Results 261 to 270 of about 161,807 (290)

Imaging in sensorineural deafness.

Acta oto-rhino-laryngologica Belgica, 2003
In this paper, the authors describe, in details, the techniques and the indication of CT scanner and MRI for the evaluation of neurosensory deafness. CT scanner allows to study bony and pneumatized structures of the ear. CT scanner is mostly indicated for the study of congenital deafness, post-trauma deafness and unilateral progressive deafness for ...
M, Decat, G, Cosnard
openaire   +1 more source

XI Unilateral Sensorineural Deafness

Annals of Otology, Rhinology & Laryngology, 1963
L W, WELSH, J J, WELSH
openaire   +2 more sources

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

Nature, 1997
D. Kelsell, J. Dunlop, H. Stevens, N. Lench, J. Liang, G. Parry, R. Mueller, I. Leigh   +7 more
semanticscholar   +1 more source

Mutation in The Nuclear‐Encoded Mitochondrial Isoleucyl–tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome

Human Mutation, 2014
J. Schwartzentruber, D. Buhas, J. Majewski, F. Sasarman, Simon Papillon-Cavanagh, Isabelle Thiffaut, Katherine M. Sheldon, C. Massicotte, Lysanne Patry, M. Simon, A. Zare, K. McKernan, J. Michaud, R. Boles, C. Deal, V. Désilets, E. Shoubridge, M. Samuels   +17 more
semanticscholar   +1 more source

Sensorineural Deafness

Archives of Otolaryngology - Head and Neck Surgery, 1965
openaire   +4 more sources

Quality-of-Life Outcomes After Bone-Anchored Hearing Device Surgery in Children With Single-Sided Sensorineural Deafness

Otology and Neurotology, 2013
J. Doshi, R. Banga, A. Child, Rebecca Lawrence, A. Reid, D. Proops, A. McDermott   +6 more
semanticscholar   +1 more source

Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3‐Methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and leigh‐Like Syndrome) caused by novel mutations in SERAC1

American Journal of Medical Genetics. Part A, 2013
O. Sarig, D. Goldsher, J. Nousbeck, D. Fuchs‐Telem, Ksenya Cohen-Katsenelson, T. Iancu, Irena Manov, Ann Saada, E. Sprecher, H. Mandel   +9 more
semanticscholar   +1 more source

An Unusual Mucocutaneous Syndrome with Sensorineural Deafness Due to Connexin 26 Mutations

Pediatric dermatology, 2013
M. M. Ibáñez, M. M. Alcalde, M. R. Jimenez, M. D. Muñoz, Francisco J. Díez‐Delgado   +4 more
semanticscholar   +1 more source

Clinical need for a Baha trial in patients with single-sided sensorineural deafness. Analysis of a Baha database of 196 patients

European Archives of Oto-Rhino-Laryngology, 2012
J. Desmet, Rajae Bouzegta, A. Hofkens, A. D. Backer, P. Lambrechts, K. Wouters, J. Claes, M. Bodt, P. Heyning   +8 more
semanticscholar   +1 more source

Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches.

Current Opinion in Neurology, 2012
C. Bonnet, A. El‐Amraoui
semanticscholar   +1 more source