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BMJ Neurology Open|December 22, 2025
Robotic thymectomy for ocular myasthenia gravis: a case series from a UK tertiary centreThomas Roberts, Stephen Cone, Jennifer Spillane, et al.
BMJ Neurology Open|December 10, 2025
Immunometabolic profiling in menopausal women with multiple sclerosis: the role of adipokines and hormone therapyLaura Juutinen, Katja Ahinko, Sanna Hagman, et al.
BMJ Neurology Open|June 23, 2025
Integrating clinical predictors and glial fibrillary acidic protein in prediction models for the prehospital identification of intracerebral haemorrhage in suspected strokeMohammed Almubayyidh, David A Jenkins, Edoardo Gaude, et al.
BMJ Neurology Open|June 23, 2025
Time to endovascular thrombectomy for acute ischaemic stroke in language other than English (LOTE) communities in South-Western SydneyVivek Pidugun, Daniel Wardman, Peter Thomas, et al.
BMJ Neurology Open|September 26, 2025
Integrated UPper limb and Language Impairment and Functional Training (UPLIFT) after stroke: study protocol for an umbrella Bayesian Optimal Phase IIa clinical trialKathryn S Hayward, Geoffrey Donnan, Erin Godecke, et al.
BMJ Neurology Open|September 26, 2025
Real-world use of disease-modifying therapy in persons with multiple sclerosis aged 55 and overMina Stanikić, Anke Salmen, Christian P Kamm, et al.
BMJ Neurology Open|May 13, 2025
Long-read sequencing for diagnosis of genetic myopathiesDennis Yeow, Laura Ivete Rudaks, Ryan Davis, et al.
BMJ Neurology Open|August 4, 2025
Efficacy and safety of oral amantadine in Parkinson's disease with dyskinesia and motor fluctuations: a systematic review and meta-analysis of randomised controlled trialsSurachet Rujirussawarawong, Saharat Aungsumart, Chayut Kasemsuk, et al.
BMJ Neurology Open|September 26, 2025
Density of routinely collected neurology data depends on patient visit type: an investigation using the observational medical outcomes partnership common data modelFran Biggin, Laura M White, Quinta Ashcroft, et al.
BMJ Neurology Open|September 26, 2025
Whole Exome Sequencing Identifies Novel Homozygous LGI1 Variant Mimicking ADAM22-Related Pathologies in a Moroccan FamilyHinde El Mouhi, Badreddine Elmakhzen, Amina Bouyahyaoui, et al.
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