Published in Int J Pediatr Otorhinolaryngol on February 18, 2010
Total and Partial Laser Arytenoidectomy for Bilateral Vocal Fold Paralysis. Biomed Res Int (2016) 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
Pharmacodynamics of the type II calcimimetic compound cinacalcet HCl. J Pharmacol Exp Ther (2003) 1.63
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
Daptomycin exerts bactericidal activity without lysis of Staphylococcus aureus. Antimicrob Agents Chemother (2008) 1.46
Role of Propranolol in the therapeutic strategy of infantile laryngotracheal hemangioma. Int J Pediatr Otorhinolaryngol (2009) 1.36
Oritavancin kills stationary-phase and biofilm Staphylococcus aureus cells in vitro. Antimicrob Agents Chemother (2008) 1.32
Functional diffusion maps (fDMs) evaluated before and after radiochemotherapy predict progression-free and overall survival in newly diagnosed glioblastoma. Neuro Oncol (2012) 1.28
Bone marrow-derived cells contribute to epithelial engraftment during wound healing. Am J Pathol (2004) 1.23
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
DNA-dependent protein kinase is a therapeutic target and an indicator of poor prognosis in B-cell chronic lymphocytic leukemia. Clin Cancer Res (2008) 1.13
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
MLD'S FUTURE? Lymphology (2015) 1.06
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
Clinical pharmacokinetic and pharmacodynamic profile of cinacalcet hydrochloride. Clin Pharmacokinet (2009) 0.97
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
Quality of life in amyotrophic lateral sclerosis/motor neuron disease: a structured review. Amyotroph Lateral Scler (2009) 0.95
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
Cochlear implant magnet displacement during magnetic resonance imaging. Otol Neurotol (2008) 0.92
Usher syndrome and cochlear implantation. Otol Neurotol (2003) 0.91
Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome. J Med Genet (2013) 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
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
Evaluation of cytomegalovirus (CMV) DNA quantification in dried blood spots: retrospective study of CMV congenital infection. J Clin Microbiol (2007) 0.87
Ultrastructural effects of oritavancin on methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus. Antimicrob Agents Chemother (2008) 0.87
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
Identification of novel candidate protein biomarkers for the post-polio syndrome - implications for diagnosis, neurodegeneration and neuroinflammation. J Proteomics (2008) 0.86
New closed skin bone-anchored implant: preliminary results in 6 children with ear atresia. Otol Neurotol (2013) 0.86
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
A novel radiotracer to image glycogen metabolism in tumors by positron emission tomography. Cancer Res (2014) 0.83
Tumor-related immunity in prostate cancer patients treated with human recombinant granulocyte monocyte-colony stimulating factor (GM-CSF). Prostate (2006) 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
Evaluation of two methods in controlling dental treatment water contamination. J Contemp Dent Pract (2011) 0.81
First successful use of eltrombopag before surgery in a child with MYH9-related thrombocytopenia. Pediatrics (2013) 0.81
A year of foot and ankle orthotic provision for adults: prospective consultations data, with patient satisfaction survey. Foot (Edinb) (2008) 0.81
Life-threatening obstructive sleep apnea caused by adenoid hypertrophy in an infant with noonan syndrome. Case Rep Pediatr (2012) 0.80
Discovery of a large deletion of KAL1 in 2 deaf brothers. Otol Neurotol (2013) 0.80
Regulation of contractile proteins and protein translational signaling in disused muscle. Cell Physiol Biochem (2012) 0.80
Public access defibrillation--designing a universal report form and database for a national programme. Resuscitation (2004) 0.80
Propranolol may become first-line treatment in obstructive subglottic infantile hemangiomas. Otolaryngol Head Neck Surg (2010) 0.80
