Published in Arch Otolaryngol Head Neck Surg on January 01, 2010
The feasibility of endoscopic transcanal approach for insertion of various cochlear electrodes: a pilot study. Eur Arch Otorhinolaryngol (2014) 1.43
Cochlear implantation in older adults: long-term analysis of complications and device survival in a consecutive series. Otol Neurotol (2013) 0.85
Cochlear implantation in a child with posttraumatic single-sided deafness. Eur Arch Otorhinolaryngol (2013) 0.83
Staphylococcus lugdunensis: Novel Organism causing Cochlear Implant Infection. Infect Dis Rep (2014) 0.81
Retaining Chorda Tympani Nerve Integrity During Cochlear Implant Surgery. Chin Med J (Engl) (2015) 0.78
A repot of surgical complications in a series of 262 consecutive pediatric cochlear implantations in iran. Iran J Pediatr (2011) 0.77
Complications requiring cochlear reimplantation. Iran J Otorhinolaryngol (2012) 0.75
Intraoperative facial nerve monitoring during cochlear implant surgery: an observational study. Medicine (Baltimore) (2015) 0.75
Comparisons of Auditory Performance and Speech Intelligibility after Cochlear Implant Reimplantation in Mandarin-Speaking Users. Biomed Res Int (2016) 0.75
GJB2 mutations and degree of hearing loss: a multicenter study. Am J Hum Genet (2005) 2.63
CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Nat Genet (2010) 2.12
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations. Eur J Hum Genet (2006) 1.69
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis. Orphanet J Rare Dis (2011) 1.57
Noninvasive positive-pressure ventilation avoids recannulation and facilitates early weaning from tracheotomy in children. Pediatr Crit Care Med (2010) 1.49
22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes. Am J Med Genet A (2005) 1.40
Role of Propranolol in the therapeutic strategy of infantile laryngotracheal hemangioma. Int J Pediatr Otorhinolaryngol (2009) 1.36
The biology and management of subglottic hemangioma: past, present, future. Laryngoscope (2004) 1.20
GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients. Arch Otolaryngol Head Neck Surg (2005) 1.19
Congenital stapes ankylosis: study of 28 cases and surgical results. Laryngoscope (2006) 1.19
Utility of radiofrequency ablation for haemorrhagic lingual lymphangioma. Int J Pediatr Otorhinolaryngol (2008) 1.17
A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E. Eur J Med Genet (2007) 1.11
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip. Eur J Hum Genet (2007) 1.10
Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patients. Clin Dysmorphol (2007) 1.07
Propranolol in the therapeutic strategy of infantile laryngotracheal hemangioma: A preliminary retrospective study of French experience. Int J Pediatr Otorhinolaryngol (2010) 1.06
Perrault syndrome: report of four new cases, review and exclusion of candidate genes. Am J Med Genet A (2008) 1.04
Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene. Eur J Hum Genet (2004) 1.04
Congenital cholesteatoma: classification, management, and outcome. Arch Otolaryngol Head Neck Surg (2002) 1.02
Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever! Biochem Biophys Res Commun (2010) 0.97
Laryngeal cleft. Otolaryngol Clin North Am (2008) 0.97
The presentation and management of laryngeal cleft: a 10-year experience. Arch Otolaryngol Head Neck Surg (2006) 0.95
Endoscopic surgical treatment of laryngotracheal clefts: indications and limitations. Arch Otolaryngol Head Neck Surg (2010) 0.94
Failures and complications of supraglottoplasty in children. Arch Otolaryngol Head Neck Surg (2003) 0.94
Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor. Eur J Hum Genet (2002) 0.93
Congenital isolated midline sinus of the upper lip: clinical and embryological approaches. Cleft Palate Craniofac J (2006) 0.92
Noninvasive positive pressure ventilation in infants with upper airway obstruction: comparison of continuous and bilevel positive pressure. Intensive Care Med (2005) 0.92
Usher syndrome and cochlear implantation. Otol Neurotol (2003) 0.91
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene. Eur J Hum Genet (2008) 0.91
Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome. J Med Genet (2013) 0.91
The natural history of congenital cholesteatoma. Arch Otolaryngol Head Neck Surg (2002) 0.91
A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss. Eur J Med Genet (2008) 0.90
Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct. Int J Pediatr Otorhinolaryngol (2010) 0.89
