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The Laryngoscope
|
October 29, 2004
Safe and reliable sound threshold measures with direct vibration of the ossicular chain
Marcus M Maassen, Jesus Rodriguez Jorge, Stephan Herberhold, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
January 12, 2011
Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing loss
Mostafa R Mohamed, Ioana Alesutan, Michael Föller, et al.
Hearing Research
|
March 22, 2006
Influence of gain of function epithelial chloride channel ClC-Kb mutation on hearing thresholds
Andreas Frey, Angelika Lampert, Siegfried Waldegger, et al.
Neurobiology of Disease
|
July 19, 2005
Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells
Lut Van Laer, Markus Pfister, Sofie Thys, et al.
Neurobiology of Disease
|
August 1, 2006
Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome
Karen Vrijens, Sofie Thys, Marcel T De Jeu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 26, 2004
Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing loss
Lukas Rüttiger, Matthias Sausbier, Ulrike Zimmermann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 27, 2009
Deafness in TRbeta mutants is caused by malformation of the tectorial membrane
Harald Winter, Lukas Rüttiger, Marcus Müller, et al.
Clinical Genetics
|
April 13, 2020
Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss
Birgit S Budde, Maha Abdelgaber Aly, Mostafa R Mohamed, et al.
American Journal of Human Genetics
|
March 12, 2004
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4)
Francesca Donaudy, Rik Snoeckx, Markus Pfister, et al.
Human Genetics
|
June 20, 2002
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations
Kim Cryns, Markus Pfister, Ronald J E Pennings, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 57) with videos related to
Sort By:
Page
of 6
The Laryngoscope
|
October 29, 2004
Safe and reliable sound threshold measures with direct vibration of the ossicular chain
Marcus M Maassen, Jesus Rodriguez Jorge, Stephan Herberhold, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
January 12, 2011
Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing loss
Mostafa R Mohamed, Ioana Alesutan, Michael Föller, et al.
Hearing Research
|
March 22, 2006
Influence of gain of function epithelial chloride channel ClC-Kb mutation on hearing thresholds
Andreas Frey, Angelika Lampert, Siegfried Waldegger, et al.
Neurobiology of Disease
|
July 19, 2005
Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells
Lut Van Laer, Markus Pfister, Sofie Thys, et al.
Neurobiology of Disease
|
August 1, 2006
Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome
Karen Vrijens, Sofie Thys, Marcel T De Jeu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 26, 2004
Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing loss
Lukas Rüttiger, Matthias Sausbier, Ulrike Zimmermann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 27, 2009
Deafness in TRbeta mutants is caused by malformation of the tectorial membrane
Harald Winter, Lukas Rüttiger, Marcus Müller, et al.
Clinical Genetics
|
April 13, 2020
Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss
Birgit S Budde, Maha Abdelgaber Aly, Mostafa R Mohamed, et al.
American Journal of Human Genetics
|
March 12, 2004
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4)
Francesca Donaudy, Rik Snoeckx, Markus Pfister, et al.
Human Genetics
|
June 20, 2002
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations
Kim Cryns, Markus Pfister, Ronald J E Pennings, et al.
Page
of 6