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Mental Retardation and Developmental Disabilities Research Reviews
|
June 30, 2006
Childhood multiple sclerosis: a review
Amy Waldman, Erin O'Connor, Gihan Tennekoon
The Pediatric Infectious Disease Journal
|
December 29, 2007
Hemosiderin-laden macrophages in the cerebrospinal fluid of a neonate after traumatic lumbar puncture
Courtney J Wusthoff, Nicholas S Abend, Gihan Tennekoon
Journal of Child Neurology
|
July 27, 2012
Unanswered questions in Friedreich ataxia
David R Lynch, Eric C Deutsch, Robert B Wilson, et al.
Journal of Neurosurgery
|
September 26, 2002
Conus medulla-cauda compression from nerve root hypertrophy in a child with Dejerine-Sottas syndrome: improvement with laminectomy and duraplasty. Case report
Kleopas A Kleopa, Leslie N Sutton, Joseph Ong, et al.
The American Journal of Occupational Therapy : Official Publication of the American Occupational Therapy Association
|
February 11, 2018
Use of the Wilmington Robotic Exoskeleton to Improve Upper Extremity Function in Patients With Duchenne Muscular Dystrophy
Timothy Estilow, Allan M Glanzman, Kacy Powers, et al.
American Journal of Physical Medicine & Rehabilitation
|
March 21, 2020
Retrospective Analysis of Fractures and Factors Causing Ambulation Loss After Lower Limb Fractures in Duchenne Muscular Dystrophy
Sulenur Yildiz, Allan M Glanzman, Tim Estilow, et al.
Journal of Neuropathology and Experimental Neurology
|
December 4, 2014
Spectrum of neuropathophysiology in spinal muscular atrophy type I
Brian N Harding, Shingo Kariya, Umrao R Monani, et al.
Journal of Neuromuscular Diseases
|
November 20, 2018
Phase 1 Study of Edasalonexent (CAT-1004), an Oral NF-κB Inhibitor, in Pediatric Patients with Duchenne Muscular Dystrophy
Erika Finanger, Krista Vandenborne, Richard S Finkel, et al.
Neurology
|
April 5, 2013
Severe congenital RYR1-associated myopathy: the expanding clinicopathologic and genetic spectrum
Diana Xerxes Bharucha-Goebel, Mariarita Santi, Livija Medne, et al.
Journal of Pediatric Rehabilitation Medicine
|
March 12, 2016
Physical therapy services received by individuals with spinal muscular atrophy (SMA)
Sally Dunaway, Jacqueline Montes, Michael P McDermott, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Mental Retardation and Developmental Disabilities Research Reviews
|
June 30, 2006
Childhood multiple sclerosis: a review
Amy Waldman, Erin O'Connor, Gihan Tennekoon
The Pediatric Infectious Disease Journal
|
December 29, 2007
Hemosiderin-laden macrophages in the cerebrospinal fluid of a neonate after traumatic lumbar puncture
Courtney J Wusthoff, Nicholas S Abend, Gihan Tennekoon
Journal of Child Neurology
|
July 27, 2012
Unanswered questions in Friedreich ataxia
David R Lynch, Eric C Deutsch, Robert B Wilson, et al.
Journal of Neurosurgery
|
September 26, 2002
Conus medulla-cauda compression from nerve root hypertrophy in a child with Dejerine-Sottas syndrome: improvement with laminectomy and duraplasty. Case report
Kleopas A Kleopa, Leslie N Sutton, Joseph Ong, et al.
The American Journal of Occupational Therapy : Official Publication of the American Occupational Therapy Association
|
February 11, 2018
Use of the Wilmington Robotic Exoskeleton to Improve Upper Extremity Function in Patients With Duchenne Muscular Dystrophy
Timothy Estilow, Allan M Glanzman, Kacy Powers, et al.
American Journal of Physical Medicine & Rehabilitation
|
March 21, 2020
Retrospective Analysis of Fractures and Factors Causing Ambulation Loss After Lower Limb Fractures in Duchenne Muscular Dystrophy
Sulenur Yildiz, Allan M Glanzman, Tim Estilow, et al.
Journal of Neuropathology and Experimental Neurology
|
December 4, 2014
Spectrum of neuropathophysiology in spinal muscular atrophy type I
Brian N Harding, Shingo Kariya, Umrao R Monani, et al.
Journal of Neuromuscular Diseases
|
November 20, 2018
Phase 1 Study of Edasalonexent (CAT-1004), an Oral NF-κB Inhibitor, in Pediatric Patients with Duchenne Muscular Dystrophy
Erika Finanger, Krista Vandenborne, Richard S Finkel, et al.
Neurology
|
April 5, 2013
Severe congenital RYR1-associated myopathy: the expanding clinicopathologic and genetic spectrum
Diana Xerxes Bharucha-Goebel, Mariarita Santi, Livija Medne, et al.
Journal of Pediatric Rehabilitation Medicine
|
March 12, 2016
Physical therapy services received by individuals with spinal muscular atrophy (SMA)
Sally Dunaway, Jacqueline Montes, Michael P McDermott, et al.
Page
of 3