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Neurology
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June 17, 2016
Disease burden and functional outcomes in congenital myotonic dystrophy: A cross-sectional study
Nicholas E Johnson, Russell Butterfield, Kiera Berggren, et al.
Developmental Medicine and Child Neurology
|
October 30, 2015
Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophy
Nicholas E Johnson, Anne-Berit Ekstrom, Craig Campbell, et al.
Developmental Medicine and Child Neurology
|
September 4, 2024
Parental diagnostic delay and developmental outcomes in congenital and childhood-onset myotonic dystrophy type 1
Federica Trucco, Emilio Albamonte, Marika Pane, et al.
BMC Neurology
|
March 16, 2024
Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD study
Amy Doody, Lindsay Alfano, Jordi Diaz-Manera, et al.
Muscle & Nerve
|
July 13, 2019
Patient-reported study of the impact of pediatric-onset myotonic dystrophy
Michael Hunter, Anne-Berit Ekstrom, Craig Campbell, et al.
Journal of Multidisciplinary Healthcare
|
October 21, 2016
Same-day physical therapy consults in an outpatient neuromuscular disease physician clinic
Evan M Pucillo, Nancy Christensen-Mayer, Shelly D Poole, et al.
Neuromuscular Disorders : NMD
|
December 28, 2021
Patient reported quality of life in limb girdle muscular dystrophy
Laurel V Kovalchick, Kameron Bates, Jeffrey Statland, et al.
Neuromuscular Disorders : NMD
|
May 21, 2022
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research Network
Pangaja Paramsothy, Yinding Wang, Bo Cai, et al.
Journal of the Peripheral Nervous System : JPNS
|
June 9, 2020
Validation of the Italian version of the Charcot-Marie-Tooth Health Index
Chiara Pisciotta, Emma Ciafaloni, Riccardo Zuccarino, et al.
Neurology. Clinical Practice
|
November 22, 2019
Consensus-based care recommendations for congenital and childhood-onset myotonic dystrophy type 1
Nicholas E Johnson, Eugenio Zapata Aldana, Nathalie Angeard, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 110) with videos related to
Sort By:
Page
of 11
Neurology
|
June 17, 2016
Disease burden and functional outcomes in congenital myotonic dystrophy: A cross-sectional study
Nicholas E Johnson, Russell Butterfield, Kiera Berggren, et al.
Developmental Medicine and Child Neurology
|
October 30, 2015
Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophy
Nicholas E Johnson, Anne-Berit Ekstrom, Craig Campbell, et al.
Developmental Medicine and Child Neurology
|
September 4, 2024
Parental diagnostic delay and developmental outcomes in congenital and childhood-onset myotonic dystrophy type 1
Federica Trucco, Emilio Albamonte, Marika Pane, et al.
BMC Neurology
|
March 16, 2024
Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD study
Amy Doody, Lindsay Alfano, Jordi Diaz-Manera, et al.
Muscle & Nerve
|
July 13, 2019
Patient-reported study of the impact of pediatric-onset myotonic dystrophy
Michael Hunter, Anne-Berit Ekstrom, Craig Campbell, et al.
Journal of Multidisciplinary Healthcare
|
October 21, 2016
Same-day physical therapy consults in an outpatient neuromuscular disease physician clinic
Evan M Pucillo, Nancy Christensen-Mayer, Shelly D Poole, et al.
Neuromuscular Disorders : NMD
|
December 28, 2021
Patient reported quality of life in limb girdle muscular dystrophy
Laurel V Kovalchick, Kameron Bates, Jeffrey Statland, et al.
Neuromuscular Disorders : NMD
|
May 21, 2022
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research Network
Pangaja Paramsothy, Yinding Wang, Bo Cai, et al.
Journal of the Peripheral Nervous System : JPNS
|
June 9, 2020
Validation of the Italian version of the Charcot-Marie-Tooth Health Index
Chiara Pisciotta, Emma Ciafaloni, Riccardo Zuccarino, et al.
Neurology. Clinical Practice
|
November 22, 2019
Consensus-based care recommendations for congenital and childhood-onset myotonic dystrophy type 1
Nicholas E Johnson, Eugenio Zapata Aldana, Nathalie Angeard, et al.
Page
of 11