2 National Center for Neurological Disorders, Shanghai, People's Republic of China 3 Rare Disease Center, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, People's Republic of ...
Objective: Parkinson’s disease (PD) is a progressive neurological disorder characterised by a large number of motor and non-motor features that can impact on function to a variable degree. This review ...
Objectives To report efficacy of adjuvant cenobamate in adults with Lennox-Gastaut syndrome (LGS) following cannabidiol. Methodology A retrospective record review was conducted of patients with LGS ...
1 Alzheimer Centre and VU University Medical Centre, Amsterdam, The Netherlands 2 Department of Neurology, VU University Medical Centre, Amsterdam, The Netherlands 3 Department of Neurology and MRI ...
1 Division of Neurology, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong 2 Department of Clinical and Experimental Epilepsy, ...
Dr Paul T Francis, Dementia Research Laboratory, Division of Biomolecular Sciences, Guy’s, King’s and St Thomas’ Schools of Biomedical Sciences, King’s College, St Thomas Street, London SE1 9RT, UK.
Background: Most studies on spinal cord infarction have been conducted in single centres; they usually consisted of case reports, or of larger series of patients recruited over a large period of time, ...
Correspondence to Dr Claudio Liguori, Department of Systems Medicine, Neurophysiopathology Unit, University of Rome “Tor Vergata”, Viale Oxford 81 Rome 00133, Italy; dott.claudioliguori{at}yahoo.it ...
Original research: Swedish nationwide study of 377 patents with non-aneurysmal subarachnoid haemorrhage: a disease with distinct demographics and risk factors (20 November, 2025) ...
The human electroencephalogram (EEG) was discovered by the German psychiatrist, Hans Berger, in 1929. Its potential applications in epilepsy rapidly became clear, when Gibbs and colleagues in Boston ...
Wilson’s disease is an autosomal–recessive disorder of copper metabolism caused by mutations in ATP7B and associated with neurological, psychiatric, ophthalmological and hepatic manifestations.
Correspondence to Emma Beeldman, Department of Neurology, Academic Medical Centre, P.O. Box 22700 DE, Amsterdam 1105 AZ, The Netherlands; e.beeldman{at}amc.uva.nl Cognitive impairment is present in ...