Richard J. H. Smith

发表

Use of portfolios in otolaryngology graduate medical education

R. Gurgel, Robert Miller, Richard J. H. Smith, 2011, The Laryngoscope.

Association of Bone Morphogenetic Proteins With Otosclerosis

J. Huyghe, M. Claustres, E. Fransen, 2007, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Respiratory Manifestations of Gastroesophageal Reflux Disease in Pediatric Patients

N. Bauman, A. Sandler, Richard J. H. Smith, 1996, The Annals of otology, rhinology, and laryngology.

Alternative Complement Pathway Inhibition With Iptacopan for the Treatment of C3 Glomerulopathy-Study Design of the APPEAR-C3G Trial

D. Kavanagh, M. Vivarelli, A. Bomback, 2022, Kidney international reports.

DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss

Adam P. DeLuca, Corey W. Goodman, Bruce W. Tompkins, 2011, Human mutation.

Degrees of dysplasia and the use of cidofovir in patients with recurrent respiratory papillomatosis

L. Karnell, H. Hoffman, Richard J. H. Smith, 2010, The Laryngoscope.

Clinical application of genetic testing for deafness

Richard J. H. Smith, 2004, American journal of medical genetics. Part A.

Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype–phenotype correlations

V. Sheffield, G. Green, R. A. Cucci, 2001, Human mutation.

Genetic heterogeneity of deafness phenotypes linked to DFNA4

H. Zenner, C. Pusch, N. Blin, 2005, American journal of medical genetics. Part A.

Amplification of mitochondrial DNA from archival temporal bone specimens

T. A. Simpson, Richard J. H. Smith, 1995, The Laryngoscope.

Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus

S. Riazuddin, Z. Ahmed, Shaheen N. Khan, 2007, Human Mutation.

A novel splice site mutation in EYA4 causes DFNA10 hearing loss

M. Bahlo, R. Gardner, H. Dahl, 2007, American journal of medical genetics. Part A.

GJB2 mutations in Iranians with autosomal recessive non‐syndromic sensorineural hearing loss

M. Farhadi, K. Kahrizi, H. Najmabadi, 2002, Human mutation.

Molecular characterization of a novel X‐linked syndrome involving developmental delay and deafness

M. Bahlo, T. Tolmachova, S. White, 2007, American journal of medical genetics. Part A.

Did the GJB2 35delG mutation originate in Iran?

K. Kahrizi, H. Najmabadi, C. Nishimura, 2011, American journal of medical genetics. Part A.

Spastic Diplegia and Other Motor Disturbances in Infants Receiving Interferon‐Alpha

N. Bauman, A. Michaud, J. Manaligod, 2004, The Laryngoscope.

COL1A1 association and otosclerosis: A meta‐analysis

E. Fransen, S. Masmoudi, G. Van Camp, 2012, American journal of medical genetics. Part A.

Genetic variants in RELN are associated with otosclerosis in a non‐European population from Tunisia

E. Fransen, S. Masmoudi, Richard J. H. Smith, 2010, Annals of human genetics.

Current treatment paradigms in the management of lymphatic malformations

Richard J. H. Smith, Richard J. H. Smith, J. Renton, 2011, The Laryngoscope.

Laryngomalacia and Its Treatment

N. Bauman, R J Smith, J. Greinwald, 1999, The Laryngoscope.

Distal Tracheal Stenosis in Neonates and Infants

N. Bauman, D. Kearns, Richard J. H. Smith, 1992, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Bipolar Hooked-Wire Electromyographic Technique in the Evaluation of Pediatric Vocal Cord Paralysis

H. Hoffman, Richard J. H. Smith, K. L. Peterson, 1993, The Annals of otology, rhinology, and laryngology.

Vocal fold Paralysis in Infants Twelve Months of Age and Younger

Richard J. H. Smith, R. I. Zbar, 1996, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Reflex laryngospasm induced by stimulation of distal esophageal afferents

N. Bauman, A. Sandler, J. Maher, 1994, The Laryngoscope.

Congenital Oral Synechiae

Richard J. H. Smith, J. Davies, Michael G. Gartlan, 1993, The Annals of otology, rhinology, and laryngology.

Mutation in the COCH gene is associated with superior semicircular canal dehiscence

Adam P. DeLuca, In Ae Hur, T. Casavant, 2009, American journal of medical genetics. Part A.

Interarytenoid Notch Height Relative to the Vocal Folds Pilot Study

N. Bauman, Richard J. H. Smith, Michael B. Neville, 1994, The Annals of otology, rhinology, and laryngology.

Mortality in the pediatric patient with tracheotomy

P. M. Palmer, J. Dutton, Richard J. H. Smith, 1995, Head & neck.

Trends in the use of tracheotomy in the pediatric patient: The Iowa experience

P. M. Palmer, J. Dutton, Richard J. H. Smith, 1995, Head & neck.

Treatment of Lymphangiomas in Children: An Update of Picibanil (OK-432) Sclerotherapy

N. Bauman, J. Greinwald, K. Kimura, 1999, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Efficacy and safety of OK‐432 immunotherapy of lymphatic malformations

Yutaka Sato, Mark C. Smith, N. Bauman, 2009, The Laryngoscope.

