Endolymphatic deafness: A particular variety of cochlear disorder

ORL

Volumn 64, Issue 2, 2002, Pages 120-124

  Tran Ba Huy, Patrice ^a  

^a HÔPITAL LARIBOISIÈRE   (France)

Author keywords

Deafness; Endolymph; Inner ear

Indexed keywords

GAP JUNCTION PROTEIN; LOOP DIURETIC AGENT; POTASSIUM; SODIUM;

ANATOMY; ARTICLE; COCHLEA; COCHLEA POTENTIAL; CONCENTRATION (PARAMETERS); CONGENITAL DISORDER; CORTI ORGAN; DISEASE COURSE; DOMINANT INHERITANCE; ELECTROCHEMISTRY; ENDOLYMPH; GENE MUTATION; GENETIC ANALYSIS; GENETIC CODE; HEARING IMPAIRMENT; HISTOLOGY; HISTOPATHOLOGY; HUMAN; INNER EAR DISEASE; PATHOGENESIS; PERCEPTION DEAFNESS; PHYSIOLOGY; PRESBYACUSIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; RECESSIVE INHERITANCE; SECRETION; STRIA VASCULARIS; SUDDEN DEAFNESS;

COCHLEA; DEAFNESS; ENDOLYMPH; ENDOLYMPHATIC HYDROPS; HEARING LOSS, SENSORINEURAL; HEARING LOSS, SUDDEN; HUMANS; LABYRINTHITIS; POTASSIUM; SPIRAL GANGLION; TEMPORAL BONE;

EID: 0036105628     PISSN: 03011569     EISSN: None     Source Type: Journal    
DOI: 10.1159/000057790     Document Type: Article

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