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Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris|March 1, 2006
[Auditory neuropathy: clinical presentation of seven cases and review of the literature]E Truy, E Ionescu, G Lina-Granade, et al.
Brain : a Journal of Neurology|June 27, 2000
Differential recruitment of the speech processing system in healthy subjects and rehabilitated cochlear implant patientsA L Giraud, E Truy, R S Frackowiak, et al.
Hearing Research|October 1, 1995
Spontaneous otoacoustic emissions in preterm neonates: prevalence and gender effectsT Morlet, A Lapillonne, C Ferber, et al.
Neuroscience Letters|December 6, 1996
Development of cochlear active mechanisms in humans differs between genderT Morlet, E Perrin, J D Durrant, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 29, 2001
[Genetic deafness:the primary cause of sensorineural hearing loss in children]G Lina-Granade, L Morlé, N Alloisio, et al.
Acta Psychiatrica Scandinavica|June 4, 2015
Childhood neglect predicts disorganization in schizophrenia through grey matter decrease in dorsolateral prefrontal cortexA Cancel, M Comte, R Truillet, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 23, 2008
The temporal relationship between speech auditory brainstem responses and the acoustic pattern of the phoneme /ba/ in normal-hearing adultsI Akhoun, S Gallégo, A Moulin, et al.
Clinical Otolaryngology and Allied Sciences|April 29, 2004
Assessment of medial olivocochlear system function in pre-term and full-term newborns using a rapid test of transient otoacoustic emissionsT Morlet, A Hamburger, J Kuint, et al.
Neuroreport|March 27, 1999
A selective imaging of tinnitusA L Giraud, S Chéry-Croze, G Fischer, et al.
Journal of Medical Genetics|May 12, 2000
A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing lossL Morlé, M Bozon, N Alloisio, et al.
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