The prevalence of mitochondrial mutations associated with aminoglycoside‐induced sensorineural hearing loss in an NICU population

K. Lynch, N. Meyer, M. Ealy, 2011, The Laryngoscope.

One-Stage Repair of Congenital Laryngeal Webs

D. Kearns, M. Biavati, Richard J. H. Smith, 1995, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Endoscopic Repair of Type IA Laryngeal Clefts

J. Bent, N. Bauman, Richard J. H. Smith, 1997, The Laryngoscope.

Genetic Testing and Genetic Counseling for Deafness: The Future Is Here

N. Robin, J. Brunger, A. Matthews, 2001, The Laryngoscope.

Flexible models for planning repair of complex tracheal anomalies

J. Reinhardt, R. Amendola, Richard J. H. Smith, 2012, The Laryngoscope.

Suprastomal Granulation Tissue and Pediatric Tracheotomy Decannulation

J. Bent, Richard J. H. Smith, R. M. Merritt, 1997, The Laryngoscope.

Microdeletion of 17q22q23.2 encompassing TBX2 and TBX4 in a patient with congenital microcephaly, thyroid duct cyst, sensorineural hearing loss, and pulmonary hypertension

V. Sheffield, S. Patil, Richard J. H. Smith, 2011, American journal of medical genetics. Part A.

Laryngotracheal stenosis: A 5‐year review

Richard J. H. Smith, Francis L. Catlin, 1991, Head & neck.

Unilateral Laryngeal Dysgenesis

Richard J. H. Smith, John P. Bent, Jose Manaligod, 1998, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1

W. Kimberling, Richard J. H. Smith, M. Hildebrand, 2008, American journal of medical genetics. Part A.

Passage to India: The Search for Genes Causing Autosomal Recessive Nonsyndromic Hearing Loss

C. Srisailapathy, A. Ramesh, K. Fukushima, 1998, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Surfactant Protein a in Rabbit Sinus and Middle Ear Mucosa

K. Goss, J. M. Snyder, J. Dutton, 1999, The Annals of otology, rhinology, and laryngology.

R. Smith, J. Skaggs, J. Manaligod, 2000, The Laryngoscope.

Mentoring in otolaryngology training programs

M. Fried, R. Gurgel, John H. Flint, 2010, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss

D. Stephan, J. Webster, M. Bahlo, 2009, The Laryngoscope.

An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss

X. Estivill, T. Speed, Justin Tan, 2008, Human mutation.

Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population

E. Stone, C. D. Della Santina, L. Minor, 2010, American journal of medical genetics. Part A.

Familial transmission of oculoauriculovertebral spectrum (Goldenhar syndrome) is not due to mutations in either EYA1 or SALL1

S. Prucka, N. Robin, J. Kohlhase, 2009, American journal of medical genetics. Part A.

Laryngeal Motion During Exercise

R. Smith, J. Wilson, M. Beaty, 1999, The Laryngoscope.

Hearing Loss in Union Army Veterans from 1862 to 1920

P. Blanck, N. Bauman, Chen Song, 2004, The Laryngoscope.

A novel mutation in COCH—implications for genotype‐phenotype correlations in DFNA9 hearing loss

D. Stephan, J. Webster, M. Bahlo, 2010, The Laryngoscope.

Hearing Genes and Cisplatin Deafness: A Pilot Study

C. Shores, J. Blatt, C. Knoll, 2006, The Laryngoscope.

Novel coding‐region polymorphisms in mitochondrial seryl‐tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness families

C. Cremers, Z. Shah, H. Jacobs, 2001, Human mutation.

Fine‐needle aspiration biopsy of subcutaneous fat necrosis of the newborn

M. Cohen, Michael B. Cohen, W. Walker, 1993, Diagnostic cytopathology.

Monitoring stress levels in postgraduate medical training

Richard J. H. Smith, Justin D. Hill, Richard J. Smith, 2009, The Laryngoscope.

In Reference to Temporal Bone Imaging in GJB2 Deafness

H. Azaiez, Richard J. H. Smith, 2007, The Laryngoscope.

Polymerase chain reaction amplification of dna from archival celloidin‐embedded human temporal bone sections

T. A. Simpson, B. Gantz, Richard J. H. Smith, 1993, The Laryngoscope.

Pathogenesis and treatment of juvenile onset recurrent respiratory papillomatosis.

R. Smith, G. Green, N. Bauman, 2000, Otolaryngologic clinics of North America.

Chronic cough and tonsillar hypertrophy: A case series

M. Weinberger, Richard J. H. Smith, R. Gurgel, 2008, Pediatric pulmonology.

Localization of the gene for branchiootorenal syndrome to chromosome 8q.

W. Kimberling, Shrawan Kumar, S. Tinley, 1992, Genomics.

Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family.

C. Cremers, W. Kimberling, Shrawan Kumar, 1992, Human molecular genetics.

Pendred Syndrome

Karen A. Kölln, Richard J. H. Smith, 2003, Handbook of Tumor Syndromes.

Branchio‐oto‐renal syndrome

W. Kimberling, Richard J. H. Smith, Amit Kochhar, 2007, American journal of medical genetics. Part A.

Branchio‐oto‐renal syndrome: The mutation spectrum in EYA1 and its phenotypic consequences

Richard J. H. Smith, N. Meyer, V. Vervoort, 2004, Human mutation.

Pediatric otolaryngologists' knowledge and understanding of genetic testing for deafness.

N. Robin, R. Smith, J. Arnold, 2001, Archives of otolaryngology--head & neck surgery.

Genetic diagnosis and renal biopsy findings in the setting of a renal genetics clinic

M. Bekheirnia, M. Braun, N. Bekheirnia, 2022, American journal of medical genetics. Part C, Seminars in medical genetics.

Degrees of dysplasia and the use of cidofovir in patients with recurrent respiratory papillomatosis

L. Karnell, R. Robinson, Hina Gupta, 2010, The Laryngoscope.

Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population

E. Stone, C. D. Della Santina, L. Minor, 2010, American journal of medical genetics. Part A.

Mentoring in otolaryngology training programs

M. Fried, R. Gurgel, John H. Flint, 2010, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.