Proukakis C - Search Results

1

A novel α-synuclein missense mutation in Parkinson disease.

Proukakis C, Dudzik CG, Brier T, MacKay DS, Cooper JM, Millhauser GL, Houlden H, Schapira AH. Proukakis C, et al. Neurology. 2013 Mar 12;80(11):1062-4. doi: 10.1212/WNL.0b013e31828727ba. Epub 2013 Feb 20. Neurology. 2013. PMID: 23427326 Free PMC article.

2

A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia.

Warner TT, Patel H, Proukakis C, Reed JA, McKie L, Wills A, Patton MA, Crosby AH. Warner TT, et al. Among authors: proukakis c. J Neurol. 2004 Sep;251(9):1068-74. doi: 10.1007/s00415-004-0401-8. J Neurol. 2004. PMID: 15372247

3

Human spastin has multiple microtubule-related functions.

Salinas S, Carazo-Salas RE, Proukakis C, Cooper JM, Weston AE, Schiavo G, Warner TT. Salinas S, et al. Among authors: proukakis c. J Neurochem. 2005 Dec;95(5):1411-20. doi: 10.1111/j.1471-4159.2005.03472.x. Epub 2005 Oct 7. J Neurochem. 2005. PMID: 16219033 Free article.

4

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35).

Dick KJ, Eckhardt M, Paisán-Ruiz C, Alshehhi AA, Proukakis C, Sibtain NA, Maier H, Sharifi R, Patton MA, Bashir W, Koul R, Raeburn S, Gieselmann V, Houlden H, Crosby AH. Dick KJ, et al. Among authors: proukakis c. Hum Mutat. 2010 Apr;31(4):E1251-60. doi: 10.1002/humu.21205. Hum Mutat. 2010. PMID: 20104589

5

Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin (SPAST) mutations is found more often in males.

Proukakis C, Moore D, Labrum R, Wood NW, Houlden H. Proukakis C, et al. J Neurol Sci. 2011 Jul 15;306(1-2):62-5. doi: 10.1016/j.jns.2011.03.043. Epub 2011 May 5. J Neurol Sci. 2011. PMID: 21546041 Review.

6

Hyposmia and cognitive impairment in Gaucher disease patients and carriers.

McNeill A, Duran R, Proukakis C, Bras J, Hughes D, Mehta A, Hardy J, Wood NW, Schapira AH. McNeill A, et al. Among authors: proukakis c. Mov Disord. 2012 Apr;27(4):526-32. doi: 10.1002/mds.24945. Epub 2012 Feb 16. Mov Disord. 2012. PMID: 22344629 Free PMC article.

7

α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?

Kiely AP, Asi YT, Kara E, Limousin P, Ling H, Lewis P, Proukakis C, Quinn N, Lees AJ, Hardy J, Revesz T, Houlden H, Holton JL. Kiely AP, et al. Among authors: proukakis c. Acta Neuropathol. 2013 May;125(5):753-69. doi: 10.1007/s00401-013-1096-7. Epub 2013 Feb 12. Acta Neuropathol. 2013. PMID: 23404372 Free PMC article.

8

α-Synuclein mutations cluster around a putative protein loop.

Kara E, Lewis PA, Ling H, Proukakis C, Houlden H, Hardy J. Kara E, et al. Among authors: proukakis c. Neurosci Lett. 2013 Jun 24;546:67-70. doi: 10.1016/j.neulet.2013.04.058. Epub 2013 May 10. Neurosci Lett. 2013. PMID: 23669636 Free PMC article.

9

Somatic alpha-synuclein mutations in Parkinson's disease: hypothesis and preliminary data.

Proukakis C, Houlden H, Schapira AH. Proukakis C, et al. Mov Disord. 2013 Jun;28(6):705-12. doi: 10.1002/mds.25502. Epub 2013 May 14. Mov Disord. 2013. PMID: 23674490 Free PMC article.

10

Genetics of Parkinson's disease: alpha-synuclein and other insights from Greece.

Proukakis C. Proukakis C. Eur J Neurol. 2014 Jul;21(7):946-7. doi: 10.1111/ene.12357. Epub 2014 Jan 25. Eur J Neurol. 2014. PMID: 24460978 No abstract available.

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