1. A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment. Issue 2 (February 2017) Authors: Wolf, Axel; Frohne, Alexandra; Allen, Matthew; Parzefall, Thomas; Koenighofer, Martin; Schreiner, Markus M.; Schoefer, Christian; Frei, Klemens; Lucas, Trevor Journal: Otology & neurotology Issue: Volume 38:Issue 2(2017) Page Start: 173 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment. Issue 2 (February 2017) Authors: Wolf, Axel; Frohne, Alexandra; Allen, Matthew; Parzefall, Thomas; Koenighofer, Martin; Schreiner, Markus M.; Schoefer, Christian; Frei, Klemens; Lucas, Trevor Journal: Otology & neurotology Issue: Volume 38:Issue 2(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity. (April 2021) Authors: Koenighofer, Martin; Parzefall, Thomas; Frohne, Alexandra; Frei, Elisabeth; Waldstein, Sebastian M.; Mitulovic, Goran; Schoefer, Christian; Frei, Klemens; Lucas, Trevor Journal: Experimental eye research Issue: Volume 205(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Effect of postoperative use of diclofenac on pharyngocutaneous fistula development after primary total laryngopharyngectomy: Results of a single‐center retrospective study. (15th December 2015) Authors: Parzefall, Thomas; Wolf, Axel; Czeiger, Shelly; Frei, Klemens; Formanek, Michael; Erovic, Boban M. Journal: Head & neck Issue: Volume 38(2016)Supplement 1 Page Start: E1515 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Epistaxis grading in Osler's disease: comparison of comprehensive scores with detailed bleeding diaries. Issue 3 (2nd November 2016) Authors: Parzefall, Thomas; Wolf, Axel; Frei, Klemens; Kaider, Alexandra; Riss, Dominik Journal: International forum of allergy & rhinology Issue: Volume 7:Issue 3(2017:Mar.) Page Start: 293 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. High Prevalence of MYO6 Variants in an Austrian Patient Cohort With Autosomal Dominant Hereditary Hearing Loss. Issue 6 (July 2021) Authors: Frohne, Alexandra; Koenighofer, Martin; Liu, David Tianxiang; Laccone, Franco; Neesen, Juergen; Gstoettner, Wolfgang; Schoefer, Christian; Lucas, Trevor; Frei, Klemens; Parzefall, Thomas Journal: Otology & neurotology Issue: Volume 42:Issue 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Incomplete penetrance of a novel SDHD variation causing familial head and neck paraganglioma. (5th May 2021) Authors: Koenighofer, Martin; Parzefall, Thomas; Frohne, Alexandra; Frei, Elisabeth; Schoefer, Christian; Laccone, Franco; Feil, Patricia; Frei, Klemens; Lucas, Trevor Journal: Clinical otolaryngology Issue: Volume 46:Number 5(2021) Page Start: 1044 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in Austria. (3rd April 2017) Authors: Parzefall, Thomas; Lucas, Trevor; Koenighofer, Martin; Ramsebner, Reinhard; Frohne, Alexandra; Czeiger, Shelly; Baumgartner, Wolf-Dieter; Schoefer, Christian; Gstoettner, Wolfgang; Frei, Klemens Journal: Acta oto-laryngologica Issue: Volume 137:Number 4(2017) Page Start: 356 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