Author/Creator: Beeson, D - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Beeson, D

1. 1106 The clinical phenotypic spectrum of GFPT1 associated congenital myasthenic syndrome. Issue 3 (9th February 2012)

Authors:: Chaouch, A; Mueller, J S; Guergueltcheva, V; Muntoni, F; Bushby, K; Straub, V; Palace, J; Beeson, D; Abicht, A; Lochmuller, H
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83:Issue 3(2012)
Page Start:: e1
Record Type:: Journal Article
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2. 172 An unusual case of congenital myasthenic syndrome: the mechanism for treatment response. Issue 3 (9th February 2012)

Authors:: Spillane, J; Kullmann, D M; Beeson, D; Howard, R S
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83:Issue 3(2012)
Page Start:: e1
Record Type:: Journal Article
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3. A treatable muscle disease. Issue 4 (16th July 2009)

Authors:: Burke, G; Hammans, S; Allen, D; Arunachalam, R; Beeson, D
Journal:: Practical neurology
Issue:: Volume 9:Issue 4(2009)
Page Start:: 233
Record Type:: Journal Article
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4. FAST CHANNEL CONGENITAL MYASTHENIA: REVIEW OF 12 CASES AND TREATMENT CHALLENGES. (29th November 2012)

Authors:: Finlayson, S; Webster, R; Beeson, D; Jayawant, S; Robb, S; Palace, J
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83(2012)Supplement 2
Page Start:: A23
Record Type:: Journal Article
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5. PONM11 "The eyes have it": initial genetic screening in suspected congenital myasthenia. Issue 11 (22nd October 2010)

Authors:: Lashley, D; Burke, G; Beeson, D; Palace, J
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 81:Issue 11(2010)
Page Start:: e63
Record Type:: Journal Article
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6. The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder. Issue 8 (30th July 2004)

Authors:: Müller, J S; Abicht, A; Burke, G; Cossins, J; Richard, P; Baumeister, S K; Stucka, R; Eymard, B; Hantaï, D; Beeson, D; Lochmüller, H
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 8(2004)
Page Start:: e104
Record Type:: Journal Article
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