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Showing results (51-60 of 92) with videos related to
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Muscle & Nerve
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February 7, 2017
The quality of life in genetic neuromuscular disease questionnaire: Rasch validation of the French version
Antoine Dany, Amandine Rapin, Brice Lavrard, et al.
BMC Neurology
|
June 16, 2026
Exploring the impact of myotonia on daily functioning in myotonic dystrophy: a patient-reported survey
Valeria A Sansone, Utkarsh J Dang, Linda Edmondson, et al.
Neurology. Clinical Practice
|
October 5, 2019
Consensus-based care recommendations for adults with myotonic dystrophy type 2
Benedikt Schoser, Federica Montagnese, Guillaume Bassez, et al.
Rheumatology (Oxford, England)
|
February 24, 2018
Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositis
Jessie Aouizerate, Marie De Antonio, Brigitte Bader-Meunier, et al.
Circulation. Cardiovascular Genetics
|
June 15, 2017
Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart Registry
Caroline Chong-Nguyen, Karim Wahbi, Vincent Algalarrondo, et al.
Neurology. Genetics
|
April 22, 2021
Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1
Stephan Wenninger, Sarah A Cumming, Kristina Gutschmidt, et al.
Journal of Neuromuscular Diseases
|
April 5, 2021
Improved Cardiac Outcomes by Early Treatment with Angiotensin-Converting Enzyme Inhibitors in Becker Muscular Dystrophy
Caroline Stalens, Leslie Motté, Anthony Béhin, et al.
Plos One
|
April 25, 2019
Diaphragm sniff ultrasound: Normal values, relationship with sniff nasal pressure and accuracy for predicting respiratory involvement in patients with neuromuscular disorders
Abdallah Fayssoil, Lee S Nguyen, Adam Ogna, et al.
Neurology
|
January 19, 2018
Hearing impairment in patients with myotonic dystrophy type 2
Judith van Vliet, Alide A Tieleman, Baziel G M van Engelen, et al.
Plos Genetics
|
December 5, 2012
Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus
Aline Huguet, Fadia Medja, Annie Nicole, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 92) with videos related to
Sort By:
Page
of 10
Muscle & Nerve
|
February 7, 2017
The quality of life in genetic neuromuscular disease questionnaire: Rasch validation of the French version
Antoine Dany, Amandine Rapin, Brice Lavrard, et al.
BMC Neurology
|
June 16, 2026
Exploring the impact of myotonia on daily functioning in myotonic dystrophy: a patient-reported survey
Valeria A Sansone, Utkarsh J Dang, Linda Edmondson, et al.
Neurology. Clinical Practice
|
October 5, 2019
Consensus-based care recommendations for adults with myotonic dystrophy type 2
Benedikt Schoser, Federica Montagnese, Guillaume Bassez, et al.
Rheumatology (Oxford, England)
|
February 24, 2018
Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositis
Jessie Aouizerate, Marie De Antonio, Brigitte Bader-Meunier, et al.
Circulation. Cardiovascular Genetics
|
June 15, 2017
Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart Registry
Caroline Chong-Nguyen, Karim Wahbi, Vincent Algalarrondo, et al.
Neurology. Genetics
|
April 22, 2021
Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1
Stephan Wenninger, Sarah A Cumming, Kristina Gutschmidt, et al.
Journal of Neuromuscular Diseases
|
April 5, 2021
Improved Cardiac Outcomes by Early Treatment with Angiotensin-Converting Enzyme Inhibitors in Becker Muscular Dystrophy
Caroline Stalens, Leslie Motté, Anthony Béhin, et al.
Plos One
|
April 25, 2019
Diaphragm sniff ultrasound: Normal values, relationship with sniff nasal pressure and accuracy for predicting respiratory involvement in patients with neuromuscular disorders
Abdallah Fayssoil, Lee S Nguyen, Adam Ogna, et al.
Neurology
|
January 19, 2018
Hearing impairment in patients with myotonic dystrophy type 2
Judith van Vliet, Alide A Tieleman, Baziel G M van Engelen, et al.
Plos Genetics
|
December 5, 2012
Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus
Aline Huguet, Fadia Medja, Annie Nicole, et al.
Page
of 10