Works matching DE "AUDITORY neuropathy"

Results: 577

Advances in Understanding the Molecular Dynamics of Autosomal Dominant Auditory Neuropathy: Unveiling a Novel DIAPH3 Gene Variant Associated With Sensorineural Hearing Loss and Bilateral Vestibular Aqueduct Enlargement.

Published in:

Journal of Audiology & Otology, 2025, v. 29, n. 2, p. 151, doi. 10.7874/jao.2024.00143

By:

Miolo, Gianmaria;
Margiotta, Francesco;
Murgia, Alessandra;
Puppa, Lara Della;
Corona, Giuseppe

Publication type:

Article

Characterisation of Patients with SH3TC2 Associated Neuropathy in an Indian Cohort.

Published in:

Neurology India, 2023, v. 71, n. 5, p. 940, doi. 10.4103/0028-3886.388101

By:

Nagappa, Madhu;
Sharma, Shivani;
Govindaraj, Periyasamy;
Chickabasaviah, Yasha T.;
Siram, Ramesh;
Shroti, Akhilesh;
Seshagiri, Doniparthi V.;
Debnath, Monojit;
Sinha, Sanjib;
Bindu, Parayil S.;
Taly, Arun B.

Publication type:

Article

A Severe Form of M - protein Negative Distal Acquired Demyelinating Symmetric Neuropathy.

Published in:

2019

By:

Ong, Tien;
Goh, Khean-Jin;
Shahrizaila, Nortina;
Wong, Kum-Thong;
Tan, Cheng-Yin;
Ong, Tien Lee

Publication type:

Case Study

Monkey see, monkey tap: mimicry of movement dynamics during coordinated tapping.

Published in:

Experimental Brain Research, 2021, v. 239, n. 5, p. 1465, doi. 10.1007/s00221-021-06061-4

By:

Kroger, Carolyn;
Kagerer, Florian A.;
McAuley, J. Devin

Publication type:

Article

A Novel Biallelic Variant in CDH23 Gene in a Family with Atypical USH1D Manifestation: A Literature Review and Investigation of Genotype-Phenotype Correlation.

Published in:

Audiology & Neurotology, 2023, v. 28, n. 4, p. 317, doi. 10.1159/000529420

By:

Khorram, Erfan;
Iravani, Omid;
Khorrami, Mehdi;
Amini, Masoomeh;
Jahanian, Sara;
Nilforoush, Mohammad Hossein;
Mousavi, Seyyed Reza;
Ehsanifard, Mahsa;
Kheirollahi, Majid

Publication type:

Article

Clinical Value of a Novel Magnetic Resonance Imaging Protocol and Prognostic Model Establishment for Sudden Sensorineural Hearing Loss: A Prospective Study.

Published in:

Audiology & Neurotology, 2023, v. 28, n. 2, p. 138, doi. 10.1159/000527738

By:

Wang, Yanjun;
Wang, Yuancheng;
Wang, Zhongjiang;
Chen, Xiaohui;
Ding, Xiaoqiong;
Ju, Shenghong

Publication type:

Article

Effects of Sequential Bilateral Cochlear Implantation in Children: Evidence from Speech-Evoked Cortical Potentials and Tests of Speech Perception.

Published in:

Audiology & Neurotology, 2022, v. 27, n. 4, p. 282, doi. 10.1159/000521600

By:

Vicente, Leticia Cristina;
Polonenko, Melissa Jane;
Gordon, Karen Ann;
Silva, Leandra Tabanez do Nascimento;
Costa, Orozimbo Alves;
Alvarenga, Kátia Freitas

Publication type:

Article

Cochlear Implant Outcomes in Patients with Neurosarcoidosis.

Published in:

Audiology & Neurotology, 2021, v. 26, n. 6, p. 454, doi. 10.1159/000514479

By:

Ebode, Dario;
Cohen-Aubart, Fleur;
Trunet, Stéphanie;
Ferrary, Evelyne;
Lahlou, Ghizlène;
Mosnier, Isabelle

Publication type:

Article

Analysis of Click and Swept-Tone Auditory Brainstem Response Results for Moderate and Severe Sensorineural Hearing Loss.

Published in:

Audiology & Neurotology, 2020, v. 25, n. 6, p. 336, doi. 10.1159/000507691

By:

Tan, Jingqian;
Luo, Jia;
Wang, Xin;
Jiang, Yanbing;
Zeng, Xiangli;
Chen, Shixiong;
Li, Peng

Publication type:

Article

Cochlear Nerve Hypoplasia: Audiological Characteristics in Children and Adults.

