Andreas Hahn

7PUBLICATIONS
56CO-AUTHORS
Cellular nervous systemGene and molecular therapyNeurology and neuromuscular diseasesPharmacogenomicsEpigenetics (incl. genome methylation and epigenomics)
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Publications (7)

|Sep 06, 2026
Epilepsy Is Part of the CNS Phenotype in Classic Infantile Pompe Disease.

|Feb 14, 2026
A roadmap for a patient-centred approach to Pompe disease management.

Benedikt Schoser, Cristina Domínguez-González, Pascal Laforet

|Jun 13, 2025
Disease-Modifying, Neuroprotective Effect of N-Acetyl-l-Leucine in Adult and Pediatric Patients With Niemann-Pick Disease Type C.

Marc C Patterson, Uma Ramaswami, Aimee Donald

|Jan 09, 2023
Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking.

Alexander H Swan, Roland F R Schindler, Marco Savarese

|May 17, 2021
Mutations in HID1 Cause Syndromic Infantile Encephalopathy and Hypopituitarism.

Anne Schänzer, Melanie T Achleitner, Dietrich Trümbach

|Apr 22, 2016
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation.

Karim Kouz, Christina Lissewski, Stephanie Spranger

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Frequent Collaborators

3 joint publications

Anne Schänzer

2 joint publications

Susanne Rinné

2 joint publications

Niels Decher

2 joint publications

Mario Sabatelli