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Clinical and Cytokine Profile in Patients with Early and Late Onset Meniere Disease.
J Clin Med. 2021 Sep 7;10(18):4052. doi: 10.3390/jcm10184052.
J Clin Med. 2021.
PMID: 34575163
Free PMC article.
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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: moleon mdc.
Ear Hear. 2020 Nov/Dec;41(6):1598-1605. doi: 10.1097/AUD.0000000000000878.
Ear Hear. 2020.
PMID: 33136635
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A Predictive Model of Bilateral Sensorineural Hearing Loss in Meniere Disease Using Clinical Data.
Moleon MDC, Torres-Garcia L, Batuecas-Caletrio A, Castillo-Ledesma N, Gonzalez-Aguado R, Magnoni L, Rossi M, Di Berardino F, Perez-Guillen V, Trinidad-Ruiz G, Lopez-Escamez JA.
Moleon MDC, et al.
Ear Hear. 2022 May/Jun;43(3):1079-1085. doi: 10.1097/AUD.0000000000001169.
Ear Hear. 2022.
PMID: 34799494
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Cytokine profiling and transcriptomics in mononuclear cells define immune variants in Meniere Disease.
Flook M, Rojano E, Gallego-Martinez A, Escalera-Balsera A, Perez-Carpena P, Moleon MDC, Gonzalez-Aguado R, Rivero de Jesus V, Domínguez-Durán E, Frejo L, G Ranea JA, Lopez-Escamez JA.
Flook M, et al. Among authors: moleon mdc.
Genes Immun. 2024 Apr;25(2):124-131. doi: 10.1038/s41435-024-00260-z. Epub 2024 Feb 23.
Genes Immun. 2024.
PMID: 38396174
Free PMC article.
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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. Among authors: moleon mdc.
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.
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