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Isabelle Rouillon

Showing results (21-30 of 32) with videos related to

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International Journal of Pediatric Otorhinolaryngology|February 6, 2023
Analysis of specific risk factors of neurodevelopmental disorder in hearing-impaired infants under ten months of age: "EnTNDre" an opening research stemming from a transdisciplinary partnershipSalomé Akrich, Erika Parlato de Oliveira, Claire Favrot-Meunier, et al.
Archives of Otolaryngology--Head & Neck Surgery|December 21, 2006
The presentation and management of laryngeal cleft: a 10-year experienceReza Rahbar, Isabelle Rouillon, Gilles Roger, et al.
Biochemical and Biophysical Research Communications|March 17, 2010
Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever!Sandrine Marlin, Delphine Feldmann, Yann Nguyen, et al.
American Journal of Medical Genetics. Part A|August 2, 2005
The GJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafnessDelphine Feldmann, Françoise Denoyelle, Hélène Blons, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 10, 2023
Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene DeletionsSophie Achard, Margaux Campion, Marine Parodi, et al.
The Journal of Pediatrics|October 25, 2025
Hearing Trajectories in Congenital Cytomegalovirus Infection: A 4-Year Follow-Up StudyHugo Delille, Marine Parodi, Jean-François Magny, 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.
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.
Neuroimage. Clinical|December 28, 2020
Arterial spin labeling brain MRI study to evaluate the impact of deafness on cerebral perfusion in 79 children before cochlear implantationArnaud Coez, Ludovic Fillon, Ana Saitovitch, et al.
Clinical Genetics|October 10, 2018
High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5Justine Lerat, Crystel Bonnet, François Cartault, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

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Pageof 4
International Journal of Pediatric Otorhinolaryngology|February 6, 2023
Analysis of specific risk factors of neurodevelopmental disorder in hearing-impaired infants under ten months of age: "EnTNDre" an opening research stemming from a transdisciplinary partnershipSalomé Akrich, Erika Parlato de Oliveira, Claire Favrot-Meunier, et al.
Archives of Otolaryngology--Head & Neck Surgery|December 21, 2006
The presentation and management of laryngeal cleft: a 10-year experienceReza Rahbar, Isabelle Rouillon, Gilles Roger, et al.
Biochemical and Biophysical Research Communications|March 17, 2010
Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever!Sandrine Marlin, Delphine Feldmann, Yann Nguyen, et al.
American Journal of Medical Genetics. Part A|August 2, 2005
The GJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafnessDelphine Feldmann, Françoise Denoyelle, Hélène Blons, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 10, 2023
Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene DeletionsSophie Achard, Margaux Campion, Marine Parodi, et al.
The Journal of Pediatrics|October 25, 2025
Hearing Trajectories in Congenital Cytomegalovirus Infection: A 4-Year Follow-Up StudyHugo Delille, Marine Parodi, Jean-François Magny, 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.
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.
Neuroimage. Clinical|December 28, 2020
Arterial spin labeling brain MRI study to evaluate the impact of deafness on cerebral perfusion in 79 children before cochlear implantationArnaud Coez, Ludovic Fillon, Ana Saitovitch, et al.
Clinical Genetics|October 10, 2018
High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5Justine Lerat, Crystel Bonnet, François Cartault, et al.
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