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International Journal of Audiology|October 5, 2019
The Oticon Medical Neuro Zti cochlear implant and the Neuro 2 sound processor: multicentric evaluation of outcomes in adults and childrenValérie Franco-Vidal, Cécile Parietti-Winkler, Nicolas Guevara, et al.
The Journal of Pediatrics|October 2, 2012
Congenital cytomegalovirus is the second most frequent cause of bilateral hearing loss in young French childrenVéronique Avettand-Fenoël, Sandrine Marlin, Christelle Vauloup-Fellous, et al.
Investigative Ophthalmology & Visual Science|April 28, 2022
Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf CohortVasily M Smirnov, Marco Nassisi, Saddek Mohand-Saïd, et al.
Human Molecular Genetics|February 4, 2020
Mutation m.3395A > G in MT-ND1 leads to variable pathologic manifestationsNicolás Gutiérrez Cortés, Claire Pertuiset, Elodie Dumon, et al.
American Journal of Medical Genetics. Part A|August 3, 2023
A 22q13.1 duplication in mosaicism including SOX10William Bertani-Torres, Margaux Serey-Gaut, Judite de Oliveira, et al.
Genes|May 27, 2026
<i>COCH</i>-Related Hearing Loss in a French Cohort: Novel Variants and Genotype-Phenotype CorrelationsRalyath Balogoun, Margaux Serey-Gaut, Véronique Pingault, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 10, 2012
European Bilateral Pediatric Cochlear Implant Forum consensus statementJames D Ramsden, Karen Gordon, Antje Aschendorff, et al.
Retina (Philadelphia, Pa.)|September 4, 2019
PHENOTYPIC CHARACTERISTICS OF ROD-CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORTSamer Khateb, Saddek Mohand-Saïd, Marco Nassisi, et al.
Human Mutation|September 22, 2016
An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the LiteratureJustine Lerat, Laurence Jonard, Natalie Loundon, et al.
European Journal of Human Genetics : EJHG|December 25, 2003
Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 geneDelphine Feldmann, Françoise Denoyelle, Natalie Loundon, et al.
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