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                             25 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Combined clotting factor deficiencies: experience at a single hemophilia treatment center O'BRIEN, S. H.
2007
13 1 p. 26-29
artikel
2 Combined factor VIII and IX inhibitors in a non-haemophilic patient: successful treatment with immunosuppressive drugs CARMASSI, F.
2007
13 1 p. 106-107
artikel
3 Confusion around the official classification of arthropathy SCHULMAN, S.
2007
13 1 p. 117-119
artikel
4 Current use of by-passing agents in Europe in the management of acute bleeds in patients with haemophilia and inhibitors ASTERMARK, J.
2007
13 1 p. 38-45
artikel
5 Cyclosporin A can achieve immune tolerance in a patient with severe haemophilia B and refractory inhibitors CROSS, D. C. A.
2007
13 1 p. 111-114
artikel
6 Defining ‘full-length’ recombinant factor VIII: a comparative structural analysis JANKOWSKI, M. A.
2007
13 1 p. 30-37
artikel
7 Definitions for haemophilia prophylaxis and its outcomes: The Canadian Consensus Study OTA, S.
2007
13 1 p. 12-20
artikel
8 Evaluation of pharmacokinetics, efficacy and safety of Immunate® solvent detergent in previously treated patients with severe haemophilia A NEMES, L.
2007
13 1 p. 9-11
artikel
9 Force fluctuations during the Maximum Isometric Voluntary Contraction of the quadriceps femoris in haemophilic patients GONZÁLEZ, L.-M.
2007
13 1 p. 65-70
artikel
10 Haemoperitoneum associated with ovulation in women with bleeding disorders: the case for conservative management and the role of the contraceptive pill PAYNE, J. H.
2007
13 1 p. 93-97
artikel
11 Haemophilia: January 2007 Lee, Christine
2007
13 1 p. 1
artikel
12 IgE-mediated anaphylactic reaction to purified and recombinant factor VIII in a patient with severe haemophilia A KADAR, J. G.
2007
13 1 p. 104-105
artikel
13 Impact of different inhibitor reactivities with commercial factor VIII concentrates on thrombin generation SALVAGNO, G. L.
2007
13 1 p. 51-56
artikel
14 In vivo recovery of factor VIII and factor IX: intra- and interindividual variance in a clinical setting BJÖRKMAN, S.
2007
13 1 p. 2-8
artikel
15 Monitoring the genotoxic effects of radiosynovectomy with Re-186 in paediatric age group undergoing therapy for haemophilic synovitis TURKMEN, C.
2007
13 1 p. 57-64
artikel
16 Osteoporosis in haemophilia – an underestimated comorbidity? WALLNY, T. A.
2007
13 1 p. 79-84
artikel
17 Pegylated interferon and ribavirin combination therapy for chronic hepatitis C in patients with congenital bleeding disorders: a single-centre experience POSTHOUWER, D.
2007
13 1 p. 98-103
artikel
18 Prevalence of sporadic and familial haemophilia KASPER, C. K.
2007
13 1 p. 90-92
artikel
19 Rituximab as an adjuvant therapy to immune tolerance in a haemophilia A boy with high inhibitor titre CHUANSUMRIT, A.
2007
13 1 p. 108-110
artikel
20 Rituximab for the treatment of patients with very high-titre acquired factor VIII inhibitors refractory to conventional chemotherapy FIELD, J. J.
2007
13 1 p. 46-50
artikel
21 Short-term oral corticosteroid therapy for acute haemarthrosis in haemophilia patients with high-titre inhibitors MEDEIROS, D.
2007
13 1 p. 85-89
artikel
22 Stayin' Alive LIPTON, R. A.
2007
13 1 p. 120
artikel
23 The Colorado Haemophilia Paediatric Joint Physical Examination Scale: normal values and interrater reliability HACKER, M. R.
2007
13 1 p. 71-78
artikel
24 Topical use of tranexamic acid to control perioperative local bleeding in gynaecology patients with clotting disorders: two cases SARRIS, I.
2007
13 1 p. 115-116
artikel
25 Von Willebrand disease within the collective of haemophilic patients as reason for unexpected bleeding episodes SIEGMUND, B.
2007
13 1 p. 21-25
artikel
                             25 gevonden resultaten
 
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