nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Acquired von Willebrand's disease associated with gastrointestinal angiodysplasia: a case report
|
GUPTA, P. K. |
|
2006 |
|
4 |
p. 452-455 |
artikel |
2 |
Analysis of Factor VIII polymorphic markers as a means for carrier detection in Brazilian families with haemophilia A
|
DE CARVALHO, F. M. |
|
2007 |
|
4 |
p. 409-412 |
artikel |
3 |
A retrospective postlicensure survey of FEIBA efficacy and safety
|
DIMICHELE, D. |
|
2006 |
|
4 |
p. 352-362 |
artikel |
4 |
Arterial and venous thrombosis in rare congenital bleeding disorders: a critical review
|
GIROLAMI, A. |
|
2006 |
|
4 |
p. 345-351 |
artikel |
5 |
C1584 in von Willebrand factor is necessary for enhanced proteolysis by ADAMTS13 in vitro
|
KEENEY, S. |
|
2007 |
|
4 |
p. 405-408 |
artikel |
6 |
Corrigendum
|
|
|
2007 |
|
4 |
p. 450 |
artikel |
7 |
Current European practice in immune tolerance induction therapy in patients with haemophilia and inhibitors
|
ASTERMARK, J. |
|
2006 |
|
4 |
p. 363-371 |
artikel |
8 |
Disability in Indian patients with haemophilia
|
KAR, A. |
|
2007 |
|
4 |
p. 398-404 |
artikel |
9 |
Erratum
|
|
|
2006 |
|
4 |
p. 456 |
artikel |
10 |
Factor VIII recovery after a single infusion of recalibrated ReFacto® in 14 severe haemophilia A patients
|
LAMBERT, T. |
|
2007 |
|
4 |
p. 357-360 |
artikel |
11 |
F8 gene mutation profile and ITT response in a cohort of Italian haemophilia A patients with inhibitors
|
SALVIATO, R. |
|
2007 |
|
4 |
p. 361-372 |
artikel |
12 |
Fibrinogen Denver: a dysfibrinogenemia associated with an abnormal Reptilase time and significant bleeding
|
WALTER, S. |
|
2006 |
|
4 |
p. 393-397 |
artikel |
13 |
Fracture neck of femur in haemophilia A – experience from a cohort of 11 patients from a tertiary centre in India
|
LEE, V. N. |
|
2007 |
|
4 |
p. 391-394 |
artikel |
14 |
Identification and management of women with inherited bleeding disorders: a survey of obstetricians and gynaecologists in the United Kingdom
|
CHI, C. |
|
2006 |
|
4 |
p. 405-412 |
artikel |
15 |
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia
|
SANTACROCE, R. |
|
2006 |
|
4 |
p. 417-422 |
artikel |
16 |
Immune tolerance induction with a high purity von Willebrand factor/VIII complex concentrate in haemophilia A patients with inhibitors at high risk of a poor response
|
GRINGERI, A. |
|
2007 |
|
4 |
p. 373-379 |
artikel |
17 |
Inhibitor development, immune tolerance and prophylaxis in haemophilia A – the need for an evidence-based approach
|
MANNUCCI, P. M. |
|
2006 |
|
4 |
p. 429-434 |
artikel |
18 |
Liver haemorrhage in haemophilia – a case report and review of the literature
|
HAMILTON, M. |
|
2006 |
|
4 |
p. 441-443 |
artikel |
19 |
Long-term major joint outcomes in young adults with haemophilia: interim data from the HGDS
|
SU, Y. |
|
2007 |
|
4 |
p. 387-390 |
artikel |
20 |
Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India
|
JAYANDHARAN, G. |
|
2007 |
|
4 |
p. 413-419 |
artikel |
21 |
Non-invasive biomarkers of liver fibrosis in haemophilia patients with hepatitis C: can you avoid liver biopsy?
