| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Achievement of immune tolerance in a patient with haemophilia B and inhibitory antibodies, complicated by an anaphylactoid reaction
|
CURRY, N. S.
|
|
2007
|
|
3 |
p. 328-330
|
artikel
|
| 2 |
A modified chromogenic assay for the measurement of very low levels of factor VIII activity (FVIII:C)
|
YATUV, R.
|
|
2006
|
|
3 |
p. 253-257
|
artikel
|
| 3 |
An illustrative case and a review on the dosing of recombinant factor VIIa in congenital factor XI deficiency
|
SCHULMAN, S.
|
|
2006
|
|
3 |
p. 223-227
|
artikel
|
| 4 |
A systematic approach to controlling problem bleeds in patients with severe congenital haemophilia A and high-titre inhibitors
|
TEITEL, J.
|
|
2007
|
|
3 |
p. 256-263
|
artikel
|
| 5 |
Comparative study of validity of clinical, X-ray and magnetic resonance imaging scores in evaluation and management of haemophilic arthropathy in children
|
PERGANTOU, H.
|
|
2006
|
|
3 |
p. 241-247
|
artikel
|
| 6 |
Continuous infusion of factor concentrates in children with haemophilia A in comparison with bolus injections
|
BIDLINGMAIER, C.
|
|
2006
|
|
3 |
p. 212-217
|
artikel
|
| 7 |
Disorders of menstruation and their effect on the quality of life in women with congenital factor VII deficiency
|
KULKARNI, A.
|
|
2006
|
|
3 |
p. 248-252
|
artikel
|
| 8 |
ELISA system for detection of immune responses to FVIII: a study of 246 samples and correlation with the Bethesda assay
|
SAHUD, M. A.
|
|
2007
|
|
3 |
p. 317-322
|
artikel
|
| 9 |
Erratum
|
|
|
2007
|
|
3 |
p. 344
|
artikel
|
| 10 |
Evaluation of the oral health situation of a group of Egyptian haemophilic children and their re-evaluation following an oral hygiene and diet education programme
|
KABIL, N.
|
|
2007
|
|
3 |
p. 287-292
|
artikel
|
| 11 |
Exercise may decrease further destruction in the adult haemophilic joint
|
HARRIS, S.
|
|
2006
|
|
3 |
p. 237-240
|
artikel
|
| 12 |
Failure of rituximab to induce immune tolerance in a boy with severe haemophilia A and an alloimmune factor VIII antibody: a case report and review of the literature
|
BISS, T. T.
|
|
2006
|
|
3 |
p. 280-284
|
artikel
|
| 13 |
Fractures of long bones in severe haemophilia
|
GHOSH, K.
|
|
2007
|
|
3 |
p. 337-339
|
artikel
|
| 14 |
Hepatotoxicity of antiretroviral drugs in HIV HCV patients with congenital coagulopathies followed at an Haemophilia Unit during a decade
|
SAULEDA, S.
|
|
2006
|
|
3 |
p. 228-236
|
artikel
|
| 15 |
Identification of factor VIII gene mutations and carrier detection in Korean haemophilia A patients
|
HAN, J.-Y.
|
|
2007
|
|
3 |
p. 331-333
|
artikel
|
| 16 |
Information and self-management needs of people living with bleeding disorders: a survey
|
BARLOW, J. H.
|
|
2007
|
|
3 |
p. 264-270
|
artikel
|
| 17 |
Insight into molecular changes of the FIX protein in a series of Italian patients with haemophilia B
|
BICOCCHI, M. P.
|
|
2006
|
|
3 |
p. 263-270
|
artikel
|
| 18 |
Meeting Report: Abstracts of the 9th World Federation of Hemophilia Musculoskeletal Congress, September 9--11, 2005, Istanbul, Turkey
|
|
|
2006
|
|
3 |
p. 289-300
|
artikel
|
| 19 |
Paediatric acquired von Willebrand Syndrome
|
WILL, A.
