Thomas Parzefall
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Explore the profile of Thomas Parzefall including associated specialties, affiliations and a list of published articles.
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Articles
36
Citations
267
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Recent Articles
1.
Usami S, Nishio S, Gavilan J, Acharya A, Hagr A, Lassaletta L, et al.
Acta Otolaryngol
. 2024 Oct;
144(11-12):602-609.
PMID: 39451138
Background: In cases of congenital sensorineural hearing loss, testing for genetic etiologies and congenital cytomegalovirus (cCMV) infection have become common practice. Aims/objectives: The purpose of this study is to determine...
2.
Frohne A, Vrabel S, Laccone F, Neesen J, Roesch S, Dossena S, et al.
Eur Arch Otorhinolaryngol
. 2024 Feb;
281(7):3577-3586.
PMID: 38400873
Purpose: Hearing loss (HL) is often monogenic. The clinical importance of genetic testing in HL may further increase when gene therapy products become available. Diagnoses are, however, complicated by a...
3.
Haas M, Lucic M, Pichler F, Brkic F, Parzefall T, Riss D, et al.
Otolaryngol Head Neck Surg
. 2023 Nov;
170(3):795-803.
PMID: 37943865
Objective: Extreme weather events are becoming more prevalent with the increasing pace of climate change. These events negatively impact human health and put considerable strain on health care resources, including...
4.
Nieratschker M, Haas M, Lucic M, Pichler F, Brkic F, Parzefall T, et al.
Front Public Health
. 2023 Jun;
11:1153111.
PMID: 37325328
Background: Climate change has been associated with a higher frequency of extreme weather events, resulting in an overall increase in morbidity and mortality. Acute otitis media (AOM) is one of...
5.
Frohne A, Koenighofer M, Cetin H, Nieratschker M, Liu D, Laccone F, et al.
Hum Genet
. 2022 Nov;
142(8):1077-1089.
PMID: 36445457
Loss-of-function variants in AP3D1 have been linked to Hermansky-Pudlak syndrome (HPS) 10, a severe multisystem disorder characterized by oculocutaneous albinism, immunodeficiency, neurodevelopmental delay, hearing loss (HL), and neurological abnormalities, fatal...
6.
Brkic F, Besser G, Schally M, Schmid E, Parzefall T, Riss D, et al.
J Med Internet Res
. 2021 Jun;
23(6):e28328.
PMID: 34185016
Background: The data retrieved with the online search engine, Google Trends, can summarize internet inquiries into specified search terms. This engine may be used for analyzing inquiry peaks for different...
7.
Parzefall T, Schnoell J, Monschein L, Foki E, Liu D, Frohne A, et al.
Cancers (Basel)
. 2021 Apr;
13(9).
PMID: 33923093
Oral tongue squamous cell carcinomas (OTSCCs) have an increasing incidence in young patients, and many have an aggressive course of disease. The objective of this study was to identify candidate...
8.
Koenighofer M, Parzefall T, Frohne A, Frei E, Schoefer C, Laccone F, et al.
Clin Otolaryngol
. 2021 Apr;
46(5):1044-1049.
PMID: 33851515
Objective: Identification of variations in tumour suppressor genes encoding the tetrameric succinate dehydrogenase (SDHx) mitochondrial enzyme complex may lead to personalised therapeutic concepts for the orphan disease, familial paraganglioma (PGL)...
9.
Frohne A, Koenighofer M, Liu D, Laccone F, Neesen J, Gstoettner W, et al.
Otol Neurotol
. 2021 Mar;
42(6):e648-e657.
PMID: 33710140
Introduction: Genetic hearing loss (HL) is often monogenic. Whereas more than half of autosomal recessive (AR) cases in Austria are caused by mutations in a single gene, no disproportionately frequent...
10.
Koenighofer M, Parzefall T, Frohne A, Frei E, Waldstein S, Mitulovic G, et al.
Exp Eye Res
. 2021 Feb;
205:108497.
PMID: 33596443
Nanophthalmos-4 is a rare autosomal dominant disorder caused by two known variations in TMEM98. An Austrian Caucasian pedigree was identified suffering from nanophthalmos and late onset angle-closure glaucoma and premature...