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Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families.
Mov Disord. 2007 Jan;22(1):55-61. doi: 10.1002/mds.21180.
Mov Disord. 2007.
PMID: 17115391
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study.
Hulihan MM, Ishihara-Paul L, Kachergus J, Warren L, Amouri R, Elango R, Prinjha RK, Upmanyu R, Kefi M, Zouari M, Sassi SB, Yahmed SB, El Euch-Fayeche G, Matthews PM, Middleton LT, Gibson RA, Hentati F, Farrer MJ.
Hulihan MM, et al. Among authors: el euch fayeche g.
Lancet Neurol. 2008 Jul;7(7):591-4. doi: 10.1016/S1474-4422(08)70116-9. Epub 2008 Jun 6.
Lancet Neurol. 2008.
PMID: 18539535
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A novel SACS gene mutation in a Tunisian family.
Bouhlal Y, El Euch-Fayeche G, Hentati F, Amouri R.
Bouhlal Y, et al. Among authors: el euch fayeche g.
J Mol Neurosci. 2009 Nov;39(3):333-6. doi: 10.1007/s12031-009-9212-9. Epub 2009 Jun 16.
J Mol Neurosci. 2009.
PMID: 19529988
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PINK1 mutations and parkinsonism.
Ishihara-Paul L, Hulihan MM, Kachergus J, Upmanyu R, Warren L, Amouri R, Elango R, Prinjha RK, Soto A, Kefi M, Zouari M, Sassi SB, Yahmed SB, El Euch-Fayeche G, Matthews PM, Middleton LT, Gibson RA, Hentati F, Farrer MJ.
Ishihara-Paul L, et al. Among authors: el euch fayeche g.
Neurology. 2008 Sep 16;71(12):896-902. doi: 10.1212/01.wnl.0000323812.40708.1f. Epub 2008 Aug 6.
Neurology. 2008.
PMID: 18685134
Free PMC article.
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Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overview.
Bouhlal Y, Amouri R, El Euch-Fayeche G, Hentati F.
Bouhlal Y, et al. Among authors: el euch fayeche g.
Parkinsonism Relat Disord. 2011 Jul;17(6):418-22. doi: 10.1016/j.parkreldis.2011.03.005. Epub 2011 Mar 30.
Parkinsonism Relat Disord. 2011.
PMID: 21450511
Review.
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Distinct phenotypes within autosomal recessive ataxias not linked to already known loci.
Bouhlal Y, El-Euch-Fayeche G, Amouri R, Hentati F.
Bouhlal Y, et al. Among authors: el euch fayeche g.
Acta Myol. 2005 Oct;24(2):155-61.
Acta Myol. 2005.
PMID: 16550933
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