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Keyword

vestibular dysfunction

Description: Impairment of the vestibular system, which supports balance and spatial orientation, studied in relation to health and functional outcomes.
Wikidata ID: wiki/Q16678483
OpenAlex ID: keywords/vestibular-dysfunction
A Clinical Sign of Canal Paresis
1988 · G. M. Halmagyi, I. S. Curthoys · Archives of Neurology · 1,286
Disorders of balance and vestibular function in US adults: data from the National Health and Nutrition Examination Survey, 2001-2004.
2009 · Yuri Agrawal, John P Carey, et al. · PubMed · 1,016
Mammalian Vestibular Physiology
1979 · Victor J. Wilson, Geoffrey Melvill Jones · Springer eBooks · 960
Natural History of Sudden Sensorineural Hearing Loss
1977 · Douglas E. Mattox, F. Blair Simmons · Annals of Otology Rhinology & Laryngology · 837
A type VII myosin encoded by the mouse deafness gene shaker-1
1995 · F. Gibson, J. Walsh, et al. · Nature · 683
Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23
2001 · Julie M. Bork, Linda M. Peters, et al. · The American Journal of Human Genetics · 555
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Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
2001 · Hanno Bolz, Benigna von Brederlow, et al. · Nature Genetics · 497
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
2000 · Elisabeth Verpy, Michel Leibovici, et al. · Nature Genetics · 471
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
1997 · Xue-Zhong Liu, James Walsh, et al. · Nature Genetics · 471
Current insights in noise-induced hearing loss: A literature review of the underlying mechanism, pathophysiology, asymmetry, and management options
2017 · Trung N. Le, Louise V. Straatman, et al. · Journal of Otolaryngology - Head and Neck Surgery · 465
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Mechanotransduction in mouse inner ear hair cells requires transmembrane channel–like genes
2011 · Yoshiyuki Kawashima, Gwenaëlle S.G. Géléoc, et al. · Journal of Clinical Investigation · 460
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The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
1997 · Dominique Weil, Polonca Küssel, et al. · Nature Genetics · 427
Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B.
1995 · T Hasson, M B Heintzelman, et al. · Proceedings of the National Academy of Sciences · 427
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Ocular torsion and tilt of subjective visual vertical are sensitive brainstem signs
1993 · Marianne Dieterich, Thomas Brandt · Annals of Neurology · 419
Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F
2001 · Zubair M. Ahmed, Saima Riazuddin, et al. · The American Journal of Human Genetics · 415
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome
2001 · L. A. Everett · Human Molecular Genetics · 415
Is Perception of Handicap Related to Functional Performance in Persons with Vestibular Dysfunction?
2004 · Susan L. Whitney, Diane M. Wrisley, et al. · Otology & Neurotology · 393
Hippocampal spatial representations require vestibular input
2002 · Robert W. Stackman, Ann S. Clark, et al. · Hippocampus · 383
Vestibular involvement in cognition: Visuospatial ability, attention, executive function, and memory
2015 · Robin T. Bigelow, Yuri Agrawal · Journal of Vestibular Research · 346
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
1998 · Nahid G. Robertson, Leonard Lu, et al. · Nature Genetics · 340
Persistent postural-perceptual dizziness (PPPD): a common, characteristic and treatable cause of chronic dizziness
2017 · Stoyan Popkirov, Jeffrey P Staab, et al. · Practical Neurology · 334
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The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
2001 · Kumar N. Alagramam, Crystal L. Murcia, et al. · Nature Genetics · 313
Molecular basis of human Usher syndrome: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease
2006 · Jan Reiners, Kerstin Nagel-Wolfrum, et al. · Experimental Eye Research · 305
Etiopathogenesis of cholesteatoma
2004 · Ewa Olszewska, Mathias Wagner, et al. · European Archives of Oto-Rhino-Laryngology · 305
Mutations affecting development of the zebrafish inner ear and lateral line
1996 · Tanya T. Whitfield, Michael Granato, et al. · Development · 302
Works count: 5,658
Citation count: 84,710
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