Beeson D - Search Results

1

The Neuromuscular Junction and Wide Heterogeneity of Congenital Myasthenic Syndromes.

Rodríguez Cruz PM, Palace J, Beeson D. Rodríguez Cruz PM, et al. Among authors: beeson d. Int J Mol Sci. 2018 Jun 5;19(6):1677. doi: 10.3390/ijms19061677. Int J Mol Sci. 2018. PMID: 29874875 Free PMC article. Review.

2

Immunogenicity of human recombinant acetylcholine receptor alpha subunit: cytoplasmic epitopes dominate the antibody response in four mouse strains.

Palace J, Vincent A, Beeson D, Newsom-Davis J. Palace J, et al. Among authors: beeson d. Autoimmunity. 1994;18(2):113-9. doi: 10.3109/08916939409007984. Autoimmunity. 1994. PMID: 7537978

3

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. Among authors: beeson d. 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.

4

Genes at the junction--candidates for congenital myasthenic syndromes.

Vincent A, Newland C, Croxen R, Beeson D. Vincent A, et al. Among authors: beeson d. Trends Neurosci. 1997 Jan;20(1):15-22. doi: 10.1016/S0166-2236(96)10066-7. Trends Neurosci. 1997. PMID: 9004414 Review.

5

Mutations in different functional domains of the human muscle acetylcholine receptor alpha subunit in patients with the slow-channel congenital myasthenic syndrome.

Croxen R, Newland C, Beeson D, Oosterhuis H, Chauplannaz G, Vincent A, Newsom-Davis J. Croxen R, et al. Among authors: beeson d. Hum Mol Genet. 1997 May;6(5):767-74. doi: 10.1093/hmg/6.5.767. Hum Mol Genet. 1997. PMID: 9158151

6

Congenital myasthenic syndromes.

Beeson D, Palace J, Vincent A. Beeson D, et al. Curr Opin Neurol. 1997 Oct;10(5):402-7. doi: 10.1097/00019052-199710000-00008. Curr Opin Neurol. 1997. PMID: 9330886 Review.

7

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.

8

Mutation of the acetylcholine receptor epsilon-subunit promoter in congenital myasthenic syndrome.

Nichols P, Croxen R, Vincent A, Rutter R, Hutchinson M, Newsom-Davis J, Beeson D. Nichols P, et al. Among authors: beeson d. Ann Neurol. 1999 Apr;45(4):439-43. Ann Neurol. 1999. PMID: 10211467

9

Association of the APOE epsilon4 allele with disease activity in multiple sclerosis.

Evangelou N, Jackson M, Beeson D, Palace J. Evangelou N, et al. Among authors: beeson d. J Neurol Neurosurg Psychiatry. 1999 Aug;67(2):203-5. doi: 10.1136/jnnp.67.2.203. J Neurol Neurosurg Psychiatry. 1999. PMID: 10406990 Free PMC article.

10

Novel functional epsilon-subunit polypeptide generated by a single nucleotide deletion in acetylcholine receptor deficiency congenital myasthenic syndrome.

Croxen R, Newland C, Betty M, Vincent A, Newsom-Davis J, Beeson D. Croxen R, et al. Among authors: beeson d. Ann Neurol. 1999 Oct;46(4):639-47. doi: 10.1002/1531-8249(199910)46:4<639::aid-ana13>3.0.co;2-1. Ann Neurol. 1999. PMID: 10514102

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