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BMC Neurology|August 17, 2023
Core protocol development for phase 2/3 clinical trials in the leukodystrophy vanishing white matter: a consensus statement by the VWM consortium and patient advocatesDaphne H Schoenmakers, Prisca S Leferink, Adeline Vanderver, et al.
BMC Neurology|August 11, 2023
Genetically predicted effects of physical activity and sedentary behavior on myasthenia gravis: evidence from mendelian randomization studyJiao Li, Fei Wang, Chen Zhang, et al.
BMC Neurology|August 14, 2023
Disease severity and mortality in Alzheimer's disease: an analysis using the U.S. National Alzheimer's Coordinating Center Uniform Data SetValerie Crowell, Adriana Reyes, Summera Qiheng Zhou, et al.
BMC Neurology|August 18, 2023
Transcranial magnetic resonance-guided focused ultrasound pallidothalamic tractotomy for patients with X-linked dystonia-parkinsonism: a study protocolRoland Dominic G Jamora, Kathleen Joy O Khu, Marie Charmaine C Sy, et al.
BMC Neurology|August 11, 2023
The "island sign" on diffusion-weighted imaging predicts early neurological deterioration in penetrating artery territory infarctions: a retrospective studyYang Yang, Zhihua Si, Dawei Wang, et al.
BMC Neurology|August 10, 2023
Intractable hiccups after VNS implantation: a case reportSusan Zhang Recio, Myriam Abdennadher
BMC Neurology|August 9, 2023
Effect of overground gait training with 'Mobility Assisted Robotic System-MARS' on gait parameters in patients with stroke: a pre-post studyAnupam Gupta, Navin B Prakash, Gourav Sannyasi, et al.
BMC Neurology|September 4, 2023
Different clinical phenotypes of AQP4-IgG positive NMOSD in two first degree relativesSalvatore Ssemmanda, Abdu Kisekka Musubire
BMC Neurology|June 30, 2023
A TRPV4 mutation caused Charcot-Marie-Tooth disease type 2C with scapuloperoneal muscular atrophy overlap syndrome and scapuloperoneal spinal muscular atrophy in one family: a case report and literature reviewHaofeng Chen, Chong Sun, Yongsheng Zheng, et al.
BMC Neurology|June 26, 2023
Epilepsy as the symptom of a spinocerebellar ataxia 13 in a patient presenting with a mutation in the KCNC3 geneShao Li, Dandan Shang, Yanjiao Du, et al.
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