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Scanning Electrochemical Microscopy as a Novel Proximity Sensor for Atraumatic Cochlear Implant Insertion

IEEE transactions on biomedical engineering, 2014-06, Vol.61 (6), p.1822-1832

2014

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Small molecule delivery across a perforated artificial membrane by thermoreversible hydrogel poloxamer 407

Colloids and surfaces, B, Biointerfaces, 2019-10, Vol.182, p.110300-110300, Article 110300

2019

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Large vestibular aqueduct syndrome and endolymphatic hydrops: two presentations of a common primary inner-ear dysfunction?

Journal of laryngology and otology, 2009-08, Vol.123 (8), p.919-921

2009

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The Cochlear-Carotid Interval: Anatomic Variation and Potential Clinical Implications

American Journal of Neuroradiology, 2006-08, Vol.27 (7), p.1486-1490

2006

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OTOF Encodes Multiple Long and Short Isoforms: Genetic Evidence That the Long Ones Underlie Recessive Deafness DFNB9

American journal of human genetics, 2000-09, Vol.67 (3), p.591-600

2000

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Cochlear gene delivery through an intact round window membrane in mouse

Human gene therapy, 2001-03, Vol.12 (5), p.539-548

2001

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Development of in vivo gene therapy for hearing disorders: introduction of adeno-associated virus into the cochlea of the guinea pig

Gene therapy, 1996-07, Vol.3 (7), p.588

1996

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Long-term in vivo cochlear transgene expression mediated by recombinant adeno-associated virus

Gene therapy, 1998-02, Vol.5 (2), p.277-281

1998

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Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment

Clinical genetics, 2003-02, Vol.63 (2), p.154-159

2003

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SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas

Clinical genetics, 2004-11, Vol.66 (5), p.461-466

2004

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Transgene expression in the guinea pig cochlea mediated by a lentivirus-derived gene transfer vector

Human gene therapy, 1999-07, Vol.10 (11), p.1867-1873

1999

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Grading venous restrictive disease in patients with dural arteriovenous fistulas of the transverse/sigmoid sinus

Journal of neurosurgery, 1993-07, Vol.79 (1), p.11-15

1993

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Utility of electronystagmography in the prediction of post-operative outcome following cochlear implantation

Journal of laryngology and otology, 2015-03, Vol.129 (3), p.238-243

2015

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Cationic liposome mediated transgene expression in the guinea pig cochlea

Hearing research, 1999-02, Vol.128 (1), p.61-69

1999

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Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33

Journal of molecular medicine (Berlin, Germany), 2004-06, Vol.82 (6), p.398-402

2004

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Human Nonsyndromic Hereditary Deafness DFNA17 Is Due to a Mutation in Nonmuscle Myosin MYH9

American journal of human genetics, 2000-11, Vol.67 (5), p.1121-1128

2000

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Transverse/Sigmoid Sinus Dural Arteriovenous Fistulas Presenting As Pulsatile Tinnitus

The Laryngoscope, 1999-01, Vol.109 (1), p.54-58

1999

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A mutation in PDS causes non-syndromic recessive deafness

Nature genetics, 1998-03, Vol.18 (3), p.215-217

1998

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Facial nerve outcome after acoustic neuroma surgery: a study from the era of cranial nerve monitoring

Otolaryngology-head and neck surgery, 1994-11, Vol.111 (5), p.561-570

1994

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Molecular Pathogenesis in Sporadic Head and Neck Paraganglioma

The Laryngoscope, 2000-08, Vol.110 (8), p.1346-1348

2000

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Meningiomas, epidermoids, and other nonacoustic tumors of the cerebellopontine angle

Otolaryngologic clinics of North America, 1992-06, Vol.25 (3), p.707-728

Lalwani, A K

1992

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Perioperative Management of von Willebrand's Disease in Otolaryngologic Surgery

The Laryngoscope, 1998-01, Vol.108 (1), p.32-36

1998

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Growth Rate Characteristics of Acoustic Neuromas Associated With Neurofibromatosis Type 2

The Laryngoscope, 1996-06, Vol.106 (6), p.694-699

1996

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A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2

American journal of human genetics, 1994-10, Vol.55 (4), p.685-694

1994

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A New Locus for Nonsyndromic Hereditary Hearing Impairment, DFNA17, Maps to Chromosome 22 and Represents a Gene for Cochleosaccular Degeneration

American journal of human genetics, 1999, Vol.64 (1), p.318-323

1999

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Scanning Electrochemical Microscopy as a Novel Proximity Sensor for Atraumatic Cochlear Implant Insertion

Small molecule delivery across a perforated artificial membrane by thermoreversible hydrogel poloxamer 407

Large vestibular aqueduct syndrome and endolymphatic hydrops: two presentations of a common primary inner-ear dysfunction?

The Cochlear-Carotid Interval: Anatomic Variation and Potential Clinical Implications

OTOF Encodes Multiple Long and Short Isoforms: Genetic Evidence That the Long Ones Underlie Recessive Deafness DFNB9

Cochlear gene delivery through an intact round window membrane in mouse

Development of in vivo gene therapy for hearing disorders: introduction of adeno-associated virus into the cochlea of the guinea pig

Long-term in vivo cochlear transgene expression mediated by recombinant adeno-associated virus

Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment

SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas

Transgene expression in the guinea pig cochlea mediated by a lentivirus-derived gene transfer vector

Grading venous restrictive disease in patients with dural arteriovenous fistulas of the transverse/sigmoid sinus

Utility of electronystagmography in the prediction of post-operative outcome following cochlear implantation

Cationic liposome mediated transgene expression in the guinea pig cochlea

Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33

Human Nonsyndromic Hereditary Deafness DFNA17 Is Due to a Mutation in Nonmuscle Myosin MYH9

Transverse/Sigmoid Sinus Dural Arteriovenous Fistulas Presenting As Pulsatile Tinnitus

A mutation in PDS causes non-syndromic recessive deafness

Facial nerve outcome after acoustic neuroma surgery: a study from the era of cranial nerve monitoring

Molecular Pathogenesis in Sporadic Head and Neck Paraganglioma

Meningiomas, epidermoids, and other nonacoustic tumors of the cerebellopontine angle

Perioperative Management of von Willebrand's Disease in Otolaryngologic Surgery

Growth Rate Characteristics of Acoustic Neuromas Associated With Neurofibromatosis Type 2

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2

A New Locus for Nonsyndromic Hereditary Hearing Impairment, DFNA17, Maps to Chromosome 22 and Represents a Gene for Cochleosaccular Degeneration

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