Lista de obras -

A case of respiratory depression in a child with ultrarapid CYP2D6 metabolism after tramadol.

artículo científico publicado en 2015

A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss

artículo científico publicado en 2008

Acquired subglottic cysts: Management and long term outcome ⬇️

artículo científico publicado el 9 de febrero de 2012

An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the Literature

artículo científico publicado en 2016

Arterial spin labeling brain MRI study to evaluate the impact of deafness on cerebral perfusion in 79 children before cochlear implantation

artículo científico publicado en 2020

Cartilage shield tympanoplasty in children: review of 268 consecutive cases

artículo científico publicado en 2011

Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene

artículo científico publicado en 2004

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

artículo científico publicado en 2011

Congenital Cytomegalovirus Is the Second Most Frequent Cause of Bilateral Hearing Loss in Young French Children

article

Congenital cholesteatoma: risk factors for residual disease and retraction pockets--a report on 117 cases

artículo científico publicado en 2007

Congenital cytomegalovirus is the second most frequent cause of bilateral hearing loss in young French children

artículo científico publicado en 2012

Craniofacial dermoids: an embryological theory unifying nasal dermoid sinus cysts

artículo científico publicado en 2005

Discovery of a large deletion of KAL1 in 2 deaf brothers

artículo científico publicado en 2013

Endoscopic surgical treatment of laryngotracheal clefts: indications and limitations

artículo científico publicado en 2010

Evaluation of cytomegalovirus (CMV) DNA quantification in dried blood spots: retrospective study of CMV congenital infection

artículo científico publicado en 2007

Failures and Complications of Supraglottoplasty in Children ⬇️

artículo científico publicado el 1 de octubre de 2003

First successful use of eltrombopag before surgery in a child with MYH9-related thrombocytopenia

artículo científico publicado en 2013

GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients.

artículo científico publicado en 2005

GJB2 mutations and degree of hearing loss: a multicenter study

artículo científico publicado en 2005

Hearing outcomes in functional surgery for middle ear malformations.

artículo científico publicado en 2013

Hearing rehabilitation with the closed skin bone-anchored implant Sophono Alpha1: results of a prospective study in 15 children with ear atresia.

artículo científico publicado en 2015

Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome

artículo científico publicado en 2013

High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5

scientific article published on 04 November 2018

Idiopathic bilateral vocal cord paralysis in infants: Case series and literature review

artículo científico publicado en 2014

Laryngeal cleft.

artículo científico publicado en 2008

Laser arytenoidectomy in the management of bilateral vocal cord paralysis in children

artículo científico publicado en 2010

Management specificities of congenital laryngeal stenosis: external and endoscopic approaches

artículo científico publicado en 2013

Mastoid fascia kite flap for cryptotia correction.

artículo científico publicado en 2016

Medical and surgical complications in paediatric cochlear implantation

artículo científico publicado el 1 de junio de 2010

Medical and surgical complications in pediatric cochlear implantation

scientific article published on 01 January 2010

Middle ear implant in conductive and mixed congenital hearing loss in children

artículo científico publicado en 2012

Neonatal vs delayed-onset fourth branchial pouch anomalies: therapeutic implications.

artículo científico publicado en 2010

New closed skin bone-anchored implant: preliminary results in 6 children with ear atresia.

artículo científico publicado en 2013

Noninvasive positive-pressure ventilation avoids recannulation and facilitates early weaning from tracheotomy in children

artículo científico publicado en 2010

Pain After Cochlear Implantation: An Unusual Complication?

artículo científico publicado en 2017

Pearls and Pitfalls in Cochlear Implantation ⬇️

artículo científico publicado el 29 de diciembre de 2011

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene

artículo científico publicado en 2008

Physiologic and clinical benefits of noninvasive ventilation in infants with Pierre Robin sequence.

artículo científico publicado en 2010

Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: A very mild phenotype ⬇️

artículo científico publicado el 23 de agosto de 2011

Propranolol in the therapeutic strategy of infantile laryngotracheal hemangioma: A preliminary retrospective study of French experience

artículo científico publicado en 2010

Propranolol may become first-line treatment in obstructive subglottic infantile hemangiomas

artículo científico publicado en 2010

Results of VSB implantation at the short process of the incus in children with ear atresia.

