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SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum.
Goizet C, Boukhris A, Maltete D, Guyant-Maréchal L, Truchetto J, Mundwiller E, Hanein S, Jonveaux P, Roelens F, Loureiro J, Godet E, Forlani S, Melki J, Auer-Grumbach M, Fernandez JC, Martin-Hardy P, Sibon I, Sole G, Orignac I, Mhiri C, Coutinho P, Durr A, Brice A, Stevanin G. Goizet C, et al. Among authors: mhiri c. Neurology. 2009 Oct 6;73(14):1111-9. doi: 10.1212/WNL.0b013e3181bacf59. Neurology. 2009. PMID: 19805727
[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. Among authors: mhiri c. 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: mhiri c. 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.
[Lupic spinal cord diseases and antiphospholipid antibodies].
Feki I, Ben Hmida M, Masmoudi H, Triki C, Bahloul Z, Hachicha J, Jlidi R, Mhiri C. Feki I, et al. Among authors: mhiri c. Rev Neurol (Paris). 1997 Mar;153(2):138-40. Rev Neurol (Paris). 1997. PMID: 9296127 French.
160 results