Origin of Vestibular Dysfunction in Usher Syndrome Type 1B-Reference-Cited by-同舟云学术

Origin of Vestibular Dysfunction in Usher Syndrome Type 1B

Published:2001-02 Issue:1 Volume:8 Page:69-77
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Sun John C.,van Alphen Adriaan M.,Wagenaar Mariette,Huygen Patrick,Hoogenraad Casper C.,Hasson Tama,Koekkoek Sebastiaan K.E.,Bohne Barbara A.,De Zeeuw Chris I.

Publisher

Elsevier BV

Subject

Neurology

Reference32 articles.

1. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells;Avraham;Nature Genet.,1995

2. Usher's syndrome: CNS defects determined by computed tomography;Bloom;Retina,1983

3. Electrical stimulation of the auditory system in animals profoundly deaf from birth;Bock;Acta Otolaryngol. Suppl. (Stockh.),1985

4. Processing and analyzing the mouse temporal bone to identify gross, cellular and subcellular pathology;Bohne;Hear. Res.,1997

5. Usher syndrome: definition and estimate of prevalence from two high-risk populations;Boughman;J. Chronic Dis.,1983

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetics of Peripheral Vestibular Dysfunction: Lessons from Mutant Mouse Strains;Journal of the American Academy of Audiology;2014-03

2. Asymmetry in semicircular canal diameters may account for circling behavior in EphB-deficient mice;The Laryngoscope;2013-12-18

3. Retinoic Acid Deficiency Impairs the Vestibular Function;Journal of Neuroscience;2013-03-27

4. “Minimized rotational vestibular testing” as a screening procedure detecting vestibular areflexy in deaf children: screening cochlear implant candidates for Usher syndrome Type I;European Archives of Oto-Rhino-Laryngology;2007-12-06

5. Hereditary Familial Vestibular Degenerative Diseases;Annals of the New York Academy of Sciences;2006-01-25