E. Cohn

发表

The M34T allele variant of connexin 26.

G. Green, G. Van Camp, P. M. Kelley, 2000, Genetic testing.

temperature-sensitive auditory neuropathy allele Running Title : A potential OTOF temperature-sensitive allele

A. Starr, C. Berlin, B. Keats, 2005 .

Menopause and benign paroxysmal positional vertigo

Kristen L. Janky, O. A. Ogun, B. Büki, 2014, Menopause.

The Genetics of Auditory Neuropathy

P. M. Kelley, E. Cohn, R. Rogers, 2002 .

Optic nerve decompression surgery for nonarteritic anterior ischemic optic neuropathy (NAION) is not effective and may be harmful. The Ischemic Optic Neuropathy Decompression Trial Research Group.

John W. Johnson, J. Horton, J. Selhorst, 1995, JAMA.

Fluctuating sensorineural hearing loss associated with enlarged vestibular aqueduct maps to 7q31, the region containing the Pendred gene.

W. Kimberling, S. Usami, S. Abe, 1999, American journal of medical genetics.

GJB2 mutations and degree of hearing loss: a multicenter study.

Mustafa Tekin, Umberto Ambrosetti, Nikolaus Blin, 2005, American journal of human genetics.

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

G. B. Schaefer, D. Harris, W. Kimberling, 1999, Pediatrics.

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

S. Leal, A. Starr, B. Keats, 2003, Journal of medical genetics.

Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children

E. Stone, W. Kimberling, R. Weleber, 2010, Genetics in Medicine.

Efficacy of glucosamine and chondroitin for treatment of osteoarthritis.

R. Smith, J. Bent, G. Green, 2000 .

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

B J Keats, L J Hood, C I Berlin, 2005, Journal of Medical Genetics.

Gender-Based Comorbidity in Benign Paroxysmal Positional Vertigo

Kristen L. Janky, O. A. Ogun, B. Büki, 2014, PloS one.

Audiological and vestibular features in affected subjects with USH3: A genotype/phenotype correlation

C. Möller, W. Kimberling, M. Sadeghi, 2005, International journal of audiology.

Connexin 26: required for normal auditory function

W. Kimberling, P. M. Kelley, E. Cohn, 2000, Brain Research Reviews.

Expressivity of hearing loss in cases with Usher syndrome type IIA

C. Möller, W. Kimberling, E. Cohn, 2013, International journal of audiology.

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

P. M. Kelley, E. Cohn, Edward S. Cohn, 1999, American journal of medical genetics.

Audiological Manifestations and Features of Connexin 26 Deafness

K. Avraham, Richard J. H. Smith, G. Green, 2003 .

Is hearing loss due to mutations in the Connexin 26 gene progressive?

W. Jesteadt, W. Kimberling, P. M. Kelley, 2008, International journal of audiology.

Audiological findings in Usher syndrome types IIa and II (non-IIa)

C. Möller, W. Kimberling, M. Sadeghi, 2004, International journal of audiology.

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

A. Starr, C. Berlin, W. Kimberling, 2005, Journal of Medical Genetics.

Hearing loss with aging: presbycusis.

E. Cohn, 1999, Clinics in geriatric medicine.