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                             42 gevonden resultaten
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
6 p. 687-689
artikel
2 Analysing two dinucleotide repeats of FVIII gene in Iranian population RABBANI, B.
2007
6 p. 740-744
artikel
3 Application of current knowledge to the management of bleeding events during immune tolerance induction DI PAOLA, J.
2006
6 p. 591-597
artikel
4 Author index 2006
6 p. 694-696
artikel
5 Coagulation deficiencies: a look to the future 1 LEE, C. A.
2007
6 p. 750-757
artikel
6 Commentary: ‘Switching between full-length and B-domain deleted Factor VIII and the risk of inhibitors’ HOOTS, W. K.
2006
6 p. 561-562
artikel
7 Comparing two measures of quality of life for children with haemophilia: the CHO-KLAT and the Haemo-QoL BRADLEY, C. S.
2006
6 p. 643-653
artikel
8 Correlation of thromboelastographic patterns with clinical presentation and rationale for use of antifibrinolytics in severe haemophilia patients GHOSH, K.
2007
6 p. 734-739
artikel
9 Epidemiology of inhibitor formation with recombinant factor VIII replacement therapy PEERLINCK, K.
2006
6 p. 579-590
artikel
10 Experience with epidural anaesthesia in pregnant women with von Willebrand disease VARUGHESE, J.
2007
6 p. 730-733
artikel
11 Factor VIII inhibitor associated with nephrotic syndrome CHANG, H.
2007
6 p. 766
artikel
12 Galectin 3-binding protein is a potential contaminant of recombinantly produced factor IX BLOSTEIN, M.
2007
6 p. 701-706
artikel
13 Haemoperitoneum in a female patient with haemophilia A caused by a ruptured ovarian follicle MARTIN-SALCES, M.
2007
6 p. 770-771
artikel
14 Health-related quality of life in chronic coagulation disorders TALAULIKAR, D.
2006
6 p. 633-642
artikel
15 Heterotropic bone formation as a complication of elective joint replacement in haemophilic patients – a case report and literature review MANN, H. A.
2006
6 p. 672-675
artikel
16 Histological changes in murine haemophilic synovitis: a quantitative grading system to assess blood-induced synovitis VALENTINO, L. A.
2006
6 p. 654-662
artikel
17 Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia FANG, Y.
2006
6 p. 615-620
artikel
18 Implementation of a hepatitis A prevention policy in haemophiliacs: results from the French cohort CHAMBOST, H.
2007
6 p. 712-721
artikel
19 Improving estimation of liver fibrosis using combination and newer noninvasive biomarker scoring systems in hepatitis C-infected haemophilia patients MAOR, Y.
2007
6 p. 722-729
artikel
20 Individualization of bypassing agent treatment for haemophilic patients with inhibitors utilizing thromboelastography YOUNG, G.
2006
6 p. 598-604
artikel
21 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
6 p. 605-614
artikel
22 Inhibitor development and successful immune tolerance in an HIV-infected patient with haemophilia A and after immune reconstitution with HAART KRUSE-JARRES, R.
2007
6 p. 707-711
artikel
23 Keyword index 2006
6 p. 692-693
artikel
24 Management of acute bleeding in a patient with congenital afibrinogenaemia VAKALOPOULOU, S.
2006
6 p. 676-678
artikel
25 Management of an acute coronary syndrome in a patient with severe haemophilia A FERRARIO, C.
2007
6 p. 763-765
artikel
26 Multiple congenital coagulopathies co-expressed with Von Willebrand’s disease: the experience of Hemophilia Region III Treatment Centers over 25 years and review of the literature ASATIANI, E.
2007
6 p. 685-696
artikel
27 Normalization of factor VIII levels in a patient with mild haemophilia A during a 35-year period MAINWARING, C. J.
2006
6 p. 668-671
artikel
28 Prenatal diagnosis of haemophilia A by using intron 1 inversion detection SALVIATO, R.
2007
6 p. 772-774
artikel
29 Rituximab treatment of mild haemophilia A with inhibitors: a proposed treatment protocol DUNKLEY, S.
2006
6 p. 663-667
artikel
30 Safety and efficacy of a plasma-derived monoclonal purified factor VIII concentrate during 10 years of follow-up MAUSER-BUNSCHOTEN, E. P.
2007
6 p. 697-700
artikel
31 Screening for factor XI deficiency amongst pregnant women of Ashkenazi Jewish origin KADIR, R. A.
2006
6 p. 625-628
artikel
32 Severe factor X deficiency due to a homozygous mutation (Cys364Arg) that disrupts a disulphide bond in the catalytic domain TODD, T.
2006
6 p. 621-624
artikel
33 Successful liver transplant in an HCV-infected haemophiliac patient with fulminant hepatic failure MANDALÀ, L.
2007
6 p. 767-769
artikel
34 Surface electrical stimulation of the quadriceps femoris in patients affected by haemophilia A QUEROL, F.
2006
6 p. 629-632
artikel
35 Switching between full-length and B-domain-deleted factor VIII and the risk of inhibitors KEELING, D.
2006
6 p. 690-691
artikel
36 The economics of haemophilia prophylaxis: governmental and insurer perspectives. PROCEEDINGS OF THE SECOND INTERNATIONAL PROPHYLAXIS STUDY GROUP (IPSG) SYMPOSIUM FELDMAN, B. M.
2007
6 p. 745-749
artikel
37 The feasibility of total ankle prosthesis for severe arthropathy in haemophilia and prothrombin deficiency VAN DER HEIDE, H. J. L.
2006
6 p. 679-682
artikel
38 The need for previously untreated patient population studies in understanding the development of factor VIII inhibitors GOMPERTS, E. D.
2006
6 p. 573-578
artikel
39 The 80th anniversary of von Willebrand's disease: history, management and research FEDERICI, A. B.
2006
6 p. 563-572
artikel
40 Torticollis as a sign of cervico-thoracic epidural haematoma in an infant with severe haemophilia A CUVELIER, G. D. E.
2006
6 p. 683-686
artikel
41 Treatment in a haemophiliac A patient with paroxysmal atrial fibrillation and ischemic heart disease CID, A. R.
2007
6 p. 760-762
artikel
42 Venous thrombosis in Glanzmann’s thrombasthenia PHILLIPS, R.
2007
6 p. 758-759
artikel
                             42 gevonden resultaten
 
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