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Contemporary Clinical Trials
|
April 29, 2017
Developing standardized corticosteroid treatment for Duchenne muscular dystrophy
Michela Guglieri, Kate Bushby, Michael P McDermott, et al.
Trials
|
May 26, 2018
A checklist for clinical trials in rare disease: obstacles and anticipatory actions-lessons learned from the FOR-DMD trial
Rebecca A Crow, Kimberly A Hart, Michael P McDermott, et al.
Human Mutation
|
January 22, 2015
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations
Catherine L Bladen, David Salgado, Soledad Monges, et al.
Journal of Neurology
|
October 29, 2013
Mapping the differences in care for 5,000 spinal muscular atrophy patients, a survey of 24 national registries in North America, Australasia and Europe
Catherine L Bladen, Rachel Thompson, Jacqueline M Jackson, et al.
Neurology. Clinical Practice
|
December 28, 2018
Consensus-based care recommendations for adults with myotonic dystrophy type 1
Tetsuo Ashizawa, Cynthia Gagnon, William J Groh, et al.
Human Mutation
|
August 6, 2013
The TREAT-NMD Duchenne muscular dystrophy registries: conception, design, and utilization by industry and academia
Catherine L Bladen, Karen Rafferty, Volker Straub, et al.
Journal of Neuromuscular Diseases
|
November 11, 2017
Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database
Zaïda Koeks, Catherine L Bladen, David Salgado, et al.
JAMA
|
April 5, 2022
Effect of Different Corticosteroid Dosing Regimens on Clinical Outcomes in Boys With Duchenne Muscular Dystrophy: A Randomized Clinical Trial
Michela Guglieri, Kate Bushby, Michael P McDermott, et al.
Page
of 19
Search research articles
Search
Showing results (181-190 of 188) with videos related to
Sort By:
Page
of 19
You have reached the last page of results.
This site can display upto 188 results.
Contemporary Clinical Trials
|
April 29, 2017
Developing standardized corticosteroid treatment for Duchenne muscular dystrophy
Michela Guglieri, Kate Bushby, Michael P McDermott, et al.
Trials
|
May 26, 2018
A checklist for clinical trials in rare disease: obstacles and anticipatory actions-lessons learned from the FOR-DMD trial
Rebecca A Crow, Kimberly A Hart, Michael P McDermott, et al.
Human Mutation
|
January 22, 2015
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations
Catherine L Bladen, David Salgado, Soledad Monges, et al.
Journal of Neurology
|
October 29, 2013
Mapping the differences in care for 5,000 spinal muscular atrophy patients, a survey of 24 national registries in North America, Australasia and Europe
Catherine L Bladen, Rachel Thompson, Jacqueline M Jackson, et al.
Neurology. Clinical Practice
|
December 28, 2018
Consensus-based care recommendations for adults with myotonic dystrophy type 1
Tetsuo Ashizawa, Cynthia Gagnon, William J Groh, et al.
Human Mutation
|
August 6, 2013
The TREAT-NMD Duchenne muscular dystrophy registries: conception, design, and utilization by industry and academia
Catherine L Bladen, Karen Rafferty, Volker Straub, et al.
Journal of Neuromuscular Diseases
|
November 11, 2017
Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database
Zaïda Koeks, Catherine L Bladen, David Salgado, et al.
JAMA
|
April 5, 2022
Effect of Different Corticosteroid Dosing Regimens on Clinical Outcomes in Boys With Duchenne Muscular Dystrophy: A Randomized Clinical Trial
Michela Guglieri, Kate Bushby, Michael P McDermott, et al.
Page
of 19