Katalin Komlosi
9PUBLICATIONS
15CO-AUTHORS
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Publications (9)
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|Mar 27, 2026
Defining Histological Patterns in Inherited Ichthyoses: Toward a Diagnostic Algorithm Based on 66 Confirmed Cases.Kira Süßmuth, Vinzenz Oji, Jacqueline Bodes
|Mar 28, 2024
Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations.Alrun Hotz, Regina Fölster-Holst, Vinzenz Oji
|Mar 29, 2023
Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis.Alrun Hotz, Julia Kopp, Emmanuelle Bourrat
|Nov 04, 2022
Acral lamellar ichthyosis with amino acid substitution in the C-terminus of keratin 2.Leonie Frommherz, Katalin Komlosi, Charlotte Hewel
|Nov 27, 2021
Marfan Syndrome Caused by Disruption of the FBN1 Gene due to A Reciprocal Chromosome Translocation.Anna Clara Schnause, Katalin Komlosi, Barbara Herr
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Frequent Collaborators
6 joint publications
Judith Fischer
4 joint publications
Alrun Hotz
3 joint publications
Andreas Zimmer
3 joint publications
Svenja Alter
1 joint publications
Andreas Tzschach
1 joint publications
Sabine Jägle
1 joint publications
Birgitta Gläser
1 joint publications
Leonie Frommherz
1 joint publications
Cristina Has
1 joint publications
Regina C Betz
