BMJ11d
Emil Adolph von Behring (1854–1917) and Shibasaburo Kitasato (1852–1931)
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BMJ11d
Papyrus of Ebers and Smith
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BMJ11d
Hyperreflexia in Guillain-Barré syndrome: relation with acute motor axonal neuropathy and anti-GM1 antibody
a Department of Neurology, Chiba University School of Medicine, Chiba, Japan, b Department of Neurology, Dokkyo University School of Medicine, Tochigi, Japan Dr Satoshi Kuwabara, Department of ...
BMJ11d
The nosological position of apathy in clinical practice
Apathy is increasingly recognised as a common behavioural syndrome in psychiatric disorders, but it is conceptually ill defined. The aim of this study was to examine the concept of apathy as it is ...
BMJ11d
Patterns of spontaneous recovery of neglect and associated disorders in acute right brain-damaged patients
Objectives: The evolutionary pattern of spontaneous recovery from acute neglect was studied by assessing cognitive deficits and motor impairments. Detailed lesion reconstruction was also performed to ...
BMJ12d
Johann Bernhard Aloys von Gudden: an outstanding scientist
Correspondence to: Dr L Sarikcioglu Department of Anatomy, Akdeniz University, Faculty of Medicine Campus, Antalya 07070, Turkey; sarikcioglu{at}akdeniz.edu.tr If you wish to reuse any or all of this ...
BMJ13d
“When the feeling’s gone”: a selective loss of musical emotion
3 Department of Speech, University of Newcastle, Newcastle-upon-Tyne, UK Correspondence to: T D Griffiths Auditory Group, University of Newcastle Medical School, Framlington Place, Newcastle-upon-Tyne ...
BMJ14d
Idiopathic generalised epilepsy in adults manifested by phantom absences, generalised tonic-clonic seizures, and frequent absence status
Department of Clinical Neurophysiology and Epilepsies, St Thomas’ Hospital, London SE1 7EH, UK Dr CP Panayiotopoulos, St Thomas’ Hospital, London SE1 7EH, UK. OBJECTIVES To describe the clinical and ...
BMJ22d
Specific phobia is a frequent non-motor feature in stiff man syndrome
Correspondence to: Dr Peter Henningsen, Department of Psychosomatic Medicine, University Hospital, Thibautstr 2, 69115 Heidelberg, Germany; peter_henningsen{at}med.uni-heidelberg.de Objective: To ...
BMJ16d
Challenges in modelling the Charcot-Marie-Tooth neuropathies for therapy development
Much has been achieved in terms of understanding the complex clinical and genetic heterogeneity of Charcot-Marie-Tooth neuropathy (CMT). Since the identification of mutations in the first CMT ...
BMJ22d
Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996–2000
Background: In recent years, there has been a paradigm shift in the method of healthcare delivery to amyotrophic lateral sclerosis (ALS) patients with the emergence of multidisciplinary ALS clinics ...
BMJ14d
Whole-exome sequencing identified novel KIF5A mutations in Chinese patients with amyotrophic lateral sclerosis and Charcot-Marie-Tooth type 2
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