Delia Kurzwelly

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients

Rebecca Schüle, Sarah Wiethoff, Peter Martus et al. · Annals of Neurology · 2016 · 298 citations

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia

Martina Minnerop, Delia Kurzwelly, Holger Wagner et al. · Brain · 2017 · 118 citations · Full text

Safety and efficacy of rasagiline as an add-on therapy to riluzole in patients with amyotrophic lateral sclerosis: a randomised, double-blind, parallel-group, placebo-controlled, phase 2 trial

Albert C. Ludolph, Joachim Schuster, Johannes Dorst et al. · The Lancet Neurology · 2018 · 78 citations · Full text

Amyotrophic Lateral Sclerosis, Neurological Disorder, Medicine +5

Primary CNS lymphoma in the elderly: temozolomide therapy and MGMT status

Delia Kurzwelly, Martin Glas, Patrick Roth et al. · Journal of Neuro-Oncology · 2009 · 77 citations

Neuro-oncology, Mgmt Status, Lymphoid Neoplasia +5

Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with <i>SPG7</i>

Giulia Coarelli, Rebecca Schüle, Bart P.C. van de Warrenburg et al. · Neurology · 2019 · 59 citations · Full text