Rebecca Schüle

Scarring Alopecia

S. Girirajan, I. Zusman, H. Meinck, 2020 .

Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia

J. Winkler, S. Klebe, P. Bauer, 2009, Journal of Neurology, Neurosurgery & Psychiatry.

Neurophysiological Markers of Novelty Processing Are Modulated by Comt and Drd4 Genotypes

T. Münte, U. Krämer, T. Cunillera, 2022 .

Amplicon‐based high‐throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients

Ludger Schöls, P. Bauer, R. Schüle, 2011, Clinical genetics.

SPG10 is a rare cause of spastic paraplegia in European families

R. Schüle, L. Schöls, J. Kassubek, 2008, Journal of Neurology, Neurosurgery, and Psychiatry.

PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

S. Züchner, Michael A. Gonzalez, E. Battaloğlu, 2017, Clinical genetics.

Consensus Recommendations for Clinical Outcome Assessments and Registry Development in Ataxias: Ataxia Global Initiative (AGI) Working Group Expert Guidance

M. Synofzik, A. Thieme, S. T. du Montcel, 2023, Cerebellum.

Unraveling Axonal Transcriptional Landscapes: Insights from iPSC-Derived Cortical Neurons and Implications for Motor Neuron Degeneration

J. Admard, S. Hauser, Maike Nagel, 2024, bioRxiv.