Results 281 to 290 of about 127,275 (301)

Connexin-26 mutations in sporadic and inherited sensorineural deafness

Lancet, The, 1998
Raquel Rabionet, Xavier Estivill i Pallejà, Paolo Gasparini   +2 more
exaly  

Sudden deafness: long-term follow-up and recurrence

Clinical Otolaryngology, 2002
Tsutomu Nakashima
exaly  

Deaf But Not Mute

AJN, American Journal of Nursing, 1976
openaire   +2 more sources

Deafness induced by Connexin 26 () deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders

Biochemical and Biophysical Research Communications, 2014
Chun Liang, Hong-Bo Zhao, Jin Chen
exaly  

Being Deaf: The Experience of Deafness

The British Journal of Sociology, 1993
Sally Sainsbury, George Taylor, Juliet Bishop   +2 more
openaire   +1 more source

Molecular Pathogenetic Mechanism of Maternally Inherited Deafness

Annals of the New York Academy of Sciences, 2004
Min-Xin Guan
exaly  

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

American Journal of Medical Genetics, Part A, 1993
Kathleen S Arnos, Walter E Nance, W E Nance   +2 more
exaly  

Mitochondrial tRNA mutations associated with deafness

Mitochondrion, 2012
Min-Xin Guan, Yanchun Ji
exaly  

Failure to Detect Critical Auditory Alerts in the Cockpit: Evidence for Inattentional Deafness

Human Factors, 2014
François Vachon, Mickaël Causse, Sébastien Tremblay   +2 more
exaly  

Central deafness: a review of past and current perspectives

International Journal of Audiology, 2019
Frank E. Musiek, Gail D. Chermak
exaly