Published in:

2019

By:

Cinar, Betul Cicek;
Tahir, Emel;
Batuk, Merve Ozbal;
Yarali, Mehmet;
Sennaroglu, Gonca;
Sennaroglu, Levent;
Cinar, Betul Cicek;
Batuk, Merve Ozbal

Publication type:

journal article

Auditory Skills following Cochlear Implantation in Children with the Charge Syndrome.

Published in:

2019

By:

Aragón-Ramos, Paula;
Pedrero-Escalas, Maria-Fernanda;
Gavilán, Javier;
Pérez-Mora, Rosa;
Herrán-Martin, Belén;
Lassaletta, Luis

Publication type:

journal article

Cochlear Nerve Aplasia with Detectable Olivocochlear Efferent Function: A Distinct Presentation of Auditory Neuropathy Spectrum Disorder.

Published in:

2018

By:

James, Adrian L.;
Dixon, Peter R.;
Harrison, Robert V.;
James, Adrian L;
Dixon, Peter R;
Harrison, Robert V

Publication type:

journal article

AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant Inheritance.

Published in:

2017

By:

Lang-Roth, Ruth;
Fischer-Krall, Eva;
Kornblum, Cornelia;
Nürnberg, Gudrun;
Meschede, Dieter;
Goebel, Ingrid;
Nürnberg, Peter;
Beutner, Dirk;
Kubisch, Christian;
Walger, Martin;
Volk, alexander E.

Publication type:

journal article

Auditory and Language Outcome in Children Using Different Hearing Devices.

Published in:

Zagazig University Medical Journal, 2024, v. 30, n. 6, p. 2290, doi. 10.21608/ZUMJ.2024.289177.3395

By:

Elbeltagy, Reem;
Hassan, Elham Magdy;
Abd Elhay, Salwa Ahmed;
Galhom, Dalia

Publication type:

Article

Auditory neuropathy in mice and humans with Friedreich ataxia.

Published in:

Annals of Clinical & Translational Neurology, 2023, v. 10, n. 6, p. 953, doi. 10.1002/acn3.51777

By:

Rance, Gary;
Carew, Peter;
Winata, Leon;
Sale, Phillip;
Delatycki, Martin;
Sly, David

Publication type:

Article

A juvenile ALS‐like phenotype dramatically improved after high‐dose riboflavin treatment.

Published in:

Annals of Clinical & Translational Neurology, 2020, v. 7, n. 2, p. 250, doi. 10.1002/acn3.50977

By:

Carreau, Christophe;
Lenglet, Timothée;
Mosnier, Isabelle;
Lahlou, Ghizlene;
Fargeot, Guillaume;
Weiss, Nicolas;
Demeret, Sophie;
Salachas, François;
Veauville‐Merllié, Alice;
Acquaviva, Cécile;
Nadjar, Yann

Publication type:

Article

Evaluation of Depression, Anxiety, and Stress in Adolescents and Young Adults with Auditory Neuropathy Spectrum Disorder.

Published in:

Scientifica, 2016, p. 1, doi. 10.1155/2016/4378269

By:

Prabhu, Prashanth

Publication type:

Article

Hearing and Balance Disorders in the State of Hawai'i: Demographics and Demand for Services.

Published in:

Hawaii Journal of Medicine & Public Health, 2017, v. 76, n. 5, p. 123

By:

Shaikh, Mohsin Ahmed M.;
Hall III, James W.;
McManus, Cindy;
Lew, Henry L.

Publication type:

Article

Hyperviscosity Syndrome Induced Bilateral Visual and Auditory Impairment in Therapy Resistant Waldenström Macroglobulinemia with MYD88 and CXCR4 Mutations.

Published in:

2023

By:

Plante, Marie M;
Kimbrough, ErinMarie O;
Agarwal, Amit K;
Jiang, Liuyan;
Bourgeois, Kirk;
Stamper, Greta C;
Stewart, Michael W;
Tun, Han W

Publication type:

Case Study

Anterior Ischemic Optic Neuropathy in a Child Receiving Chronic Hemodialysis.

Published in:

Case Reports in Nephrology, 2020, p. 1, doi. 10.1155/2020/7012586

By:

Moore, Joyce;
Klowak, Jennifer;
Isaza, Gloria;
Arora, Steven;
Belostotsky, Vladimir;
Stein, Nina;
Chanchlani, Rahul

Publication type:

Article

Investigation of high‐frequency hearing loss and outer hair cell function of the cochlea in patients with psoriasis: a case–control study.

