日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Preservation of Distortion Product Otoacoustic Emissions in OTOF -Related Hearing Impairment

耳声发射相关听力障碍中畸变产物耳声发射的保留

期刊:Ear and Hearing
影响因子:2.8
doi:10.1097/AUD.0000000000001421
Santarelli, Rosamaria; Scimemi, Pietro; Cama, Elona; Domínguez-Ruiz, María; Bonora, Chiara; Gallo, Chiara; Rodríguez-Ballesteros, Montserrat; Del Castillo, Ignacio
发表日期：2024
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Telemedicine for hearing-impaired patients in Italy

意大利为听障患者提供的远程医疗服务

期刊:Acta Otorhinolaryngologica Italica
影响因子:2.1
doi:10.14639/0392-100X-N3116
Ghiselli, Sara; Sorrentino, Flavia; Lazzerini, Francesco; Rabito, Chiara; Murri, Alessandra; Scimemi, Pietro
发表日期：2024
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Cochlear Synaptopathy due to Mutations in OTOF Gene May Result in Stable Mild Hearing Loss and Severe Impairment of Speech Perception

OTOF基因突变引起的耳蜗突触病变可能导致稳定的轻度听力损失和严重的言语感知障碍

期刊:Ear and Hearing
影响因子:2.8
doi:10.1097/AUD.0000000000001052
Santarelli, Rosamaria; Scimemi, Pietro; Costantini, Marco; Domínguez-Ruiz, María; Rodríguez-Ballesteros, Montserrat; Del Castillo, Ignacio
神经科学
发表日期：2021
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Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 Gene

OTOF 或 OPA1 基因突变相关听觉神经病的耳蜗电图检查

期刊:Audiology Research
影响因子:1.8
doi:10.3390/audiolres11040059
Santarelli, Rosamaria; Scimemi, Pietro; La Morgia, Chiara; Cama, Elona; Del Castillo, Ignacio; Carelli, Valerio
OPA1
发表日期：2021
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An audiological perspective on ''Two further patients with Warsaw breakage syndrome. Is a mild phenotype possible?"

从听力学角度探讨“又两例华沙断裂综合征患者。是否存在轻型表型？”

期刊:Molecular Genetics & Genomic Medicine
影响因子:1.6
doi:10.1002/mgg3.1283
Brotto, Davide; Manara, Renzo; Scimemi, Pietro; Sorrentino, Flavia; Montino, Silvia; Maritan, Francesca; Caserta, Ezio; Lovo, Elisa; Martini, Alessandro; Santarelli, Rosamaria; Trevisi, Patrizia
发表日期：2020
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BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice.

BAAV介导的GJB2基因转移恢复了来自耳聋Cx26Sox10Cre小鼠的耳蜗器官型培养物的间隙连接耦合

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0023279
Crispino Giulia, Di Pasquale Giovanni, Scimemi Pietro, Rodriguez Laura, Galindo Ramirez Fabian, De Siati Romolo Daniele, Santarelli Rosa Maria, Arslan Edoardo, Bortolozzi Mario, Chiorini John A, Mammano Fabio
免疫/内分泌
耳聋耳鸣
发表日期：2011
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The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.

人类耳聋相关的连接蛋白 30 T5M 突变会导致轻度听力损失，并降低敲入小鼠耳蜗非感觉细胞之间的生化耦合

期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddq402
Schütz Melanie, Scimemi Pietro, Majumder Paromita, De Siati Romolo Daniele, Crispino Giulia, Rodriguez Laura, Bortolozzi Mario, Santarelli Rosamaria, Seydel Anke, Sonntag Stephan, Ingham Neil, Steel Karen P, Willecke Klaus, Mammano Fabio
细胞生物学
耳聋耳鸣
Human
发表日期：2010
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