Detalhe da pesquisa
1.
Liver-related complications before and after successful treatment of chronic hepatitis C virus infection in people with inherited bleeding disorders.
Haemophilia
; 29(1): 106-114, 2023 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-36184751
2.
Viral hepatitis in haemophilia: historical perspective and current management.
Br J Haematol
; 195(2): 174-185, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-33955555
3.
Antifibrinolytic therapy for preventing oral bleeding in patients with haemophilia or Von Willebrand disease undergoing minor oral surgery or dental extractions.
Cochrane Database Syst Rev
; 4: CD011385, 2019 04 19.
Artigo
Inglês
| MEDLINE | ID: mdl-31002742
4.
Antifibrinolytic therapy for preventing oral bleeding in people on anticoagulants undergoing minor oral surgery or dental extractions.
Cochrane Database Syst Rev
; 7: CD012293, 2018 07 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29963686
5.
Bleeding spectrum in children with moderate or severe von Willebrand disease: Relevance of pediatric-specific bleeding.
Am J Hematol
; 90(12): 1142-8, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26375306
6.
Antifibrinolytic therapy for preventing oral bleeding in patients with haemophilia or Von Willebrand disease undergoing minor oral surgery or dental extractions.
Cochrane Database Syst Rev
; (12): CD011385, 2015 Dec 24.
Artigo
Inglês
| MEDLINE | ID: mdl-26704192
7.
Inhibitor incidence after intensive FVIII replacement for surgery in mild and moderate haemophilia A: a prospective national study in the Netherlands.
Br J Haematol
; 157(6): 747-52, 2012 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-22533635
8.
Socioeconomic participation of persons with hemophilia: Results from the sixth hemophilia in the Netherlands study.
Res Pract Thromb Haemost
; 6(6): e12741, 2022 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-36051543
9.
How I treat age-related morbidities in elderly persons with hemophilia.
Blood
; 114(26): 5256-63, 2009 Dec 17.
Artigo
Inglês
| MEDLINE | ID: mdl-19837978
10.
Health and treatment outcomes of patients with hemophilia in the Netherlands, 1972-2019.
J Thromb Haemost
; 19(10): 2394-2406, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34117710
11.
Mortality, life expectancy, and causes of death of persons with hemophilia in the Netherlands 2001-2018.
J Thromb Haemost
; 19(3): 645-653, 2021 03.
Artigo
Inglês
| MEDLINE | ID: mdl-33217158
12.
ADAMTS-13 and bleeding phenotype in von Willebrand disease.
Res Pract Thromb Haemost
; 4(8): 1331-1339, 2020 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-33313472
13.
Desmopressin treatment combined with clotting factor VIII concentrates in patients with non-severe haemophilia A: protocol for a multicentre single-armed trial, the DAVID study.
BMJ Open
; 9(4): e022719, 2019 04 23.
Artigo
Inglês
| MEDLINE | ID: mdl-31015264
14.
IgG subclasses of anti-FVIII antibodies during immune tolerance induction in patients with hemophilia A.
Br J Haematol
; 142(4): 644-52, 2008 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-18510679
15.
Circulating Angiogenic Mediators in Patients with Moderate and Severe von Willebrand Disease: A Multicentre Cross-Sectional Study.
Thromb Haemost
; 118(1): 152-160, 2018 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29304535
16.
Management of cardiovascular disease in aging persons with haemophilia.
Hamostaseologie
; 37(3): 196-201, 2017 Aug 07.
Artigo
Inglês
| MEDLINE | ID: mdl-27966004
17.
Nonacog beta pegol (N9-GP) in haemophilia B: A multinational phase III safety and efficacy extension trial (paradigm™4).
Thromb Res
; 141: 69-76, 2016 May.
Artigo
Inglês
| MEDLINE | ID: mdl-26970716
18.
Discontinuing early prophylaxis in severe haemophilia leads to deterioration of joint status despite low bleeding rates.
Thromb Haemost
; 115(5): 931-8, 2016 05 02.
Artigo
Inglês
| MEDLINE | ID: mdl-26791021
19.
[Von Willebrand disease in the Netherlands: the WiN study]. / De ziekte van von Willebrand in Nederland: de WiN-studie.
Ned Tijdschr Geneeskd
; 158: A6518, 2014.
Artigo
Holandês
| MEDLINE | ID: mdl-24800796
20.
Inhibition of fibrinolysis by recombinant factor VIIa in plasma from patients with severe hemophilia A.
Blood
; 99(1): 175-9, 2002 Jan 01.
Artigo
Inglês
| MEDLINE | ID: mdl-11756168