Published in:

Clinical & Experimental Dermatology, 2019, v. 44, n. 5, p. 520, doi. 10.1111/ced.13805

By:

Vir, D.;
Sharma, P.;
Mahajan, R.;
Dogra, S.;
Bakshi, J.;
Panda, N. K.

Publication type:

Article

Magnetic resonance spectroscopy and auditory brain-stem response audiometry as predictors of bilirubin-induced neurologic dysfunction in full-term jaundiced neonates.

Published in:

European Journal of Pediatrics, 2024, v. 183, n. 2, p. 727, doi. 10.1007/s00431-023-05246-z

By:

Zidan, Lamiaa Khaled;
Rowisha, Mohamed Ahmed;
Nassar, Mohammed Abd Ellatif;
Elshafey, Rasha Ahmed;
El Mahallawi, Trandil Hassan;
Elmahdy, Heba Saied

Publication type:

Article

Permanent childhood hearing impairment in infants admitted to the neonatal intensive care unit: nested case–control study.

Published in:

European Journal of Pediatrics, 2021, v. 180, n. 7, p. 2083, doi. 10.1007/s00431-021-03983-7

By:

Nair, Vrinda;
Janakiraman, Sundaram;
Whittaker, Sarah;
Quail, Jenna;
Foster, Trevor;
Loganathan, Prakash Kannan

Publication type:

Article

Auditory neuropathy spectrum disorder (ANSD) in referrals from neonatal hearing screening at a well-baby clinic.

Published in:

2016

By:

Boudewyns, A.;
Declau, Frank;
Ende, Jenneke;
Hofkens, Anouk;
Dirckx, Sara;
Heyning, Paul;
van den Ende, Jenneke;
Van de Heyning, Paul

Publication type:

journal article

Editorial: Biomarkers of peripheral and central auditory system integrity and function.

Published in:

Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1374844

By:

Weder, Stefan;
Bester, Christo William;
O'Leary, Stephen

Publication type:

Article

Vestibular assessment in children with sensorineural hearing loss: diagnostic accuracy and proposal for a diagnostic algorithm.

Published in:

Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1349554

By:

Gerdsen, Max;
Hundscheid, Tamara Maria;
Boudewyns, An;
Van Rompaey, Vincent;
Van De Berg, Raymond;
Colette Widdershoven, Josine Christine

Publication type:

Article

Perilymphatic fistula with characteristic findings of the inner ear by contrast-enhanced magnetic resonance imaging: a case report.

Published in:

Frontiers in Neurology, 2023, p. 01, doi. 10.3389/fneur.2023.1276991

By:

Yusuke Ito;
Toru Seo;
Yoshiyuki Sasano;
Fumihiro Mochizuki;
Izumi Koizuka

Publication type:

Article

Neuroinflammatory disorders of the brain and inner ear: a systematic review of auditory function in patients with migraine, multiple sclerosis, and neurodegeneration to support the idea of an innovative 'window of discovery'.

Published in:

Frontiers in Neurology, 2023, p. 1, doi. 10.3389/fneur.2023.1204132

By:

Di Stadio, Arianna;
De Luca, Pietro;
Koohi, Nehzat;
Kaski, Diego;
Ralli, Massimo;
Giesemann, Anja;
Hartung, Hans-Peter;
Altieri, Marta;
Messineo, Daniela;
Warnecke, Athanasia;
Frohman, Teresa;
Frohman, Elliot M.

Publication type:

Article

Case report: Mohr-Tranebjaerg syndrome: hearing impairment as the onset of an insidious disorder with high recurrence risk.

Published in:

Frontiers in Neurology, 2023, p. 01, doi. 10.3389/fneur.2023.1161940

By:

Sousa, Eulalia;
Abreu, Maria;
Tkachenko, Nataliya;
Rocha, João;
Falcão Reis, Cláudia

Publication type:

Article

Case report: Novel compound heterozygosity for pathogenic variants in MED23 in a syndromic patient with postnatal microcephaly.

Published in:

Frontiers in Neurology, 2023, v. 14, p. 1, doi. 10.3389/fneur.2023.1090082

By:

Salzano, Emanuela;
Niceta, Marcello;
Pizzi, Simone;
Radio, Francesca Clementina;
Busè, Martina;
Mercadante, Francesca;
Barresi, Sabina;
Ferrara, Arturo;
Mancini, Cecilia;
Tartaglia, Marco;
Piccione, Maria

Publication type:

Article

Vincristine-induced neurotoxicity in pediatric patients with rhabdomyosarcoma: A retrospective analysis of clinical features and outcome.

