Congenital hereditary endothelial dystrophy with progressive sensorineural deafness: a case report of Harboyan syndrome. [PDF]
Karataş E, Utine CA.
europepmc +1 more source
[A case report of congenital sensorineural deafness caused by novel mutation in Usher1C and related literature analysis]. [PDF]
Guo M, Han W, Li S.
europepmc +1 more source
Evaluation of the Auditory Performance in Noise of Bone-Anchored Hearing System in Patients With Single Side Sensorineural Deafness. [PDF]
Baguant A +6 more
europepmc +1 more source
Acute Low-Tone Sensorineural Hearing Loss-With Nation-Wide Epidemiological Study of Sudden Deafness.
K. Matsuda +4 more
openalex +2 more sources
Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia [PDF]
Safarina G. Malik +4 more
openalex +1 more source
A novel GATA3 frameshift mutation causes hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome. [PDF]
Huang B +8 more
europepmc +1 more source
Prevalence of congenital sensorineural deafness in a population of client-owned purebred kittens in the United Kingdom. [PDF]
Mari L +3 more
europepmc +1 more source

