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Reinhard Ramsebner

Showing results (1-10 of 17) with videos related to

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Wiener Klinische Wochenschrift|November 21, 2014
Delayed auditory pathway maturation and prematurityMartin Koenighofer, Thomas Parzefall, Reinhard Ramsebner, et al.
The American Journal of Tropical Medicine and Hygiene|February 1, 2017
Progressive Perforation of the Nasal Septum Due to <i>Leishmania major</i>: A Case of Mucosal Leishmaniasis in a TravelerNicole Harrison, Julia Walochnik, 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|July 11, 2012
Endolymphatic sac tumor and angiomatous lesions of the nasal and pharyngeal mucosa as a first manifestation of von Hippel-Lindau diseaseClemens Honeder, Wolfgang Gstoettner, Christian Matula, et al.
Hearing Research|October 7, 2004
Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern AustriaKlemens Frei, Reinhard Ramsebner, Trevor Lucas, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 24, 2007
Relevance of the A1555G mutation in the 12S rRNA gene for hearing impairment in AustriaReinhard Ramsebner, Trevor Lucas, Christian Schoefer, et al.
Audiology & Neuro-Otology|May 8, 2014
A novel missense NDP mutation [p.(Cys93Arg)] with a manifesting carrier in an austrian family with Norrie diseaseThomas Parzefall, Trevor Lucas, Markus Ritter, et al.
Hearing Research|July 28, 2004
Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in AustriaKlemens Frei, Reinhard Ramsebner, Gertrude Hamader, et al.
European Journal of Human Genetics : EJHG|September 28, 2006
Vasoactive intestinal peptide gene alterations in patients with idiopathic pulmonary arterial hypertensionInes Haberl, Klemens Frei, Reinhard Ramsebner, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 21, 2007
Relevance of the A1555G Mutation in the 12S rRNA Gene for Hearing Impairment in AustriaReinhard Ramsebner, Trevor Lucas, Christian Schoefer, et al.
Pageof 2

Showing results (1-10 of 17) 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.
The American Journal of Tropical Medicine and Hygiene|February 1, 2017
Progressive Perforation of the Nasal Septum Due to <i>Leishmania major</i>: A Case of Mucosal Leishmaniasis in a TravelerNicole Harrison, Julia Walochnik, 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|July 11, 2012
Endolymphatic sac tumor and angiomatous lesions of the nasal and pharyngeal mucosa as a first manifestation of von Hippel-Lindau diseaseClemens Honeder, Wolfgang Gstoettner, Christian Matula, et al.
Hearing Research|October 7, 2004
Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern AustriaKlemens Frei, Reinhard Ramsebner, Trevor Lucas, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 24, 2007
Relevance of the A1555G mutation in the 12S rRNA gene for hearing impairment in AustriaReinhard Ramsebner, Trevor Lucas, Christian Schoefer, et al.
Audiology & Neuro-Otology|May 8, 2014
A novel missense NDP mutation [p.(Cys93Arg)] with a manifesting carrier in an austrian family with Norrie diseaseThomas Parzefall, Trevor Lucas, Markus Ritter, et al.
Hearing Research|July 28, 2004
Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in AustriaKlemens Frei, Reinhard Ramsebner, Gertrude Hamader, et al.
European Journal of Human Genetics : EJHG|September 28, 2006
Vasoactive intestinal peptide gene alterations in patients with idiopathic pulmonary arterial hypertensionInes Haberl, Klemens Frei, Reinhard Ramsebner, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 21, 2007
Relevance of the A1555G Mutation in the 12S rRNA Gene for Hearing Impairment in AustriaReinhard Ramsebner, Trevor Lucas, Christian Schoefer, et al.
Pageof 2