Pediatric Otolaryngology,
Head and Neck Surgery Department,
AP-HP,
Pediatric Otolaryngology, Head and neck surgery department, AP-HP
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Evaluation of cytomegalovirus (CMV) DNA quantification in dried blood spots: retrospective study of CMV congenital infection.
Journal of clinical microbiology Nov, 2007 | Pubmed ID: 17898161
Discovery of a large deletion of KAL1 in 2 deaf brothers.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology Dec, 2013 | Pubmed ID: 24232061
Pediatric cochlear implantation in residual hearing candidates.
The Annals of otology, rhinology, and laryngology Jun, 2015 | Pubmed ID: 25586946
A case of mild CHARGE syndrome associated with a splice site mutation in CHD7.
European journal of medical genetics Apr, 2016 | Pubmed ID: 26921530
Efficiency of Melatonin as Compared to Pentobarbital for Audiometry Brainstem Response in Children With Associated Disorders.
American journal of audiology Sep, 2016 | Pubmed ID: 27598454
International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient.
International journal of pediatric otorhinolaryngology Nov, 2016 | Pubmed ID: 27729144
Noonan Syndrome: An Underestimated Cause of Severe to Profound Sensorineural Hearing Impairment. Which Clues to Suspect the Diagnosis?
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology Sep, 2017 | Pubmed ID: 28742629
Mutations in TUBB4B Cause a Distinctive Sensorineural Disease.
American journal of human genetics Dec, 2017 | Pubmed ID: 29198720
Intra-cochlear electrode tip fold-over.
Cochlear implants international Jul, 2018 | Pubmed ID: 29363410
Mutation m.3395A > G in MT-ND1 leads to variable pathologic manifestations.
Human molecular genetics Apr, 2020 | Pubmed ID: 32011699
Pediatric sudden sensorineural hearing loss: Experience in a pediatric ENT emergency care center.
International journal of pediatric otorhinolaryngology Aug, 2020 | Pubmed ID: 32408010
PRPS1 loss-of-function variants, from isolated hearing loss to severe congenital encephalopathy: New cases and literature review.
European journal of medical genetics Nov, 2020 | Pubmed ID: 32781272
The French Cochlear Implant Registry (EPIIC): Perception and language results in infants with cochlear implantation under the age of 24 months.
European annals of otorhinolaryngology, head and neck diseases Sep, 2020 | Pubmed ID: 32863156
Arterial spin labeling brain MRI study to evaluate the impact of deafness on cerebral perfusion in 79 children before cochlear implantation.
NeuroImage. Clinical , 2021 | Pubmed ID: 33369563
Long-term outcomes of cartilage tympanoplasty in 139 ears in children.
Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery Nov, 2021 | Pubmed ID: 33993647
[Neonatal hearing screening].
Medecine sciences : M/S May, 2021 | Pubmed ID: 34003098
French adaptation and validation of parents' evaluation of aural/oral performance of children (PEACH) scale in children.
International journal of audiology Jun, 2023 | Pubmed ID: 35533092
French adaptation and validation of the Speech, Spatial and Qualities of Hearing scale for Parents (SSQ-P) and for Children (SSQ-Ch).
International journal of audiology Aug, 2023 | Pubmed ID: 35671326
Long-term outcomes of retrospective case series of middle ear implantation with Vibrant Soundbridge in children with congenital aural atresia.
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 Apr, 2023 | Pubmed ID: 36098862
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 partnership.
International journal of pediatric otorhinolaryngology Mar, 2023 | Pubmed ID: 36746056
Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene Deletions.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology Apr, 2023 | Pubmed ID: 36764706
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment.
Audiology research May, 2023 | Pubmed ID: 37218840
A 22q13.1 duplication in mosaicism including SOX10.
American journal of medical genetics. Part A Dec, 2023 | Pubmed ID: 37533297
RIPOR2: A new gene of non-syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models.
Clinical genetics Dec, 2023 | Pubmed ID: 37864412
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