Robb S - Search Results

1

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: robb s. Neurology. 2003 Sep 23;61(6):826-8. doi: 10.1212/01.wnl.0000085865.55513.ae. Neurology. 2003. PMID: 14504330

2

Circulating T cell subsets in the Lambert-Eaton myasthenic syndrome.

Robb SA, Bowley TJ, Willcox HN, Newsom-Davis J. Robb SA, et al. J Neurol Neurosurg Psychiatry. 1985 Jun;48(6):501-5. doi: 10.1136/jnnp.48.6.501. J Neurol Neurosurg Psychiatry. 1985. PMID: 2989435 Free PMC article.

3

Acetylcholine receptor antibodies in the elderly and in Down's syndrome.

Robb SA, Vincent A, McGregor MA, McGregor AM, Newsom-Davis JM. Robb SA, et al. J Neuroimmunol. 1985 Aug;9(3-4):139-46. doi: 10.1016/s0165-5728(85)80014-x. J Neuroimmunol. 1985. PMID: 3160723

4

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: robb s. Neuromuscul Disord. 2004 Jun;14(6):356-64. doi: 10.1016/j.nmd.2004.03.005. Neuromuscul Disord. 2004. PMID: 15145336 Clinical Trial.

5

Congenital myasthenic syndromes in childhood: diagnostic and management challenges.

Kinali M, Beeson D, Pitt MC, Jungbluth H, Simonds AK, Aloysius A, Cockerill H, Davis T, Palace J, Manzur AY, Jimenez-Mallebrera C, Sewry C, Muntoni F, Robb SA. Kinali M, et al. Among authors: robb sa. J Neuroimmunol. 2008 Sep 15;201-202:6-12. doi: 10.1016/j.jneuroim.2008.06.026. Epub 2008 Aug 15. J Neuroimmunol. 2008. PMID: 18707767

6

The use of rituximab in myasthenia gravis and Lambert-Eaton myasthenic syndrome.

Maddison P, McConville J, Farrugia ME, Davies N, Rose M, Norwood F, Jungbluth H, Robb S, Hilton-Jones D. Maddison P, et al. Among authors: robb s. J Neurol Neurosurg Psychiatry. 2011 Jun;82(6):671-3. doi: 10.1136/jnnp.2009.197632. Epub 2010 Apr 14. J Neurol Neurosurg Psychiatry. 2011. PMID: 20392977

7

Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7.

Lashley D, Palace J, Jayawant S, Robb S, Beeson D. Lashley D, et al. Among authors: robb s. Neurology. 2010 May 11;74(19):1517-23. doi: 10.1212/WNL.0b013e3181dd43bf. Neurology. 2010. PMID: 20458068 Free PMC article. Clinical Trial.

8

Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myasthenia.

Munot P, Lashley D, Jungbluth H, Feng L, Pitt M, Robb SA, Palace J, Jayawant S, Kennet R, Beeson D, Cullup T, Abbs S, Laing N, Sewry C, Muntoni F. Munot P, et al. Among authors: robb sa. Neuromuscul Disord. 2010 Dec;20(12):796-800. doi: 10.1016/j.nmd.2010.07.274. Epub 2010 Oct 14. Neuromuscul Disord. 2010. PMID: 20951040

9

Clinical features in a series of fast channel congenital myasthenia syndrome.

Palace J, Lashley D, Bailey S, Jayawant S, Carr A, McConville J, Robb S, Beeson D. Palace J, et al. Among authors: robb s. Neuromuscul Disord. 2012 Feb;22(2):112-7. doi: 10.1016/j.nmd.2011.08.002. Epub 2011 Sep 21. Neuromuscul Disord. 2012. PMID: 21940170

10

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. Among authors: robb s. 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

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