Melanie Kellner
Tuebingen, BW, Germany
Last Updated: 09/26/2026
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Found 8 publications
Natural History of Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP): A Retrospective Patient Cohort Study.
Journal: Neurology and therapy
Published: November 13, 2025
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.
Journal: Nature communications
Published: March 31, 2025
Mobile digital gait analysis captures effects of botulinum toxin in hereditary spastic paraplegia.
Journal: European journal of neurology
Published: December 28, 2023
Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.
Journal: Nature medicine
Published: May 01, 2023
Early-Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 11, 2022
The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15.
Journal: Brain : a journal of neurology
Published: June 23, 2022
Showing 1-8 of 8
Last Updated: 09/26/2026