Musculoskeletal syndromes

0830 Help! I've become shorter than my wife: a treatable cause of camptocormia
S Slaght, I Galea, S O'Connell, S R Hammans

Journal of Neurology, Neurosurgery & Psychiatry Mar 2012, 83 (3) e1; DOI: 10.1136/jnnp-2011-301993.38
0906 A new clinical variant of the post-malaria neurological syndrome
A Pace, S Edwards

Journal of Neurology, Neurosurgery & Psychiatry Mar 2012, 83 (3) e1; DOI: 10.1136/jnnp-2011-301993.41
1106 The clinical phenotypic spectrum of GFPT1 associated congenital myasthenic syndrome
A Chaouch, J S Mueller, V Guergueltcheva, F Muntoni, K Bushby, V Straub, J Palace, D Beeson, A Abicht, H Lochmuller

Journal of Neurology, Neurosurgery & Psychiatry Mar 2012, 83 (3) e1; DOI: 10.1136/jnnp-2011-301993.17
016 A case of reversible dementia
K Ali, R Corkill

Journal of Neurology, Neurosurgery & Psychiatry Mar 2012, 83 (3) e1; DOI: 10.1136/jnnp-2011-301993.58
1130 Clinical features and clinical course of sporadic inclusion body myositis (IBM): a prospective cohort study: IBM-net
A Cortese, P Machado, A Miller, S Brady, D Hilton-Jones, J Morrow, A Hiscock, E Dewar, M Parton, M Hanna

Journal of Neurology, Neurosurgery & Psychiatry Mar 2012, 83 (3) e1; DOI: 10.1136/jnnp-2011-301993.19
014 Prevalence study of skeletal muscle channelopathies in England
A Horga, D L Raja Rayan, E Matthews, D Fialho, R Sud, A Haworth, S Portaro, J Burge, M B Davis, M G Hanna

Journal of Neurology, Neurosurgery & Psychiatry Mar 2012, 83 (3) e1; DOI: 10.1136/jnnp-2011-301993.56
1154 Skeletal muscle chloride channel gene (CLCN1) copy number variation can cause myotonia congenita
D Raja Rayan, A Haworth, R Sud, E Matthews, D Fialho, J Burge, S Portaro, A Toscano, M D Davis, M G Hanna

Journal of Neurology, Neurosurgery & Psychiatry Mar 2012, 83 (3) e1; DOI: 10.1136/jnnp-2011-301993.21
020 WITHDRAWN
Journal of Neurology, Neurosurgery & Psychiatry Mar 2012, 83 (3) e1; DOI: 10.1136/jnnp-2011-301993.62
1700 Expanding the phenotypic spectrum of progressive encephalomyelitis with rigidity and myoclonus syndrome (PERMS) associated with glycine receptor antibody: clinical and laboratory study of 20 patients
M I Leite, P Waters, A Carvajal, M Woodhall, A Vincent

Journal of Neurology, Neurosurgery & Psychiatry Mar 2012, 83 (3) e1; DOI: 10.1136/jnnp-2011-301993.26
015 Identifying the cause of phenotypic variability in a family with non-dystrophic myotonia
D Raja Rayan, A Haworth, R Sud, S McCall, S V Tan, S Durran, M Davis, M G Hanna

Journal of Neurology, Neurosurgery & Psychiatry Mar 2012, 83 (3) e1; DOI: 10.1136/jnnp-2011-301993.57

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