Isabelle Rouillon

ORCID: 0000-0002-8051-468X
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About
Contact & Profiles
Research Areas
  • Hearing, Cochlea, Tinnitus, Genetics
  • Hearing Loss and Rehabilitation
  • Ear Surgery and Otitis Media
  • Vestibular and auditory disorders
  • Hearing Impairment and Communication
  • Tumors and Oncological Cases
  • Head and Neck Anomalies
  • Tracheal and airway disorders
  • Cytomegalovirus and herpesvirus research
  • Infant Health and Development
  • Congenital Ear and Nasal Anomalies
  • Neuroscience of respiration and sleep
  • Teratomas and Epidermoid Cysts
  • Language Development and Disorders
  • Noise Effects and Management
  • Neonatal Respiratory Health Research
  • Obstructive Sleep Apnea Research
  • Voice and Speech Disorders
  • Herpesvirus Infections and Treatments
  • Airway Management and Intubation Techniques
  • Neuroscience and Music Perception
  • Connexins and lens biology
  • Cleft Lip and Palate Research
  • Parvovirus B19 Infection Studies
  • Connective tissue disorders research

Assistance Publique – Hôpitaux de Paris
2006-2024

Hôpital Necker-Enfants Malades
2015-2024

Google (United States)
2023-2024

Université Paris Cité
2013-2017

Hôpital Armand-Trousseau
2005-2013

Hôpital Antoine-Béclère
2013

Sorbonne Université
2005-2013

Inserm
2010-2013

Université Laval
2013

Hôpital d'Enfants
2005-2012

Objective: To review the presentation and associated

10.1001/archotol.132.12.1335 article EN Archives of Otolaryngology - Head and Neck Surgery 2006-12-01

<b><i>Objective:</i></b> Unilateral sensorineural hearing loss (USNHL) is known to impact on school performance and social skills during childhood, but the etiologies remain unclear. The aim of this study was assess various clinical contexts in population. <b><i>Methods:</i></b> a retrospective review. Characteristics (HL), audiometric parameters, imaging, genetic medical were analyzed. <b><i>Results:</i></b> Eighty...

10.1159/000474928 article EN Audiology and Neurotology 2017-01-01

To evaluate surgical aspects and results of cochlear implantation in inner ear malformations.Retrospective cohort study.Ear, nose, throat department a tertiary referral hospital.Out 260 implanted children, 18 (6.9%) had malformations: complex cochleovestibular malformation (n = 11), common cavity 1), enlarged vestibular aqueduct (EVA) 6). Deafness was progressive 12 cases (G1) congenital 6 (G2). Genetics lead to diagnosis 13 cases: PSD mutation Waardenburg syndrome negative (1). Mean age at...

10.1097/01.mao.0000178126.58859.a9 article EN Otology & Neurotology 2005-07-01

Objective Magnet displacement is a rare but possible complication in patients with cochlear implants. We report 1 case young child that occurred during magnetic resonance imaging scanning, despite precautionary measures taken by the surgeon and radiographer. Study Design Retrospective report. Setting This presented ENT Department of Armand Trousseau Paediatrics Hospital, Paris, France. Patient An 8-year-old child, implanted Freedom Contour Nucleus implant, was referred for 1.5-T cerebral...

10.1097/mao.0b013e3181825695 article EN Otology & Neurotology 2008-08-20

10.1016/s1632-3475(25)50352-1 article ES EMC - Otorrinolaringología 2025-04-01

Objective The nasal dermoid sinus cyst (NDSC) is an uncommon congenital lesion presenting as a large panel of midline craniofacial anomalies. objective this study was to review and reanalyze embryological hypotheses concerning NDSCs propose theory unifying the various anatomical characteristics these lesions. first case frontal localization NDSC extending within diploetic bone in 9-month-old boy, median fistula with recurrent swelling, 6 months after mild trauma presented. Results Complete...

