Detalhe da pesquisa
1.
Diagnostic utility of bleeding assessment tools in congenital fibrinogen deficiencies.
Haemophilia
; 29(3): 827-835, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36897560
2.
IgG subclasses as biomarkers for persistence of factor VIII inhibitors in previously untreated patients with severe haemophilia A.
Br J Haematol
; 192(3): 621-625, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33316077
3.
Performance of a clinical risk prediction model for inhibitor formation in severe haemophilia A.
Haemophilia
; 27(4): e441-e449, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33988289
4.
An international registry of patients with plasminogen deficiency (HISTORY).
Haematologica
; 105(3): 554-561, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32001536
5.
Genetic risk stratification to reduce inhibitor development in the early treatment of hemophilia A: a SIPPET analysis.
Blood
; 130(15): 1757-1759, 2017 10 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28768627
6.
Nonneutralizing antibodies against factor VIII and risk of inhibitor development in severe hemophilia A.
Blood
; 129(10): 1245-1250, 2017 03 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28034891
7.
Rare bleeding disorders: diagnosis and treatment.
Blood
; 125(13): 2052-61, 2015 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-25712993
8.
Hemostatic alterations in COVID-19.
Haematologica
; 106(5): 1472-1475, 2021 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32855280
9.
Role of factor VIII-binding capacity of endogenous von Willebrand factor in the development of factor VIII inhibitors in patients with severe hemophilia A.
Haematologica
; 104(8): e369-e372, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30705098
10.
Congenital thrombotic thrombocytopenic purpura with novel mutations in three unrelated Turkish children.
Pediatr Blood Cancer
; 61(3): 558-61, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24115559
11.
Predictive parameters for spontaneous joint bleeding during emicizumab prophylaxis.
Blood Adv
; 8(11): 2901-2907, 2024 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38531053
12.
Predicting inhibitor development using a random peptide phage-display library approach in the SIPPET cohort.
Blood Adv
; 8(11): 2880-2889, 2024 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38593222
13.
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
Blood Adv
; 8(6): 1392-1404, 2024 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38286442
14.
Rare bleeding disorders: worldwide efforts for classification, diagnosis, and management.
Semin Thromb Hemost
; 39(6): 579-84, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23888434
15.
Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for ultra-rare inherited bleeding disorders.
Expert Rev Hematol
; 16(sup1): 55-70, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36920862
16.
No changes of parameters nor coagulation activation in healthy subjects vaccinated for SARS-Cov-2.
Thromb Update
; 4: 100059, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-38620667
17.
ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura.
Hum Mutat
; 31(1): 11-9, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19847791
18.
Different clinical severity of first episodes and recurrences of thrombotic thrombocytopenic purpura.
Br J Haematol
; 151(5): 488-94, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20955397
19.
Clinical and laboratory diagnosis of rare coagulation disorders (RCDs).
Thromb Res
; 196: 603-608, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31515069
20.
Introduction. Rare bleeding disorders: general aspects of clinical features, diagnosis, and management.
Semin Thromb Hemost
; 35(4): 349-55, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19598063