domain deleted Factor VIII and the risk of inhibitors’
|
HOOTS, W. K.
|
|
2006
|
12 |
6 |
p. 561-562
|
artikel
|
| 5 |
Comparing two measures of quality of life for children with haemophilia: the CHO-KLAT and the Haemo-QoL
|
BRADLEY, C. S.
|
|
2006
|
12 |
6 |
p. 643-653
|
artikel
|
| 6 |
Epidemiology of inhibitor formation with recombinant factor VIII replacement therapy
|
PEERLINCK, K.
|
|
2006
|
12 |
6 |
p. 579-590
|
artikel
|
| 7 |
Health-related quality of life in chronic coagulation disorders
|
TALAULIKAR, D.
|
|
2006
|
12 |
6 |
p. 633-642
|
artikel
|
| 8 |
Heterotropic bone formation as a complication of elective joint replacement in haemophilic patients – a case report and literature review
|
MANN, H. A.
|
|
2006
|
12 |
6 |
p. 672-675
|
artikel
|
| 9 |
Histological changes in murine haemophilic synovitis: a quantitative grading system to assess blood-induced synovitis
|
VALENTINO, L. A.
|
|
2006
|
12 |
6 |
p. 654-662
|
artikel
|
| 10 |
Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia
|
FANG, Y.
|
|
2006
|
12 |
6 |
p. 615-620
|
artikel
|
| 11 |
Individualization of bypassing agent treatment for haemophilic patients with inhibitors utilizing thromboelastography
|
YOUNG, G.
|
|
2006
|
12 |
6 |
p. 598-604
|
artikel
|
| 12 |
Influence of factor VIII on overall coagulability and fibrinolytic potential of haemophilic plasma as measured by global assay: monitoring in haemophilia A
|
GOLDENBERG, N. A.
|
|
2006
|
12 |
6 |
p. 605-614
|
artikel
|
| 13 |
Keyword index
|
|
|
2006
|
12 |
6 |
p. 692-693
|
artikel
|
| 14 |
Management of acute bleeding in a patient with congenital afibrinogenaemia
|
VAKALOPOULOU, S.
|
|
2006
|
12 |
6 |
p. 676-678
|
artikel
|
| 15 |
Normalization of factor VIII levels in a patient with mild haemophilia A during a 35-year period
|
MAINWARING, C. J.
|
|
2006
|
12 |
6 |
p. 668-671
|
artikel
|
| 16 |
Rituximab treatment of mild haemophilia A with inhibitors: a proposed treatment protocol
|
DUNKLEY, S.
|
|
2006
|
12 |
6 |
p. 663-667
|
artikel
|
| 17 |
Screening for factor XI deficiency amongst pregnant women of Ashkenazi Jewish origin
|
KADIR, R. A.
|
|
2006
|
12 |
6 |
p. 625-628
|
artikel
|
| 18 |
Severe factor X deficiency due to a homozygous mutation (Cys364Arg) that disrupts a disulphide bond in the catalytic domain
|
TODD, T.
|
|
2006
|
12 |
6 |
p. 621-624
|
artikel
|
| 19 |
Surface electrical stimulation of the quadriceps femoris in patients affected by haemophilia A
|
QUEROL, F.
|
|
2006
|
12 |
6 |
p. 629-632
|
artikel
|
| 20 |
Switching between full-length and B-domain-deleted factor VIII and the risk of inhibitors
|
KEELING, D.
|
|
2006
|
12 |
6 |
p. 690-691
|
artikel
|
| 21 |
The feasibility of total ankle prosthesis for severe arthropathy in haemophilia and prothrombin deficiency
|
VAN DER HEIDE, H. J. L.
|
|
2006
|
12 |
6 |
p. 679-682
|
artikel
|
| 22 |
The need for previously untreated patient population studies in understanding the development of factor VIII inhibitors
|
GOMPERTS, E. D.
|
|
2006
|
12 |
6 |
p. 573-578
|
artikel
|
| 23 |
The 80th anniversary of von Willebrand's disease: history, management and research
|
FEDERICI, A. B.
|
|
2006
|
12 |
6 |
p. 563-572
|
artikel
|
| 24 |
Torticollis as a sign of cervico-thoracic epidural haematoma in an infant with severe haemophilia A
|
CUVELIER, G. D. E.
|
|
2006
|
12 |
6 |
p. 683-686
|
artikel
|
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