Published in:

Pediatric Hematology & Oncology, 2022, v. 39, n. 7, p. 644, doi. 10.1080/08880018.2022.2047849

By:

Dakik, Lama;
Basbous, Maya;
Tamim, Hani;
Moubarak, Yacoub;
Tarek, Nidale;
Hamideh, Dima;
Muwakkit, Samar;
Abboud, Miguel;
Saab, Raya

Publication type:

Article

Auditory Neuropathy Caused by a Structural Variation in the OTOF Gene, Identified Using Oxford Nanopore Adaptive Sampling.

Published in:

Genes, 2025, v. 16, n. 2, p. 116, doi. 10.3390/genes16020116

By:

Kumai, Takumi;
Nishio, Shin-ya;
Moteki, Hideaki;
Katada, Akihiro;
Usami, Shin-ichi

Publication type:

Article

FDXR -Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population.

Published in:

Genes, 2023, v. 14, n. 4, p. 952, doi. 10.3390/genes14040952

By:

Yi, Shutong;
Zheng, Yuxi;
Yi, Zhen;
Wang, Yingwei;
Jiang, Yi;
Ouyang, Jiamin;
Li, Shiqiang;
Xiao, Xueshan;
Sun, Wenmin;
Wang, Panfeng;
Zhang, Qingjiong

Publication type:

Article

Genetics of Hearing Impairment.

Published in:

Genes, 2022, v. 13, n. 5, p. 852, doi. 10.3390/genes13050852

By:

Kremer, Hannie;
del Castillo, Ignacio

Publication type:

Article

Novel Pathogenic Variants in PJVK , the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum Disorder.

Published in:

Genes, 2022, v. 13, n. 1, p. 149, doi. 10.3390/genes13010149

By:

Domínguez-Ruiz, María;
Rodríguez-Ballesteros, Montserrat;
Gandía, Marta;
Gómez-Rosas, Elena;
Villamar, Manuela;
Scimemi, Pietro;
Mancini, Patrizia;
Rendtorff, Nanna D.;
Moreno-Pelayo, Miguel A.;
Tranebjaerg, Lisbeth;
Medà, Carme;
Santarelli, Rosamaria;
del Castillo, Ignacio

Publication type:

Article

Identification of a novel pathogenic OTOF variant causative of nonsyndromic hearing loss with high frequency in the Ashkenazi Jewish population.

Published in:

Application of Clinical Genetics, 2016, v. 9, p. 141, doi. 10.2147/TACG.S113828

By:

Fedick, Anastasia M.;
Jalas, Chaim;
Swaroop, Ananya;
Smouha, Eric E.;
Webb, Bryn D.

Publication type:

Article

Elucidating the causes of post SARS‐CoV‐2 neuropathy / myopathy requires comprehensive investigations because of the broad spectrum of different etiologies.

Published in:

International Journal of Rheumatic Diseases, 2023, v. 26, n. 5, p. 982, doi. 10.1111/1756-185X.14499

By:

Finsterer, Josef

Publication type:

Article

Complex auditory impairment with peduncular hallucinosis due to pontine haemorrhage – a case report.

Published in:

2021

By:

Negrilă, Anca;
Terecoasă, Elena Oana;
Radu, Răzvan Alexandru;
Cășaru, Bogdan;
Marinescu, Andreea Nicoleta;
Tiu, Cristina

Publication type:

Case Study

Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family.

Published in:

Neural Plasticity, 2020, p. 1, doi. 10.1155/2020/6350479

By:

Wang, Longhao;
Zhao, Lin;
Peng, Hu;
Xu, Jun;
Lin, Yun;
Yang, Tao;
Wu, Hao

Publication type:

Article

Auditory Neuropathy Spectrum Disorder due to Two Novel Compound Heterozygous OTOF Mutations in Two Chinese Families.

Published in:

Neural Plasticity, 2019, p. 1, doi. 10.1155/2019/9765276

By:

Qiu, Yue;
Chen, Sen;
Xie, Le;
Xu, Kai;
Lin, Yi;
Bai, Xue;
Zhang, Hui-Min;
Liu, Xiao-Zhou;
Jin, Yuan;
Sun, Yu;
Kong, Wei-Jia

Publication type:

Article

Is There a Relationship between Psychotic Disorders and the Radicalization Process? A Systematic Review.

