Gallego-Martinez A - Search Results

1

Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease.

Gallego-Martinez A, Requena T, Roman-Naranjo P, Lopez-Escamez JA. Gallego-Martinez A, et al. Front Genet. 2019 Feb 15;10:76. doi: 10.3389/fgene.2019.00076. eCollection 2019. Front Genet. 2019. PMID: 30828346 Free PMC article.

2

A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.

Martín-Sierra C, Requena T, Frejo L, Price SD, Gallego-Martinez A, Batuecas-Caletrio A, Santos-Pérez S, Soto-Varela A, Lysakowski A, Lopez-Escamez JA. Martín-Sierra C, et al. Hum Mol Genet. 2016 Aug 15;25(16):3407-3415. doi: 10.1093/hmg/ddw183. Epub 2016 Jun 21. Hum Mol Genet. 2016. PMID: 27329761 Free PMC article.

3

Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease.

Martín-Sierra C, Gallego-Martinez A, Requena T, Frejo L, Batuecas-Caletrío A, Lopez-Escamez JA. Martín-Sierra C, et al. Eur J Hum Genet. 2017 Feb;25(2):200-207. doi: 10.1038/ejhg.2016.154. Epub 2016 Nov 23. Eur J Hum Genet. 2017. PMID: 27876815 Free PMC article.

4

A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasets.

Requena T, Gallego-Martinez A, Lopez-Escamez JA. Requena T, et al. Hum Genomics. 2017 May 22;11(1):11. doi: 10.1186/s40246-017-0107-5. Hum Genomics. 2017. PMID: 28532469 Free PMC article.

5

Genetics of vestibular syndromes.

Roman-Naranjo P, Gallego-Martinez A, Lopez Escamez JA. Roman-Naranjo P, et al. Curr Opin Neurol. 2018 Feb;31(1):105-110. doi: 10.1097/WCO.0000000000000519. Curr Opin Neurol. 2018. PMID: 29095749 Review.

6

Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease.

Frejo L, Requena T, Okawa S, Gallego-Martinez A, Martinez-Bueno M, Aran I, Batuecas-Caletrio A, Benitez-Rosario J, Espinosa-Sanchez JM, Fraile-Rodrigo JJ, García-Arumi AM, González-Aguado R, Marques P, Martin-Sanz E, Perez-Fernandez N, Pérez-Vázquez P, Perez-Garrigues H, Santos-Perez S, Soto-Varela A, Tapia MC, Trinidad-Ruiz G, Del Sol A, Alarcon Riquelme ME, Lopez-Escamez JA. Frejo L, et al. Front Immunol. 2017 Dec 13;8:1739. doi: 10.3389/fimmu.2017.01739. eCollection 2017. Front Immunol. 2017. PMID: 29326686 Free PMC article.

7

Genetic contribution to vestibular diseases.

Gallego-Martinez A, Espinosa-Sanchez JM, Lopez-Escamez JA. Gallego-Martinez A, et al. J Neurol. 2018 Oct;265(Suppl 1):29-34. doi: 10.1007/s00415-018-8842-7. Epub 2018 Mar 26. J Neurol. 2018. PMID: 29582143 Review.

8

Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

Ahmad H, Requena T, Frejo L, Cobo M, Gallego-Martinez A, Martin F, Lopez-Escamez JA, Bronstein AM. Ahmad H, et al. Front Genet. 2018 Mar 23;9:85. doi: 10.3389/fgene.2018.00085. eCollection 2018. Front Genet. 2018. PMID: 29628936 Free PMC article.

9

Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease.

Frejo L, Gallego-Martinez A, Requena T, Martin-Sanz E, Amor-Dorado JC, Soto-Varela A, Santos-Perez S, Espinosa-Sanchez JM, Batuecas-Caletrio A, Aran I, Fraile J, Rossi-Izquierdo M, Lopez-Escamez JA. Frejo L, et al. Sci Rep. 2018 Apr 13;8(1):5974. doi: 10.1038/s41598-018-23911-4. Sci Rep. 2018. PMID: 29654306 Free PMC article.

10

Bioinformatic Integration of Molecular Networks and Major Pathways Involved in Mice Cochlear and Vestibular Supporting Cells.

Requena T, Gallego-Martinez A, Lopez-Escamez JA. Requena T, et al. Front Mol Neurosci. 2018 Apr 5;11:108. doi: 10.3389/fnmol.2018.00108. eCollection 2018. Front Mol Neurosci. 2018. PMID: 29674954 Free PMC article.

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