Investigador Ramon y Cajal

Investigador Ramón y Cajal

Foto de Investigador Ramon y Cajal

Foto de Salam

Salam
Salloum Asfar

Salam Salloum Asfar-rekin lankidetzan egindako argitalpenak (6)

2020

When genetic and surname analyses meet historical sources: The C56R mutation associated with factor XI deficiency as a marker of human migration during the Spanish Reconquista
Medical Hypotheses, Vol. 141

2019

Archeogenetics of F11 p.Cys38Arg: A 5400-year-old mutation identified in different southwestern European countries
Blood
Gynaecological and obstetrical bleeding in Caucasian women with congenital factor XI deficiency: Results from a twenty-year, retrospective, observational study
Medicina Clinica, Vol. 153, Núm. 10, pp. 373-379

2018

Assessment of two contact activation reagents for the diagnosis of congenital factor XI deficiency
Thrombosis Research, Vol. 163, pp. 64-70

2017

High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study
Haemophilia, Vol. 23, Núm. 6, pp. e488-e496

2013

Control of post-translational modifications in antithrombin during murine post-natal development by miR-200a
Journal of Biomedical Science, Vol. 20, Núm. 1