Alberto López-Lera
6PUBLICATIONS
27CO-AUTHORS
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Publications (6)
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|Jun 27, 2024
Altered levels of phospholipases C, diacylglycerols, endocannabinoids, and N-acylethanolamines in patients with hereditary angioedema due to FXII mutation.Anne Lise Ferrara, Francesco Palestra, Fabiana Piscitelli
|Mar 16, 2021
Thrombin in the Activation of the Fluid Contact Phase in Patients with Hereditary Angioedema Carrying the F12 P.Thr309Lys Variant.R López-Gálvez, M E de la Morena-Barrio, A Miñano
|Jan 20, 2021
In Search of an Association Between Genotype and Phenotype in Hereditary Angioedema due to C1-INH Deficiency.David Loli-Ausejo, Alberto López-Lera, Christian Drouet
|May 24, 2020
Novel homozygous variants in the SERPING1 gene in two Turkish families with hereditary angioedema of recessive inheritance.Nihal Mete Gökmen, César Rodríguez-Alcalde, Okan Gülbahar
|Sep 14, 2019
SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes.Denise Ponard, Christine Gaboriaud, Delphine Charignon
|Aug 10, 2019
Serum complexes between C1INH and C1INH autoantibodies for the diagnosis of acquired angioedema.A López-Lera, S Garrido, P Nozal
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Frequent Collaborators
2 joint publications
Margarita López-Trascasa
2 joint publications
Christian Drouet
2 joint publications
Teresa Caballero
1 joint publications
Christine Gaboriaud
1 joint publications
Delphine Charignon
1 joint publications
Arije Ghannam
1 joint publications
Ineke G A Wagenaar-Bos
1 joint publications
Nihal Mete Gökmen
1 joint publications
Okan Gülbahar
1 joint publications
Hüseyin Onay
