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Annals of Neurology|November 11, 2008
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic strokeSolveig Gretarsdottir, Gudmar Thorleifsson, Andrei Manolescu, et al.Parkinsonism & Related Disorders|October 23, 2016
Knowledge gaps and research recommendations for essential tremorFranziska Hopfner, Dietrich Haubenberger, Wendy R Galpern, et al.Nature Genetics|September 28, 2005
Mutations in SEPT9 cause hereditary neuralgic amyotrophyGregor Kuhlenbäumer, Mark C Hannibal, Eva Nelis, et al.JAMA Neurology|August 4, 2025
Early Treatment With Intravenous Immunoglobulins and Outcomes of Patients With Anti-IgLON5 DiseaseThomas Grüter, Carles Gaig, Yvette S Crijnen, et al.Translational Neurodegeneration|April 16, 2019
No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptorsFranziska Hopfner, Stefanie H Müller, Dagmar Steppat, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.Frontiers in Immunology|July 25, 2024
HLA and KIR genetic association and NK cells in anti-NMDAR encephalitisVicente Peris Sempere, Guo Luo, Sergio Muñiz-Castrillo, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2024
Large-Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia GenesMirja Thomsen, Katrin Marth, Sebastian Loens, et al.Neurology(R) Neuroimmunology & Neuroinflammation|September 15, 2025
Risk of Epilepsy and Factors Associated With Time to Seizure Remission in Anti-LGI1 Encephalitis: Long-Term Outcome in 236 PatientsTobias Baumgartner, Moritz Freyberg, Lucia Campetella, et al.Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.Pageof 10