Otologic features in children with primary ciliary dyskinesia. Arch Otolaryngol Head Neck Surg (2010) 0.89
Physiologic and clinical benefits of noninvasive ventilation in infants with Pierre Robin sequence. Pediatrics (2010) 0.89
Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: a very mild phenotype. Eur J Med Genet (2011) 0.87
Evaluation of cytomegalovirus (CMV) DNA quantification in dried blood spots: retrospective study of CMV congenital infection. J Clin Microbiol (2007) 0.87
Cidofovir plasma assays after local injection in respiratory papillomatosis. Laryngoscope (2004) 0.86
Treatment of anterior skull base defects by a transnasal endoscopic approach in children. J Neurosurg Pediatr (2010) 0.86
Craniofacial dermoids: an embryological theory unifying nasal dermoid sinus cysts. Cleft Palate Craniofac J (2005) 0.85
Cricotracheal resection in children weighing less than 10 kg. Arch Otolaryngol Head Neck Surg (2005) 0.84
Acquired subglottic cysts: management and long term outcome. Int J Pediatr Otorhinolaryngol (2012) 0.83
Middle ear implant in conductive and mixed congenital hearing loss in children. Int J Pediatr Otorhinolaryngol (2012) 0.83
Cartilage shield tympanoplasty in children: review of 268 consecutive cases. Arch Otolaryngol Head Neck Surg (2011) 0.82
Neonatal vs delayed-onset fourth branchial pouch anomalies: therapeutic implications. Arch Otolaryngol Head Neck Surg (2010) 0.82
Eye lens radiation exposure and repeated head CT scans: A problem to keep in mind. Eur J Radiol (2011) 0.81
First successful use of eltrombopag before surgery in a child with MYH9-related thrombocytopenia. Pediatrics (2013) 0.81
Discovery of a large deletion of KAL1 in 2 deaf brothers. Otol Neurotol (2013) 0.80
Propranolol may become first-line treatment in obstructive subglottic infantile hemangiomas. Otolaryngol Head Neck Surg (2010) 0.80
Congenital cholesteatoma: risk factors for residual disease and retraction pockets--a report on 117 cases. Laryngoscope (2007) 0.78
Autologous fat transfer in velopharyngeal insufficiency: indications and results of a 25 procedures series. Int J Pediatr Otorhinolaryngol (2011) 0.78
Laser arytenoidectomy in the management of bilateral vocal cord paralysis in children. Int J Pediatr Otorhinolaryngol (2010) 0.78
The GJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafness. Am J Med Genet A (2005) 0.78
Mucocele after transnasal endoscopic repair of traumatic anterior skull base fistula in children. Int J Pediatr Otorhinolaryngol (2011) 0.77
Screening to detect permanent childhood hearing impairment in neonates transferred from the newborn nursery. Int J Pediatr Otorhinolaryngol (2009) 0.76
Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: genotypic and phenotypic analysis. Am J Med Genet A (2004) 0.76
Congenital cytomegalovirus is the second most frequent cause of bilateral hearing loss in young French children. J Pediatr (2012) 0.76
Velopharyngoplasty for noncleft velopharyngeal insufficiency: results in relation to 22q11 microdeletion. Arch Otolaryngol Head Neck Surg (2009) 0.76
Pain After Cochlear Implantation: An Unusual Complication? Otol Neurotol (2017) 0.75
[Subglottic hemangioma in the infant]. Ann Otolaryngol Chir Cervicofac (2008) 0.75
[Otalgia and otitis in children and adults]. Rev Prat (2003) 0.75
Propranolol therapy for hemorrhagic lymphangioma of the tongue. Arch Otolaryngol Head Neck Surg (2011) 0.75
Stapedectomy in children: causes and surgical results in 35 cases. Arch Otolaryngol Head Neck Surg (2010) 0.75
Unilateral Sensorineural Hearing Loss: Medical Context and Etiology. Audiol Neurootol (2017) 0.75
Traumatic intravestibular luxation of the stapes highlighted by computed tomographic scan oblique multiplanar reconstructions. Otol Neurotol (2010) 0.75
Results of myringoplasty in children with cleft palate: a patient-matched study. Otol Neurotol (2014) 0.75
Pearls and pitfalls in cochlear implantation. Int J Otolaryngol (2011) 0.75
[Genetic deafness in adults]. Rev Prat (2009) 0.75
Slide tracheoplasty in infant with congenital tracheal stenosis and tracheomalacia after esophageal atresia with tracheoesophageal fistula repair. J Pediatr Surg (2009) 0.75
Management specificities of congenital laryngeal stenosis: external and endoscopic approaches. Laryngoscope (2013) 0.75
[Hereditary deafness: molecular genetics]. Med Sci (Paris) (2004) 0.75
Medical and surgical complications in paediatric cochlear implantation. Cochlear Implants Int (2010) 0.75