Natalie Loundon

Evaluation of cytomegalovirus (CMV) DNA quantification in dried blood spots: retrospective study of CMV congenital infection.

Discovery of a large deletion of KAL1 in 2 deaf brothers.

Pediatric cochlear implantation in residual hearing candidates.

A case of mild CHARGE syndrome associated with a splice site mutation in CHD7.

Efficiency of Melatonin as Compared to Pentobarbital for Audiometry Brainstem Response in Children With Associated Disorders.

International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient.

Noonan Syndrome: An Underestimated Cause of Severe to Profound Sensorineural Hearing Impairment. Which Clues to Suspect the Diagnosis?

Mutations in TUBB4B Cause a Distinctive Sensorineural Disease.

Intra-cochlear electrode tip fold-over.

Mutation m.3395A > G in MT-ND1 leads to variable pathologic manifestations.

Pediatric sudden sensorineural hearing loss: Experience in a pediatric ENT emergency care center.

PRPS1 loss-of-function variants, from isolated hearing loss to severe congenital encephalopathy: New cases and literature review.

The French Cochlear Implant Registry (EPIIC): Perception and language results in infants with cochlear implantation under the age of 24 months.

Arterial spin labeling brain MRI study to evaluate the impact of deafness on cerebral perfusion in 79 children before cochlear implantation.

Long-term outcomes of cartilage tympanoplasty in 139 ears in children.

[Neonatal hearing screening].

French adaptation and validation of parents' evaluation of aural/oral performance of children (PEACH) scale in children.

French adaptation and validation of the Speech, Spatial and Qualities of Hearing scale for Parents (SSQ-P) and for Children (SSQ-Ch).

Long-term outcomes of retrospective case series of middle ear implantation with Vibrant Soundbridge in children with congenital aural atresia.

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.

Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene Deletions.

Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment.

A 22q13.1 duplication in mosaicism including SOX10.

RIPOR2: A new gene of non-syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models.