Lera, Alberto López: search on Z-Library

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1

Disease-modifying factors in hereditary angioedema: an RNA expression-based screening

Alberto López-Lera, Fátima Sánchez Cabo, Sofía Garrido…

Journal:

Orphanet Journal of Rare Diseases

Year:

2013

Language:

english

File:

PDF, 326 KB

english, 2013

2

Analysis of SERPING1 expression on hereditary angioedema patients: Quantitative analysis of full-length and exon 3 splicing variants

Rocío Mena de la Cruz, Alberto López-Lera, Margarita López-Trascasa

Journal:

Immunology Letters

Year:

2012

Language:

english

File:

PDF, 258 KB

english, 2012

3

Expression of theSERPING1gene is not regulated by promoter hypermethylation in peripheral blood mononuclear cells from patients with hereditary angioedema due to C1-inhibitor deficiency

Alberto López-Lera,Olga Pernia…

Journal:

Orphanet Journal of Rare Diseases

Year:

2014

Language:

english

File:

PDF, 944 KB

english, 2014

4

SERPING1 mutations in 59 families with hereditary angioedema

Alberto López-Lera, Sofía Garrido, Olga Roche, Margarita López-Trascasa

Journal:

Molecular Immunology

Year:

2011

Language:

english

File:

PDF, 780 KB

english, 2011

5

Complement factor I deficiency: a not so rare immune defect. Characterization of new mutations and the first large gene deletion

María Alba-Domínguez, Alberto López-Lera, Sofía Garrido, Pilar Nozal, Ignacio González-Granado, Josefa Melero, Pere Soler-Palacín, Carmen Cámara, Margarita López-Trascasa

Journal:

Orphanet Journal of Rare Diseases

Year:

2012

Language:

english

File:

PDF, 574 KB

english, 2012

6

Perceived performance effects of ICT in manufacturing SMEs

Bayo‐Moriones, Alberto, Billón, Margarita, Lera‐López, Fernando

Journal:

Industrial Management & Data Systems

Year:

2013

Language:

english

File:

PDF, 346 KB

english, 2013

7

Immunological features of patients affected by Barraquer-Simons syndrome

Corvillo, Fernando, Ceccarini, Giovanni, Nozal, Pilar, Magno, Silvia, Pelosini, Caterina, Garrido, Sofía, López-Lera, Alberto, Moraru, Manuela, Vilches, Carlos, Fornaciari, Silvia, Gabbriellini, Sabri

Journal:

Orphanet Journal of Rare Diseases

Year:

2020

Language:

english

File:

PDF, 647 KB

english, 2020

8

A firm-level analysis of determinants of ICT adoption in Spain

Alberto Bayo-Moriones, Fernando Lera-López

Journal:

Year:

2007

Language:

english

File:

PDF, 312 KB

english, 2007

9

Analysis of natural allelic variation inin vitroorganogenesis ofArabidopsis thaliana

Ignacio Velázquez, Silvia Valencia, Alberto López-Lera, Alicia de la Peña, Milagros Candela

Journal:

Year:

2004

Language:

english

File:

PDF, 301 KB

english, 2004

10

Human plasma C3 is essential for the development of memory B, but not T, lymphocytes

Jiménez-Reinoso, Anaïs, Marin, Ana V., Subias, Marta, López-Lera, Alberto, Román-Ortiz, Elena, Payne, Kathryn, Ma, Cindy S., Arbore, Giuseppina, Kolev, Martin, Freeley, Simon J., Kemper, Claudia, Tang

Journal:

Journal of Allergy and Clinical Immunology

Year:

2017

Language:

english

File:

PDF, 3.87 MB

english, 2017

11

High frequency in the delay in primary tooth loss in X-linked chronic granulomatous disease

de Diego, Rebeca Pérez, Lera, Alberto López, Cerdán, Antonio Ferreira

Journal:

Clinical Immunology

Year:

2012

Language:

english

File:

PDF, 285 KB

english, 2012

12

Molecular characterisation of a C5 deficiency caused by a de novo mutation

Alberto Lopez-Lera, Sofia Garrido-Herrero, Rocio Mena de la Cruz, Jose Manuel Ramos, Gumersindo Fontan, Margarita Lopez-Trascasa

Journal:

Molecular Immunology

Year:

2008

Language:

english

File:

PDF, 83 KB

english, 2008

13

Hereditary angioedema caused by the p.Thr309Lys mutation in the F12 gene: A multifactorial disease

Gómez-Traseira, Carmen, López-Lera, Alberto, Drouet, Christian, López-Trascasa, Margarita, Pérez-Fernández, Elia, Favier, Bertrand, Prior, Nieves, Caballero, Teresa

Journal:

Journal of Allergy and Clinical Immunology

Year:

2013

Language:

english

File:

PDF, 765 KB

english, 2013

14

Clinical, biochemical, and genetic characterization of type III hereditary angioedema in 13 Northwest Spanish families

Marcos, Carmen, López Lera, Alberto, Varela, Susana, Liñares, Tania, Alvarez-Eire, Marimar G., López-Trascasa, Margarita

Journal:

Annals of Allergy, Asthma & Immunology

Year:

2012

Language:

english

File:

PDF, 298 KB

english, 2012

15

Splicing variants in C1 inhibitor gene: Quantitative study in hereditary angioedema patients

Rocio Mena de la Cruz, Alberto Lopez-Lera, Sofia Garrido-Herrero, Gumersindo Fontan, Margarita Lopez-Trascasa

Journal:

Molecular Immunology

Year:

2008

Language:

english

File:

PDF, 66 KB

english, 2008

16

Molecular characterization of three new mutations causing C5 deficiency in two non-related families

