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2001 1
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Page 1
[Isoniazid-induced myopathy].
Chaouch N, Mejid M, Zarrouk M, Racil H, Rouhou SC, El Euch G, Chabbou A. Chaouch N, et al. Among authors: el euch g. Rev Pneumol Clin. 2011 Dec;67(6):354-8. doi: 10.1016/j.pneumo.2010.05.001. Epub 2010 Dec 3. Rev Pneumol Clin. 2011. PMID: 22137279 French.
Ataxia with vitamin E deficiency and abetalipoproteinemia.
Hentati F, El-Euch G, Bouhlal Y, Amouri R. Hentati F, et al. Among authors: el euch g. Handb Clin Neurol. 2012;103:295-305. doi: 10.1016/B978-0-444-51892-7.00018-8. Handb Clin Neurol. 2012. PMID: 21827896 Review. No abstract available.
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa.
Jasinska-Myga B, Kachergus J, Vilariño-Güell C, Wider C, Soto-Ortolaza AI, Kefi M, Middleton LT, Ishihara-Paul L, Gibson RA, Amouri R, Yahmed SB, Sassi SB, Zouari M, El Euch G, Ross OA, Hentati F, Farrer MJ. Jasinska-Myga B, et al. Among authors: el euch g. Mov Disord. 2010 Oct 15;25(13):2052-8. doi: 10.1002/mds.23283. Mov Disord. 2010. PMID: 20721913
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease.
Nishioka K, Kefi M, Jasinska-Myga B, Wider C, Vilariño-Güell C, Ross OA, Heckman MG, Middleton LT, Ishihara-Paul L, Gibson RA, Amouri R, Ben Yahmed S, Ben Sassi S, Zouari M, El Euch G, Farrer MJ, Hentati F. Nishioka K, et al. Among authors: el euch g. J Neurol Neurosurg Psychiatry. 2010 Apr;81(4):391-5. doi: 10.1136/jnnp.2009.185231. Epub 2009 Sep 2. J Neurol Neurosurg Psychiatry. 2010. PMID: 19726410
Aprataxin gene mutations in Tunisian families.
Amouri R, Moreira MC, Zouari M, El Euch G, Barhoumi C, Kefi M, Belal S, Koenig M, Hentati F. Amouri R, et al. Among authors: el euch g. Neurology. 2004 Sep 14;63(5):928-9. doi: 10.1212/01.wnl.0000137044.06573.46. Neurology. 2004. PMID: 15365154