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Items: 1 to 20 of 25

1.
A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings
Naomi F Bramhall, Jeremy C Kallman, Aimee M Verrall, Valerie A Street
BMC Med Genet. 2008; 9: 48. Published online 2008 Jun 2. doi: 10.1186/1471-2350-9-48
PMCID:
PMC2435521
AbstractArticlePDF–805K
2.
A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss
Paula Robles-Bolivar, David Bächinger, Alberto M. Parra-Perez, Pablo Román-Naranjo, Alba Escalera-Balsera, Alvaro Gallego-Martinez, Andreas H. Eckhard, Jose A. Lopez-Escamez
Eur J Hum Genet. 2022 Nov; 30(11): 1301–1305. Published online 2022 Sep 7. doi: 10.1038/s41431-022-01184-w
PMCID:
PMC9626507
AbstractArticlePDF–734K
3.
A Novel Missense WFS1 Variant: Expanding the Mutational Spectrum Associated with Nonsyndromic Low-Frequency Sensorineural Hearing Loss
Jingyu Ma, Rongrong Wang, Li Zhang, Shanshan Wang, Shuqing Tong, Xiaohui Bai, Zhiming Lu
Biomed Res Int. 2022; 2022: 5068869. Published online 2022 Oct 3. doi: 10.1155/2022/5068869
PMCID:
PMC9550458
AbstractArticlePDF–2.4M
4.
Low-Frequency Sensorineural Hearing Loss Associated With Iron-Deficiency Anemia
Masakatsu Taki, Tatsuhisa Hasegawa, Yuzuru Ninoyu, Hiroaki Mohri, Shigeru Hirano
J Int Adv Otol. 2021 Sep; 17(5): 465–467. Published online 2021 Sep 1. doi: 10.5152/iao.2021.9369
PMCID:
PMC8975401
AbstractArticlePDF–5.9M
5.
Clinical Characteristics and Short-term Outcomes of Acute Low Frequency Sensorineural Hearing Loss With Vertigo
Myung Jin Park, Sang Hoon Kim, Sung Su Kim, Seung Geun Yeo
Clin Exp Otorhinolaryngol. 2018 Jun; 11(2): 96–101. Published online 2018 Jan 10. doi: 10.21053/ceo.2017.00948
PMCID:
PMC5951067
AbstractArticlePDF–348K
6.
Association Between Sigmoid Sinusoidal Tinnitus and Low-Frequency Sensorineural Hearing Loss: A Retrospective Study at a Single Center
Siji Wang, Jiaqiu Dai, Changchao Xiang, Ziqi Chen, Xi Ouyang, Lin Zhu, Fenghui Yu, Xiaofang Zong, Houyong Kang
Med Sci Monit. 2021; 27: e929300-1–e929300-9. Prepublished online 2021 Jan 23. Published online 2021 Mar 21. doi: 10.12659/MSM.929300
PMCID:
PMC7992498
AbstractArticlePDF–1.0M
7.
Mutations in the Wolfram Syndrome Type 1 Gene (WFSI) Define a Clinical Entity of Dominant Low-Frequency Sensorineural Hearing Loss
Marci M. Lesperance, James W. Hall, III, Theresa B. San Agustin, Suzanne M. Leal
Arch Otolaryngol Head Neck Surg. Author manuscript; available in PMC 2018 Sep 19.
Published in final edited form as: Arch Otolaryngol Head Neck Surg. 2003 Apr; 129(4): 411–420. doi: 10.1001/archotol.129.4.411
PMCID:
PMC6145174
AbstractArticlePDF–705K
8.
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss
Irina N. Bespalova, Guy Van Camp, Steven J.H. Bom, David J. Brown, Kim Cryns, Andrew T. DeWan, Ayse E. Erson, Kris Flothmann, Henricus P.M. Kunst, Purnima Kurnool, Theru A. Sivakumaran, Cor W.R.J. Cremers, Suzanne M. Leal, Margit Burmeister, Marci M. Lesperance
Hum Mol Genet. Author manuscript; available in PMC 2018 Oct 23.
Published in final edited form as: Hum Mol Genet. 2001 Oct 15; 10(22): 2501–2508. doi: 10.1093/hmg/10.22.2501
PMCID:
PMC6198816
AbstractArticlePDF–1.1M
9.
A novel mutation in the WFS1 gene identified in a Taiwanese family with low-frequency hearing impairment
Hsun-Tien Tsai, Ying-Piao Wang, Shing-Fang Chung, Hung-Ching Lin, Guan-Min Ho, Min-Tsan Shu
BMC Med Genet. 2007; 8: 26. Published online 2007 May 22. doi: 10.1186/1471-2350-8-26
PMCID:
PMC1890544
AbstractArticlePDF–692K
10.
Autoimmune Disease in a DFNA6/14/38 Family carrying a Novel Missense Mutation in WFS1
Michael S. Hildebrand, Jessica L. Sorensen, Maren Jensen, William J. Kimberling, Richard J.H. Smith
Am J Med Genet A. Author manuscript; available in PMC 2009 Sep 1.
