Saskia Elgün

Phenotypic variation between siblings with Metachromatic Leukodystrophy

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2019, Orphanet Journal of Rare Diseases.

Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? - Chances and challenges.

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2022, Molecular genetics and metabolism.

Association of Age at Onset and First Symptoms With Disease Progression in Patients With Metachromatic Leukodystrophy

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2020, Neurology.

Recognizing early MRI signs (or their absence) is crucial in diagnosing metachromatic leukodystrophy

S. Groeschel, I. Krägeloh-Mann, M. S. van der Knaap, 2022, Annals of clinical and translational neurology.