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Markus Pfister

Showing results (1-10 of 57) with videos related to

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International Journal of Molecular Medicine|June 7, 2011
The otoferlin interactome in neurosensory hair cells: significance for synaptic vesicle release and trans-Golgi network (Review)Magdalena Zak, Markus Pfister, Nikolaus Blin
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 30, 2006
Tinnitus sensitization: Sensory and psychophysiological aspects of a new pathway of acquired centralization of chronic tinnitusHans P Zenner, Markus Pfister, Niels Birbaumer
Neurosurgical Focus|August 27, 2004
Anatomy involved in the jugular foramen approach for jugulotympanic paraganglioma resectionMichelle M Inserra, Markus Pfister, Robert K Jackler
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 20, 2011
Temporal expression pattern of Fkbp8 in rodent cochleaMagdalena Zak, Andreas Bress, Markus Pfister, et al.
International Journal of Molecular Medicine|December 7, 2002
Uncommon cytidine-homopolymer dimorphism in 5'-UTR of the human otoferlin geneFarhad Mirghomizadeh, Markus Pfister, Nikolaus Blin, et al.
International Journal of Pediatric Otorhinolaryngology|July 27, 2005
Phenotypic characterization of a DFNA6 family showing progressive low-frequency sensorineural hearing impairmentTímea Tóth, Markus Pfister, Hans-Peter Zenner, et al.
Orvosi Hetilap|November 8, 2002
[Frequency of the Connexin26/35delG mutation and its characteristic phenotype in patients with hearing impairment and controls in Northeastern Hungary]Tímea Tóth, Susan Kupka, Nicolaus Blin, et al.
International Journal of Molecular Medicine|June 6, 2007
A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndromeSibylle Brosch, Manuela Baur, Nikolaus Blin, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|January 27, 2007
The aborted early history of the translabyrinthine approach: a victim of suppression or technical prematurity?Anh T Nguyen-Huynh, Robert K Jackler, Markus Pfister, et al.
Acta Oto-Laryngologica|October 16, 2008
Impact of genotype and mutation type on health-related quality of life in patients with hereditary hemorrhagic telangiectasiaMarkus Pfister, Ilse M Zalaman, Gunnar Blumenstock, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
International Journal of Molecular Medicine|June 7, 2011
The otoferlin interactome in neurosensory hair cells: significance for synaptic vesicle release and trans-Golgi network (Review)Magdalena Zak, Markus Pfister, Nikolaus Blin
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 30, 2006
Tinnitus sensitization: Sensory and psychophysiological aspects of a new pathway of acquired centralization of chronic tinnitusHans P Zenner, Markus Pfister, Niels Birbaumer
Neurosurgical Focus|August 27, 2004
Anatomy involved in the jugular foramen approach for jugulotympanic paraganglioma resectionMichelle M Inserra, Markus Pfister, Robert K Jackler
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 20, 2011
Temporal expression pattern of Fkbp8 in rodent cochleaMagdalena Zak, Andreas Bress, Markus Pfister, et al.
International Journal of Molecular Medicine|December 7, 2002
Uncommon cytidine-homopolymer dimorphism in 5'-UTR of the human otoferlin geneFarhad Mirghomizadeh, Markus Pfister, Nikolaus Blin, et al.
International Journal of Pediatric Otorhinolaryngology|July 27, 2005
Phenotypic characterization of a DFNA6 family showing progressive low-frequency sensorineural hearing impairmentTímea Tóth, Markus Pfister, Hans-Peter Zenner, et al.
Orvosi Hetilap|November 8, 2002
[Frequency of the Connexin26/35delG mutation and its characteristic phenotype in patients with hearing impairment and controls in Northeastern Hungary]Tímea Tóth, Susan Kupka, Nicolaus Blin, et al.
International Journal of Molecular Medicine|June 6, 2007
A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndromeSibylle Brosch, Manuela Baur, Nikolaus Blin, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|January 27, 2007
The aborted early history of the translabyrinthine approach: a victim of suppression or technical prematurity?Anh T Nguyen-Huynh, Robert K Jackler, Markus Pfister, et al.
Acta Oto-Laryngologica|October 16, 2008
Impact of genotype and mutation type on health-related quality of life in patients with hereditary hemorrhagic telangiectasiaMarkus Pfister, Ilse M Zalaman, Gunnar Blumenstock, et al.
Pageof 6