Maxwell S - Search Results

1

Antibodies to GABAA receptor α1 and γ2 subunits: clinical and serologic characterization.

Pettingill P, Kramer HB, Coebergh JA, Pettingill R, Maxwell S, Nibber A, Malaspina A, Jacob A, Irani SR, Buckley C, Beeson D, Lang B, Waters P, Vincent A. Pettingill P, et al. Among authors: maxwell s. Neurology. 2015 Mar 24;84(12):1233-41. doi: 10.1212/WNL.0000000000001326. Epub 2015 Jan 30. Neurology. 2015. PMID: 25636713 Free PMC article.

2

Rapsyn mutations in hereditary myasthenia: distinct early- and late-onset phenotypes.

Burke G, Cossins J, Maxwell S, Owens G, Vincent A, Robb S, Nicolle M, Hilton-Jones D, Newsom-Davis J, Palace J, Beeson D. Burke G, et al. Among authors: maxwell s. Neurology. 2003 Sep 23;61(6):826-8. doi: 10.1212/01.wnl.0000085865.55513.ae. Neurology. 2003. PMID: 14504330

3

Distinct phenotypes of congenital acetylcholine receptor deficiency.

Burke G, Cossins J, Maxwell S, Robb S, Nicolle M, Vincent A, Newsom-Davis J, Palace J, Beeson D. Burke G, et al. Among authors: maxwell s. Neuromuscul Disord. 2004 Jun;14(6):356-64. doi: 10.1016/j.nmd.2004.03.005. Neuromuscul Disord. 2004. PMID: 15145336 Clinical Trial.

4

A mouse model of AChR deficiency syndrome with a phenotype reflecting the human condition.

Cossins J, Webster R, Maxwell S, Burke G, Vincent A, Beeson D. Cossins J, et al. Among authors: maxwell s. Hum Mol Genet. 2004 Dec 1;13(23):2947-57. doi: 10.1093/hmg/ddh320. Epub 2004 Oct 7. Hum Mol Genet. 2004. PMID: 15471888

5

Dok-7 mutations underlie a neuromuscular junction synaptopathy.

Beeson D, Higuchi O, Palace J, Cossins J, Spearman H, Maxwell S, Newsom-Davis J, Burke G, Fawcett P, Motomura M, Müller JS, Lochmüller H, Slater C, Vincent A, Yamanashi Y. Beeson D, et al. Among authors: maxwell s. Science. 2006 Sep 29;313(5795):1975-8. doi: 10.1126/science.1130837. Epub 2006 Aug 17. Science. 2006. PMID: 16917026

6

Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutations.

Cossins J, Burke G, Maxwell S, Spearman H, Man S, Kuks J, Vincent A, Palace J, Fuhrer C, Beeson D. Cossins J, et al. Among authors: maxwell s. Brain. 2006 Oct;129(Pt 10):2773-83. doi: 10.1093/brain/awl219. Epub 2006 Aug 31. Brain. 2006. PMID: 16945936 Free article.

7

Clinical features of the DOK7 neuromuscular junction synaptopathy.

Palace J, Lashley D, Newsom-Davis J, Cossins J, Maxwell S, Kennett R, Jayawant S, Yamanashi Y, Beeson D. Palace J, et al. Among authors: maxwell s. Brain. 2007 Jun;130(Pt 6):1507-15. doi: 10.1093/brain/awm072. Epub 2007 Apr 23. Brain. 2007. PMID: 17452375

8

Congenital myasthenic syndromes and the formation of the neuromuscular junction.

Beeson D, Webster R, Cossins J, Lashley D, Spearman H, Maxwell S, Slater CR, Newsom-Davis J, Palace J, Vincent A. Beeson D, et al. Among authors: maxwell s. Ann N Y Acad Sci. 2008;1132:99-103. doi: 10.1196/annals.1405.049. Ann N Y Acad Sci. 2008. PMID: 18567858

9

Aquaporin-4 antibodies in neuromyelitis optica and longitudinally extensive transverse myelitis.

Waters P, Jarius S, Littleton E, Leite MI, Jacob S, Gray B, Geraldes R, Vale T, Jacob A, Palace J, Maxwell S, Beeson D, Vincent A. Waters P, et al. Among authors: maxwell s. Arch Neurol. 2008 Jul;65(7):913-9. doi: 10.1001/archneur.65.7.913. Arch Neurol. 2008. PMID: 18625857

10

N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes.

Irani SR, Bera K, Waters P, Zuliani L, Maxwell S, Zandi MS, Friese MA, Galea I, Kullmann DM, Beeson D, Lang B, Bien CG, Vincent A. Irani SR, et al. Among authors: maxwell s. Brain. 2010 Jun;133(Pt 6):1655-67. doi: 10.1093/brain/awq113. Brain. 2010. PMID: 20511282 Free PMC article.

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