Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Bulletin De L'Academie Nationale De Medecine|September 17, 2004
[The early medico-social center for hearing loss (Nantes University Hospital). A twenty two years experience]François Legent, Catherine Calais
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|April 20, 2010
Systematic screening for nonspecific autoantibodies in idiopathic sensorineural hearing loss: no association with steroid responseBaptiste Hervier, Philippe Bordure, Marie Audrain, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|March 19, 2021
Evaluation of vestibular function following endolymphatic sac surgeryAdrien Gendre, Kinnie Bourget-Aguilar, Catherine Calais, et al.
International Journal of Pediatric Otorhinolaryngology|July 13, 2010
Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueductLaurence Jonard, Magali Niasme-Grare, Crystel Bonnet, et al.
European Journal of Human Genetics : EJHG|March 30, 2006
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populationsSébastien Albert, Hélène Blons, Laurence Jonard, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: genotypic and phenotypic analysisDelphine Feldmann, Françoise Denoyelle, Pierre Chauvin, et al.
Archives of Otolaryngology--Head & Neck Surgery|June 22, 2005
GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patientsSandrine Marlin, Delphine Feldmann, Hélène Blons, et al.
Orphanet Journal of Rare Diseases|May 17, 2011
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosisCrystel Bonnet, M'hamed Grati, Sandrine Marlin, et al.
Pageof 1