Association Between Orthonasal Olfaction and Chemosensory Perception in Patients With Smell Loss

Autor Liu, David T., Besser, Gerold, Prem, Bernhard, Sharma, Gunjan, Koenighofer, Martin, Renner, Bertold, Mueller, Christian A.
Vydáno v Laryngoscope (2020)

Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation

Autor Parzefall, Thomas, Frohne, Alexandra, Koenighofer, Martin, Kirchnawy, Andreas, Streubel, Berthold, Schoefer, Christian, Frei, Klemens, Lucas, Trevor
Vydáno v Eur Arch Otorhinolaryngol (2017)

Carrageenan nasal spray in virus confirmed common cold: individual patient data analysis of two randomized controlled trials

Autor Koenighofer, Martin, Lion, Thomas, Bodenteich, Angelika, Prieschl-Grassauer, Eva, Grassauer, Andreas, Unger, Hermann, Mueller, Christian A, Fazekas, Tamás
Vydáno v Multidiscip Respir Med (2014)

Identification of a rare COCH mutation by whole-exome sequencing: Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal domina...

Autor Parzefall, Thomas, Frohne, Alexandra, Koenighofer, Martin, Kirchnawy, Andreas, Streubel, Berthold, Schoefer, Christian, Gstoettner, Wolfgang, Frei, Klemens, Lucas, Trevor
Vydáno v Wien Klin Wochenschr (2017)

Spectrum of Novel Hereditary Hemorrhagic Telangiectasia Variants in an Austrian Patient Cohort

Autor Koenighofer, Martin, Parzefall, Thomas, Frohne, Alexandra, Allen, Matthew, Unterberger, Ursula, Laccone, Franco, Schoefer, Christian, Frei, Klemens, Lucas, Trevor
Vydáno v Clin Exp Otorhinolaryngol (2019)

Body-Mass-Index Associated Differences in Ortho- and Retronasal Olfactory Function and the Individual Significance of Olfaction in Health and Disease

Autor Besser, Gerold, Erlacher, Brigitte, Aydinkoc-Tuzcu, Kadriye, Liu, David T., Pablik, Eleonore, Niebauer, Verena, Koenighofer, Martin, Renner, Bertold, Mueller, Christian A.
Vydáno v J Clin Med (2020)

A Novel Variant in the TBC1D24 Lipid-Binding Pocket Causes Autosomal Dominant Hearing Loss: Evidence for a Genotype-Phenotype Correlation

Autor Parzefall, Thomas, Frohne, Alexandra, Koenighofer, Martin, Neesen, Juergen, Laccone, Franco, Eckl-Dorna, Julia, Waters, Jonathan J., Schreiner, Markus, Amr, Sami Samir, Ashton, Emma, Schoefer, Christian, Gstœttner, Wolfgang, Frei, Klemens, Lucas, Trevor
Vydáno v Front Cell Neurosci (2020)

Mutations in RIT1 cause Noonan syndrome – additional functional evidence and expanding the clinical phenotype

Autor Koenighofer, Martin, Hung, Christina Y., McCauley, Jacob L., Dallman, Julia, Back, Emma J., Mihalek, Ivana, Gripp, Karen W., Sol-Church, Katia, Rusconi, Paolo, Zhang, Zhaiyi, Shi, Geng-Xian, Andres, Douglas A., Bodamer, Olaf A.
Vydáno v Clin Genet (2015)