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Thomas Parzefall

7PUBLICATIONS
31CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsDisease surveillanceGene mappingPredictive and prognostic markers
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Publications (7)

Sort by Publication Date:
|Feb 24, 2024
Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria.

Alexandra Frohne, Sybille Vrabel, Franco Laccone

|Nov 29, 2022
A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestation.

Alexandra Frohne, Martin Koenighofer, Hakan Cetin

|Jun 29, 2021
Biannual Differences in Interest Peaks for Web Inquiries Into Ear Pain and Ear Drops: Infodemiology Study.

Faris F Brkic, Gerold Besser, Martin Schally

|Apr 14, 2021
Incomplete penetrance of a novel SDHD variation causing familial head and neck paraganglioma.

Martin Koenighofer, Thomas Parzefall, Alexandra Frohne

|Oct 30, 2019
Lymph node ratio as a prognostic marker in advanced laryngeal and hypopharyngeal carcinoma after primary total laryngopharyngectomy.

Stefan Grasl, Stefan Janik, Thomas Parzefall

|May 03, 2019
Post-laryngectomy adjuvant radiotherapy in patients with pharyngocutaneous fistulae: Treatment regimens, outcomes and complications in 67 patients.

Thomas Parzefall, Axel Wolf, Stefan Grasl

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Frequent Collaborators

3 joint publications

Alexandra Frohne

3 joint publications

Christian Schoefer

3 joint publications

Franco Laccone

3 joint publications

Klemens Frei

2 joint publications

Juergen Neesen

2 joint publications

Stefan Janik

2 joint publications

Stefan Grasl

2 joint publications

Martin Koenighofer

2 joint publications

David T Liu

1 joint publications

Silvia Dossena

Frequent Collaborators

3 joint publications

Alexandra Frohne

3 joint publications

Christian Schoefer

3 joint publications

Franco Laccone

3 joint publications

Klemens Frei

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