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Clinical Genetics|January 11, 2011
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutationsA Arnoldi, C Crimella, E Tenderini, et al.Journal of Autoimmunity|January 28, 2009
Neurolupus is associated with anti-ribosomal P protein antibodies: an inception cohort studyC Briani, M Lucchetta, A Ghirardello, et al.Neurology|March 15, 2006
Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutationR Del Bo, F Locatelli, S Corti, et al.Neurology|July 30, 2008
The extracellular matrix affects axonal regeneration in peripheral neuropathiesS C Previtali, M C Malaguti, N Riva, et al.Clinical Genetics|June 1, 2011
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2C Crimella, C Baschirotto, A Arnoldi, et al.Pageof 2