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Matrix Biology : Journal of the International Society for Matrix Biology
|
June 23, 2018
Extracellular matrix-driven congenital muscular dystrophies
Payam Mohassel, A Reghan Foley, Carsten G Bönnemann
Neurology. Genetics
|
April 12, 2016
Next-generation sequencing still needs our generation's clinicians
A Reghan Foley, Sandra Donkervoort, Carsten G Bönnemann
Pediatric Neurology
|
August 4, 2018
Dramatic Improvement of a Rare Syndrome With High Dose Riboflavin Treatment
Eva B Forman, A Reghan Foley, Mary D King
Current Opinion in Genetics & Development
|
March 15, 2011
Dystroglycanopathies: coming into focus
Caroline Godfrey, A Reghan Foley, Emma Clement, et al.
Neurology
|
November 22, 2012
Spontaneous keloid formation in patients with Bethlem myopathy
James Collins, A Reghan Foley, Volker Straub, et al.
Neuromuscular Disorders : NMD
|
October 17, 2025
283rd ENMC international workshop: Establishing expert care recommendations for LAMA2-RD: A prototype for the development of congenital muscular dystrophy subtype-specific care guidelines. Hoofddorp, The Netherlands, January 17th-19th 2025
Alberto Andrea Zambon, Andrea Klein, Anna Sarkozy, et al.
Seminars in Pediatric Neurology
|
May 8, 2019
The Use of Muscle Ultrasound in the Diagnosis and Differential Diagnosis of Congenital Disorders of Muscle in the Age of Next Generation Genetics
Dimah N Saade, Sarah B Neuhaus, A Reghan Foley, et al.
Muscle & Nerve
|
September 10, 2019
Utility of neuromuscular ultrasound for electromyographic needle localization within diseased muscle
Omar F Ahmad, Dimah Saade, A Reghan Foley, et al.
Frontiers in Molecular Neuroscience
|
August 28, 2020
LAMA2-Related Dystrophies: Clinical Phenotypes, Disease Biomarkers, and Clinical Trial Readiness
Anna Sarkozy, A Reghan Foley, Alberto A Zambon, et al.
Journal of Neuromuscular Diseases
|
May 26, 2019
MuscleViz: Free Open-Source Software for Muscle Weakness Visualization
Jason D Wittenbach, Benjamin T Cocanougher, Pomi Yun, et al.
Page
of 12
Search research articles
Search
Showing results (1-10 of 114) with videos related to
Sort By:
Page
of 12
Matrix Biology : Journal of the International Society for Matrix Biology
|
June 23, 2018
Extracellular matrix-driven congenital muscular dystrophies
Payam Mohassel, A Reghan Foley, Carsten G Bönnemann
Neurology. Genetics
|
April 12, 2016
Next-generation sequencing still needs our generation's clinicians
A Reghan Foley, Sandra Donkervoort, Carsten G Bönnemann
Pediatric Neurology
|
August 4, 2018
Dramatic Improvement of a Rare Syndrome With High Dose Riboflavin Treatment
Eva B Forman, A Reghan Foley, Mary D King
Current Opinion in Genetics & Development
|
March 15, 2011
Dystroglycanopathies: coming into focus
Caroline Godfrey, A Reghan Foley, Emma Clement, et al.
Neurology
|
November 22, 2012
Spontaneous keloid formation in patients with Bethlem myopathy
James Collins, A Reghan Foley, Volker Straub, et al.
Neuromuscular Disorders : NMD
|
October 17, 2025
283rd ENMC international workshop: Establishing expert care recommendations for LAMA2-RD: A prototype for the development of congenital muscular dystrophy subtype-specific care guidelines. Hoofddorp, The Netherlands, January 17th-19th 2025
Alberto Andrea Zambon, Andrea Klein, Anna Sarkozy, et al.
Seminars in Pediatric Neurology
|
May 8, 2019
The Use of Muscle Ultrasound in the Diagnosis and Differential Diagnosis of Congenital Disorders of Muscle in the Age of Next Generation Genetics
Dimah N Saade, Sarah B Neuhaus, A Reghan Foley, et al.
Muscle & Nerve
|
September 10, 2019
Utility of neuromuscular ultrasound for electromyographic needle localization within diseased muscle
Omar F Ahmad, Dimah Saade, A Reghan Foley, et al.
Frontiers in Molecular Neuroscience
|
August 28, 2020
LAMA2-Related Dystrophies: Clinical Phenotypes, Disease Biomarkers, and Clinical Trial Readiness
Anna Sarkozy, A Reghan Foley, Alberto A Zambon, et al.
Journal of Neuromuscular Diseases
|
May 26, 2019
MuscleViz: Free Open-Source Software for Muscle Weakness Visualization
Jason D Wittenbach, Benjamin T Cocanougher, Pomi Yun, et al.
Page
of 12