artículo científico publicado en 2016

Role of Propranolol in the therapeutic strategy of infantile laryngotracheal hemangioma.

artículo científico publicado en 2009

Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct

artículo científico publicado en 2010

Stapedectomy in children: causes and surgical results in 35 cases

artículo científico publicado en 2010

Subglottic hemangioma in the infant

artículo científico publicado en 2008

Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever!

artículo científico publicado en 2010

The presentation and management of laryngeal cleft: a 10-year experience.

artículo científico publicado en 2006

TheGJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafness

artículo científico publicado en 2005

Total ossiculoplasty in children: predictive factors and long-term follow-up

artículo científico

Unilateral Sensorineural Hearing Loss: Medical Context and Etiology

artículo científico publicado en 2017

[Genetic deafness in adults]

artículo científico publicado en 2009

Lista de obras de

A case of respiratory depression in a child with ultrarapid CYP2D6 metabolism after tramadol.

A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss

Acquired subglottic cysts: Management and long term outcome ⬇️

An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the Literature

Arterial spin labeling brain MRI study to evaluate the impact of deafness on cerebral perfusion in 79 children before cochlear implantation

Cartilage shield tympanoplasty in children: review of 268 consecutive cases

Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

Congenital Cytomegalovirus Is the Second Most Frequent Cause of Bilateral Hearing Loss in Young French Children

Congenital cholesteatoma: risk factors for residual disease and retraction pockets--a report on 117 cases

Congenital cytomegalovirus is the second most frequent cause of bilateral hearing loss in young French children

Craniofacial dermoids: an embryological theory unifying nasal dermoid sinus cysts

Discovery of a large deletion of KAL1 in 2 deaf brothers

Endoscopic surgical treatment of laryngotracheal clefts: indications and limitations

Evaluation of cytomegalovirus (CMV) DNA quantification in dried blood spots: retrospective study of CMV congenital infection

Failures and Complications of Supraglottoplasty in Children ⬇️

First successful use of eltrombopag before surgery in a child with MYH9-related thrombocytopenia

GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients.

GJB2 mutations and degree of hearing loss: a multicenter study

Hearing outcomes in functional surgery for middle ear malformations.

Hearing rehabilitation with the closed skin bone-anchored implant Sophono Alpha1: results of a prospective study in 15 children with ear atresia.

Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome

High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5

Idiopathic bilateral vocal cord paralysis in infants: Case series and literature review

Laryngeal cleft.

Laser arytenoidectomy in the management of bilateral vocal cord paralysis in children

Management specificities of congenital laryngeal stenosis: external and endoscopic approaches

Mastoid fascia kite flap for cryptotia correction.

Medical and surgical complications in paediatric cochlear implantation

Medical and surgical complications in pediatric cochlear implantation

Middle ear implant in conductive and mixed congenital hearing loss in children

Neonatal vs delayed-onset fourth branchial pouch anomalies: therapeutic implications.

New closed skin bone-anchored implant: preliminary results in 6 children with ear atresia.

Noninvasive positive-pressure ventilation avoids recannulation and facilitates early weaning from tracheotomy in children

Pain After Cochlear Implantation: An Unusual Complication?

Pearls and Pitfalls in Cochlear Implantation ⬇️

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene

Physiologic and clinical benefits of noninvasive ventilation in infants with Pierre Robin sequence.

Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: A very mild phenotype ⬇️

Propranolol in the therapeutic strategy of infantile laryngotracheal hemangioma: A preliminary retrospective study of French experience

Propranolol may become first-line treatment in obstructive subglottic infantile hemangiomas

Results of VSB implantation at the short process of the incus in children with ear atresia.

Role of Propranolol in the therapeutic strategy of infantile laryngotracheal hemangioma.

Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct

Stapedectomy in children: causes and surgical results in 35 cases

Subglottic hemangioma in the infant

Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever!

The presentation and management of laryngeal cleft: a 10-year experience.

TheGJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafness

Total ossiculoplasty in children: predictive factors and long-term follow-up

Unilateral Sensorineural Hearing Loss: Medical Context and Etiology

[Genetic deafness in adults]