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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.
Azzedine H, Ravisé N, Verny C, Gabrëels-Festen A, Lammens M, Grid D, Vallat JM, Durosier G, Senderek J, Nouioua S, Hamadouche T, Bouhouche A, Guilbot A, Stendel C, Ruberg M, Brice A, Birouk N, Dubourg O, Tazir M, LeGuern E. Azzedine H, et al. Among authors: tazir m. Neurology. 2006 Aug 22;67(4):602-6. doi: 10.1212/01.wnl.0000230225.19797.93. Neurology. 2006. PMID: 16924012
Autosomal-recessive Charcot-Marie-Tooth diseases.
Vallat JM, Tazir M, Magdelaine C, Sturtz F, Grid D. Vallat JM, et al. Among authors: tazir m. J Neuropathol Exp Neurol. 2005 May;64(5):363-70. doi: 10.1093/jnen/64.5.363. J Neuropathol Exp Neurol. 2005. PMID: 15892292 Review.
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease.
Dubourg O, Azzedine H, Verny C, Durosier G, Birouk N, Gouider R, Salih M, Bouhouche A, Thiam A, Grid D, Mayer M, Ruberg M, Tazir M, Brice A, LeGuern E. Dubourg O, et al. Among authors: tazir m. Neuromolecular Med. 2006;8(1-2):75-86. doi: 10.1385/nmm:8:1-2:75. Neuromolecular Med. 2006. PMID: 16775368 Review.
[Autosomal recessive forms of Charcot-Marie-Tooth disease].
Vallat JM, Grid D, Magdelaine C, Sturtz F, Levy N, Tazir M. Vallat JM, et al. Among authors: tazir m. Bull Acad Natl Med. 2005 Jan;189(1):55-68; discussion 68-9. Bull Acad Natl Med. 2005. PMID: 16119880 Review. French.
113 results