López-Trascasa M - Search Results

1

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

Loules G, Zamanakou M, Parsopoulou F, Vatsiou S, Psarros F, Csuka D, Porebski G, Obtulowicz K, Valerieva A, Staevska M, López-Lera A, López-Trascasa M, Moldovan D, Magerl M, Maurer M, Speletas M, Farkas H, Germenis AE. Loules G, et al. Gene. 2018 Aug 15;667:76-82. doi: 10.1016/j.gene.2018.05.029. Epub 2018 May 16. Gene. 2018. PMID: 29753808

2

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

de la Cruz RM, López-Lera A, López-Trascasa M. de la Cruz RM, et al. Immunol Lett. 2012 Jan 30;141(2):158-64. doi: 10.1016/j.imlet.2011.07.011. Epub 2011 Oct 4. Immunol Lett. 2012. PMID: 22001489

3

SERPING1 mutations in 59 families with hereditary angioedema.

López-Lera A, Garrido S, Roche O, López-Trascasa M. López-Lera A, et al. Mol Immunol. 2011 Oct;49(1-2):18-27. doi: 10.1016/j.molimm.2011.07.010. Epub 2011 Aug 23. Mol Immunol. 2011. PMID: 21864911

4

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

López-Lera A, Cabo FS, Garrido S, Dopazo A, López-Trascasa M. López-Lera A, et al. Orphanet J Rare Dis. 2013 May 20;8:77. doi: 10.1186/1750-1172-8-77. Orphanet J Rare Dis. 2013. PMID: 23688356 Free PMC article.

5

Expression of the SERPING1 gene is not regulated by promoter hypermethylation in peripheral blood mononuclear cells from patients with hereditary angioedema due to C1-inhibitor deficiency.

López-Lera A, Pernia O, López-Trascasa M, Ibanez de Caceres I. López-Lera A, et al. Orphanet J Rare Dis. 2014 Jul 22;9:103. doi: 10.1186/s13023-014-0103-y. Orphanet J Rare Dis. 2014. PMID: 25053016 Free PMC article.

6

Complement Study Versus CINH Gene Testing for the Diagnosis of Type I Hereditary Angioedema in Children.

Pedrosa M, Phillips-Angles E, López-Lera A, López-Trascasa M, Caballero T. Pedrosa M, et al. J Clin Immunol. 2016 Jan;36(1):16-8. doi: 10.1007/s10875-015-0222-9. Epub 2015 Dec 10. J Clin Immunol. 2016. PMID: 26661330 No abstract available.

7

Novel homozygous variants in the SERPING1 gene in two Turkish families with hereditary angioedema of recessive inheritance.

Mete Gökmen N, Rodríguez-Alcalde C, Gülbahar O, Lopez-Trascasa M, Onay H, López-Lera A. Mete Gökmen N, et al. Immunol Cell Biol. 2020 Sep;98(8):693-699. doi: 10.1111/imcb.12362. Epub 2020 Jul 12. Immunol Cell Biol. 2020. PMID: 32445210

8

Serum complexes between C1INH and C1INH autoantibodies for the diagnosis of acquired angioedema.

López-Lera A, Garrido S, Nozal P, Skatum L, Bygum A, Caballero T, López Trascasa M. López-Lera A, et al. Clin Exp Immunol. 2019 Dec;198(3):341-350. doi: 10.1111/cei.13361. Epub 2019 Sep 17. Clin Exp Immunol. 2019. PMID: 31397881 Free PMC article.

9

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

Marcos C, López Lera A, Varela S, Liñares T, Alvarez-Eire MG, López-Trascasa M. Marcos C, et al. Ann Allergy Asthma Immunol. 2012 Sep;109(3):195-200.e2. doi: 10.1016/j.anai.2012.05.022. Epub 2012 Jun 27. Ann Allergy Asthma Immunol. 2012. PMID: 22920075

10

SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes.

Ponard D, Gaboriaud C, Charignon D, Ghannam A, Wagenaar-Bos IGA, Roem D, López-Lera A, López-Trascasa M, Tosi M, Drouet C. Ponard D, et al. Hum Mutat. 2020 Jan;41(1):38-57. doi: 10.1002/humu.23917. Epub 2019 Oct 22. Hum Mutat. 2020. PMID: 31517426 Free article. Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

142 results

Search Page

Filters