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Human Molecular Genetics|December 1, 1994
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene intervalH Chaïb, G Lina-Granade, P Guilford, et al.
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.
B-ENT|October 28, 2008
Cochlear implantation in 3 adults with auditory neuropathy/auditory dys-synchronyE M R De Leenheer, I J M Dhooge, E Veuillet, 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.
European Annals of Otorhinolaryngology, Head and Neck Diseases|December 19, 2025
Cochlear implantation in the very elderly: Longitudinal assessment of device use and outcomesT Bocquillon, I Mosnier, M Marx, et al.
International Journal of Pediatric Otorhinolaryngology|November 6, 1998
Comprehension of language in congenitally deaf children with and without cochlear implantsE Truy, G Lina-Granade, A M Jonas, et al.
Revue De Laryngologie - Otologie - Rhinologie|December 29, 1998
[Language comprehension by children with profound congenital deafness after cochlear implant]E Truy, G Lina-Granade, A M Jonas, et al.
Orphanet Journal of Rare Diseases|February 1, 2021
Long term disease burden post-transplantation: three decades of observations in 25 Hurler patients successfully treated with hematopoietic stem cell transplantation (HSCT)N Guffon, M Pettazzoni, N Pangaud, 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.
European Journal of Human Genetics : EJHG|April 10, 1999
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing lossN Alloisio, L Morlé, M Bozon, et al.
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