Spacey S - Search Results

1

Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation.

Sheerin UM, Stamelou M, Charlesworth G, Shiner T, Spacey S, Valente EM, Wood NW, Bhatia KP. Sheerin UM, et al. Among authors: spacey s. J Neurol. 2013 Feb;260(2):656-60. doi: 10.1007/s00415-012-6747-4. Epub 2012 Nov 24. J Neurol. 2013. PMID: 23180180 Free PMC article. No abstract available.

2

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.

Gardiner AR, Bhatia KP, Stamelou M, Dale RC, Kurian MA, Schneider SA, Wali GM, Counihan T, Schapira AH, Spacey SD, Valente EM, Silveira-Moriyama L, Teive HA, Raskin S, Sander JW, Lees A, Warner T, Kullmann DM, Wood NW, Hanna M, Houlden H. Gardiner AR, et al. Among authors: spacey sd. Neurology. 2012 Nov 20;79(21):2115-21. doi: 10.1212/WNL.0b013e3182752c5a. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077024 Free PMC article.

3

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.

Valente EM, Spacey SD, Wali GM, Bhatia KP, Dixon PH, Wood NW, Davis MB. Valente EM, et al. Among authors: spacey sd. Brain. 2000 Oct;123 ( Pt 10):2040-5. doi: 10.1093/brain/123.10.2040. Brain. 2000. PMID: 11004121

4

The genetics of Parkinson's disease.

Spacey SD, Wood NW. Spacey SD, et al. Curr Opin Neurol. 1999 Aug;12(4):427-32. doi: 10.1097/00019052-199908000-00009. Curr Opin Neurol. 1999. PMID: 10555831 Review.

5

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.

Spacey SD, Valente EM, Wali GM, Warner TT, Jarman PR, Schapira AH, Dixon PH, Davis MB, Bhatia KP, Wood NW. Spacey SD, et al. Mov Disord. 2002 Jul;17(4):717-25. doi: 10.1002/mds.10126. Mov Disord. 2002. PMID: 12210861

6

Mutation analysis of the sodium/hydrogen exchanger gene (NHE5) in familial paroxysmal kinesigenic dyskinesia.

Spacey SD, Szczygielski BI, McRory JE, Wali GM, Wood NW, Snutch TP. Spacey SD, et al. J Neural Transm (Vienna). 2002 Sep;109(9):1189-94. doi: 10.1007/s00702-002-0750-3. J Neural Transm (Vienna). 2002. PMID: 12203045

7

Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia.

Spacey SD, Materek LA, Szczygielski BI, Bird TD. Spacey SD, et al. Arch Neurol. 2005 Feb;62(2):314-6. doi: 10.1001/archneur.62.2.314. Arch Neurol. 2005. PMID: 15710862

8

Pseudomigraine with lymphocytic pleocytosis: a calcium channelopathy? Clinical description of 10 cases and genetic analysis of the familial hemiplegic migraine gene CACNA1A.

Chapman KM, Szczygielski BI, Toth C, Woolfenden A, Robinson G, Snutch TP, Spacey SD. Chapman KM, et al. Headache. 2003 Sep;43(8):892-5. doi: 10.1046/j.1526-4610.2003.03168.x. Headache. 2003. PMID: 12940811

9

Malaysian siblings with friedreich ataxia and chorea: a novel deletion in the frataxin gene.

Spacey SD, Szczygielski BI, Young SP, Hukin J, Selby K, Snutch TP. Spacey SD, et al. Can J Neurol Sci. 2004 Aug;31(3):383-6. doi: 10.1017/s0317167100003498. Can J Neurol Sci. 2004. PMID: 15376485

10

Functional implications of a novel EA2 mutation in the P/Q-type calcium channel.

Spacey SD, Hildebrand ME, Materek LA, Bird TD, Snutch TP. Spacey SD, et al. Ann Neurol. 2004 Aug;56(2):213-20. doi: 10.1002/ana.20169. Ann Neurol. 2004. PMID: 15293273

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