Natalie Loundon

Pediatric Otolaryngology, Hôpital Necker-Enfants Malades

Affiliated withHôpital Necker-Enfants Malades

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 3	2023

Other Publications

Article	Year
Evaluation of cytomegalovirus (CMV) DNA quantification in dried blood spots: retrospective study of CMV congenital infection. Journal of clinical microbiology\| PubMed ID: 17898161	2007
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\| PubMed ID: 24232061	2013
Pediatric cochlear implantation in residual hearing candidates. The Annals of otology, rhinology, and laryngology\| PubMed ID: 25586946	2015
A case of mild CHARGE syndrome associated with a splice site mutation in CHD7. European journal of medical genetics\| PubMed ID: 26921530	2016
Efficiency of Melatonin as Compared to Pentobarbital for Audiometry Brainstem Response in Children With Associated Disorders. American journal of audiology\| PubMed ID: 27598454	2016
International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient. International journal of pediatric otorhinolaryngology\| PubMed ID: 27729144	2016
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\| PubMed ID: 28742629	2017
Mutations in TUBB4B Cause a Distinctive Sensorineural Disease. American journal of human genetics\| PubMed ID: 29198720	2017
Intra-cochlear electrode tip fold-over. Cochlear implants international\| PubMed ID: 29363410	2018
Mutation m.3395A > G in MT-ND1 leads to variable pathologic manifestations. Human molecular genetics\| PubMed ID: 32011699	2020
Pediatric sudden sensorineural hearing loss: Experience in a pediatric ENT emergency care center. International journal of pediatric otorhinolaryngology\| PubMed ID: 32408010	2020
PRPS1 loss-of-function variants, from isolated hearing loss to severe congenital encephalopathy: New cases and literature review. European journal of medical genetics\| PubMed ID: 32781272	2020
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\| PubMed ID: 32863156	2020
Arterial spin labeling brain MRI study to evaluate the impact of deafness on cerebral perfusion in 79 children before cochlear implantation. NeuroImage. Clinical\| PubMed ID: 33369563	2021
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\| PubMed ID: 33993647	2021
[Neonatal hearing screening]. Medecine sciences : M/S\| PubMed ID: 34003098	2021
French adaptation and validation of parents' evaluation of aural/oral performance of children (PEACH) scale in children. International journal of audiology\| PubMed ID: 35533092	2023
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\| PubMed ID: 35671326	2023
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\| PubMed ID: 36098862	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 partners... International journal of pediatric otorhinolaryngology\| PubMed ID: 36746056	2023
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\| PubMed ID: 36764706	2023
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment. Audiology research\| PubMed ID: 37218840	2023
A 22q13.1 duplication in mosaicism including SOX10. American journal of medical genetics. Part A\| PubMed ID: 37533297	2023
RIPOR2: A new gene of non-syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models. Clinical genetics\| PubMed ID: 37864412	2023