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BMC Musculoskeletal Disorders
|
November 27, 2007
LGMD2I in a North American population
Peter B Kang, Chris A Feener, Elicia Estrella, et al.
Genetics in Medicine Open
|
December 13, 2024
The diagnosis communication process in spinal muscular atrophy: A cross-cutting view of the new challenges facing the therapeutic era
Eulàlia Rovira-Moreno, Anna Abulí, Patricia Muñoz-Cabello, et al.
Pediatric Neurology
|
May 13, 2014
Cross-sectional evaluation of electrical impedance myography and quantitative ultrasound for the assessment of Duchenne muscular dystrophy in a clinical trial setting
Seward B Rutkove, Tom R Geisbush, Aleksandar Mijailovic, et al.
Muscle & Nerve
|
May 28, 2014
Quantitative muscle ultrasound in Duchenne muscular dystrophy: a comparison of techniques
Irina Shklyar, Tom R Geisbush, Aleksandar S Mijialovic, et al.
CNS Drugs
|
August 18, 2019
An Integrated Safety Analysis of Infants and Children with Symptomatic Spinal Muscular Atrophy (SMA) Treated with Nusinersen in Seven Clinical Trials
Basil T Darras, Michelle A Farrar, Eugenio Mercuri, et al.
JAMA Neurology
|
March 5, 2014
Comparison of plasmapheresis and intravenous immunoglobulin as maintenance therapies for juvenile myasthenia gravis
Wendy K M Liew, Christine A Powell, Steven R Sloan, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
April 26, 2021
Putting the patient first: The validity and value of surface-based electrical impedance myography techniques
Seward B Rutkove, Pushpa Narayanaswami, W David Arnold, et al.
Muscle & Nerve
|
July 21, 2018
Deflazacort versus prednisone/prednisolone for maintaining motor function and delaying loss of ambulation: A post HOC analysis from the ACT DMD trial
Perry B Shieh, Joseph Mcintosh, Fengbin Jin, et al.
Journal of Comparative Effectiveness Research
|
October 25, 2021
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy
Perry B Shieh, Gary Elfring, Panayiota Trifillis, et al.
Neuromuscular Disorders : NMD
|
April 28, 2018
Comprehensive nutritional and metabolic assessment in patients with spinal muscular atrophy: Opportunity for an individualized approach
Enid E Martinez, Nicolle Quinn, Kayla Arouchon, et al.
Page
of 23
Search research articles
Search
Showing results (91-100 of 222) with videos related to
Sort By:
Page
of 23
BMC Musculoskeletal Disorders
|
November 27, 2007
LGMD2I in a North American population
Peter B Kang, Chris A Feener, Elicia Estrella, et al.
Genetics in Medicine Open
|
December 13, 2024
The diagnosis communication process in spinal muscular atrophy: A cross-cutting view of the new challenges facing the therapeutic era
Eulàlia Rovira-Moreno, Anna Abulí, Patricia Muñoz-Cabello, et al.
Pediatric Neurology
|
May 13, 2014
Cross-sectional evaluation of electrical impedance myography and quantitative ultrasound for the assessment of Duchenne muscular dystrophy in a clinical trial setting
Seward B Rutkove, Tom R Geisbush, Aleksandar Mijailovic, et al.
Muscle & Nerve
|
May 28, 2014
Quantitative muscle ultrasound in Duchenne muscular dystrophy: a comparison of techniques
Irina Shklyar, Tom R Geisbush, Aleksandar S Mijialovic, et al.
CNS Drugs
|
August 18, 2019
An Integrated Safety Analysis of Infants and Children with Symptomatic Spinal Muscular Atrophy (SMA) Treated with Nusinersen in Seven Clinical Trials
Basil T Darras, Michelle A Farrar, Eugenio Mercuri, et al.
JAMA Neurology
|
March 5, 2014
Comparison of plasmapheresis and intravenous immunoglobulin as maintenance therapies for juvenile myasthenia gravis
Wendy K M Liew, Christine A Powell, Steven R Sloan, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
April 26, 2021
Putting the patient first: The validity and value of surface-based electrical impedance myography techniques
Seward B Rutkove, Pushpa Narayanaswami, W David Arnold, et al.
Muscle & Nerve
|
July 21, 2018
Deflazacort versus prednisone/prednisolone for maintaining motor function and delaying loss of ambulation: A post HOC analysis from the ACT DMD trial
Perry B Shieh, Joseph Mcintosh, Fengbin Jin, et al.
Journal of Comparative Effectiveness Research
|
October 25, 2021
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy
Perry B Shieh, Gary Elfring, Panayiota Trifillis, et al.
Neuromuscular Disorders : NMD
|
April 28, 2018
Comprehensive nutritional and metabolic assessment in patients with spinal muscular atrophy: Opportunity for an individualized approach
Enid E Martinez, Nicolle Quinn, Kayla Arouchon, et al.
Page
of 23