Detalhe da pesquisa
1.
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis.
Am J Hum Genet
; 102(5): 995-1007, 2018 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29656858
2.
Managing women-specific bleeding in inherited bleeding disorders: A multidisciplinary approach.
Haemophilia
; 27(3): 463-469, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33314402
3.
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis.
Am J Hum Genet
; 103(4): 631, 2018 10 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30290155
4.
History of non-fatal cardiovascular disease in a cohort of Dutch and British patients with haemophilia.
Eur J Haematol
; 89(4): 336-9, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22775476
5.
Successful treatment of fetal hemolytic disease due to glucose phosphate isomerase deficiency (GPI) using repeated intrauterine transfusions: a case report.
Clin Case Rep
; 3(10): 862-5, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26509025
6.
Unfavourable cardiovascular disease risk profiles in a cohort of Dutch and British haemophilia patients.
Thromb Haemost
; 109(1): 16-23, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23138324
7.
Non-fatal cardiovascular disease, malignancies, and other co-morbidity in adult haemophilia patients.
Thromb Res
; 130(2): 157-62, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22209337
8.
Increased prevalence of hypertension in haemophilia patients.
Thromb Haemost
; 108(4): 750-5, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22955860