Natalie Loundon

Hôpital Necker-Enfants Malades — France

Neuroscience · Life Sciences

32h-index3.0kcitations177works1.82yr avg
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Research Topics

Hearing, Cochlea, Tinnitus, Genetics(78), Hearing Loss and Rehabilitation(68), Ear Surgery and Otitis Media(40), Vestibular and auditory disorders(28), Hearing Impairment and Communication(20)

Publications176 total

Amélioration du bain langagier chez les enfants implantés cochléaires utilisant le système d’analyse du langage et de l’environnement (LENA) – analyse CONSORT
Annales françaises d Oto-rhino-laryngologie et de Pathologie Cervico-faciale·2025
Vestibular Deficit in Patients with Waardenburg Syndrome
Biomedicines·2025Open Access
Bilateral Enlarged Vestibular Aqueduct: Auditory, Genetic and Radiological Characterization, and Benefits of Cochlear Implants
Otolaryngology·2025Open Access
Improving the language environment for children with cochlear implants, using the LENA language and environment analysis system – A CONSORT analysis
European Annals of Otorhinolaryngology Head and Neck Diseases·2025
Implantación coclear en niños
EMC - Otorrinolaringología·2025
Unilateral, bilateral symmetric or asymmetric isolated hearing loss in patients with heterozygous KITLG variants
Human Genetics·2025
Disparities among Different Countries in Access for Diagnosis and Treatment of Pediatric Sensorineural Hearing Loss
Otology & Neurotology·2024· 2 cited
<scp>EAONO</scp>/<scp>JOS</scp>, <scp>STAMCO</scp>, <scp>ChOLE</scp> &amp; Potsic Staging of 271 Pediatric Cholesteatoma: Evidence‐Based Mod‐Pot Staging System
The Laryngoscope·2024· 7 citedOpen Access
<scp>HDR</scp> syndrome: Large cohort and systematic review
Clinical Genetics·2024· 6 citedOpen Access
Author response for "&lt;scp&gt;HDR&lt;/scp&gt; syndrome: Large cohort and systematic review"
2024
Pediatric Cholesteatoma Follow‐Up: Residual and Recurrence in 239 Cases with Over 5‐Year Hindsight
The Laryngoscope·2024· 10 cited
Author response for "&lt;scp&gt;HDR&lt;/scp&gt; syndrome: Large cohort and systematic review"
2024
Analyse qualitative des profils développementaux d’une cohorte de bébés de moins de dix mois atteints de surdité congénitale
Contraste·2024
Traduction et validation des questionnaires PVSQ et DHI-PC dans les vertiges de l’enfant
Annales françaises d Oto-rhino-laryngologie et de Pathologie Cervico-faciale·2024
JoVE Video Dataset
2023
Robot-Assisted Transcanal Endoscopic Ear Surgery for Congenital Cholesteatoma
Journal of Visualized Experiments·2023· 3 cited
<scp>RIPOR2</scp> : A new gene of non‐syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models
Clinical Genetics·2023Open Access
Surdités de perception de l’enfant
Contraste·2023· 1 cited
Author response for "&lt;scp&gt;RIPOR2&lt;/scp&gt;: A new gene of non‐syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models"
2023
A 22q13.1 duplication in mosaicism including <i>SOX10</i>
American Journal of Medical Genetics Part A·2023Open Access
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Frequent Co-authors

Sandrine Marlin(25), Françoise Denoyelle(23), Isabelle Rouillon(19), E.N. Garabédian(15), Christine Petit(8), Éréa-Noël Garabédian(8), Marine Parodi(8), Laurence Jonard(7), Nicolas Leboulanger(6), Marion Blanchard(5), Gilles Roger(5), Delphine Feldmann(5), Rémy Couderc(5), Valérie Drouin‐Garraud(5), Briac Thierry(5), Vincent Couloigner(5), Hubert Journel(4), Hélène Catros(4), Crystel Bonnet(4), Véronique Pingault(4)