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Parkinsonism & Related Disorders|January 20, 2023
Management of rare movement diseases in different world regionsCelia Painous, Maria J Martí, Holm Graessner, et al.
Neurology|April 7, 2017
Clinical manifestations of the anti-IgLON5 diseaseCarles Gaig, Francesc Graus, Yarko Compta, et al.
Human Molecular Genetics|July 19, 2015
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremorHyun Hor, Ludmila Francescatto, Luca Bartesaghi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 17, 2020
Fosmetpantotenate Randomized Controlled Trial in Pantothenate Kinase-Associated NeurodegenerationThomas Klopstock, Aleksandar Videnovic, Almut Turid Bischoff, et al.
JAMA Network Open|April 29, 2022
Diagnostic Accuracy of Magnetic Resonance Imaging Measures of Brain Atrophy Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal DegenerationIgnacio Illán-Gala, Salvatore Nigro, Lawren VandeVrede, et al.
The Lancet. Neurology|November 22, 2024
Sensitivity and specificity of a seed amplification assay for diagnosis of multiple system atrophy: a multicentre cohort studyYihua Ma, Carly M Farris, Sandrina Weber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 29, 2025
Barcelona Progressive Supranuclear Palsy (PSP) Registry: Clinical, Oculomotor, and Cerebrospinal Fluid Markers; from Suggestive to Definite CasesCelia Painous, Manel Fernández, Ana Cámara, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2022
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System AtrophyFranziska Hopfner, Anja K Tietz, Viktoria C Ruf, et al.
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