Published in Otolaryngol Head Neck Surg on March 01, 2010
Initiation and use of propranolol for infantile hemangioma: report of a consensus conference. Pediatrics (2012) 1.91
Treatment with propranolol for infantile hemangiomas: A case series of 106 infants. Exp Ther Med (2015) 0.75
GJB2 mutations and degree of hearing loss: a multicenter study. Am J Hum Genet (2005) 2.63
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
GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients. Arch Otolaryngol Head Neck Surg (2005) 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
Medical and surgical complications in pediatric cochlear implantation. Arch Otolaryngol Head Neck Surg (2010) 1.02
Laryngeal cleft. Otolaryngol Clin North Am (2008) 0.97
Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever! Biochem Biophys Res Commun (2010) 0.97
Endoscopic surgical treatment of laryngotracheal clefts: indications and limitations. Arch Otolaryngol Head Neck Surg (2010) 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
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
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
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
Craniofacial dermoids: an embryological theory unifying nasal dermoid sinus cysts. Cleft Palate Craniofac J (2005) 0.85
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
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
Congenital cholesteatoma: risk factors for residual disease and retraction pockets--a report on 117 cases. Laryngoscope (2007) 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
Laser arytenoidectomy in the management of bilateral vocal cord paralysis in children. Int J Pediatr Otorhinolaryngol (2010) 0.78
Autologous fat transfer in velopharyngeal insufficiency: indications and results of a 25 procedures series. Int J Pediatr Otorhinolaryngol (2011) 0.78
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
Pearls and pitfalls in cochlear implantation. Int J Otolaryngol (2011) 0.75
Propranolol therapy for hemorrhagic lymphangioma of the tongue. Arch Otolaryngol Head Neck Surg (2011) 0.75
Pain After Cochlear Implantation: An Unusual Complication? Otol Neurotol (2017) 0.75
Unilateral Sensorineural Hearing Loss: Medical Context and Etiology. Audiol Neurootol (2017) 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
Results of myringoplasty in children with cleft palate: a patient-matched study. Otol Neurotol (2014) 0.75
[Genetic deafness in adults]. Rev Prat (2009) 0.75
[Subglottic hemangioma in the infant]. Ann Otolaryngol Chir Cervicofac (2008) 0.75
Management specificities of congenital laryngeal stenosis: external and endoscopic approaches. Laryngoscope (2013) 0.75