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N Merchant

Showing results (241-250 of 252) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 28, 2008
Human temporal bone consortium for research resource enhancementSaumil N Merchant, Michael J McKenna, Joe C Adams, et al.
The Laryngoscope|August 5, 2003
Temporal bone histopathological and quantitative analysis of mitochondrial DNA in MELASKatsumasa Takahashi, Saumil N Merchant, Tetsuo Miyazawa, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 31, 2014
Power reflectance as a screening tool for the diagnosis of superior semicircular canal dehiscenceGabrielle R Merchant, Christof Röösli, Marlien E F Niesten, et al.
The Laryngoscope|August 4, 2006
Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndromeAndrew J Griffith, Yandan Yang, Shannon P Pryor, et al.
Journal of the American College of Surgeons|September 26, 2020
Technical Evidence Review for Emergency Major Abdominal Operation Conducted for the AHRQ Safety Program for Improving Surgical Care and RecoveryQ Lina Hu, Michael C Grant, Melissa A Hornor, et al.
Human Molecular Genetics|July 1, 1996
A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13E N Manolis, N Yandavi, J B Nadol, et al.
Early Human Development|November 21, 2009
A patient care system for early 3.0 Tesla magnetic resonance imaging of very low birth weight infantsN Merchant, A Groves, D J Larkman, et al.
Brain : a Journal of Neurology|February 1, 2013
Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degenerationMariam B Totonchy, Deborah Tamura, Matthew S Pantell, et al.
Nature Genetics|November 7, 1998
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunctionN G Robertson, L Lu, S Heller, et al.
Human Molecular Genetics|February 17, 2006
Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunctionNahid G Robertson, Cor W R J Cremers, Patrick L M Huygen, et al.
Pageof 26

Showing results (241-250 of 252) with videos related to

Sort By:
Pageof 26
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 28, 2008
Human temporal bone consortium for research resource enhancementSaumil N Merchant, Michael J McKenna, Joe C Adams, et al.
The Laryngoscope|August 5, 2003
Temporal bone histopathological and quantitative analysis of mitochondrial DNA in MELASKatsumasa Takahashi, Saumil N Merchant, Tetsuo Miyazawa, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 31, 2014
Power reflectance as a screening tool for the diagnosis of superior semicircular canal dehiscenceGabrielle R Merchant, Christof Röösli, Marlien E F Niesten, et al.
The Laryngoscope|August 4, 2006
Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndromeAndrew J Griffith, Yandan Yang, Shannon P Pryor, et al.
Journal of the American College of Surgeons|September 26, 2020
Technical Evidence Review for Emergency Major Abdominal Operation Conducted for the AHRQ Safety Program for Improving Surgical Care and RecoveryQ Lina Hu, Michael C Grant, Melissa A Hornor, et al.
Human Molecular Genetics|July 1, 1996
A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13E N Manolis, N Yandavi, J B Nadol, et al.
Early Human Development|November 21, 2009
A patient care system for early 3.0 Tesla magnetic resonance imaging of very low birth weight infantsN Merchant, A Groves, D J Larkman, et al.
Brain : a Journal of Neurology|February 1, 2013
Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degenerationMariam B Totonchy, Deborah Tamura, Matthew S Pantell, et al.
Nature Genetics|November 7, 1998
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunctionN G Robertson, L Lu, S Heller, et al.
Human Molecular Genetics|February 17, 2006
Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunctionNahid G Robertson, Cor W R J Cremers, Patrick L M Huygen, et al.
Pageof 26