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Martin Koenighofer

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Wiener Klinische Wochenschrift|November 21, 2014
Delayed auditory pathway maturation and prematurityMartin Koenighofer, Thomas Parzefall, Reinhard Ramsebner, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 3, 2014
The promoter mutation c.-259C>T (-3438C>T) is not a common cause of non-syndromic hearing impairment in AustriaMartin Koenighofer, Trevor Lucas, Thomas Parzefall, et al.
The Laryngoscope|June 4, 2020
Association Between Orthonasal Olfaction and Chemosensory Perception in Patients With Smell LossDavid T Liu, Gerold Besser, Bernhard Prem, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 19, 2016
A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing ImpairmentAxel Wolf, Alexandra Frohne, Matthew Allen, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 20, 2017
Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutationThomas Parzefall, Alexandra Frohne, Martin Koenighofer, et al.
Clinical and Experimental Otorhinolaryngology|June 22, 2019
Spectrum of Novel Hereditary Hemorrhagic Telangiectasia Variants in an Austrian Patient CohortMartin Koenighofer, Thomas Parzefall, Alexandra Frohne, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|April 14, 2021
Incomplete penetrance of a novel SDHD variation causing familial head and neck paragangliomaMartin Koenighofer, Thomas Parzefall, Alexandra Frohne, et al.
Wiener Klinische Wochenschrift|July 23, 2017
Identification of a rare COCH mutation by whole-exome sequencing : Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing lossThomas Parzefall, Alexandra Frohne, Martin Koenighofer, et al.
Multidisciplinary Respiratory Medicine|November 21, 2014
Carrageenan nasal spray in virus confirmed common cold: individual patient data analysis of two randomized controlled trialsMartin Koenighofer, Thomas Lion, Angelika Bodenteich, et al.
Acta Oto-Laryngologica|November 10, 2016
The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in AustriaThomas Parzefall, Trevor Lucas, Martin Koenighofer, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Wiener Klinische Wochenschrift|November 21, 2014
Delayed auditory pathway maturation and prematurityMartin Koenighofer, Thomas Parzefall, Reinhard Ramsebner, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 3, 2014
The promoter mutation c.-259C>T (-3438C>T) is not a common cause of non-syndromic hearing impairment in AustriaMartin Koenighofer, Trevor Lucas, Thomas Parzefall, et al.
The Laryngoscope|June 4, 2020
Association Between Orthonasal Olfaction and Chemosensory Perception in Patients With Smell LossDavid T Liu, Gerold Besser, Bernhard Prem, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 19, 2016
A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing ImpairmentAxel Wolf, Alexandra Frohne, Matthew Allen, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 20, 2017
Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutationThomas Parzefall, Alexandra Frohne, Martin Koenighofer, et al.
Clinical and Experimental Otorhinolaryngology|June 22, 2019
Spectrum of Novel Hereditary Hemorrhagic Telangiectasia Variants in an Austrian Patient CohortMartin Koenighofer, Thomas Parzefall, Alexandra Frohne, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|April 14, 2021
Incomplete penetrance of a novel SDHD variation causing familial head and neck paragangliomaMartin Koenighofer, Thomas Parzefall, Alexandra Frohne, et al.
Wiener Klinische Wochenschrift|July 23, 2017
Identification of a rare COCH mutation by whole-exome sequencing : Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing lossThomas Parzefall, Alexandra Frohne, Martin Koenighofer, et al.
Multidisciplinary Respiratory Medicine|November 21, 2014
Carrageenan nasal spray in virus confirmed common cold: individual patient data analysis of two randomized controlled trialsMartin Koenighofer, Thomas Lion, Angelika Bodenteich, et al.
Acta Oto-Laryngologica|November 10, 2016
The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in AustriaThomas Parzefall, Trevor Lucas, Martin Koenighofer, et al.
Pageof 2