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European Journal of Neurology
|
June 27, 2025
Longitudinal Assessment of 4-Year HFMSE Changes in SMA II and III Patients Treated With Nusinersen
Giorgia Coratti, Francesca Bovis, Marika Pane, et al.
Journal of Neuromuscular Diseases
|
March 1, 2024
Disease Trajectories in the Revised Hammersmith Scale in a Cohort of Untreated Patients with Spinal Muscular Atrophy types 2 and 3
Amy Wolfe, Georgia Stimpson, Danielle Ramsey, et al.
Muscle & Nerve
|
July 30, 2021
Different trajectories in upper limb and gross motor function in spinal muscular atrophy
Giorgia Coratti, Maria Carmela Pera, Jacqueline Montes, et al.
Neuromuscular Disorders : NMD
|
January 4, 2022
Revised upper limb module in type II and III spinal muscular atrophy: 24-month changes
Giorgia Coratti, Maria Carmela Pera, Jacqueline Montes, et al.
American Journal of Human Genetics
|
November 26, 2013
Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy
Vandana A Gupta, Gianina Ravenscroft, Ranad Shaheen, et al.
European Journal of Neurology
|
October 11, 2024
Long-term natural history in type II and III spinal muscular atrophy: a 4-year international study on the Hammersmith Functional Motor Scale Expanded
Giorgia Coratti, Francesca Bovis, Maria Carmela Pera, et al.
Journal of Comparative Effectiveness Research
|
August 28, 2020
Meta-analyses of ataluren randomized controlled trials in nonsense mutation Duchenne muscular dystrophy
Craig Campbell, Richard J Barohn, Enrico Bertini, et al.
Acta Neuropathologica
|
February 17, 2023
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy
Andres Nascimento, Christine C Bruels, Sandra Donkervoort, et al.
American Journal of Human Genetics
|
October 1, 1989
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion
M Koenig, A H Beggs, M Moyer, et al.
Neuromuscular Disorders : NMD
|
June 4, 2013
Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network
Anne M Connolly, Julaine M Florence, Mary M Cradock, et al.
Page
of 31
Search research articles
Search
Showing results (281-290 of 303) with videos related to
Sort By:
Page
of 31
European Journal of Neurology
|
June 27, 2025
Longitudinal Assessment of 4-Year HFMSE Changes in SMA II and III Patients Treated With Nusinersen
Giorgia Coratti, Francesca Bovis, Marika Pane, et al.
Journal of Neuromuscular Diseases
|
March 1, 2024
Disease Trajectories in the Revised Hammersmith Scale in a Cohort of Untreated Patients with Spinal Muscular Atrophy types 2 and 3
Amy Wolfe, Georgia Stimpson, Danielle Ramsey, et al.
Muscle & Nerve
|
July 30, 2021
Different trajectories in upper limb and gross motor function in spinal muscular atrophy
Giorgia Coratti, Maria Carmela Pera, Jacqueline Montes, et al.
Neuromuscular Disorders : NMD
|
January 4, 2022
Revised upper limb module in type II and III spinal muscular atrophy: 24-month changes
Giorgia Coratti, Maria Carmela Pera, Jacqueline Montes, et al.
American Journal of Human Genetics
|
November 26, 2013
Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy
Vandana A Gupta, Gianina Ravenscroft, Ranad Shaheen, et al.
European Journal of Neurology
|
October 11, 2024
Long-term natural history in type II and III spinal muscular atrophy: a 4-year international study on the Hammersmith Functional Motor Scale Expanded
Giorgia Coratti, Francesca Bovis, Maria Carmela Pera, et al.
Journal of Comparative Effectiveness Research
|
August 28, 2020
Meta-analyses of ataluren randomized controlled trials in nonsense mutation Duchenne muscular dystrophy
Craig Campbell, Richard J Barohn, Enrico Bertini, et al.
Acta Neuropathologica
|
February 17, 2023
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy
Andres Nascimento, Christine C Bruels, Sandra Donkervoort, et al.
American Journal of Human Genetics
|
October 1, 1989
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion
M Koenig, A H Beggs, M Moyer, et al.
Neuromuscular Disorders : NMD
|
June 4, 2013
Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network
Anne M Connolly, Julaine M Florence, Mary M Cradock, et al.
Page
of 31