Design, Control and Applications of Mechatronic Systems in Engineering 2017
DOI: 10.5772/67458
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Design and Motion Control of a Lower Limb Robotic Exoskeleton

Abstract: This chapter presents the results of research work on design, actuator selection and motion control of a lower extremity exoskeleton developed to provide legged mobility to spinal cord injured (SCI) individuals. The exoskeleton has two degrees of freedom per leg. Hip and knee joints are actuated in the sagittal plane by using DC servomotors. Additional effort supplied by user's arms through crutches is defined as user support rate (USR). Experimentally determined USR values are considered in actuator torque co… Show more

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Cited by 12 publications
(5 citation statements)
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“…Connecting Cables are linked with sensor placement. An IMU is mounted on each joint of the exoskeleton which are securely attached and aligned with the axis of rotation of the joint [17].…”
Section: Introductionmentioning
confidence: 99%
“…Connecting Cables are linked with sensor placement. An IMU is mounted on each joint of the exoskeleton which are securely attached and aligned with the axis of rotation of the joint [17].…”
Section: Introductionmentioning
confidence: 99%
“…The origin of ALS in 5-10% of the cases is familial (fALS), while the rest of the patients diagnosed with ALS have a sporadic disease (sALS) [84]. However, the two are clinically undistinguishable from each other [85]. The survival time after first symptoms for 50% of the patients is below 30 months, while only 20% of patients survive after 5 years and a small percentage live for more than 10 years [86].…”
Section: Ii2 Amyotrophic Lateral Sclerosismentioning
confidence: 99%
“…The scientific interest to investigate the disease started to raise in the 90"s, after some new insights in the glutamate neurotransmitter system and the discovery of genes linked to the development of familial ALS [84]. Since then several genetic studies have dealt with the ALS, revealing the involvement of mutations in the genes of SOD1, TARDBP and FUS, but also a genetic defect in a noncoding nucleotide sequence was associated with ALS [85].…”
Section: Ii2 Amyotrophic Lateral Sclerosismentioning
confidence: 99%
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