Alberto López-Lera, Sofía Garrido, Rocío Mena de la Cruz, Gumersindo Fontán, Margarita López-Trascasa

Journal:

Molecular Immunology

Year:

2009

Language:

english

File:

PDF, 876 KB

english, 2009

17

Similar percentages in most abundant chronic granulomatous disease autosomal recessive forms in a Spanish cohort

Pérez de Diego, Rebeca, López-Lera, Alberto, Ferreira, Antonio

Journal:

Clinical Immunology

Year:

2015

Language:

english

File:

PDF, 231 KB

english, 2015

18

Serum complexes between C1 INH and C1 INH ‐autoantibodies for the diagnosis of Acquired Angioedema

López‐Lera, Alberto, Garrido, Sofía, Nozal, Pilar, Skatum, Lillemor, Bygum, Anette, Caballero, Teresa, López Trascasa, Margarita

Journal:

Clinical & Experimental Immunology

Year:

2019

Language:

english

File:

PDF, 444 KB

english, 2019

19

Are new work practices applied together with ICT and AMT?

Bayo-Moriones, Alberto, Billon, Margarita, Lera-López, Fernando

Journal:

International Journal of Human Resource Management

Year:

2015

Language:

english

File:

PDF, 1.64 MB

english, 2015

20

The relationship between ICTs and HPWPs across occupations

Bayo-Moriones, Alberto, Calleja-Blanco, Jonathan, Lera-López, Fernando

Journal:

International Journal of Manpower

Year:

2015

Language:

english

File:

PDF, 222 KB

english, 2015

21

Hereditary Angioedema: Insights into inflammation and allergy

Maas, Coen, López-Lera, Alberto

Journal:

Molecular Immunology

Year:

2019

Language:

english

File:

PDF, 632 KB

english, 2019

22

Complement as a diagnostic tool in immunopathology

López-Lera, Alberto, Corvillo, Fernando, Nozal, Pilar, Regueiro, José R., Sánchez-Corral, Pilar, López-Trascasa, Margarita

Journal:

Seminars in Cell & Developmental Biology

Year:

2018

Language:

english

File:

PDF, 2.15 MB

english, 2018

23

Skills, technology and organisational innovation in Spanish firms

Bayo‐Moriones, Alberto, Billón, Margarita, Lera‐López, Fernando

Journal:

International Journal of Manpower

Year:

2008

Language:

english

File:

PDF, 291 KB

english, 2008

24

A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation

López-Lera, Alberto, Favier, Bertrand, de la Cruz, Rocío Mena, Garrido, Sofía, Drouet, Christian, López-Trascasa, Margarita

Journal:

Journal of Allergy and Clinical Immunology

Year:

2010

Language:

english

File:

PDF, 480 KB

english, 2010

25

Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency

Loules, Gedeon, Zamanakou, Maria, Parsopoulou, Faidra, Vatsiou, Sofia, Psarros, Fotis, Csuka, Dorottya, Porebski, Grzegorz, Obtulowicz, Krystyna, Valerieva, Anna, Staevska, Maria, López-Lera, Alberto,

Journal:

Year:

2018

Language:

english

File:

PDF, 941 KB

english, 2018

26

Autoantibodies Against Perilipin 1 as a Cause of Acquired Generalized Lipodystrophy

Corvillo, Fernando, Aparicio, Verónica, López-Lera, Alberto, Garrido, Sofía, Araújo-Vilar, David, de Miguel, María P., López-Trascasa, Margarita

Journal:

Frontiers in Immunology

Year:

2018

Language:

english

File:

PDF, 4.41 MB

english, 2018

27

Rothmund–Thomson Syndrome and Glomerulonephritis in a Homozygous C1q-Deficient Patient Due to a Gly164Ser C1qC Mutation

López-Lera, Alberto, M. Torres-Canizales, Juan, Garrido, Sofía, Morales, Adelaida, López-Trascasa, Margarita

Journal:

The Journal of Investigative Dermatology

Year:

2014

Language:

english

File:

PDF, 214 KB

english, 2014

28

Complement Study VersusCINHGene Testing for the Diagnosis of Type I Hereditary Angioedema in Children

Pedrosa, María, Phillips-Angles, Elsa, López-Lera, Alberto, López-Trascasa, Margarita, Caballero, Teresa

Journal:

Journal of Clinical Immunology

Year:

2016

Language:

english

File:

PDF, 228 KB

english, 2016

29

Proteomics-based discovery of an abnormal, internally duplicated CFHR1 protein which associates with renal pathology in a Spanish family

Cynthia Abarrategui-Garrido, Rubén Martínez-Barricarte, Alberto López-Lera, Elena Fariza-Requejo, Carolina Ruivo, Rafael Bedoya-Pérez, Santiago Rodríguez de Córdoba, Margarita López-Trascasa, Pilar Sá

Journal:

Molecular Immunology

Year:

2010

Language:

english

File:

PDF, 75 KB

english, 2010

30

Common and rare genetic variants of complement components in human disease

Goicoechea de Jorge, Elena, López Lera, Alberto, Bayarri-Olmos, Rafael, Yebenes, Hugo, Lopez-Trascasa, Margarita, Rodríguez de Córdoba, Santiago

Journal:

Molecular Immunology

Year:

2018

Language:

english

File:

PDF, 1.31 MB

english, 2018

31

High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3*B

Pouw, Richard B., Gómez Delgado, Irene, López Lera, Alberto, Rodríguez de Córdoba, Santiago, Wouters, Diana, Kuijpers, Taco W., Sánchez-Corral, Pilar

Journal:

Frontiers in Immunology

Year:

2018

Language:

english

File:

PDF, 1.76 MB

english, 2018

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