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Page 1
A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.
Boukhris A, Feki I, Elleuch N, Miladi MI, Boland-Augé A, Truchetto J, Mundwiller E, Jezequel N, Zelenika D, Mhiri C, Brice A, Stevanin G. Boukhris A, et al. Among authors: miladi mi. Neurogenetics. 2010 Oct;11(4):441-8. doi: 10.1007/s10048-010-0249-2. Epub 2010 Jul 1. Neurogenetics. 2010. PMID: 20593214
[Cardiac involvement in Steinert myotonic dystrophy].
Miladi MI, Charfeddine H, Feki I, Turki E, Elleuch N, Trabelsi I, Krichène S, Kammoun S, Mhiri C. Miladi MI, et al. Rev Med Interne. 2009 Jul;30(7):573-7. doi: 10.1016/j.revmed.2009.01.017. Epub 2009 Mar 14. Rev Med Interne. 2009. PMID: 19286286 French.
[Multiple arterial thrombosis in Behçet's disease].
Kallel A, Miladi MI, Marzouk S, Feki I, Bahloul Z, Mhiri C. Kallel A, et al. Among authors: miladi mi. Rev Med Interne. 2010 Jun;31(6):e1-4. doi: 10.1016/j.revmed.2009.05.012. Epub 2010 Apr 1. Rev Med Interne. 2010. PMID: 20362364 French.
14 results