|
MAOR, Y. |
|
2006 |
|
4 |
p. 372-379 |
artikel |
22 |
Operative treatment of anterior heterotopic bone formation of the elbow in a patient with severe haemophilia A
|
MORTAZAVI, S. M. J. |
|
2006 |
|
4 |
p. 444-447 |
artikel |
23 |
Orthopaedic limb salvage with a mega prosthesis in a patient with haemophilia A and inhibitors – a case report
|
STUMPF, U. C. |
|
2007 |
|
4 |
p. 435-439 |
artikel |
24 |
Pain relief after knee replacement in patients with a bleeding disorder
|
VANARASE, M. Y. |
|
2007 |
|
4 |
p. 395-397 |
artikel |
25 |
Percutaneous coronary intervention with stent implantation in haemophilic A patient with unstable angina
|
SMOLKA, G. |
|
2007 |
|
4 |
p. 428-431 |
artikel |
26 |
Periodontal status and IOTN interventions among young hemophiliacs
|
AZHAR, S. |
|
2006 |
|
4 |
p. 401-404 |
artikel |
27 |
Pregnancy in women with congenital factor VII deficiency
|
KULKARNI, A. A. |
|
2006 |
|
4 |
p. 413-416 |
artikel |
28 |
Preliminary results of HBV DNA testing of Polish haemophilia patients – lack of occult HBV infection
|
WINDYGA, J. |
|
2006 |
|
4 |
p. 380-383 |
artikel |
29 |
Primary malignancies mistaken for pseudotumours in haemophilic patients
|
ALLEN, D. J. |
|
2007 |
|
4 |
p. 383-386 |
artikel |
30 |
RCTs and observational studies to determine the effect of prophylaxis in severe haemophilia
|
FISCHER, K. |
|
2007 |
|
4 |
p. 345-350 |
artikel |
31 |
Safety and efficacy of a sucrose-formulated recombinant factor VIII product for the treatment of previously treated patients with haemophilia A in China
|
SHI, J. |
|
2007 |
|
4 |
p. 351-356 |
artikel |
32 |
Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N
|
BERBER, E. |
|
2006 |
|
4 |
p. 398-400 |
artikel |
33 |
Severe factor V deficiency presenting with intracranial haemorrhage during gestation
|
ELLESTAD, S. C. |
|
2007 |
|
4 |
p. 432-434 |
artikel |
34 |
Spinal epidural haematoma in a patient with haemophilia B
|
BALKAN, C. |
|
2006 |
|
4 |
p. 437-440 |
artikel |
35 |
Successful concurrent triple surgery in an adolescent patient with haemophilia A and inhibitors treated with recombinant factor VIIa
|
JANIC, D. |
|
2007 |
|
4 |
p. 447-449 |
artikel |
36 |
The haemophilic ankle
|
RODRIGUEZ-MERCHAN, E. C. |
|
2006 |
|
4 |
p. 337-344 |
artikel |
37 |
The Haemo-QoL Index: developing a short measure for health-related quality of life assessment in children and adolescents with haemophilia
|
POLLAK, E. |
|
2006 |
|
4 |
p. 384-392 |
artikel |
38 |
The incidence and outcome of intracranial haemorrhage in newborns with haemophilia: analysis of the Nationwide Inpatient Sample database
|
TARANTINO, M. D. |
|
2007 |
|
4 |
p. 380-382 |
artikel |
39 |
The molecular aetiology of haemophilia A in a New Zealand patient group
|
LAURIE, A. D. |
|
2007 |
|
4 |
p. 420-427 |
artikel |
40 |
The obstetric and gynaecological management of women with inherited bleeding disorders – review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors’ Organization
|
LEE, C. A. |
|
2006 |
|
4 |
p. 301-336 |
artikel |
41 |
The use of topical crushed tranexamic acid tablets to control bleeding after dental surgery and from skin ulcers in haemophilia
|
COETZEE, M. J. |
|
2007 |
|
4 |
p. 443-444 |
artikel |
42 |
Treatment and outcome of acquired haemophilia A with a standard conventional regimen in a cohort without associated conditions
|
NG, H. J. |
|
2006 |
|
4 |
p. 423-428 |
artikel |
43 |
True radial artery aneurysm in a mild haemophilia A patient
|
FILIS, K. |
|
2007 |
|
4 |
p. 440-442 |
artikel |
44 |
Tyr2105Cys mutation in exon 22 of FVIII gene is a risk factor for the development of inhibitors in patients with mild/moderate haemophilia A
|
FRANCHINI, M. |
|
2006 |
|
4 |
p. 448-451 |
artikel |
45 |
Urgent arterial: venous fistula to secure vascular access in a patient with severe factor V deficiency and intracranial haemorrhage
|
PEAKE, L. |
|
2007 |
|
4 |
p. 445-446 |
artikel |
46 |
Use of factor VIII replacement during open heart surgery in a patient with haemophilia A
|
STINE, K. C. |
|
2006 |
|
4 |
p. 435-436 |
artikel |