Search Results - "Cohn, Edward S."

Gender-based comorbidity in benign paroxysmal positional vertigo by Ogun, Oluwaseye Ayoola, Janky, Kristen L, Cohn, Edward S, Büki, Bela, Lundberg, Yunxia Wang

“…It has been noted that benign paroxysmal positional vertigo (BPPV) may be associated with certain disorders and medical procedures. However, most studies to…”
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Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children by Kimberling, William J., Hildebrand, Michael S., Shearer, A. Eliot, Jensen, Maren L., Halder, Jennifer A., Trzupek, Karmen, Cohn, Edward S., Weleber, Richard G., Stone, Edwin M., Smith, Richard J.H.

“…Usher syndrome is a major cause of genetic deafness and blindness. The hearing loss is usually congenital and the retinitis pigmentosa is progressive and first…”
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Menopause and benign paroxysmal positional vertigo by Ogun, Oluwaseye Ayoola, Büki, Bela, Cohn, Edward S, Janky, Kristen L, Lundberg, Yunxia Wang

“…OBJECTIVEThis study was designed to examine the age and sex distribution and the effects of menopause in a large cohort of participants diagnosed with benign…”
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Is hearing loss due to mutations in the Connexin 26 gene progressive? by Gopalarao, Deepika, Kimberling, William J., Jesteadt, Walt, Kelley, Philip M., Beauchaine, Kathryn L., Cohn, Edward S.

“…Serial audiograms were analysed for seven subjects, who were homozygous for the 35delG GJB2 mutation. The criterion for determining progression of hearing loss…”
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Expressivity of hearing loss in cases with Usher syndrome type IIA by Sadeghi, André M., Cohn, Edward S., Kimberling, William J., Halvarsson, Glenn, Möller, Claes

“…Abstract Objective: The purpose of this study was to compare the genotype/phenotype relationship between siblings with identical USH2A pathologic mutations and…”
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Clinical Studies of Families With Hearing Loss Attributable to Mutations in the Connexin 26 Gene (GJB2/DFNB1) by Cohn, Edward S, Kelley, Philip M, Fowler, Thomas W, Gorga, Michael P, Lefkowitz, David M, Kuehn, Harold J, Schaefer, G. Bradley, Gobar, Lisa S, Hahn, Francis J, Harris, Djuana J, Kimberling, William J

“…This retrospective study describes the phenotype associated with the single most common cause of genetic hearing loss. The frequency of childhood deafness is…”
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Audiological and vestibular features in affected subjects with USH3: A genotype/phenotype correlation by Sadeghi, Mehdi, Cohn, Edward S., Kimberling, William J., Tranebjærg, Lisbeth, Möller, Claes

“…The aims were to compare the genotype/phenotype relationship between USH3 mutations and the consequent hearing and vestibular phenotype; and to compare hearing…”
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Genetic Testing to Identify Deaf Newborns by Green, Glenn E, Smith, Richard J. H, Bent, John P, Cohn, Edward S

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Audiological findings in Usher syndrome types IIa and II (non-IIa) by Sadeghi, Mehdi, Cohn, Edward S., Kelly, William J., Kimberling, William J., Tranebjoerg, Lisbeth, Möller, Claes

“…The aim was to define the natural history of hearing lossin Usher syndrome type IIa compared to non-IIa. Peoplewith Usher syndrome type II show…”
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GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study by Snoeckx, Rikkert L., Huygen, Patrick L.M., Feldmann, Delphine, Marlin, Sandrine, Denoyelle, Françoise, Waligora, Jaroslaw, Mueller-Malesinska, Malgorzata, Pollak, Agneszka, Ploski, Rafal, Murgia, Alessandra, Orzan, Eva, Castorina, Pierangela, Ambrosetti, Umberto, Nowakowska-Szyrwinska, Ewa, Bal, Jerzy, Wiszniewski, Wojciech, Janecke, Andreas R., Nekahm-Heis, Doris, Seeman, Pavel, Bendova, Olga, Kenna, Margaret A., Frangulov, Anna, Rehm, Heidi L., Tekin, Mustafa, Incesulu, Armagan, Dahl, Hans-Henrik M., du Sart, Desirée, Jenkins, Lucy, Lucas, Deirdre, Bitner-Glindzicz, Maria, Avraham, Karen B., Brownstein, Zippora, del Castillo, Ignacio, Moreno, Felipe, Blin, Nikolaus, Pfister, Markus, Sziklai, Istvan, Toth, Timea, Kelley, Philip M., Cohn, Edward S., Van Maldergem, Lionel, Hilbert, Pascale, Roux, Anne-Françoise, Mondain, Michel, Hoefsloot, Lies H., Cremers, Cor W.R.J., Löppönen, Tuija, Löppönen, Heikki, Parving, Agnete, Gronskov, Karen, Schrijver, Iris, Roberson, Joseph, Gualandi, Francesca, Martini, Alessandro, Lina-Granade, Geneviève, Pallares-Ruiz, Nathalie, Correia, Céu, Fialho, Graça, Cryns, Kim, Hilgert, Nele, Van de Heyning, Paul, Nishimura, Carla J., Smith, Richard J.H., Van Camp, Guy

