Detalhe da pesquisa
1.
Increased galactose expression and enhanced clearance in patients with low von Willebrand factor.
Blood
; 133(14): 1585-1596, 2019 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30770394
2.
Guideline for laboratory diagnosis and monitoring of von Willebrand disease: A joint guideline from the United Kingdom Haemophilia Centre Doctors' Organisation and the British Society for Haematology.
Br J Haematol
; 204(5): 1714-1731, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38532595
3.
Catalogue of inherited disorders found among the Irish Traveller population.
J Med Genet
; 55(4): 233-239, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29358271
4.
Management of a patient with acute myeloid leukaemia with a diagnosis of type 2 von Willebrand disease and a novel variant within the von Willebrand factor (VWF) gene.
Br J Haematol
; 199(2): e5-e7, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35903954
5.
Management of combined factor V and factor VIII deficiency in pregnancy.
J Obstet Gynaecol
; 39(2): 271-272, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29667457
6.
Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation framework.
J Thromb Haemost
; 22(3): 645-665, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38016518
7.
Heterogeneity in the half-life of factor VIII concentrate in patients with hemophilia A is due to variability in the clearance of endogenous von Willebrand factor.
J Thromb Haemost
; 21(5): 1123-1134, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36775768
8.
Clinical utility gene card for: haemophilia B.
Eur J Hum Genet
; 20(5)2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22274582