Published in:

Medicina (1010660X), 2024, v. 60, n. 6, p. 926, doi. 10.3390/medicina60060926

By:

Catapano, Pierluigi;
Cipolla, Salvatore;
De Rosa, Corrado;
Milano, Stefania;
Vozza, Daniela;
Guadagno, Davide;
Perris, Francesco;
Sampogna, Gaia;
Fiorillo, Andrea

Publication type:

Article

The Relationship between the Ewing Test, Sudoscan Cardiovascular Autonomic Neuropathy Score and Cardiovascular Risk Score Calculated with SCORE2-Diabetes.

Published in:

Medicina (1010660X), 2024, v. 60, n. 5, p. 828, doi. 10.3390/medicina60050828

By:

Nica, Andra-Elena;
Rusu, Emilia;
Dobjanschi, Carmen;
Rusu, Florin;
Sivu, Claudia;
Parlițeanu, Oana Andreea;
Radulian, Gabriela

Publication type:

Article

Polyphenols in Inner Ear Neurobiology, Health and Disease: From Bench to Clinics.

Published in:

Medicina (1010660X), 2023, v. 59, n. 11, p. 2045, doi. 10.3390/medicina59112045

By:

Osakabe, Naomi;
Modafferi, Sergio;
Ontario, Maria Laura;
Rampulla, Francesco;
Zimbone, Vincenzo;
Migliore, Maria Rita;
Fritsch, Tilman;
Abdelhameed, Ali S.;
Maiolino, Luigi;
Lupo, Gabriella;
Anfuso, Carmelina Daniela;
Genovese, Elisabetta;
Monzani, Daniele;
Wenzel, Uwe;
Calabrese, Edward J.;
Vabulas, R. Martin;
Calabrese, Vittorio

Publication type:

Article

Repulsive Guidance Molecule-A as a Therapeutic Target Across Neurological Disorders: An Update.

Published in:

International Journal of Molecular Sciences, 2025, v. 26, n. 7, p. 3221, doi. 10.3390/ijms26073221

By:

Tseriotis, Vasilis-Spyridon;
Liampas, Andreas;
Lazaridou, Irene Zacharo;
Karachrysafi, Sofia;
Vavougios, George D.;
Hadjigeorgiou, Georgios M.;
Papamitsou, Theodora;
Kouvelas, Dimitrios;
Arnaoutoglou, Marianthi;
Pourzitaki, Chryssa;
Mavridis, Theodoros

Publication type:

Article

A TRPV4 mutation caused Charcot-Marie-Tooth disease type 2C with scapuloperoneal muscular atrophy overlap syndrome and scapuloperoneal spinal muscular atrophy in one family: a case report and literature review.

Published in:

BMC Neurology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12883-023-03260-0

By:

Chen, Haofeng;
Sun, Chong;
Zheng, Yongsheng;
Yin, Junxiong;
Gao, Mingshi;
Zhao, Chongbo;
Lin, Jie

Publication type:

Article

Activity Limitation and Participation Restriction in Adults with Auditory Neuropathy Spectrum Disorder.

Published in:

International Journal of Community Health & Medical Research, 2017, v. 3, n. 2, p. 21

By:

Sonawane, Anuja;
Nandurkar, Aparna

Publication type:

Article

Bilateral intracochlear hemorrhage: A rare onset of chronic myelogenous leukemia.

Published in:

2024

By:

Flahat, Babak;
Bonnard, Åsa;
Arebro, Julia

Publication type:

Case Study

Poly‐D,L‐lactic acid polymer and cochlear implantation.

Published in:

2022

By:

Di Berardino, Federica;
Messina, Federica;
Conte, Giorgio;
Cavicchiolo, Sara;
Rossi, Diego;
Giannì, Aldo Bruno;
Pignataro, Lorenzo;
Zanetti, Diego

Publication type:

Case Study

Two Rare Cases of Long Surviving Riboflavin Transporter Deficiency with Co-Existing Adenosine Monophosphate Deaminase (AMP) Deficiency.

Published in:

2022

By:

Zhang, Lin;
Thyagarajan, Dominic

Publication type:

Case Study

A Retrospective Evaluation to Assess Reliability of Electrophysiological Methods for Diagnosis of Hearing Loss in Infants.

Published in:

Brain Sciences (2076-3425), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/brainsci12070950

By:

Mandalà, Marco;
Mazzocchin, Luca;
Ward, Bryan Kevin;
Viberti, Francesca;
Bindi, Ilaria;
Salerni, Lorenzo;
Colletti, Giacomo;
Colletti, Liliana;
Colletti, Vittorio

Publication type:

Article