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Randomized, controlled, phase 3 study to evaluate the safety and efficacy of fibrin sealant VH S/D 4 s-apr (Artiss) to improve tissue adherence in subjects undergoing rhytidectomy

Aesthetic surgery journal, 2013-05, Vol.33 (4), p.487-496

2013

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Exploratory, randomized, controlled, phase 2 study to evaluate the safety and efficacy of adjuvant fibrin sealant VH S/D 4 S-Apr (ARTISS) in patients undergoing rhytidectomy

Aesthetic surgery journal, 2013-03, Vol.33 (3), p.323-333

2013

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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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Anticipation and management of the emergency airway in the cosmetic patient during office-based surgery

Plastic and reconstructive surgery (1963), 2008-12, Vol.122 (6), p.230e-232e

2008

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The Dimpleplasty: A New Streamlined Approach to Surgical Creation of Dynamic Facial Dimples, Our Experience, and Results

The American journal of cosmetic surgery, 2019-09, Vol.36 (3), p.138-142

2019

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Incidence of vocal fold paralysis in infants undergoing ligation of patent ductus arteriosus

The Annals of thoracic surgery, 1996-03, Vol.61 (3), p.814-816

1996

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Altering brow contour with botulinum toxin

Facial plastic surgery clinics of North America, 2003-11, Vol.11 (4), p.457-464

2003

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Total Face Rejuvenation: Simultaneous 3-Plane Surgical Approach Combined with Ablative Laser Resurfacing

The American journal of cosmetic surgery, 2014-09, Vol.31 (3), p.183-188

2014

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Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q

Human molecular genetics, 1995-09, Vol.4 (9), p.1643-1648

1995

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Treatment of Large Keloids with Secondary-Intention Healing

The American journal of cosmetic surgery, 2013-09, Vol.30 (3), p.193-199

2013

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Chondroid syringoma of the head and neck: clinical management and literature review

Ear, nose, & throat journal, 1996-02, Vol.75 (2), p.104-108

1996

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MYO1F as a candidate gene for nonsyndromic deafness, DFNB15

Archives of otolaryngology--head & neck surgery, 2001-08, Vol.127 (8), p.921

2001

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Repair of the Pixie Ear Deformity with Modified V to Y Plasty during Rhytidectomy

The American journal of cosmetic surgery, 2007-09, Vol.24 (3), p.146-149

2007

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Linkage of a gene for dominant non-syndromic deafness to chromosome 19

Human molecular genetics, 1995-06, Vol.4 (6), p.1073-1076

1995

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Phenotypic manifestations of branchiootorenal syndrome

American journal of medical genetics, 1995-09, Vol.58 (4), p.365-370

1995

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A Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10, Maps to Chromosome 6

Human molecular genetics, 1996-06, Vol.5 (6), p.853-856

1996

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A Gene for Recessive Nonsyndromic Sensorineural Deafness (DFNB18) Maps to the Chromosomal Region 11p14–p15.1 Containing the Usher Syndrome Type 1C Gene

Genomics (San Diego, Calif.), 1998-06, Vol.50 (2), p.290-292

1998

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Physical mapping of the deafness gene DFNA 10

Otolaryngology-head and neck surgery, 1999-08, Vol.121 (2), p.P80-P80

1999

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Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping

Archives of otolaryngology--head & neck surgery, 1998-01, Vol.124 (1), p.20

1998

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Laryngeal Cancer Cost Analysis: Association of Case-Mix and Treatment Characteristics With Medical Charges

The Laryngoscope, 2000-01, Vol.110 (1), p.1-7

2000

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The incidence of postoperative vocal fold paralysis in infants less than or equal to one year of age undergoing ligation of patent ductus arteriosus

Otolaryngology-head and neck surgery, 1995, Vol.113 (2), p.P208-P209

1995

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169 The Incidence of Postoperative Vocal Fold Paralysis in Infants Less Than or Equal to One Year of Age Undergoing Ligation of Patent Ductus Arteriosus

Otolaryngology-head and neck surgery, 1995-08, Vol.113 (2), p.P208-P208

1995

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非症候性常染色体優性遺伝性難聴の連鎖解析-DFNA4のマッピング

日本耳鼻咽喉科学会会報, 1996-05, Vol.99 (suppl-5), p.782-782

1996

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Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31

American journal of medical genetics, 1998-06, Vol.78 (2), p.107-113

1998

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New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p

American journal of medical genetics, 1997-09, Vol.71 (4), p.467-471

1997

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Ear, Auditive Nerve, Cochleovestibular Tract, Facial Nerve: Diseases, Semeiology
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Randomized, controlled, phase 3 study to evaluate the safety and efficacy of fibrin sealant VH S/D 4 s-apr (Artiss) to improve tissue adherence in subjects undergoing rhytidectomy

Exploratory, randomized, controlled, phase 2 study to evaluate the safety and efficacy of adjuvant fibrin sealant VH S/D 4 S-Apr (ARTISS) in patients undergoing rhytidectomy

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

Anticipation and management of the emergency airway in the cosmetic patient during office-based surgery

The Dimpleplasty: A New Streamlined Approach to Surgical Creation of Dynamic Facial Dimples, Our Experience, and Results

Incidence of vocal fold paralysis in infants undergoing ligation of patent ductus arteriosus

Altering brow contour with botulinum toxin

Total Face Rejuvenation: Simultaneous 3-Plane Surgical Approach Combined with Ablative Laser Resurfacing

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q

Treatment of Large Keloids with Secondary-Intention Healing

Chondroid syringoma of the head and neck: clinical management and literature review

MYO1F as a candidate gene for nonsyndromic deafness, DFNB15

Repair of the Pixie Ear Deformity with Modified V to Y Plasty during Rhytidectomy

Linkage of a gene for dominant non-syndromic deafness to chromosome 19

Phenotypic manifestations of branchiootorenal syndrome

A Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10, Maps to Chromosome 6

A Gene for Recessive Nonsyndromic Sensorineural Deafness (DFNB18) Maps to the Chromosomal Region 11p14–p15.1 Containing the Usher Syndrome Type 1C Gene

Physical mapping of the deafness gene DFNA 10

Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping

Laryngeal Cancer Cost Analysis: Association of Case-Mix and Treatment Characteristics With Medical Charges

The incidence of postoperative vocal fold paralysis in infants less than or equal to one year of age undergoing ligation of patent ductus arteriosus

169 The Incidence of Postoperative Vocal Fold Paralysis in Infants Less Than or Equal to One Year of Age Undergoing Ligation of Patent Ductus Arteriosus

非症候性常染色体優性遺伝性難聴の連鎖解析-DFNA4のマッピング

Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31

New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p

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