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Neurogenetics|May 18, 1999
Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmissionC Bessou, J B Giugia, C J Franks, et al.
Neurogenetics|May 10, 2008
ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxiaSascha Vermeer, Rowdy P P Meijer, Benjamin J Pijl, et al.
Neurogenetics|April 3, 2025
The association of SCN1A polymorphisms with epilepsy and drug resistance: a systematic review and meta-analysisIda Mohammadi, Shahryar Rajai Firouzabadi, Aryan Aarabi, et al.
Neurogenetics|April 3, 2025
Genetic variants associated with idiopathic Parkinson's disease in Latin America: A systematic reviewFelipe Duarte-Zambrano, David Felipe Alfonso-Cedeño, Jorge A Barrero, et al.
Neurogenetics|April 1, 2025
Multi-target approach to Alzheimer's disease prevention and treatment: antioxidant, anti-inflammatory, and amyloid- modulating mechanismsKashif Abbas, Mohd Mustafa, Mudassir Alam, et al.
Neurogenetics|January 16, 2026
ADK deficiency without hypermethioninemia presenting as intractable epilepsy: a rare neurometabolic case and literature reviewAgung Triono, Kristy Iskandar, Neti Nurani, et al.
Neurogenetics|January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
Neurogenetics|March 5, 2013
Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in FinlandMari Auranen, Emil Ylikallio, Jussi Toppila, et al.
Neurogenetics|April 19, 2013
CCM molecular screening in a diagnosis context: novel unclassified variants leading to abnormal splicing and importance of large deletionsFlorence Riant, Michaelle Cecillon, Pascale Saugier-Veber, et al.
Neurogenetics|December 6, 2005
Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern BrazilHsin F Chien, Christan F Rohé, Maria D L Costa, et al.
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