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

Year Number of Results
1998 2
1999 2
2000 1
2001 2
2002 3
2003 2
2004 1
2008 2
2009 1
2010 1
2011 4
2012 2
2015 1
2024 0

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Page 1
[Superoxyde dismutase 1 gene abnormalities in familial amyotrophic lateral sclerosis: phenotype/genotype correlations. The French experience and review of the literature].
Jafari-Schluep HF, Khoris J, Mayeux-Portas V, Hand C, Rouleau G, Camu W; Groupe Français d'Etude des Maladies du Motoneurone. Jafari-Schluep HF, et al. Among authors: khoris j. Rev Neurol (Paris). 2004 Jan;160(1):44-50. doi: 10.1016/s0035-3787(04)70846-2. Rev Neurol (Paris). 2004. PMID: 14978393 Review. French.
How to Capitalize on the Retest Effect in Future Trials on Huntington's Disease.
Schramm C, Katsahian S, Youssov K, Démonet JF, Krystkowiak P, Supiot F, Verny C, Cleret de Langavant L, Bachoud-Lévi AC; European Huntington's Disease Initiative Study Group and the Multicentre Intracerebral Grafting in Huntington's Disease Group. Schramm C, et al. PLoS One. 2015 Dec 29;10(12):e0145842. doi: 10.1371/journal.pone.0145842. eCollection 2015. PLoS One. 2015. PMID: 26714284 Free PMC article. Clinical Trial.
A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.
Hand CK, Khoris J, Salachas F, Gros-Louis F, Lopes AA, Mayeux-Portas V, Brewer CG, Brown RH Jr, Meininger V, Camu W, Rouleau GA. Hand CK, et al. Among authors: khoris j. Am J Hum Genet. 2002 Jan;70(1):251-6. doi: 10.1086/337945. Epub 2001 Nov 9. Am J Hum Genet. 2002. PMID: 11706389 Free PMC article.
Absence of mutations in the hypoxia response element of VEGF in ALS.
Gros-Louis F, Laurent S, Lopes AA, Khoris J, Meininger V, Camu W, Rouleau GA. Gros-Louis F, et al. Among authors: khoris j. Muscle Nerve. 2003 Dec;28(6):774-5. doi: 10.1002/mus.10498. Muscle Nerve. 2003. PMID: 14639597 No abstract available.
21 results