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Down syndrome: An electrophysiological and radiological profile

The Laryngoscope, 2014-04, Vol.124 (4), p.E141-E147

2014

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Molecular genetics of the Usher syndrome in Lebanon: identification of 11 novel protein truncating mutations by whole exome sequencing

PloS one, 2014-09, Vol.9 (9), p.e107326-e107326

2014

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A mutation in OTOF , encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

Nature genetics, 1999-04, Vol.21 (4), p.363-369

1999

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A Pilot Study to Assess the Vestibular Apparatus Function with Videonystagmography During Chronic Otitis Media with Effusion

Current pediatric reviews, 2015-01, Vol.11 (2), p.135-140

2015

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Nicotine Addiction and Hearing Loss in Young Subjects From Beirut, Lebanon

International journal of high risk behaviors & addiction, 2016-06, Vol.5 (4)

2016

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Measures of the electrically evoked compound action potential threshold and slope in HiRes 90K(TM) users

Cochlear implants international, 2014-01, Vol.15 (1), p.53-60

2014

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Measures of the electrically evoked compound action potential threshold and slope in HiRes 90K TM users

Cochlear implants international, 2014-01, Vol.15 (1), p.53-60

2014

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Measures of the electrically evoked compound action potential threshold and slope in HiRes 90KTM users

Cochlear implants international, 2014-01, Vol.15 (1), p.53-60

2014

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A novel 5-bp deletion in Clarin 1 in a family with Usher syndrome

Ophthalmic genetics, 2011-11, Vol.32 (4), p.245-249

2011

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An α-Tectorin Gene Defect Causes a Newly Identified Autosomal Recessive Form of Sensorineural Pre-Lingual Non-Syndromic Deafness, DFNB21

Human molecular genetics, 1999-03, Vol.8 (3), p.409-412

1999

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Map refinement of the Usher syndrome type 1B gene, MYO7A, relative to 11q13.5 microsatellite markers

Clinical genetics, 1998-08, Vol.54 (2), p.155-158

1998

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Molecular Genetics of the Usher Syndrome in Lebanon: Identification of 11 Novel Protein Truncating Mutations by Whole Exome Sequencing: e107326

PloS one, 2014-09, Vol.9 (9)

2014

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A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22–23

Human molecular genetics, 1996-01, Vol.5 (1), p.155-158

1996

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Mapping of DFNB12, a Gene for a Non-Syndromal Autosomal Recessive Deafness, to Chromosome 10q21–22

Human molecular genetics, 1996-07, Vol.5 (7), p.1061-1064

1996

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A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36

European journal of human genetics : EJHG, 1998-05, Vol.6 (3), p.245-250

1998

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Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness

European journal of human genetics : EJHG, 1998-11, Vol.6 (6), p.548-551

1998

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Automated classification of electrically-evoked compound action potentials

2015 7th International IEEE/EMBS Conference on Neural Engineering (NER), 2015, p.687-690

2015

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An [alpha]-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21

Human molecular genetics, 1999-03, Vol.8 (3), p.409

1999

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A novel 5-bp deletion in Clarin 1 in a family with Usher syndrome

Ophthalmic Genetics, 2011, Vol.32 (4), p.245-249

2011

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Deficits héréditaires de l'audition chez l'enfant

Annales de l'Institut Pasteur. Actualités, 1995, Vol.6 (4), p.304-309

1995

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Déficits héréditaires de l'audition chez l'enfant: Les maladies génétiques sensorielles

Annales de l'Institut Pasteur. Actualités, 1995, Vol.6 (4), p.304-309

1995

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Deafness - Genetics
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Ear, Auditive Nerve, Cochleovestibular Tract, Facial Nerve: Diseases, Semeiology
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Down syndrome: An electrophysiological and radiological profile

Molecular genetics of the Usher syndrome in Lebanon: identification of 11 novel protein truncating mutations by whole exome sequencing

A mutation in OTOF , encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

A Pilot Study to Assess the Vestibular Apparatus Function with Videonystagmography During Chronic Otitis Media with Effusion

Nicotine Addiction and Hearing Loss in Young Subjects From Beirut, Lebanon

Measures of the electrically evoked compound action potential threshold and slope in HiRes 90K(TM) users

Measures of the electrically evoked compound action potential threshold and slope in HiRes 90K TM users

Measures of the electrically evoked compound action potential threshold and slope in HiRes 90KTM users

A novel 5-bp deletion in Clarin 1 in a family with Usher syndrome

An α-Tectorin Gene Defect Causes a Newly Identified Autosomal Recessive Form of Sensorineural Pre-Lingual Non-Syndromic Deafness, DFNB21

Map refinement of the Usher syndrome type 1B gene, MYO7A, relative to 11q13.5 microsatellite markers

Molecular Genetics of the Usher Syndrome in Lebanon: Identification of 11 Novel Protein Truncating Mutations by Whole Exome Sequencing: e107326

A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22–23

Mapping of DFNB12, a Gene for a Non-Syndromal Autosomal Recessive Deafness, to Chromosome 10q21–22

A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36

Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness

Automated classification of electrically-evoked compound action potentials

An [alpha]-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21

A novel 5-bp deletion in Clarin 1 in a family with Usher syndrome

Deficits héréditaires de l'audition chez l'enfant

Déficits héréditaires de l'audition chez l'enfant: Les maladies génétiques sensorielles

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