Detalhe da pesquisa
1.
Evaluation of procoagulant imbalance in Cushing's syndrome after short- and long-term remission of disease.
J Endocrinol Invest
; 45(1): 9-16, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34115342
2.
A comparative evaluation of a new fully automated assay for von Willebrand factor collagen binding activity to an established method.
Haemophilia
; 24(1): 156-161, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29168270
3.
First-year results of an expanded humanitarian aid programme for haemophilia in resource-constrained countries.
Haemophilia
; 24(2): 229-235, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29537123
4.
Ageing successfully with haemophilia: A multidisciplinary programme.
Haemophilia
; 24(1): 57-62, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28780767
5.
"In vitro" correction of the severe factor V deficiency-related coagulopathy by a novel plasma-derived factor V concentrate.
Haemophilia
; 24(4): 648-656, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29578313
6.
Molecular diagnosis of von Willebrand disease.
Haemophilia
; 23(2): 188-197, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28220580
7.
Incidence of low-titre factor VIII inhibitors in patients with haemophilia A: meta-analysis of observational studies.
Haemophilia
; 23(2): e87-e92, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28220685
8.
SIPPET: methodology, analysis and generalizability.
Haemophilia
; 23(3): 353-361, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28306186
9.
New findings on inhibitor development: from registries to clinical studies.
Haemophilia
; 23 Suppl 1: 4-13, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27990784
10.
Involvement of the IgE-basophil system and mild complement activation in haemophilia B with anti-factor IX neutralizing antibodies and anaphylaxis.
Haemophilia
; 23(4): e348-e353, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28594432
11.
Kreuth IV: European consensus proposals for treatment of haemophilia with coagulation factor concentrates.
Haemophilia
; 23(3): 370-375, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28401658
12.
Genomic approaches to bleeding disorders.
Haemophilia
; 22 Suppl 5: 42-5, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27405675
13.
Baseline factor VIII plasma levels and age at first bleeding in patients with severe forms of von Willebrand disease.
Haemophilia
; 22(4): 564-9, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26843468
14.
Efficacy, safety and pharmacokinetics of a new high-purity factor X concentrate in subjects with hereditary factor X deficiency.
Haemophilia
; 22(3): 419-25, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27197801
15.
von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients.
Haemophilia
; 22(6): e502-e511, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27785872
16.
The thrombin generation assay distinguishes inhibitor from non-inhibitor patients with severe haemophilia A.
Haemophilia
; 22(4): e286-91, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27166132
17.
Low thrombin generation during major orthopaedic surgery fails to predict the bleeding risk in inhibitor patients treated with bypassing agents.
Haemophilia
; 22(4): e292-300, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27197961
18.
Long-term prophylaxis in severe factor VII deficiency.
Haemophilia
; 21(6): 812-9, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25952977
19.
Research in haemophilia B--approaching the request for high evidence levels in a rare disease.
Haemophilia
; 21(1): 4-20, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25495927
20.
Rare bleeding disorders - bleeding assessment tools, laboratory aspects and phenotype and therapy of FXI deficiency.
Haemophilia
; 20 Suppl 4: 71-5, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24762279