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2011 | 3 |
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Page 1
MFN2 mutations cause severe phenotypes in most patients with CMT2A.
Neurology. 2011 May 17;76(20):1690-6. doi: 10.1212/WNL.0b013e31821a441e. Epub 2011 Apr 20.
Neurology. 2011.
PMID: 21508331
Free PMC article.
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations.
Polke JM, Laurá M, Pareyson D, Taroni F, Milani M, Bergamin G, Gibbons VS, Houlden H, Chamley SC, Blake J, Devile C, Sandford R, Sweeney MG, Davis MB, Reilly MM.
Polke JM, et al. Among authors: gibbons vs.
Neurology. 2011 Jul 12;77(2):168-73. doi: 10.1212/WNL.0b013e3182242d4d. Epub 2011 Jun 29.
Neurology. 2011.
PMID: 21715711
Free PMC article.
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Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.
Catarino CB, Liu JY, Liagkouras I, Gibbons VS, Labrum RW, Ellis R, Woodward C, Davis MB, Smith SJ, Cross JH, Appleton RE, Yendle SC, McMahon JM, Bellows ST, Jacques TS, Zuberi SM, Koepp MJ, Martinian L, Scheffer IE, Thom M, Sisodiya SM.
Catarino CB, et al. Among authors: gibbons vs.
Brain. 2011 Oct;134(Pt 10):2982-3010. doi: 10.1093/brain/awr129. Epub 2011 Jun 29.
Brain. 2011.
PMID: 21719429
Free PMC article.
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In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2.
Tomlinson SE, Tan SV, Burke D, Labrum RW, Haworth A, Gibbons VS, Sweeney MG, Griggs RC, Kullmann DM, Bostock H, Hanna MG.
Tomlinson SE, et al. Among authors: gibbons vs.
Brain. 2016 Feb;139(Pt 2):380-91. doi: 10.1093/brain/awv380.
Brain. 2016.
PMID: 26912519
Free PMC article.
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GJB1 gene mutations in suspected inflammatory demyelinating neuropathies not responding to treatment.
Michell AW, Laura M, Blake J, Lunn MP, Cox A, Gibbons VS, Davis MB, Wood NW, Manji H, Houlden H, Murray NM, Reilly MM.
Michell AW, et al. Among authors: gibbons vs.
J Neurol Neurosurg Psychiatry. 2009 Jun;80(6):699-700. doi: 10.1136/jnnp.2008.150557.
J Neurol Neurosurg Psychiatry. 2009.
PMID: 19448103
No abstract available.
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