TY  - JOUR 
AU  - Egido Turrión, Cristina
AU  - Rossi, Elisa
AU  - Ollauri Ibáñez, Claudia
AU  - Pérez García, María Luisa
AU  - Sevilla Toral, María Ángeles
AU  - Bastida Bermejo, José María
AU  - González Porras, José Ramón
AU  - Rodríguez Barbero, Alicia
AU  - Bernabeu, Carmelo
AU  - López-Novoa, José M.
AU  - Pericacho Bustos, Miguel
PY  - 2022
SN  - 2296-858X
UR  - http://hdl.handle.net/10366/154602
AB  - [EN] Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal-dominant genetic disorder involving defects in two predominant genes known as endoglin (ENG; HHT-1) and activin receptor-like kinase 1 (ACVRL1/ALK1; HHT-2). It is characterized by...
LA  - eng
PB  - Frontiers
KW  - Rendu-Osler Disease
KW  - Bleeding
KW  - ALK1 (ACVRL1)
KW  - Hereditary Hemorrhagic Telangiectasia (HHT)
KW  - Epistaxis
KW  - Hemostasia
KW  - Endoglin (CD105)
KW  - Epistaxis
KW  - Telangiectasia, Hereditary Hemorrhagic
KW  - Bleeding Time
KW  - Hemostasis
TI  - Functional Alterations Involved in Increased Bleeding in Hereditary Hemorrhagic Telangiectasia Mouse Models.
DO  - 10.3389/fmed.2022.871903
T2  - Frontiers in medicine
VL  - 9
M2  - 871903
ER  -