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Human Mutation|October 29, 2002
Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutationsAlvaro Blanch, Olga Roche, Eduardo López-Granados, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|May 7, 2005
Hereditary angioedema due to C1 inhibitor deficiency: patient registry and approach to the prevalence in SpainOlga Roche, Alvaro Blanch, Teresa Caballero, et al.
Human Mutation|June 23, 2005
Hereditary angioedema: the mutation spectrum of SERPING1/C1NH in a large Spanish cohortOlga Roche, Alvaro Blanch, Christiane Duponchel, et al.
Plos One|June 27, 2013
Eukaryotic translation elongation factor 1-alpha 1 inhibits p53 and p73 dependent apoptosis and chemotherapy sensitivityAlvaro Blanch, Fiona Robinson, Ian R Watson, et al.
The Journal of Allergy and Clinical Immunology|December 2, 2006
First case of homozygous C1 inhibitor deficiencyAlvaro Blanch, Olga Roche, Ignacio Urrutia, et al.
The Journal of Biological Chemistry|September 19, 2006
Mdm2-mediated NEDD8 modification of TAp73 regulates its transactivation functionIan R Watson, Alvaro Blanch, Dan C C Lin, et al.
Oncotarget|January 7, 2014
Anti-tumor activity of the beta-adrenergic receptor antagonist propranolol in neuroblastomaJennifer K Wolter, Nikolaus E Wolter, Alvaro Blanch, et al.
The Journal of Allergy and Clinical Immunology|September 10, 2004
Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyondAngelo Agostoni, Emel Aygören-Pürsün, Karen E Binkley, et al.
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