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Improving the electrophysiological measurement of REM without atonia in the diagnosis of REM sleep behaviour disorder
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Posted in Clinical Review Article
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20th Jan 2014
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Samuel Bolitho and Simon JG Lewis
Posted in Clinical Review Article
20th Jan 2014
Samuel Bolitho and Simon JG Lewis
Posted in Clinical Review Article
07th Nov 2013
Karen P Steel
Posted in Clinical Review Article
06th Nov 2013
James M Shine and Simon JG Lewis
Posted in Clinical Review Article
20th Sep 2013
Edward Roberts, Adolfo Bronstein, Barry M Seemungal
Posted in Clinical Review Article
10th Sep 2013
Laura Gasparini and Andrea Constestablie
Posted in Clinical Review Article
10th Sep 2013
Florence R Fricker and David Bennett
Posted in Clinical Review Article
19th Jun 2013
What’s in a name? Words used to describe patients with functional neurological symptoms suggest either that we know clearly what the mechanism is (psychogenic,psychosomatic, conversion disorder), or that we have no idea (medically unexplained). Added to this is a pervasive colloquial use of terms in doctor-to-doctor communication about patients with functional neurological symptoms which betrays […]
Posted in Clinical Review Article
19th Jun 2013
It is forty years since the first full report of long-term potentiation (LTP), a presumed cellular substrate for learning and memory. This review will provide an update on some recent advances in our understanding of the mechanisms underlying hippocampal LTP and address their potential clinical relevance. Introduction The hippocampus plays a fundamental role in learning […]
Posted in Clinical Review Article
13th Mar 2013
The diagnosis of Susac’s syndrome has been facilitated greatly by appreciation of distinctive magnetic resonance imaging (MRI) findings. As a result there is now increased recognition of what was once thought to be a very rare disease. The aim of this review is to provide an update on the latest developments in Susac’s syndrome and […]
Posted in Clinical Review Article
31st Jan 2013
The last two decades have witnessed a rapid increase in the number of inherited disorders caused by ion channel mutations. One of the major challenges is to delineate the full clinical spectrum of these ‘channelopathies’. Among this expanding group, neurological ion channel disorders are among the best characterised, reflecting the fundamental importance of electrical excitability […]