Structure-function relationships of the outer membrane translocon Wza investigated by cryo-electron microscopy and mutagenesis. J Struct Biol (2009) 0.79
Cochlear implant and inner ear malformation. Proposal for an hyperosmolar therapy at surgery. Int J Pediatr Otorhinolaryngol (2008) 0.79
The use of gene expression analysis and proteomic databases in the development of a screening system to determine the value of natural medicinal products. Evid Based Complement Alternat Med (2006) 0.79
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
The GJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafness. Am J Med Genet A (2005) 0.78
Design and evaluation of International Video Teleconference (iVTC) for orthopedic trauma education. AMIA Annu Symp Proc (2006) 0.78
Hearing outcomes in functional surgery for middle ear malformations. Otol Neurotol (2013) 0.78
Effect of hypercapnia on intracellular pH regulation in a rainbow trout hepatoma cell line, RTH 149. J Comp Physiol B (2011) 0.77
Cholesteatoma secondary to temporal bone involvement by Langerhans cell histiocytosis: a complication amenable to curative surgery. Otol Neurotol (2009) 0.77
The Amyotrophic Lateral Sclerosis Assessment Questionnaire (ALSAQ-40): evidence for a method of imputing missing data. Amyotroph Lateral Scler (2007) 0.77
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
Optimizing pneumococcal vaccination for paediatric cochlear implant recipients using the cochlear implant pneumococcal vaccination flowchart. Cochlear Implants Int (2012) 0.76
Regioselective silylation of sugars through palladium nanoparticle-catalyzed silane alcoholysis. J Am Chem Soc (2002) 0.76
The calcineurin inhibitor tacrolimus as a new therapy in severe cherubism. J Bone Miner Res (2015) 0.76
Immunological effects of granulocyte-macrophage colony-stimulating factor and autologous tumor vaccine in patients with renal cell carcinoma. J Urol (2004) 0.76
Rehabilitation of congenital facial palsy with temporalis flap--case series and literature review. Int J Pediatr Otorhinolaryngol (2012) 0.76
Congenital cytomegalovirus is the second most frequent cause of bilateral hearing loss in young French children. J Pediatr (2012) 0.76
Continuous positive airway pressure titration in infants with severe upper airway obstruction or bronchopulmonary dysplasia. Crit Care (2013) 0.76
Continuous Positive Airway Pressure for Upper Airway Obstruction in Infants with Pierre Robin Sequence. Plast Reconstr Surg (2016) 0.76
Treatment of pancreatic and periampullary cancers at a community hospital: successful application of tertiary care treatment standards. Int J Surg Oncol (2011) 0.76
Velopharyngoplasty for noncleft velopharyngeal insufficiency: results in relation to 22q11 microdeletion. Arch Otolaryngol Head Neck Surg (2009) 0.76
Capacity for intracellular pH compensation during hypercapnia in white sturgeon primary liver cells. J Comp Physiol B (2011) 0.75
Silicone in HIV-1-infected patients: a cause of misdiagnosed granulomatous disease. Int J Infect Dis (2010) 0.75
Lymphatic Malformations: A Case-Based Overview. Ultrasound Q (2016) 0.75
Cochlear implantation in a patient with combined renal and liver transplantation. Cochlear Implants Int (2014) 0.75
[Genetic deafness in adults]. Rev Prat (2009) 0.75
Injuries of the head from backface deformation of ballistic protective helmets under ballistic impact. J Forensic Sci (2014) 0.75
[Subglottic hemangioma in the infant]. Ann Otolaryngol Chir Cervicofac (2008) 0.75
Effects of calcium carbonate, sevelamer hydrochloride or pantoprazole on the pharmacokinetics of cinacalcet. Clin Drug Investig (2014) 0.75
[Hereditary deafness: molecular genetics]. Med Sci (Paris) (2004) 0.75
Unilateral Sensorineural Hearing Loss: Medical Context and Etiology. Audiol Neurootol (2017) 0.75
[Nasal obstruction and mouth breathing: the ENT's point of view]. Orthod Fr (2013) 0.75
Stapedectomy in children: causes and surgical results in 35 cases. Arch Otolaryngol Head Neck Surg (2010) 0.75
Effect of hand position on EMG activity of the posterior shoulder musculature during a horizontal abduction exercise. J Strength Cond Res (2013) 0.75