Alexandra Frohne
6PUBLICATIONS
79CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (6)
Sort by Publication Date:
|Nov 22, 2024
LTβR deficiency causes lymph node aplasia and impaired B cell differentiation.Bernhard Ransmayr, Sevgi Köstel Bal, Marini Thian
|Apr 27, 2024
Very-early-onset Inflammatory Bowel Disease in an Infant with a Partial RIPK1 Deletion.Ceyda Tuna Kırsaçlıoğlu, Alexandra Frohne, Zarife Kuloğlu
|Feb 24, 2024
Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria.Alexandra Frohne, Sybille Vrabel, Franco Laccone
|May 30, 2023
Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis.Sevgi Kostel Bal, Sarah Giuliani, Jana Block
|Nov 29, 2022
A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestation.Alexandra Frohne, Martin Koenighofer, Hakan Cetin
|Apr 14, 2021
Incomplete penetrance of a novel SDHD variation causing familial head and neck paraganglioma.Martin Koenighofer, Thomas Parzefall, Alexandra Frohne
Pageof 1
Frequent Collaborators
3 joint publications
Thomas Parzefall
3 joint publications
Kaan Boztug
3 joint publications
Christian Schoefer
3 joint publications
Franco Laccone
3 joint publications
Klemens Frei
2 joint publications
Martin Koenighofer
2 joint publications
Jana Block
2 joint publications
Cheryl van de Wetering
2 joint publications
Sevgi Kostel Bal
2 joint publications
Juergen Neesen
