Newsom-Davis J - Search Results

1

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

2

Pathogenic autoantibodies in the lambert-eaton myasthenic syndrome.

Lang B, Pinto A, Giovannini F, Newsom-Davis J, Vincent A. Lang B, et al. Ann N Y Acad Sci. 2003 Sep;998:187-95. doi: 10.1196/annals.1254.019. Ann N Y Acad Sci. 2003. PMID: 14592874

3

Antibodies in myasthenia gravis and related disorders.

Vincent A, McConville J, Farrugia ME, Bowen J, Plested P, Tang T, Evoli A, Matthews I, Sims G, Dalton P, Jacobson L, Polizzi A, Blaes F, Lang B, Beeson D, Willcox N, Newsom-Davis J, Hoch W. Vincent A, et al. Ann N Y Acad Sci. 2003 Sep;998:324-35. doi: 10.1196/annals.1254.036. Ann N Y Acad Sci. 2003. PMID: 14592891 Review.

4

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. Science. 2006 Sep 29;313(5795):1975-8. doi: 10.1126/science.1130837. Epub 2006 Aug 17. Science. 2006. PMID: 16917026

5

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. Brain. 2007 Jun;130(Pt 6):1507-15. doi: 10.1093/brain/awm072. Epub 2007 Apr 23. Brain. 2007. PMID: 17452375

6

Myasthenia gravis seronegative for acetylcholine receptor antibodies.

Vincent A, Leite MI, Farrugia ME, Jacob S, Viegas S, Shiraishi H, Benveniste O, Morgan BP, Hilton-Jones D, Newsom-Davis J, Beeson D, Willcox N. Vincent A, et al. Ann N Y Acad Sci. 2008;1132:84-92. doi: 10.1196/annals.1405.020. Ann N Y Acad Sci. 2008. PMID: 18567857

7

Structural abnormalities of the AChR caused by mutations underlying congenital myasthenic syndromes.

Beeson D, Webster R, Ealing J, Croxen R, Brownlow S, Brydson M, Newsom-Davis J, Slater C, Hatton C, Shelley C, Colquhoun D, Vincent A. Beeson D, et al. Ann N Y Acad Sci. 2003 Sep;998:114-24. doi: 10.1196/annals.1254.013. Ann N Y Acad Sci. 2003. PMID: 14592868

8

Myasthenia gravis in a woman with congenital AChR deficiency due to epsilon-subunit mutations.

Croxen R, Vincent A, Newsom-Davis J, Beeson D. Croxen R, et al. Neurology. 2002 May 28;58(10):1563-5. doi: 10.1212/wnl.58.10.1563. Neurology. 2002. PMID: 12034803

9

Clinical and experimental observations in patients with congenital myasthenic syndromes.

Vincent A, Newsom-Davis J, Wray D, Shillito P, Harrison J, Betty M, Beeson D, Mills K, Palace J, Molenaar P, et al. Vincent A, et al. Ann N Y Acad Sci. 1993 Jun 21;681:451-60. doi: 10.1111/j.1749-6632.1993.tb22929.x. Ann N Y Acad Sci. 1993. PMID: 7689312 No abstract available.

10

Congenital myasthenic syndromes. Studies of the AChR and other candidate genes.

Beeson D, Newland C, Croxen R, Buckel A, Li FY, Larsson C, Tariq M, Vincent A, Newsom-Davis J. Beeson D, et al. Ann N Y Acad Sci. 1998 May 13;841:181-3. doi: 10.1111/j.1749-6632.1998.tb10924.x. Ann N Y Acad Sci. 1998. PMID: 9668236 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

322 results

Search Page

Filters