Alfonso Pérez-Molino

Mutation study of Spanish patients with Hereditary Hemorrhagic Telangiectasia

F. Blanco, Africa Fernández-L, C. Bernabéu, 2008, BMC Medical Genetics.

Blood outgrowth endothelial cells from Hereditary Haemorrhagic Telangiectasia patients reveal abnormalities compatible with vascular lesions.

R. Hebbel, Africa Fernández-L, F. Sanz‐Rodríguez, 2005, Cardiovascular research.

Mutation analysis in Spanish patients with hereditary hemorrhagic telangiectasia: deficient endoglin up-regulation in activated monocytes.

E. Coto, Africa Fernández-L, F. Sanz‐Rodríguez, 2004, Clinical chemistry.

Therapeutic action of tranexamic acid in hereditary haemorrhagic telangiectasia (HHT): Regulation of ALK-1/endoglin pathway in endothelial cells

Africa Fernández-L, F. Sanz‐Rodríguez, C. Bernabéu, 2007, Thrombosis and Haemostasis.

Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1

E. Coto, Africa Fernández-L, C. Restrepo, 2006, Human mutation.

Mutation study of Spanish patients with Hereditary Hemorrhagic Telangiectasia

F. Blanco, Africa Fernández-L, C. Bernabéu, 2008, BMC Medical Genetics.