| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Blastocystis hominis colitis in a haemophilic patient as a cause of lower gastrointestinal bleeding
|
LUCÍA, J. F.
|
|
2007
|
13 |
2 |
p. 224-225
|
artikel
|
| 2 |
Communicating about haemophilia within the family: the importance of context and of experience
|
GREGORY, M.
|
|
2007
|
13 |
2 |
p. 189-198
|
artikel
|
| 3 |
Different clinical phenotype in triplets with haemophilia A
|
BARNES, C.
|
|
2007
|
13 |
2 |
p. 202-205
|
artikel
|
| 4 |
Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A
|
CHALMERS, E. A.
|
|
2007
|
13 |
2 |
p. 149-155
|
artikel
|
| 5 |
Efficacy and safety of a high purity, double virus inactivated factor VIII/von Willebrand factor concentrate (Biostate®) in patients with von Willebrand disorder requiring invasive or surgical procedures
|
SHORTT, J.
|
|
2007
|
13 |
2 |
p. 144-148
|
artikel
|
| 6 |
Efficacy, safety and tolerability of recombinant factor VIII (REFACTO®) in patients with haemophilia A: interim data from a postmarketing surveillance study in Germany and Austria
|
POLLMANN, H.
|
|
2007
|
13 |
2 |
p. 131-143
|
artikel
|
| 7 |
Factor VIII Inhibitor Associated with Peginterferon – A Follow Up
|
HERMAN, C. H.
|
|
2007
|
13 |
2 |
p. 213
|
artikel
|
| 8 |
Hepatitis C virus genotypes among patients with thalassemia and inherited bleeding disorders in Markazi province, Iran
|
SAMIMI-RAD, K.
|
|
2007
|
13 |
2 |
p. 156-163
|
artikel
|
| 9 |
Inhibitor development in one patient and laboratory discrepancies in several families with both mild haemophilia and Arg531Cys mutation
|
CID, A. R.
|
|
2007
|
13 |
2 |
p. 206-208
|
artikel
|
| 10 |
Is primary postpartum haemorrhage a good predictor of inherited bleeding disorders?
|
KADIR, R. A.
|
|
2007
|
13 |
2 |
p. 178-181
|
artikel
|
| 11 |
Molecular characterization of a novel mutation in the factor XIII A subunit gene associated with a severe defect and an adulthood diagnosis
|
TRIGUI, N.
|
|
2007
|
13 |
2 |
p. 221-222
|
artikel
|
| 12 |
Multicentric giant cell tumours in an adolescent with haemophilia
|
CHANG, C.-C.
|
|
2007
|
13 |
2 |
p. 199-201
|
artikel
|
| 13 |
32P colloid radiosynovectomy in treatment of chronic haemophilic synovitis: Iran experience
|
MORTAZAVI, S. M. J.
|
|
2007
|
13 |
2 |
p. 182-188
|
artikel
|
| 14 |
Percutaneous liver biopsy in adult haemophiliacs with hepatitis C virus: safety of outpatient procedure and impact of human immunodeficiency virus coinfection on the spectrum of liver disease
|
STERLING, R. K.
|
|
2007
|
13 |
2 |
p. 164-171
|
artikel
|
| 15 |
Pharmacovigilance studies in haemophilia
|
INGERSLEV, J.
|
|
2007
|
13 |
2 |
p. 121-123
|
artikel
|
| 16 |
ReFacto® 1 and Advate® 2: a single-dose, randomized, two-period crossover pharmacokinetics study in subjects with haemophilia A
|
DI PAOLA, J.
|
|
2007
|
13 |
2 |
p. 124-130
|
artikel
|
| 17 |
Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders
|
SHETTY, S.
|
|
2007
|
13 |
2 |
p. 172-177
|
artikel
|
| 18 |
Successful combination therapy of a proximal haemophilic pseudotumour with surgery, radiation and embolization in a child with mild haemophilia A
|
AHUJA, S. P.
|
|
2007
|
13 |
2 |
p. 209-212
|
artikel
|
| 19 |
Successful concurrent triple surgery in an adolescent patient with haemophilia A and inhibitors treated with recombinant factor VIIa
|
JANIC, D.
|
|
2007
|
13 |
2 |
p. 214-216
|
artikel
|
| 20 |
The coagulation laboratory needs to move out of the middle age
|
LIPTON, R.
|
|
2007
|
13 |
2 |
p. 223
|
artikel
|
| 21 |
The haemophilic pseudotumour – surgical treatment by excision and filling the defect with calcium-phosphate cement granules
|
MOHANTY, S. S.
|
|
2007
|
13 |
2 |
p. 217-220
|
artikel
|
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