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Manoj P Menezes

Showing results (21-30 of 68) with videos related to

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Neuromuscular Disorders : NMD|January 25, 2015
ResponseManoj P Menezes, Leigh Waddell, Guy M Lenk, et al.
Muscle & Nerve|September 29, 2018
Magnetic resonance imaging of the anterior compartment of the lower leg is a biomarker for weakness, disability, and impaired gait in childhood Charcot-Marie-Tooth diseaseKayla M D Cornett, Elizabeth Wojciechowski, Amy D Sman, et al.
Journal of Foot and Ankle Research|February 19, 2019
Feasibility of designing, manufacturing and delivering 3D printed ankle-foot orthoses: a systematic reviewElizabeth Wojciechowski, Angela Y Chang, Daniel Balassone, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 21, 2015
Pathophysiology of motor dysfunction in a childhood motor neuron disease caused by mutations in the riboflavin transporterManoj P Menezes, Michelle A Farrar, Richard Webster, et al.
Neuromuscular Disorders : NMD|March 23, 2024
Rare homozygous disease-associated sequence variants in children with spinal muscular atrophy: a phenotypic description and review of the literatureLimin Li, Manoj P Menezes, Melanie Smith, et al.
Gait & Posture|May 21, 2022
Replicating and redesigning ankle-foot orthoses with 3D printing for children with Charcot-Marie-Tooth diseaseElizabeth A Wojciechowski, Tegan L Cheng, Sean M Hogan, et al.
Developmental Medicine and Child Neurology|January 28, 2016
Eye movement disorders are an early manifestation of CACNA1A mutations in childrenEsther M Tantsis, Deepak Gill, Lyn Griffiths, et al.
Neuromuscular Disorders : NMD|March 16, 2013
Rapidly progressive asymmetrical weakness in Charcot-Marie-Tooth disease type 4J resembles chronic inflammatory demyelinating polyneuropathyEllen Cottenie, Manoj P Menezes, Alexander M Rossor, et al.
Mitochondrion|August 1, 2016
Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial diseaseManoj P Menezes, Shamima Rahman, Kaustuv Bhattacharya, et al.
Annals of Clinical and Translational Neurology|February 19, 2026
Ketogenic Diet as an Epigenetic Therapy in SETD1B-Related EpilepsyErica Tsang, Brian S Gloss, Jessica P Hayes, et al.
Pageof 7

Showing results (21-30 of 68) with videos related to

Sort By:
Pageof 7
Neuromuscular Disorders : NMD|January 25, 2015
ResponseManoj P Menezes, Leigh Waddell, Guy M Lenk, et al.
Muscle & Nerve|September 29, 2018
Magnetic resonance imaging of the anterior compartment of the lower leg is a biomarker for weakness, disability, and impaired gait in childhood Charcot-Marie-Tooth diseaseKayla M D Cornett, Elizabeth Wojciechowski, Amy D Sman, et al.
Journal of Foot and Ankle Research|February 19, 2019
Feasibility of designing, manufacturing and delivering 3D printed ankle-foot orthoses: a systematic reviewElizabeth Wojciechowski, Angela Y Chang, Daniel Balassone, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 21, 2015
Pathophysiology of motor dysfunction in a childhood motor neuron disease caused by mutations in the riboflavin transporterManoj P Menezes, Michelle A Farrar, Richard Webster, et al.
Neuromuscular Disorders : NMD|March 23, 2024
Rare homozygous disease-associated sequence variants in children with spinal muscular atrophy: a phenotypic description and review of the literatureLimin Li, Manoj P Menezes, Melanie Smith, et al.
Gait & Posture|May 21, 2022
Replicating and redesigning ankle-foot orthoses with 3D printing for children with Charcot-Marie-Tooth diseaseElizabeth A Wojciechowski, Tegan L Cheng, Sean M Hogan, et al.
Developmental Medicine and Child Neurology|January 28, 2016
Eye movement disorders are an early manifestation of CACNA1A mutations in childrenEsther M Tantsis, Deepak Gill, Lyn Griffiths, et al.
Neuromuscular Disorders : NMD|March 16, 2013
Rapidly progressive asymmetrical weakness in Charcot-Marie-Tooth disease type 4J resembles chronic inflammatory demyelinating polyneuropathyEllen Cottenie, Manoj P Menezes, Alexander M Rossor, et al.
Mitochondrion|August 1, 2016
Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial diseaseManoj P Menezes, Shamima Rahman, Kaustuv Bhattacharya, et al.
Annals of Clinical and Translational Neurology|February 19, 2026
Ketogenic Diet as an Epigenetic Therapy in SETD1B-Related EpilepsyErica Tsang, Brian S Gloss, Jessica P Hayes, et al.
Pageof 7