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Acta Oto-Laryngologica Volume 123, 2003 - Issue 6
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Audiology

Familial Early-onset Progressive Vestibulopathy Without Hearing Impairment

Krister Brantberg Department of Audiology, Karolinska Hospital, Stockholm, Sweden
Pages 713-717 | Received 04 Sep 2002, Accepted 12 Dec 2002, Published online: 21 Nov 2014

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Daniele Monzani, Tatiana Fancello, Matteo Alicandri-Ciufelli, Elisabetta Genovese, Patrizia Tarugi, Elisa Aggazzotti Cavazza & Antonio Percesepe. (2016) Mutation screening of the Otop1 gene in familial benign positional paroxysmal vertigo. Hearing, Balance and Communication 14:1, pages 1-7.
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Rose Marie Rine. (2009) Growing evidence for balance and vestibular problems in children. Audiological Medicine 7:3, pages 138-142.
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Andreas Traschütz, Felix HeindlMuhammad BilalAnnette M. HartmannClaudia DufkeOlaf RiessAndreas ZwergalDan RujescuTobias HaackMatthis Synofzik & Michael Strupp. (2023) Frequency and Phenotype of RFC1 Repeat Expansions in Bilateral Vestibulopathy . Neurology 101:10.
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Fabrizio Salvinelli, Francesca Bonifacio, Claudia Beccaria, Fabio Greco, Valeria Frari, Francesco Iafrati & Maurizio Trivelli. (2022) Minimal invasive resurfacing: an innovative technique for the superior semicircular canal dehiscence. A case series. Journal of Surgical Case Reports 2022:5.
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Christine Mei, Hongsong Dong, Eric Nisenbaum, Torin Thielhelm, Aida Nourbakhsh, Denise Yan, Molly Smeal, Yesha Lundberg, Michael E. Hoffer, Simon Angeli, Fred Telischi, Guohui Nie, Susan H. Blanton & Xuezhong Liu. (2021) Genetics and the Individualized Therapy of Vestibular Disorders. Frontiers in Neurology 12.
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Mingzhu Deng, Chen Liu, Weiqing Jiang, Fei Wang, Juan Zhou, Dong Wang & Yonggang Wang. (2020) A novel genetic variant associated with benign paroxysmal positional vertigo within the LOXL1 . Molecular Genetics & Genomic Medicine 8:10.
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Sally M. Rosengren, James G. Colebatch, Allison S. Young, Sendhil Govender & Miriam S. Welgampola. (2019) Vestibular evoked myogenic potentials in practice: Methods, pitfalls and clinical applications. Clinical Neurophysiology Practice 4, pages 47-68.
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Carina Frykholm, Joakim Klar, Tatjana Tomanovic, Adam Ameur & Niklas Dahl. (2018) Stereocilin gene variants associated with episodic vertigo: expansion of the DFNB16 phenotype. European Journal of Human Genetics 26:12, pages 1871-1874.
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Sally M. Rosengren, Miriam S. Welgampola & Rachael L. Taylor. (2018) Vestibular-Evoked Myogenic Potentials in Bilateral Vestibulopathy. Frontiers in Neurology 9.
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Yoon-Hee Cha. (2012) Less Common Neuro-otologic Disorders. CONTINUUM: Lifelong Learning in Neurology 18, pages 1142-1157.
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Kevin A. Kerber & Robert W. Baloh. 2012. Neurology in Clinical Practice. Neurology in Clinical Practice 644 667 .
Robert W. Eppsteiner & Richard J.H. Smith. (2011) Genetic disorders of the vestibular system. Current Opinion in Otolaryngology & Head & Neck Surgery 19:5, pages 397-402.
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Joanna C. Jen & Robert W. Baloh. 2010. Vertigo and Imbalance: Clinical Neurophysiologyof the Vestibular System. Vertigo and Imbalance: Clinical Neurophysiologyof the Vestibular System 433 439 .
Joanna C Jen. (2008) Recent advances in the genetics of recurrent vertigo and vestibulopathy. Current Opinion in Neurology 21:1, pages 3-7.
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J. C. JenH. WangH. LeeC. SabattiR. TrentI. HanniganK. BrantbergG. M. HalmagyiS. F. NelsonR. W. Baloh. (2004) Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy. Neurology 63:12, pages 2376-2379.
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