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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 2
1997 1
1998 1
2000 4
2001 1
2002 1
2003 5
2004 1
2005 2
2006 3
2007 2
2008 5
2009 4
2010 7
2011 6
2012 5
2013 6
2014 4
2015 1
2016 2
2017 1
2019 1
2020 1
2022 1
2023 3
2024 4

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64 results

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Page 1
Giant axonal neuropathy.
Hentati F, Hentati E, Amouri R. Hentati F, et al. Among authors: amouri r. Handb Clin Neurol. 2013;115:933-8. doi: 10.1016/B978-0-444-52902-2.00052-7. Handb Clin Neurol. 2013. PMID: 23931822 Review.
A Tunisian patient with CLCN2-related leukoencephalopathy.
Ben Mohamed D, Saied Z, Ben Sassi S, Ben Said M, Nabli F, Achouri A, Jeridi C, Masmoudi S, Amouri R. Ben Mohamed D, et al. Among authors: amouri r. Clin Case Rep. 2022 Dec 26;10(12):e6737. doi: 10.1002/ccr3.6737. eCollection 2022 Dec. Clin Case Rep. 2022. PMID: 36583195 Free PMC article.
Ataxia with vitamin E deficiency and abetalipoproteinemia.
Hentati F, El-Euch G, Bouhlal Y, Amouri R. Hentati F, et al. Among authors: amouri r. 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.
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: amouri r. 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.
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase.
Gustavsson EK, Follett J, Trinh J, Barodia SK, Real R, Liu Z, Grant-Peters M, Fox JD, Appel-Cresswell S, Stoessl AJ, Rajput A, Rajput AH, Auer R, Tilney R, Sturm M, Haack TB, Lesage S, Tesson C, Brice A, Vilariño-Güell C, Ryten M, Goldberg MS, West AB, Hu MT, Morris HR, Sharma M, Gan-Or Z, Samanci B, Lis P, Tocino T, Amouri R, Sassi SB, Hentati F; Global Parkinson’s Genetics Program (GP2); Tonelli F, Alessi DR, Farrer MJ. Gustavsson EK, et al. Among authors: amouri r. medRxiv [Preprint]. 2024 Jan 18:2024.01.17.24300927. doi: 10.1101/2024.01.17.24300927. medRxiv. 2024. PMID: 38293014 Free PMC article. Preprint.
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: amouri r. 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.
64 results