Cossins J - Search Results

1

Passive and active immunization models of MuSK-Ab positive myasthenia: electrophysiological evidence for pre and postsynaptic defects.

Viegas S, Jacobson L, Waters P, Cossins J, Jacob S, Leite MI, Webster R, Vincent A. Viegas S, et al. Among authors: cossins j. Exp Neurol. 2012 Apr;234(2):506-12. doi: 10.1016/j.expneurol.2012.01.025. Epub 2012 Feb 3. Exp Neurol. 2012. PMID: 22326541 Free 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: cossins j. 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: cossins j. Neuromuscul Disord. 2004 Jun;14(6):356-64. doi: 10.1016/j.nmd.2004.03.005. Neuromuscul Disord. 2004. PMID: 15145336 Clinical Trial.

4

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: cossins j. Ann N Y Acad Sci. 2008;1132:99-103. doi: 10.1196/annals.1405.049. Ann N Y Acad Sci. 2008. PMID: 18567858

5

The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome.

Cossins J, Liu WW, Belaya K, Maxwell S, Oldridge M, Lester T, Robb S, Beeson D. Cossins J, et al. Hum Mol Genet. 2012 Sep 1;21(17):3765-75. doi: 10.1093/hmg/dds198. Epub 2012 Jun 1. Hum Mol Genet. 2012. PMID: 22661499

6

Presence and pathogenic relevance of antibodies to clustered acetylcholine receptor in ocular and generalized myasthenia gravis.

Jacob S, Viegas S, Leite MI, Webster R, Cossins J, Kennett R, Hilton-Jones D, Morgan BP, Vincent A. Jacob S, et al. Among authors: cossins j. Arch Neurol. 2012 Aug;69(8):994-1001. doi: 10.1001/archneurol.2012.437. Arch Neurol. 2012. PMID: 22689047

7

Antibodies identified by cell-based assays in myasthenia gravis and associated diseases.

Vincent A, Waters P, Leite MI, Jacobson L, Koneczny I, Cossins J, Beeson D. Vincent A, et al. Among authors: cossins j. Ann N Y Acad Sci. 2012 Dec;1274:92-8. doi: 10.1111/j.1749-6632.2012.06789.x. Ann N Y Acad Sci. 2012. PMID: 23252902

8

The search for new antigenic targets in myasthenia gravis.

Cossins J, Belaya K, Zoltowska K, Koneczny I, Maxwell S, Jacobson L, Leite MI, Waters P, Vincent A, Beeson D. Cossins J, et al. Ann N Y Acad Sci. 2012 Dec;1275:123-8. doi: 10.1111/j.1749-6632.2012.06833.x. Ann N Y Acad Sci. 2012. PMID: 23278587 Review.

9

The role of muscle-specific tyrosine kinase (MuSK) and mystery of MuSK myasthenia gravis.

Koneczny I, Cossins J, Vincent A. Koneczny I, et al. Among authors: cossins j. J Anat. 2014 Jan;224(1):29-35. doi: 10.1111/joa.12034. Epub 2013 Mar 4. J Anat. 2014. PMID: 23458718 Free PMC article. Review.

10

Mutations in GFPT1 that underlie limb-girdle congenital myasthenic syndrome result in reduced cell-surface expression of muscle AChR.

Zoltowska K, Webster R, Finlayson S, Maxwell S, Cossins J, Müller J, Lochmüller H, Beeson D. Zoltowska K, et al. Among authors: cossins j. Hum Mol Genet. 2013 Jul 15;22(14):2905-13. doi: 10.1093/hmg/ddt145. Epub 2013 Apr 8. Hum Mol Genet. 2013. PMID: 23569079

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