|
|
2006
|
|
3 |
p. 287-288
|
artikel
|
| 20 |
Participation in sports and physical activity of haemophilia patients
|
FROMME, A.
|
|
2007
|
|
3 |
p. 323-327
|
artikel
|
| 21 |
Predicting severity of haemophilia A and B splicing mutations by information analysis
|
KODOLITSCH, Y.
|
|
2006
|
|
3 |
p. 258-262
|
artikel
|
| 22 |
Prophylactic treatment with activated prothrombin complex concentrate (FEIBA®) reduces the frequency of bleeding episodes in paediatric patients with haemophilia A and inhibitors
|
LEISSINGER, C. A.
|
|
2007
|
|
3 |
p. 249-255
|
artikel
|
| 23 |
Prophylaxis in the haemophilia population-optimizing therapy
|
CARCAO, M. D.
|
|
2007
|
|
3 |
p. 227-232
|
artikel
|
| 24 |
Psychological aspects and coping styles of parents with Haemophilic child undergoing a programme of counselling and psychological support
|
BOTTOS, A. M.
|
|
2007
|
|
3 |
p. 305-310
|
artikel
|
| 25 |
Reduced bone density in individuals with combined factor V and VIII deficiency
|
MANSOURITORGHABEH, H.
|
|
2007
|
|
3 |
p. 340-343
|
artikel
|
| 26 |
Reformulated B eneF ix®: efficacy and safety in previously treated patients with moderately severe to severe haemophilia B
|
LAMBERT, T.
|
|
2007
|
|
3 |
p. 233-243
|
artikel
|
| 27 |
Rituximab for adolescents with haemophilia and high titre inhibitors
|
FOX, R. A.
|
|
2006
|
|
3 |
p. 218-222
|
artikel
|
| 28 |
Sequential therapy with activated prothrombin complex concentrates and recombinant FVIIa in patients with severe haemophilia and inhibitors: update of our previous experience
|
SCHNEIDERMAN, J.
|
|
2007
|
|
3 |
p. 244-248
|
artikel
|
| 29 |
Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment
|
INGERSLEV, J.
|
|
2007
|
|
3 |
p. 334-336
|
artikel
|
| 30 |
Sonography for assessment of haemophilic arthropathy in children: a systematic protocol
|
ZUKOTYNSKI, K.
|
|
2007
|
|
3 |
p. 293-304
|
artikel
|
| 31 |
Spectrum of mutations in Albanian patients with haemophilia A: identification of ten novel mutations in the factor VIII gene
|
CASTAMAN, G.
|
|
2007
|
|
3 |
p. 311-316
|
artikel
|
| 32 |
Sustained expression of Epstein–Barr virus episomal vector mediated factor VIII in vivo following muscle electroporation
|
MEI, W.-H.
|
|
2006
|
|
3 |
p. 271-279
|
artikel
|
| 33 |
Trends in the utilization and wastage of coagulation factor concentrates: the application of a regional tracking programme
|
ARNOLD, D. M.
|
|
2007
|
|
3 |
p. 271-278
|
artikel
|
| 34 |
Unresolved issues in diagnosis and management of inherited bleeding disorders in the perinatal period: A White Paper of the Perinatal Task Force of the Medical and Scientific Advisory Council of the National Hemophilia Foundation, USA
|
KULKARNI, R.
|
|
2006
|
|
3 |
p. 205-211
|
artikel
|
| 35 |
Upper gastrointestinal bleeding in haemophiliacs: incidence and relation to use of non-steroidal anti-inflammatory drugs
|
EYSTER, M. E.
|
|
2007
|
|
3 |
p. 279-286
|
artikel
|
| 36 |
Von Willebrand's disease and angiodysplasia treated with thalidomide
|
HIRRI, H. M.
|
|
2006
|
|
3 |
p. 285-286
|
artikel
|
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