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 |
13 |
3 |
p. 328-330 |
artikel |
2 |
A systematic approach to controlling problem bleeds in patients with severe congenital haemophilia A and high-titre inhibitors
|
TEITEL, J. |
|
2007 |
13 |
3 |
p. 256-263 |
artikel |
3 |
ELISA system for detection of immune responses to FVIII: a study of 246 samples and correlation with the Bethesda assay
|
SAHUD, M. A. |
|
2007 |
13 |
3 |
p. 317-322 |
artikel |
4 |
Erratum
|
|
|
2007 |
13 |
3 |
p. 344 |
artikel |
5 |
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 |
13 |
3 |
p. 287-292 |
artikel |
6 |
Fractures of long bones in severe haemophilia
|
GHOSH, K. |
|
2007 |
13 |
3 |
p. 337-339 |
artikel |
7 |
Identification of factor VIII gene mutations and carrier detection in Korean haemophilia A patients
|
HAN, J.-Y. |
|
2007 |
13 |
3 |
p. 331-333 |
artikel |
8 |
Information and self-management needs of people living with bleeding disorders: a survey
|
BARLOW, J. H. |
|
2007 |
13 |
3 |
p. 264-270 |
artikel |
9 |
Participation in sports and physical activity of haemophilia patients
|
FROMME, A. |
|
2007 |
13 |
3 |
p. 323-327 |
artikel |
10 |
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 |
13 |
3 |
p. 249-255 |
artikel |
11 |
Prophylaxis in the haemophilia population-optimizing therapy
|
CARCAO, M. D. |
|
2007 |
13 |
3 |
p. 227-232 |
artikel |
12 |
Psychological aspects and coping styles of parents with Haemophilic child undergoing a programme of counselling and psychological support
|
BOTTOS, A. M. |
|
2007 |
13 |
3 |
p. 305-310 |
artikel |
13 |
Reduced bone density in individuals with combined factor V and VIII deficiency
|
MANSOURITORGHABEH, H. |
|
2007 |
13 |
3 |
p. 340-343 |
artikel |
14 |
Reformulated B eneF ix®: efficacy and safety in previously treated patients with moderately severe to severe haemophilia B
|
LAMBERT, T. |
|
2007 |
13 |
3 |
p. 233-243 |
artikel |
15 |
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 |
13 |
3 |
p. 244-248 |
artikel |
16 |
Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment
|
INGERSLEV, J. |
|
2007 |
13 |
3 |
p. 334-336 |
artikel |
17 |
Sonography for assessment of haemophilic arthropathy in children: a systematic protocol
|
ZUKOTYNSKI, K. |
|
2007 |
13 |
3 |
p. 293-304 |
artikel |
18 |
Spectrum of mutations in Albanian patients with haemophilia A: identification of ten novel mutations in the factor VIII gene
|
CASTAMAN, G. |
|
2007 |
13 |
3 |
p. 311-316 |
artikel |
19 |
Trends in the utilization and wastage of coagulation factor concentrates: the application of a regional tracking programme
|
ARNOLD, D. M. |
|
2007 |
13 |
3 |
p. 271-278 |
artikel |
20 |
Upper gastrointestinal bleeding in haemophiliacs: incidence and relation to use of non-steroidal anti-inflammatory drugs
|
EYSTER, M. E. |
|
2007 |
13 |
3 |
p. 279-286 |
artikel |