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Page 1
Did you mean israel aaran (3 results)?
Defective α-tectorin may involve tectorial membrane in familial Meniere disease.
Roman-Naranjo P, Parra-Perez AM, Escalera-Balsera A, Soto-Varela A, Gallego-Martinez A, Aran I, Perez-Fernandez N, Bächinger D, Eckhard AH, Gonzalez-Aguado R, Frejo L, Lopez-Escamez JA. Roman-Naranjo P, et al. Among authors: aran i. Clin Transl Med. 2022 Jun;12(6):e829. doi: 10.1002/ctm2.829. Clin Transl Med. 2022. PMID: 35653455 Free PMC article. No abstract available.
Clinical Subgroups in Bilateral Meniere Disease.
Frejo L, Soto-Varela A, Santos-Perez S, Aran I, Batuecas-Caletrio A, Perez-Guillen V, Perez-Garrigues H, Fraile J, Martin-Sanz E, Tapia MC, Trinidad G, García-Arumi AM, González-Aguado R, Espinosa-Sanchez JM, Marques P, Perez P, Benitez J, Lopez-Escamez JA. Frejo L, et al. Among authors: aran i. Front Neurol. 2016 Oct 24;7:182. doi: 10.3389/fneur.2016.00182. eCollection 2016. Front Neurol. 2016. PMID: 27822199 Free PMC article.
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. Among authors: aran i. Front Immunol. 2019 Jun 4;10:1229. doi: 10.3389/fimmu.2019.01229. eCollection 2019. Front Immunol. 2019. PMID: 31214186 Free PMC article.
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. Among authors: aran i. Ear Hear. 2020 Nov/Dec;41(6):1598-1605. doi: 10.1097/AUD.0000000000000878. Ear Hear. 2020. PMID: 33136635
Clinical and Cytokine Profile in Patients with Early and Late Onset Meniere Disease.
Moleon MD, Martinez-Gomez E, Flook M, Peralta-Leal A, Gallego JA, Sanchez-Gomez H, Montilla-Ibañez MA, Dominguez-Durán E, Soto-Varela A, Aran I, Frejo L, Lopez-Escamez JA. Moleon MD, et al. Among authors: aran i. J Clin Med. 2021 Sep 7;10(18):4052. doi: 10.3390/jcm10184052. J Clin Med. 2021. PMID: 34575163 Free PMC article.
Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study.
Amanat S, Gallego-Martinez A, Sollini J, Perez-Carpena P, Espinosa-Sanchez JM, Aran I, Soto-Varela A, Batuecas-Caletrio A, Canlon B, May P, Cederroth CR, Lopez-Escamez JA. Amanat S, et al. Among authors: aran i. EBioMedicine. 2021 Apr;66:103309. doi: 10.1016/j.ebiom.2021.103309. Epub 2021 Apr 1. EBioMedicine. 2021. PMID: 33813136 Free PMC article.
21 results