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Articles (206)

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1-10 of 206 results for Sensorineural deafness

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Select article: Epilepsy,ataxia,sensorineural deafness,tubulopathy syndrome in a European child with KCNJ10 mutations: A case report

Open access

Case report

First published 2017

Epilepsy,ataxia,sensorineural deafness,tubulopathy syndrome in a European child with KCNJ10 mutations: A case report

Antigone Papavasiliou, Katerina Foska, John Ioannou [...]

Sage Open Medical Case Reports

Select article: Unilateral Sensorineural Deafness in Children

Retricted access

Research article

First published 1988-12

Unilateral Sensorineural Deafness in Children

Izak H. Kielmovitch, William H. Friedman

Otolaryngology–Head and Neck Surgery

Select article: Profound Sensorineural Deafness: A Histopathologic Study

Retricted access

Research article

First published 1987-1

Profound Sensorineural Deafness: A Histopathologic Study

R. Hinojosa, R. R. Blough, E. E. Mhoon

Annals of Otology,Rhinology & Laryngology

Select article: Case Report Antiphospholipid Syndrome in Rheumatoid Arthritis Presenting with Sensorineural Deafness

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Other

First published 1994-02

Case Report Antiphospholipid Syndrome in Rheumatoid Arthritis Presenting with Sensorineural Deafness

J. Etherington, A. Cooper, N. Buchanan

Lupus

Select article: Complete Biotinidase Deficiency Presenting as Reversible Progressive Ataxia and Sensorineural Deafness

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Other

First published 2002-02

Complete Biotinidase Deficiency Presenting as Reversible Progressive Ataxia and Sensorineural Deafness

Chang Y Tsao, C. Lawrence Kien

Journal of Child Neurology

Select article: Keratoderma Hereditarium Mutilans (Vohwinkel's Syndrome) Associated with Sensorineural Deafness in an HIV Positive Man: A Case Report

Free access

Letter

First published 2003-1

Keratoderma Hereditarium Mutilans (Vohwinkel's Syndrome) Associated with Sensorineural Deafness in an HIV Positive Man: A Case Report

L. Boccia, M. Perrella, P. Donofrio

European Journal of Inflammation

Select article: Evaluation of dHPLC for CX26 Mutation Screening in Patients from Southern France with Sensorineural Deafness

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Brief report

First published 2001-12

Evaluation of dHPLC for CX26 Mutation Screening in Patients from Southern France with Sensorineural Deafness

Nathalie Pallares-Ruiz, Patricia Blanchet, Michel Mondain [...]

Genetic Testing and Molecular Biomarkers

Select article: Sudden Sensorineural Deafness

Free access

Meeting report

First published 1976-8

Sudden Sensorineural Deafness

R. F. McCall

Journal of the Royal Society of Medicine

Select article: Sudden Sensorineural Deafness

Free access

Meeting report

First published 1976-8

Sudden Sensorineural Deafness

Andrew W Morrison

Journal of the Royal Society of Medicine

Select article: Sudden Sensorineural Deafness

Free access

Meeting report

First published 1976-8

Sudden Sensorineural Deafness

Victor Goodhill

Journal of the Royal Society of Medicine

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