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Pediatric Bronchogenic Cysts: A Case Series of Six Patients Highlighting Diagnosis and Management

Journal of investigative surgery, 2020-07, Vol.33 (6), p.568-573

2020

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OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

Journal of medical genetics, 2006-07, Vol.43 (7), p.576-581

2006

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Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene

Journal of medical genetics, 2003-01, Vol.40 (1), p.45-50

2003

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Novel case examples of the submental island flap in pediatric head and neck reconstruction

International journal of pediatric otorhinolaryngology, 2017-06, Vol.97, p.51-54

2017

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In Reference to “Informed Consent in Pediatric Otolaryngology: What Risks and Benefits Do Parents Recall?”

Otolaryngology-head and neck surgery, 2017-02, Vol.156 (2), p.385-385

2017

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Outcome of Reproductive Age Women with Stage IA or IC Invasive Epithelial Ovarian Cancer Treated with Fertility-Sparing Therapy

Gynecologic oncology, 2002-10, Vol.87 (1), p.1-7

2002

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Blood Pressure Screening of School Children in a Multiracial School District: The Healthy Kids Project

American journal of hypertension, 2009-04, Vol.22 (4), p.351-356

2009

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Incidental mastoid opacification on computed tomography in the pediatric population

International journal of pediatric otorhinolaryngology, 2020-01, Vol.128, p.109688-109688, Article 109688

2020

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Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)

Pediatrics (Evanston), 1999-03, Vol.103 (3), p.546-550

1999

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Contraception methods used among women with HIV starting antiretroviral therapy in a large United States clinical trial, 2009–2011

Contraception (Stoneham), 2021-04, Vol.103 (4), p.225-231

2021

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Novel technique for nasal septal button insertion: The sutured rosette

Clinical otolaryngology, 2019-11, Vol.44 (6), p.1221-1223

2019

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Otitis Media and Hearing Loss in Patients With Nonsyndromic Craniosynostosis: A Multicenter Study

The Cleft palate-craniofacial journal, 2022-05, Vol.59 (5), p.652-658

2022

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Ending the evidence gap for pregnancy, HIV and co‐infections: ethics guidance from the PHASES project

Journal of the International AIDS Society, 2021-12, Vol.24 (12), p.e25846-n/a

2021

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Repair of a Secondary Cleft Lip Deformity With the Abbé Flap in a Pediatric Patient

Ear, nose, & throat journal, 2019-06, Vol.98 (5), p.265-267

2019

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Castleman Disease Presenting as a Supraclavicular Neck Mass in a Child

Ear, nose, & throat journal, 2020-02, Vol.99 (2), p.99-100

2020

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Parent perspectives of occupational therapy using a sensory integration approach

The American journal of occupational therapy, 2001-05, Vol.55 (3), p.285-294

Cohn, E S

2001

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Chest Pain in Young Patients in an Office Setting: Cardiac Diagnoses, Outcomes, and Test Burden

Clinical pediatrics, 2012-09, Vol.51 (9), p.877-883

2012

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From waiting to relating: parents' experiences in the waiting room of an occupational therapy clinic

The American journal of occupational therapy, 2001-03, Vol.55 (2), p.167-174

Cohn, E S

2001

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Urinary Incontinence in the CKiD Cohort and Health Related Quality of Life

The Journal of urology, 2009-10, Vol.182 (4), p.2007-2014

2009

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Expressivity of hearing loss in cases with Usher syndrome type IIA

International journal of audiology, 2013-12, Vol.52 (12), p.832-837

2013

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Including the family perspective in sensory integration outcomes research

The American journal of occupational therapy, 1998-07, Vol.52 (7), p.540-546

1998

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Parental hopes for therapy outcomes: children with sensory modulation disorders

The American journal of occupational therapy, 2000-01, Vol.54 (1), p.36-43

2000

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Exploring parents' use of strategies to promote social participation of school-age children with acquired brain injuries

The American journal of occupational therapy, 2005-05, Vol.59 (3), p.273-284

2005

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Are rods and cones of dyslexics anomalous?

Perceptual and motor skills, 1989-08, Vol.69 (1), p.91-94

Cohn, T E

1989

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Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss

American journal of medical genetics, 1999-09, Vol.89 (3), p.130-136

1999

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Pediatric Bronchogenic Cysts: A Case Series of Six Patients Highlighting Diagnosis and Management

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene

Novel case examples of the submental island flap in pediatric head and neck reconstruction

In Reference to “Informed Consent in Pediatric Otolaryngology: What Risks and Benefits Do Parents Recall?”

Outcome of Reproductive Age Women with Stage IA or IC Invasive Epithelial Ovarian Cancer Treated with Fertility-Sparing Therapy

Blood Pressure Screening of School Children in a Multiracial School District: The Healthy Kids Project

Incidental mastoid opacification on computed tomography in the pediatric population

Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)

Contraception methods used among women with HIV starting antiretroviral therapy in a large United States clinical trial, 2009–2011

Novel technique for nasal septal button insertion: The sutured rosette

Otitis Media and Hearing Loss in Patients With Nonsyndromic Craniosynostosis: A Multicenter Study

Ending the evidence gap for pregnancy, HIV and co‐infections: ethics guidance from the PHASES project

Repair of a Secondary Cleft Lip Deformity With the Abbé Flap in a Pediatric Patient

Castleman Disease Presenting as a Supraclavicular Neck Mass in a Child

Parent perspectives of occupational therapy using a sensory integration approach

Chest Pain in Young Patients in an Office Setting: Cardiac Diagnoses, Outcomes, and Test Burden

From waiting to relating: parents' experiences in the waiting room of an occupational therapy clinic

Urinary Incontinence in the CKiD Cohort and Health Related Quality of Life

Expressivity of hearing loss in cases with Usher syndrome type IIA

Including the family perspective in sensory integration outcomes research

Parental hopes for therapy outcomes: children with sensory modulation disorders

Exploring parents' use of strategies to promote social participation of school-age children with acquired brain injuries

Are rods and cones of dyslexics anomalous?

Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss

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