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Sent: Monday, May 31, 2010 8:10 AM
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Subject: Neuromuscular Disorders: Table of Contents - May 31, 2010
Neuromuscular Disorders
Neuromuscular Disorders - Table of Contents E-mail Alert - May 31, 2010
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Dear Mr. Meir Weiss,
The following table of contents from Neuromuscular Disorders (Vol 20, No 6) is now available:
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Editorial Board
page IFC
http://www.nmd-journal.com/article/S0960-8966%2810%2900205-1/abstract
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Research papers
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Drosophila indirect flight muscle specific Act88F actin mutants as a model system for studying congenital myopathies of the human ACTA1 skeletal muscle actin gene
Sarah E. Haigh, Sheetal S. Salvi, Maria Sevdali, Meg Stark, David Goulding, Jonathan D. Clayton, Belinda Bullard, John C. Sparrow, Upendra Nongthomba
pages 363-374
http://www.nmd-journal.com/article/S0960-8966%2810%2900128-8/abstract
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Novel molecular diagnostic approaches for X-linked centronuclear (myotubular) myopathy reveal intronic mutations
Valérie Tosch, Nasim Vasli, Christine Kretz, Anne-Sophie Nicot, Claire Gasnier, Nicolas Dondaine, Denis Oriot, Magalie Barth, Hugues Puissant, Norma B. Romero, Carsten G. Bönnemann, Betty Heller, Gilles Duval, Valérie Biancalana, Jocelyn Laporte
pages 375-381
http://www.nmd-journal.com/article/S0960-8966%2810%2900164-1/abstract
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Oral dexamethasone pulse therapy versus daily prednisolone in sub-acute onset myositis, a randomised clinical trial
J. van de Vlekkert, J.E. Hoogendijk, R.J. de Haan, A. Algra, I. van der Tweel, W.L. van der Pol, E.V. Uijtendaal, M. de Visser, on behalf of the Dexa Myositis Trial
pages 382-389
http://www.nmd-journal.com/article/S0960-8966%2810%2900131-8/abstract
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A novel heterozygous deletion–insertion mutation (2695–2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family
Xinghua Luan, Daojun Hong, Wei Zhang, Zhaoxia Wang, Yun Yuan
pages 390-396
http://www.nmd-journal.com/article/S0960-8966%2810%2900129-X/abstract
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Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene
Hasan O. Akman, Guido Davidzon, Kurenai Tanji, Emma J. MacDermott, Louann Larsen, Mercy M. Davidson, Ronald G. Haller, Lidia S. Szczepaniak, Thomas J.A. Lehman, Michio Hirano, Salvatore DiMauro
pages 397-402
http://www.nmd-journal.com/article/S0960-8966%2810%2900185-9/abstract
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The pathogenic m.3243A>T mitochondrial DNA mutation is associated with a variable neurological phenotype
Charlotte L. Alston, Andreas Bender, Iain P. Hargreaves, Helen Mundy, Charulata Deshpande, Thomas Klopstock, Robert McFarland, Rita Horvath, Robert W. Taylor
pages 403-406
http://www.nmd-journal.com/article/S0960-8966%2810%2900183-5/abstract
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Calpainopathy presenting as foot drop in a 41 year old
G. Burke, C. Hillier, J. Cole, M. Sampson, L. Bridges, K. Bushby, R. Barresi, S.R. Hammans
pages 407-410
http://www.nmd-journal.com/article/S0960-8966%2810%2900187-2/abstract
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Nephrogenic systemic fibrosis presenting as myopathy: A case report with histopathologic correlation
Eric Edgar, Randy Woltjer, Ruth Whitham, S. Humayun Gultekin, Suzanne Watnick, Edward J. Cupler
pages 411-413
http://www.nmd-journal.com/article/S0960-8966%2810%2900166-5/abstract
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Workshop reports
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International Workshop on Inclusion Body Myositis held at the Institute of Myology, Paris, on 29 May 2009
Olivier Benveniste, David Hilton-Jones
pages 414-421
http://www.nmd-journal.com/article/S0960-8966%2810%2900163-X/abstract
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Best Practice Guidelines on molecular diagnostics in Duchenne/Becker muscular dystrophies
Stephen Abbs, Sylvie Tuffery-Giraud, Egbert Bakker, Alessandra Ferlini, Thomas Sejersen, Clemens R. Mueller
pages 422-427
http://www.nmd-journal.com/article/S0960-8966%2810%2900186-0/abstract
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WMS 2010
page I
http://www.nmd-journal.com/article/S0960-8966%2810%2900208-7/abstract
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WMS online application form
page II
http://www.nmd-journal.com/article/S0960-8966%2810%2900209-9/abstract
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WMS News
pages III-IV
http://www.nmd-journal.com/article/S0960-8966%2810%2900210-5/abstract
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The complete editorial board is available at http://www.nmd-journal.com/edboard
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