X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (157) 157
hematology (137) 137
adult (99) 99
male (83) 83
adolescent (77) 77
middle aged (77) 77
index medicus (75) 75
hemophilia (73) 73
child (58) 58
aged (55) 55
hemophilia a - complications (51) 51
female (50) 50
child, preschool (42) 42
haemophilia (40) 40
von willebrand disease (37) 37
young adult (34) 34
hemophilia a - drug therapy (33) 33
peripheral vascular disease (33) 33
hemophilia a - immunology (31) 31
infant (30) 30
netherlands (30) 30
aged, 80 and over (29) 29
risk factors (28) 28
arthropathy (27) 27
hemophilia a - therapy (27) 27
factor viii - immunology (26) 26
factor viii - therapeutic use (25) 25
prevalence (25) 25
prophylaxis (25) 25
cohort studies (24) 24
diagnosis (23) 23
von willebrand factor (23) 23
management (22) 22
quality-of-life (22) 22
blood coagulation factor viii (21) 21
hepatitis c (21) 21
factor viii - administration & dosage (20) 20
treatment outcome (20) 20
hemophilia a - blood (18) 18
factor-viii (17) 17
hemophilia a - epidemiology (17) 17
mortality (17) 17
adult patients (16) 16
bleeding (16) 16
retrospective studies (16) 16
age factors (15) 15
care and treatment (15) 15
cross-sectional studies (15) 15
follow-up studies (15) 15
hemophilia b - complications (15) 15
phenotype (15) 15
quality of life (15) 15
surveys and questionnaires (15) 15
children (14) 14
hepatitis c virus (14) 14
inhibitors (14) 14
haemophilia a (13) 13
immune tolerance (13) 13
moderate (13) 13
netherlands - epidemiology (13) 13
risk (13) 13
analysis (12) 12
hemophilia a - genetics (12) 12
hepatitis c, chronic - complications (12) 12
mutation (12) 12
prospective studies (12) 12
antibodies (11) 11
cardiovascular disease (11) 11
comorbidity (11) 11
factor ix - therapeutic use (11) 11
genetic aspects (11) 11
risk-factors (11) 11
severity of illness index (11) 11
therapy (11) 11
umcg approved (11) 11
von willebrand diseases - complications (11) 11
bleeding disorders (10) 10
blood coagulation factors - therapeutic use (10) 10
disease (10) 10
factor viii (10) 10
hemophilia b - drug therapy (10) 10
hemorrhage - etiology (10) 10
hemorrhage - prevention & control (10) 10
hepatitis c, chronic - drug therapy (10) 10
journal article (10) 10
time factors (10) 10
age (9) 9
cohort (9) 9
fibrinolysis (9) 9
health aspects (9) 9
hemophilia-a (9) 9
hemorrhage (9) 9
medicine, general & internal (9) 9
population (9) 9
reliability (9) 9
surgery (9) 9
antiviral agents - therapeutic use (8) 8
atherosclerosis (8) 8
factor viii - genetics (8) 8
factor-viii inhibitors (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Haemophilia, ISSN 1351-8216, 09/2016, Volume 22, Issue 6, p. 943–948
INTRODUCTION: Musculoskeletal impact of haemophilia justifies physiotherapy throughout life. Recently the Dutch Health Care Institute constrained their 'list... 
cost-effectiveness | evidence | physiotherapy | science | outcome | Journal Article
Journal Article
Journal of thrombosis and haemostasis, ISSN 1538-7933, 2013, Volume 11, Issue 5, pp. 845 - 854
Journal Article
Blood, ISSN 0006-4971, 12/2009, Volume 114, Issue 26, pp. 5256 - 5263
In persons with hemophilia, life expectancy is now approaching that of the general male population, at least in countries that can afford regular replacement... 
SEROTONIN REUPTAKE INHIBITORS | RISK-FACTORS | INHERITED BLEEDING DISORDERS | FACTOR-VIII INHIBITORS | ANTITHROMBOTIC THERAPY | MULTICENTER COHORT | HEMATOLOGY | THROMBOLYTIC THERAPY | LIFE EXPECTANCY | ACTIVATED FACTOR-VII | ATRIAL-FIBRILLATION | Hemophilia A - diet therapy | Comorbidity - trends | Humans | Aging | Male | Aged | Hemophilia A - epidemiology
Journal Article
Journal of thrombosis and haemostasis, ISSN 1538-7933, 2015, Volume 13, Issue 7, pp. 1217 - 1225
Journal Article
Journal of thrombosis and haemostasis, ISSN 1538-7933, 2018, Volume 16, Issue 12, pp. 2413 - 2424
Essentials It is unclear whether there are differences between von Willebrand factor (VWF) activity assays. We compared the four most used VWF activity assays... 
blood coagulation disorders | subtype classification | von Willebrand disease | clinical laboratory techniques | von Willebrand factor | PANEL | VWF | PERFORMANCE | CLASSIFICATION | DISEASE | PERIPHERAL VASCULAR DISEASE | RISTOCETIN COFACTOR | HEMATOLOGY | BINDING | PROPEPTIDE | Monoclonal antibodies | Von Willebrand factor | Platelets | Health risk assessment | Ristocetin | Classification
Journal Article