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Alberto López-Lera

6PUBLICATIONS

27CO-AUTHORS

HaematologyCardiology (incl. cardiovascular diseases)Autoimmunity

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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

Frequent Collaborators

2 joint publications

Margarita López-Trascasa

2 joint publications

Christian Drouet

2 joint publications

Teresa Caballero

1 joint publications

Christine Gaboriaud

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