10.1597/03-106.1 article EN The Cleft Palate-Craniofacial Journal 2005-01-01

To propose categories for the various types of residual hearing in children and to review outcomes cochlear implantation (CI) with these different conditions.We identified 53 who had received a implant. Five groups were arbitrarily defined based on auditory features: G1, characterized by low-frequency (n=5); G2, severe sensorineural loss (SNHL) low speech discrimination (n=12); G3, asymmetric SNHL (n=9); G4, progressive (n=15); G5, fluctuating (n=12). The main audiometric features...

10.1177/0003489414566121 article EN Annals of Otology Rhinology & Laryngology 2015-01-13

10.1016/j.anorl.2018.09.004 article EN publisher-specific-oa European Annals of Otorhinolaryngology Head and Neck Diseases 2018-10-09

<h3>Objective</h3> To evaluate the results of velopharyngoplasty for velopharyngeal insufficiency (VPI) in relation to 22q11 deletion or nonsyndromic VPI. <h3>Design</h3> Retrospective study. <h3>Setting</h3> Academic medical center. <h3>Patients</h3> Eleven 45 patients with microdeletion (group 1) and 9 without 2) noncleft VPI (hypoplastic velum hypodynamic velopharynx deep pharynx) underwent (midline pharyngeal flap superior pedicle). Exclusion criteria included cleft palate, submucous all...

10.1001/archoto.2009.64 article EN Archives of Otolaryngology - Head and Neck Surgery 2009-07-01

The purpose of the study was to define boundaries between endocochlear hearing loss and auditory neuropathy in children with congenital profound positive otoacoustic emissions.A child presented bilateral loss, which confirmed by absence evoked potentials at 110 dB conserved emissions. lack any relevant medical history, a normal neurologic pediatric examination, improvement obtained powerful aids suggested an cause. Genetic testing identified mutations OTOF, responsible for DFNB9 recessive...

10.1097/01.mao.0000169044.63970.4a article EN Otology & Neurotology 2005-07-01

Abstract Objective: The objective of this study was to analyze functional results after stapes surgery in patients with congenital nonprogressive conductive deafness resulting from an isolated fixation the according age and surgical procedure. Study Design: authors conducted a retrospective case series March 1993 December 2003 two tertiary referral centers. Methods: Twenty‐eight were operated on by stapedotomy or partial stapedectomy using Teflon prostheses. median at 14.2 years (range,...

10.1097/01.mlg.0000227501.78004.f6 article EN The Laryngoscope 2006-07-01

Objective: To analyze clinical signs and better define the underestimated long-term pain after implantation, to discuss etiological hypothesis, propose our department treatment algorithm results. Study Design Setting: Retrospective review of children implanted with complaints atypical in area device not immediate postoperative period, more than or equal 4 on Visual Analog Pain Scale (VAPS: 0–10) ENT pediatric Trousseau Necker Enfants Malades Hospitals between 1998 2015. Patients: All...

10.1097/mao.0000000000001451 article EN Otology & Neurotology 2017-06-09

Cochlear implantation has been performed safely for over two decades but still various minor and major complications. We report cases of an unusual complication electrode implantation: tip fold-over the array within cochlea. Both required undergoing explantation re-implantation. The frequent use fine pre-curved electrodes particularly with insertion tool necessitates routine postoperative radiological evaluation array. Our demonstrate benefit systematic imaging including possible Cone Beam...

10.1080/14670100.2018.1427823 article EN Cochlear Implants International 2018-01-24

10.1016/j.anorl.2018.05.002 article EN publisher-specific-oa European Annals of Otorhinolaryngology Head and Neck Diseases 2018-06-01

To study children who had undergone stapedectomy at an age younger than 16 years to determine the causes (particularly frequency of congenital anomalies vs otosclerosis) and analyze functional results over short-term, 1-year, long-term postsurgery time course.Ten-year retrospective covering 1998 2008.Pediatric tertiary care centers.A total 33 patients (35 ears) underwent stapes surgery from October 2008.Sex, age, preoperative postoperative audiometric test results, associated anomalies, type...

10.1001/archoto.2010.170 article EN Archives of Otolaryngology - Head and Neck Surgery 2010-10-18

10.1016/j.anorl.2016.05.004 article EN publisher-specific-oa European Annals of Otorhinolaryngology Head and Neck Diseases 2016-07-22
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