Published in final edited form as: Am J Med Genet A. 2008 Sep 1; 146A(17): 2258–2265. doi: 10.1002/ajmg.a.32449
PMCID:
PMC2586182
AbstractArticlePDF–493K
11.
Hearing loss in a mouse model of Muenke syndrome
Suzanne L. Mansour, Stephen R.F. Twigg, Rowena M. Freeland, Steven A. Wall, Chaoying Li, Andrew O.M. Wilkie
Hum Mol Genet. 2009 Jan 1; 18(1): 43–50. Published online 2008 Sep 25. doi: 10.1093/hmg/ddn311
PMCID:
PMC2644644
AbstractArticlePDF–1.0M
12.
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene
H Eiberg, L Hansen, B Kjer, T Hansen, O Pedersen, M Bille, T Rosenberg, L Tranebjærg
J Med Genet. 2006 May; 43(5): 435–440. doi: 10.1136/jmg.2005.034892
PMCID:
PMC2649014
AbstractArticlePDF–646K
13.
Early Detection of Endolymphatic Hydrops using the Auditory Nerve Overlapped Waveform (ANOW)
C Lee, CV Valenzuela, SS Goodman, D Kallogjeri, CA Buchman, JT Lichtenhan
Neuroscience. Author manuscript; available in PMC 2021 Jan 15.
Published in final edited form as: Neuroscience. 2020 Jan 15; 425: 251–266. Published online 2019 Dec 3. doi: 10.1016/j.neuroscience.2019.11.004
PMCID:
PMC6935415
AbstractArticlePDF–1.2M
14.
MR Imaging of Cochlear Modiolus and Endolymphatic Hydrops in Patients With Menière's Disease
Rita Sousa, Carla Guerreiro, Tiago Eça, Jorge Campos, Leonel Luis
Front Surg. 2021; 8: 667248. Published online 2021 Jul 20. doi: 10.3389/fsurg.2021.667248
PMCID:
PMC8329086
AbstractArticlePDF–1.0M
15.
The Auditory Nerve Overlapped Waveform (ANOW) Detects Small Endolymphatic Manipulations That May Go Undetected by Conventional Measurements
Jeffery T. Lichtenhan, Choongheon Lee, Farah Dubaybo, Kaitlyn A. Wenrich, Uzma S. Wilson
Front Neurosci. 2017; 11: 405. Published online 2017 Jul 18. doi: 10.3389/fnins.2017.00405
PMCID:
PMC5513905
AbstractArticlePDF–1.8M
16.
How Often Does Stapedectomy for Otosclerosis Result in Endolymphatic Hydrops?
Reuven Ishai, Christopher Halpin, Michael J. McKenna, Alicia M. Quesnel
Otol Neurotol. Author manuscript; available in PMC 2017 Aug 1.
Published in final edited form as: Otol Neurotol. 2016 Aug; 37(7): 984–990. doi: 10.1097/MAO.0000000000001116
PMCID:
PMC5040166
AbstractArticlePDF–2.6M
17.
A Challenging Form of Non-autoimmune Insulin-Dependent Diabetes in a Wolfram Syndrome Patient with a Novel Sequence Variant
Liliana P Paris, Yoshihiko Usui, Josefina Serino, Joaquim Sá, Martin Friedlander
J Diabetes Metab. Author manuscript; available in PMC 2016 Jan 25.
Published in final edited form as: J Diabetes Metab. 2015 Jun; 6(7): 1–5. doi: 10.4172/2155-6156.1000561
PMCID:
PMC4725320
AbstractArticlePDF–319K
18.
TEMPORAL BONE FINDINGS IN A CASE OF SUSAC’S SYNDROME
Howard W. Francis, Chadi Makary, Christopher Halpin, Benjamin T. Crane, Saumil N. Merchant
Otol Neurotol. Author manuscript; available in PMC 2012 Oct 1.
Published in final edited form as: Otol Neurotol. 2011 Oct; 32(8): 1198–1204. doi: 10.1097/MAO.0b013e31822e9665
PMCID:
PMC3177404
AbstractArticlePDF–1.8M
19.
Effects of degree and configuration of hearing loss on the contribution of high- and low-frequency speech information to bilateral speech understanding
Benjamin W. Y. Hornsby, Earl E. Johnson, Erin Picou
Ear Hear. Author manuscript; available in PMC 2012 Sep 1.
Published in final edited form as: Ear Hear. 2011 Sep-Oct; 32(5): 543–555. doi: 10.1097/AUD.0b013e31820e5028
PMCID:
PMC3113662
AbstractArticlePDF–1.1M
20.
Case reports on two patients with episodic vertigo, fluctuating hearing loss and migraine responding to prophylactic drugs for migraine. Menière’s disease or migraine-associated vertigo?
R. TEGGI, B. FABIANO, P. RECANATI, P. LIMARDO, M. BUSSI
Acta Otorhinolaryngol Ital. 2010 Aug; 30(4): 217.
PMCID:
PMC3008148
AbstractArticlePDF–143K

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