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, 2002
Christos Proukakis   +2 more
exaly  

Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene

European Journal of Neurology, 2017
M. Krenn   +9 more
semanticscholar   +1 more source

Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms

Lancet Neurology, The, 2008
Sara Salinas   +2 more
exaly  

Heart rate and oxygen demand of powered exoskeleton-assisted walking in persons with paraplegia.

Journal of rehabilitation research and development, 2015
P. Asselin   +6 more
semanticscholar   +1 more source

Intention-based walking support for paraplegia patients with Robot Suit HAL

Advanced Robotics, 2007
Hiroaki Kawamoto   +2 more
exaly  

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)

Human Mutation, 2010
Matthias Eckhardt   +2 more
exaly  

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