Lopez-Escamez JA - Search Results

1

DNA Methylation Signature in Mononuclear Cells and Proinflammatory Cytokines May Define Molecular Subtypes in Sporadic Meniere Disease.

Flook M, Escalera-Balsera A, Gallego-Martinez A, Espinosa-Sanchez JM, Aran I, Soto-Varela A, Lopez-Escamez JA. Flook M, et al. Biomedicines. 2021 Oct 25;9(11):1530. doi: 10.3390/biomedicines9111530. Biomedicines. 2021. PMID: 34829759 Free PMC article.

2

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.

3

Differential Proinflammatory Signature in Vestibular Migraine and Meniere Disease.

Flook M, Frejo L, Gallego-Martinez A, Martin-Sanz E, Rossi-Izquierdo M, Amor-Dorado JC, Soto-Varela A, Santos-Perez S, Batuecas-Caletrio A, Espinosa-Sanchez JM, Pérez-Carpena P, Martinez-Martinez M, Aran I, Lopez-Escamez JA. Flook M, et al. Front Immunol. 2019 Jun 4;10:1229. doi: 10.3389/fimmu.2019.01229. eCollection 2019. Front Immunol. 2019. PMID: 31214186 Free PMC article.

4

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.

5

Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere's disease.

Gallego-Martinez A, Requena T, Roman-Naranjo P, May P, Lopez-Escamez JA. Gallego-Martinez A, et al. J Med Genet. 2020 Feb;57(2):82-88. doi: 10.1136/jmedgenet-2019-106159. Epub 2019 Sep 7. J Med Genet. 2020. PMID: 31494579

6

Systematic Review of Sequencing Studies and Gene Expression Profiling in Familial Meniere Disease.

Escalera-Balsera A, Roman-Naranjo P, Lopez-Escamez JA. Escalera-Balsera A, et al. Genes (Basel). 2020 Nov 27;11(12):1414. doi: 10.3390/genes11121414. Genes (Basel). 2020. PMID: 33260921 Free PMC article.

7

[No title available]

[No authors listed] [No authors listed] PMID: 32251013

8

Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease.

Roman-Naranjo P, Gallego-Martinez A, Soto-Varela A, Aran I, Moleon MDC, Espinosa-Sanchez JM, Amor-Dorado JC, Batuecas-Caletrio A, Perez-Vazquez P, Lopez-Escamez JA. Roman-Naranjo P, et al. Ear Hear. 2020 Nov/Dec;41(6):1598-1605. doi: 10.1097/AUD.0000000000000878. Ear Hear. 2020. PMID: 33136635

9

Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease.

Roman-Naranjo P, Moleon MDC, Aran I, Escalera-Balsera A, Soto-Varela A, Bächinger D, Gomez-Fiñana M, Eckhard AH, Lopez-Escamez JA. Roman-Naranjo P, et al. Hear Res. 2021 Sep 15;409:108329. doi: 10.1016/j.heares.2021.108329. Epub 2021 Aug 2. Hear Res. 2021. PMID: 34391192 Free article.

10

Familial clustering and genetic heterogeneity in Meniere's disease.

Requena T, Espinosa-Sanchez JM, Cabrera S, Trinidad G, Soto-Varela A, Santos-Perez S, Teggi R, Perez P, Batuecas-Caletrio A, Fraile J, Aran I, Martin E, Benitez J, Pérez-Fernández N, Lopez-Escamez JA. Requena T, et al. Clin Genet. 2014 Mar;85(3):245-52. doi: 10.1111/cge.12150. Epub 2013 Apr 9. Clin Genet. 2014. PMID: 23521103

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