BMJ1d
The Tolosa-Hunt syndrome
aDepartment of Ophthalmology, University of Alabama School of Medicine, 601 700 South 18th Street, Birmingham, Alabama, USA, bNeuro-ophthalmology Unit, University of California School of Medicine, San ...
BMJ2d
Hypothyroidism is associated with prolonged COVID-19-induced anosmia: a case–control study
Correspondence to Dr Georgios Tsivgoulis, Second Department of Neurology, National and Kapodistrian University of Athens School of Medicine, Athens 15344, Attica, Greece; tsivgoulisgiorg{at}yahoo.gr ...
BMJ2d
Acute small fibre sensory neuropathy: another variant of Guillain-Barré syndrome?
Six patients who presented with acute sensory neuropathy were studied. All patients underwent detailed clinical assessment along with electrophysiological tests and relevant laboratory investigations.
BMJ2d
Use of 14–3–3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease
OBJECTIVES The detection of the protein 14–3–3 in the CSF has been shown to be a reliable and sensitive marker for sporadic Creutzfeldt-Jakob disease (CJD). Other brain-specific proteins such as ...
BMJ2d
Overlapping CNS inflammatory diseases: differentiating features of NMO and MS
Correspondence to Jacqueline Palace, Department of Neurology, Oxford University Hospitals NHS Trust, West Wing Level 3, John Radcliffe Hospital, Oxford, OX39DU, UK; jacqueline.palace{at}ndcn.ox.ac.uk ...
BMJ3d
Timing of surgery for supratentorial aneurysmal subarachnoid haemorrhage: report of a prospective study
University Department of Neurosurgery, Box 167, Block A, Level 4, Addenbrookes Hospital, Cambridge CB2 2QQ, UK Correspondence to: Dr P J Kirkpatrick, University Department of Neurosurgery, Box 167, ...
BMJ3d
Hypermetabolism in motor neurone disease is associated with a greater functional decline but not weight loss
2 Centre for Clinical Research (CCR), University of Queensland, Brisbane, QLD, Australia 3 School of Medicine, University of Queensland, Brisbane, QLD, Australia 4 School of Biomedical Sciences, ...
BMJ3d
Hereditary spastic paraparesis: a review of new developments
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BMJ3d
Variant Creutzfeldt-Jakob disease in older patients
1 National CJD Research & Surveillance Unit, University of Edinburgh, Western General Hospital, Edinburgh, UK 2 Department of Clinical Neurosciences, Western General Hospital, Edinburgh, UK ...
BMJ4d
Disability and survival in Duchenne muscular dystrophy
Zurich Centre for Integrative Human Physiology, University of Zurich, Switzerland Dr K E Bloch, Pulmonary Division, University Hospital of Zurich, Raemistrasse 100, 8091 Zurich, Switzerland; ...
BMJ4d
Does the primary literature provide support for clinical signs used to distinguish psychogenic nonepileptic seizures from epileptic seizures?
Psychogenic non-epileptic seizures (PNES) represent a diagnostic challenge. When trying to distinguish between PNES and epileptic seizures (ES), clinicians rely on the presence or absence of several ...
BMJ4d
Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis
Background The population rate of familial amyotrophic lateral sclerosis (FALS) is frequently reported as 10%. However, a systematic review and meta-analysis of the true population based frequency of ...