Detalhe da pesquisa
1.
Platelet function and filamin A expression in two families with novel FLNA gene mutations associated with periventricular nodular heterotopia and panlobular emphysema.
Am J Med Genet A
; 188(6): 1716-1722, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35156755
2.
Characterisation of healthcare utilisation and cost of haemophilia care in real-life: A 4-year follow-up study in Finland.
Haemophilia
; 27(1): e30-e39, 2021 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-33216410
3.
Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders.
Int J Mol Sci
; 22(5)2021 Feb 25.
Artigo
Inglês
| MEDLINE | ID: mdl-33668986
4.
Interleukin-6 increases expression of serine protease inhibitor Kazal type 1 through STAT3 in colorectal adenocarcinoma.
Mol Carcinog
; 55(12): 2010-2023, 2016 12.
Artigo
Inglês
| MEDLINE | ID: mdl-26663388
5.
Intravenous immunoglobulin treatment in a type 3 von Willebrand disease patient with alloantibodies and a life-threatening gastrointestinal bleed.
Haemophilia
; 25(4): e291-e293, 2019 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-31050121
6.
Novel missense mutations affecting the structure of the conserved fibrinogen Bß C-terminal domain cause congenital hypofibrinogenemia.
Thromb Res
; 206: 5-8, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34352655