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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: rouleau ga. Muscle Nerve. 2003 Dec;28(6):774-5. doi: 10.1002/mus.10498. Muscle Nerve. 2003. PMID: 14639597 No abstract available.
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: rouleau ga. 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.
[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. 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.
Genetics of familial and sporadic amyotrophic lateral sclerosis.
Gros-Louis F, Gaspar C, Rouleau GA. Gros-Louis F, et al. Among authors: rouleau ga. Biochim Biophys Acta. 2006 Nov-Dec;1762(11-12):956-72. doi: 10.1016/j.bbadis.2006.01.004. Epub 2006 Feb 10. Biochim Biophys Acta. 2006. PMID: 16503123 Free article. Review.
826 results