Clinical Trials on Rare Diseases in Austria 2011-2021
Ursula Unterberger, Julie Bruyere-Zrelli, Trevor Lucas, Till Voigtländer et autres
0 citationsZenodo (CERN European Organization for Nuclear Research)
Trevor Lucas
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
101Publications signalées
3167Citations signalées
1Affiliations récentes
Institutions déclarées
Domaines associés
Hearing, Cochlea, Tinnitus, GeneticsConnexins and lens biologyCell death mechanisms and regulationRNA Interference and Gene DeliveryDental materials and restorations
Publications récentes
Clinical Trials on Rare Diseases in Austria 2011-2021
Ursula Unterberger, Julie Bruyere-Zrelli, Trevor Lucas, Till Voigtländer et autres
0 citationsZenodo (CERN European Organization for Nuclear Research)
Adenocarcinoma de Cólon em Paciente de 19 Anos: Diagnóstico de Síndrome de Lynch com Mutação no Gene PMS2
D. Neves, Renato de Souza Melo, Trevor Lucas, L. V.P. Dias et autres
0 citationsJournal of Coloproctology
PRKCA Overexpression Is Frequent in Young Oral Tongue Squamous Cell Carcinoma Patients and Is Associated with Poor Prognosis
Thomas Parzefall, Julia Schnoell, Laura Monschein, Elisabeth Foki et autres
19 citationsCancers
Incomplete penetrance of a novel SDHD variation causing familial head and neck paraganglioma
Martin Koenighofer, Thomas Parzefall, Alexandra Frohne, Elisabeth Frei et autres
4 citationsClinical Otolaryngology
High Prevalence of MYO6 Variants in an Austrian Patient Cohort With Autosomal Dominant Hereditary Hearing Loss
Alexandra Frohne, Martin Koenighofer, David T. Liu, Franco Laccone et autres
4 citationsOtology & Neurotology
A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Martin Koenighofer, Thomas Parzefall, Alexandra Frohne, Elisabeth Frei et autres
4 citationsExperimental Eye Research
A Novel Variant in the TBC1D24 Lipid-Binding Pocket Causes Autosomal Dominant Hearing Loss: Evidence for a Genotype-Phenotype Correlation
Thomas Parzefall, Alexandra Frohne, Martin Koenighofer, Juergen Neesen et autres
15 citationsFrontiers in Cellular Neuroscience
PRKCA overexpression is frequent in young oral tongue squamous cell carcinoma patients and is associated with poor prognosis
Thomas Parzefall, Julia Schnoell, Laura Monschein, Elisabeth Foki et autres
1 citationmedRxiv
Overexpression of LAPTM4B-35 is a negative prognostic factor in head and neck squamous cell carcinoma
Ulana Kotowski, Lorenz Kadletz, Sven Schneider, Felicitas Oberndorfer et autres
7 citationsScientific Reports
Plasma VEGF - a candidate biomarker for response to treatment with bevacizumab in HHT patients
David T. Liu, Alexandra Frohne, Martin Koenighofer, Karl Frei et autres
7 citationsRhinology Journal
Spectrum of Novel Hereditary Hemorrhagic Telangiectasia Variants in an Austrian Patient Cohort
Martin Koenighofer, Thomas Parzefall, Alexandra Frohne, Matthew J. Allen et autres
5 citationsClinical and Experimental Otorhinolaryngology
BNTIC News n’est pas le producteur de ces données. Recherche à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, ROR et la Banque mondiale, sans clé ; OpenAlex reste optionnel. Aucun service payant requis, aucune donnée externe enregistrée en base. Sources et limites.