Alvaro Blanch

Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

A Agostoni, Emel Aygören‐Pürsün, Karen Binkley et al. · Journal of Allergy and Clinical Immunology · 2004 · 640 citations · Full text

Hereditary angioedema due to C1 inhibitor deficiency: patient registry and approach to the prevalence in Spain

O. Roche, Alvaro Blanch, Teresa Caballero et al. · Annals of Allergy Asthma & Immunology · 2005 · 209 citations

Patient Registry, Cardiovascular Disease, C1 Inhibitor Deficiency +7

Mdm2-mediated NEDD8 Modification of TAp73 Regulates Its Transactivation Function

Ian R. Watson, Alvaro Blanch, Dan Lin et al. · Journal of Biological Chemistry · 2006 · 116 citations · Full text

Molecular Regulation, Molecular Biology, Cysteine Protease +17

Hereditary angioedema: The mutation spectrum of<i>SERPING1/C1NH</i>in a large Spanish cohort

O. Roche, Alvaro Blanch, Christiane Duponchel et al. · Human Mutation · 2005 · 79 citations

First case of homozygous C1 inhibitor deficiency

Alvaro Blanch, O. Roche, Inés Urrutia et al. · Journal of Allergy and Clinical Immunology · 2006 · 77 citations

Mendelian Disorder, Genetic Disorder, Medicine +5