Elisabetta Indelicato

36PUBLICATIONS
78CO-AUTHORS
Developmental genetics (incl. sex determination)Computational linguisticsNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Peripheral nervous system
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Publications (36)

|Jun 03, 2026
Atypical Atypical MECP2-Related Rett Syndrome Presenting with Movement Disorders- Predominating Phenotype.

|May 22, 2026
A Patient-Reported Outcome Measure of Communication Difficulties in Friedreich Ataxia: COMATAX.

|Mar 03, 2026
Genotype and Age at Onset Drive Vermis Atrophy in CACNA1A- and GAA-FGF14-related Ataxias.

Elisabetta Indelicato, Wolfgang Nachbauer, Matthias Amprosi

|Feb 02, 2026
Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia Cohort.

Alice Saparov, Ivana Dzinovic, Theresa Brunet

|Jan 26, 2026
Natural history in hereditary spastic paraplegias: real-world data from an Austrian cohort.

Matthias Amprosi, Elisabetta Indelicato, Andreas Eigentler

|Jan 16, 2026
Efficacy of Deep Brain Stimulation for the Treatment of Monogenic Dystonia Symptoms: A Systematic Review.

Elisabetta Indelicato, Beatriz Carmona-Hidalgo, Javier Quintero

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Frequent Collaborators

9 joint publications

Michael Zech

9 joint publications

Sylvia M Boesch

4 joint publications

Matthis Synofzik

3 joint publications

Henry Houlden