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Middle ear cholesteatoma: non-echo-planar diffusion-weighted MR imaging versus delayed gadolinium-enhanced T1-weighted MR imaging--value in detection

Radiology, 2010-06, Vol.255 (3), p.866-872

2010

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A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family

American journal of human genetics, 2008-04, Vol.82 (4), p.982-991

2008

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Value of high-resolution computed tomography and magnetic resonance imaging in the detection of residual cholesteatomas in primary bony obliterated mastoids

American journal of otolaryngology, 2007-07, Vol.28 (4), p.230-234

2007

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Subarcuate Supralabyrinthine Approach for Supralabyrinthine Petrosal Cholesteatoma

Annals of otology, rhinology & laryngology, 2010, Vol.119 (1), p.42-46

2010

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Handling an Isolated Malleus Handle Fracture: Current Diagnostic Work-up and Treatment Options

Annals of otology, rhinology & laryngology, 2015-03, Vol.124 (3), p.244-249

2015

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Consensus Statements on the BAHA System: Where Do We Stand at Present?

Annals of otology, rhinology & laryngology, 2005-12, Vol.114 (12_suppl), p.2-12

2005

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Outcome evaluation of the dizziness handicap inventory in an outpatient vestibular clinic

Journal of vestibular research, 2016-01, Vol.26 (5-6), p.479-486

2016

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Statistical analysis of otosclerosis surgery performed by Jean Marquet

Annals of otology, rhinology & laryngology, 1994-12, Vol.103 (12), p.945-951

1994

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The coding polymorphism T263I in TGF-β1 is associated with otosclerosis in two independent populations

Human molecular genetics, 2007-09, Vol.16 (17), p.2021-2030

2007

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Association of Bone Morphogenetic Proteins With Otosclerosis

Journal of bone and mineral research, 2008-04, Vol.23 (4), p.507-516

2008

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Chronic Petrous Apicitis with Pericarotid Extension into the Neck in a Child

Annals of otology, rhinology & laryngology, 2001-10, Vol.110 (10), p.988-991

2001

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Box and whisker plots for graphic presentation of audiometric results of conductive hearing loss treatment

Otolaryngology-head and neck surgery, 1998-06, Vol.118 (6), p.892-895

1998

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Stapedotomy with Microdrill or Carbon Dioxide Laser: Influence on Inner Ear Function

Annals of otology, rhinology & laryngology, 2006-12, Vol.115 (12), p.880-885

2006

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A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family

American journal of human genetics, 2008-09, Vol.83 (3), p.424-424

2008

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Aplasia and hypoplasia of the vestibulocochlear nerve: diagnosis with MR imaging

Radiology, 1997-03, Vol.202 (3), p.773-781

1997

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Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Nature genetics, 1998-05, Vol.19 (1), p.60-62

1998

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Results, Hearing Rehabilitation, and Follow-up with Magnetic Resonance Imaging after Tympanomastoid Exenteration, Obliteration, and External Canal Overclosure for Severe Chronic Otitis Media

Annals of otology, rhinology & laryngology, 2007-09, Vol.116 (9), p.705-711

2007

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A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36

American journal of human genetics, 2001-02, Vol.68 (2), p.495-500

2001

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Stapedotomy With Microdrill or Carbon Dioxide Laser: Influence on Inner Ear Function/Commentary on "Stapedotomy With Microdrill or Carbon Dioxide Laser: Influence on Inner Ear Function"

Annals of otology, rhinology & laryngology, 2006-12, Vol.115 (12), p.880

2006

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The coding polymorphism T263I in TGF-[beta]1 is associated with otosclerosis in two independent populations

Human molecular genetics, 2007-09, Vol.16 (17), p.2021-2030

2007

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The coding polymorphism T263I in TGF-beta1 is associated with otosclerosis in two independent populations

Human molecular genetics, 2007-09, Vol.16 (17), p.2021-2030

2007

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The coding polymorphism T2631 in TGF-β1 is associated with otosclerosis in two independent populations

Human molecular genetics, 2007, Vol.16 (17), p.2021-2030

2007

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A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24

American journal of human genetics, 1997-05, Vol.60 (5), p.1168-1173

1997

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Imaging case study of the month: Chronic petrous apicitis with pericarotid extension into the neck in a child

Annals of otology, rhinology & laryngology, 2001-10, Vol.110 (10), p.988

2001

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Allograft tympanoplasty type 1 in the childhood population

Annals of otology, rhinology & laryngology, 1996-11, Vol.105 (11), p.871-876

1996

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Antineoplastic Combined Chemotherapy Protocols - Therapeutic Use
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Ear, Auditive Nerve, Cochleovestibular Tract, Facial Nerve: Diseases, Semeiology
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Middle ear cholesteatoma: non-echo-planar diffusion-weighted MR imaging versus delayed gadolinium-enhanced T1-weighted MR imaging--value in detection

A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family

Value of high-resolution computed tomography and magnetic resonance imaging in the detection of residual cholesteatomas in primary bony obliterated mastoids

Subarcuate Supralabyrinthine Approach for Supralabyrinthine Petrosal Cholesteatoma

Handling an Isolated Malleus Handle Fracture: Current Diagnostic Work-up and Treatment Options

Consensus Statements on the BAHA System: Where Do We Stand at Present?

Outcome evaluation of the dizziness handicap inventory in an outpatient vestibular clinic

Statistical analysis of otosclerosis surgery performed by Jean Marquet

The coding polymorphism T263I in TGF-β1 is associated with otosclerosis in two independent populations

Association of Bone Morphogenetic Proteins With Otosclerosis

Chronic Petrous Apicitis with Pericarotid Extension into the Neck in a Child

Box and whisker plots for graphic presentation of audiometric results of conductive hearing loss treatment

Stapedotomy with Microdrill or Carbon Dioxide Laser: Influence on Inner Ear Function

A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family

Aplasia and hypoplasia of the vestibulocochlear nerve: diagnosis with MR imaging

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Results, Hearing Rehabilitation, and Follow-up with Magnetic Resonance Imaging after Tympanomastoid Exenteration, Obliteration, and External Canal Overclosure for Severe Chronic Otitis Media

A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36

Stapedotomy With Microdrill or Carbon Dioxide Laser: Influence on Inner Ear Function/Commentary on "Stapedotomy With Microdrill or Carbon Dioxide Laser: Influence on Inner Ear Function"

The coding polymorphism T263I in TGF-[beta]1 is associated with otosclerosis in two independent populations

The coding polymorphism T263I in TGF-beta1 is associated with otosclerosis in two independent populations

The coding polymorphism T2631 in TGF-β1 is associated with otosclerosis in two independent populations

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24

Imaging case study of the month: Chronic petrous apicitis with pericarotid extension into the neck in a child

Allograft tympanoplasty type 1 in the childhood population

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