Results 301 to 310 of about 113,489 (310)
Some of the next articles are maybe not open access.
SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia
Nature Genetics, 2002Christos Proukakis +2 more
exaly
Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms
Lancet Neurology, The, 2008Sara Salinas +2 more
exaly
Heart rate and oxygen demand of powered exoskeleton-assisted walking in persons with paraplegia.
Journal of rehabilitation research and development, 2015P. Asselin +6 more
semanticscholar +1 more source
Intention-based walking support for paraplegia patients with Robot Suit HAL
Advanced Robotics, 2007Hiroaki Kawamoto +2 more
exaly
Structural basis of microtubule severing by the hereditary spastic paraplegia protein spastin
Nature, 2008Antonina Roll-Mecak
exaly
Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)
Human Mutation, 2010Matthias Eckhardt +2 more
exaly