“…Hearing impairment (HI) affects 1 in 650 newborns, which makes it the most common congenital sensory impairment. Despite extraordinary genetic heterogeneity,…”
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Ethacrynic Acid Effect on the Composition of Cochlear Fluids by Cohn, Edward S., Gordes, Ellen H., Brusilow, Saul W.

“…Ethacrynic acid, when administered to six dogs, caused a fall in the concentration of potassium in endolymph from 145 to 21 milliequivalents per liter and a…”
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Transsphenoidal approach to the sella: the Johns Hopkins experience by Kennedy, D W, Cohn, E S, Papel, I D, Holliday, M J

“…The transsphenoidal hypophysectomy has become a relatively frequent procedure in recent years, with the otolaryngologist playing a major role in its renewed…”
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Audiological and vestibular features in affected subjects with USH3: A genotype/phenotype correlation: Aspectos audiológicos y vestibulares en sujetos afectados con USH3: una correlación de genotipo/fenotipo by Sadeghi, Mehdi, Cohn, Edward S., Kimberling, William J., Tranebjærg, Lisbeth, Möller, Claes

“…The aims were to compare the genotype/phenotype relationship between USH3 mutations and the consequent hearing and vestibular phenotype; and to compare hearing…”
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Hallazgos audiologicos en el sindrome de Usher tipo IIa y II (no IIa). Audiological findings in Usher syndrome types IIa and II (non-IIa) by Cohn, Edward S, Kelly, William J, Kimberling, William J, Moller, Claes, Sadeghi, Mehdi, Tranebjaerg, Lisbeth

“…The aim was to define the natural history of hearing loss in Usher syndrome type IIa compared to non-IIa. People with Usher syndrome type II show…”
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Ethacrynic acid by Cohn, E S

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Hearing loss with aging: presbycusis by Cohn, E S

“…Older adults with presbycusis have varied presentations. Early identification requires sensitivity to communication problems described by patients and their…”
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Ca 2+-dependence and nifedipine-sensitivity of vascular tone and contractility in the isolated superfused spiral modiolar artery in vitro by Wangemann, Philine, Cohn, Edward S, Gruber, Daniel D, Gratton, Michael Anne

“…The regulation of the vascular diameter of the spiral modiolar artery may play a major role in the regulation of cochlear blood flow and tissue oxygenation…”
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Ca2+-dependence and nifedipine-sensitivity of vascular tone and contractility in the isolated superfused spiral modiolar artery in vitro by WANGEMANN, P, COHN, E. S, GRUBER, D. D, GRATTON, M. A

“…The regulation of the vascular diameter of the spiral modiolar artery may play a major role in the regulation of cochlear blood flow and tissue oxygenation…”
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Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss by Cohn, Edward S., Kelley, Philip M.

“…Mutations in the gene for connexin 26, GJB2, are the most common cause of hearing loss in American and European populations, with a carrier rate of about 3%—a…”
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Tone burst auditory brain stem response latency estimates of cochlear travel time in Meniere's disease, cochlear hearing loss, and normal ears by MURRAY, J. G, COHN, E. S, HARKER, L. A, GORGA, M. P

“…The current study sought to determine whether tone burst auditory brain stem response (ABR) latencies could be used to detect an increase in the cochlear…”
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