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Growth pattern trajectories in boys with Duchenne muscular dystrophy

Orphanet journal of rare diseases, 2022-01, Vol.17 (1), p.20-20, Article 20

2022

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Long term noninvasive ventilation and continuous positive airway pressure in children with neuromuscular diseases in France

Neuromuscular disorders : NMD, 2022-12, Vol.32 (11-12), p.886-892

2022

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Interventions for preventing and treating cardiac complications in Duchenne and Becker muscular dystrophy and X-linked dilated cardiomyopathy

Cochrane database of systematic reviews, 2018-10, Vol.10 (10), p.CD009068

2018

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Surgery for scoliosis in Duchenne muscular dystrophy

Cochrane database of systematic reviews, 2007-01 (1), p.CD005375

2007

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Effects of systemic multiexon skipping with peptide-conjugated morpholinos in the heart of a dog model of Duchenne muscular dystrophy

Proceedings of the National Academy of Sciences - PNAS, 2017-04, Vol.114 (16), p.4213-4218

2017

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Cardiac Pathophysiology and the Future of Cardiac Therapies in Duchenne Muscular Dystrophy

International journal of molecular sciences, 2019-08, Vol.20 (17), p.4098

2019

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Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care

Lancet neurology, 2010-02, Vol.9 (2), p.177-189

2010

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Cardiac Management of the Patient With Duchenne Muscular Dystrophy

Pediatrics (Evanston), 2018-10, Vol.142 (Suppl 2), p.S72

2018

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Relationships between DMD mutations and neurodevelopment in dystrophinopathy

Neurology, 2019-10, Vol.93 (17), p.e1597

2019

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The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID‐19 pandemic

Muscle & nerve, 2020-07, Vol.62 (1), p.41-45

2020

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Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations

Developmental medicine and child neurology, 2016-01, Vol.58 (1), p.77-84

2016

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Diaphragm muscle fibrosis involves changes in collagen organization with mechanical implications in Duchenne muscular dystrophy

Journal of applied physiology (1985), 2022-03, Vol.132 (3), p.653-672

2022

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Hereditary muscular dystrophies and the heart

Neuromuscular disorders : NMD, 2010-08, Vol.20 (8), p.479-492

2010

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Bone Health and Osteoporosis Management of the Patient With Duchenne Muscular Dystrophy

Pediatrics (Evanston), 2018-10, Vol.142 (Suppl 2), p.S34

2018

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Absence of full-length dystrophin impairs normal maturation and contraction of cardiomyocytes derived from human-induced pluripotent stem cells

Cardiovascular research, 2020-02, Vol.116 (2), p.368-382

2020

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Efficacy of idebenone on respiratory function in patients with Duchenne muscular dystrophy not using glucocorticoids (DELOS): a double-blind randomised placebo-controlled phase 3 trial

The Lancet (British edition), 2015-05, Vol.385 (9979), p.1748-1757

2015

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Different bone health progression patterns and early-stage risk marker in glucocorticoid-treated ambulatory Duchenne muscular dystrophy

Osteoporosis international, 2024-06, Vol.35 (6), p.997-1005

2024

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Cardiac and skeletal muscle effects in the randomized HOPE-Duchenne trial

Neurology, 2019-02, Vol.92 (8), p.e866

2019

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Evaluation of effects of continued corticosteroid treatment on cardiac and pulmonary function in non‐ambulatory males with Duchenne muscular dystrophy from MD STARnet

Muscle & nerve, 2022-07, Vol.66 (1), p.15-23

2022

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One in five patients with Duchenne muscular dystrophy dies from other causes than cardiac or respiratory failure

European journal of epidemiology, 2022-02, Vol.37 (2), p.147-156

2022

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Genetic therapies and respiratory outcomes in patients with neuromuscular disease

Current opinion in pediatrics, 2024-06, Vol.36 (3), p.296

2024

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Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy

PloS one, 2015-10, Vol.10 (10), p.e0141240-e0141240

2015

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

Nature cell biology, 2013-08, Vol.15 (8), p.895

2013

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Pilot study of a virtual weight management program for Duchenne muscular dystrophy

Muscle & nerve, 2024-04, Vol.69 (4), p.459-466

2024

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Growth pattern trajectories in boys with Duchenne muscular dystrophy

Long term noninvasive ventilation and continuous positive airway pressure in children with neuromuscular diseases in France

Interventions for preventing and treating cardiac complications in Duchenne and Becker muscular dystrophy and X-linked dilated cardiomyopathy

Surgery for scoliosis in Duchenne muscular dystrophy

Effects of systemic multiexon skipping with peptide-conjugated morpholinos in the heart of a dog model of Duchenne muscular dystrophy

Cardiac Pathophysiology and the Future of Cardiac Therapies in Duchenne Muscular Dystrophy

Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care

Cardiac Management of the Patient With Duchenne Muscular Dystrophy

Relationships between DMD mutations and neurodevelopment in dystrophinopathy

The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID‐19 pandemic

Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations

Diaphragm muscle fibrosis involves changes in collagen organization with mechanical implications in Duchenne muscular dystrophy

Hereditary muscular dystrophies and the heart

Bone Health and Osteoporosis Management of the Patient With Duchenne Muscular Dystrophy

Absence of full-length dystrophin impairs normal maturation and contraction of cardiomyocytes derived from human-induced pluripotent stem cells

Efficacy of idebenone on respiratory function in patients with Duchenne muscular dystrophy not using glucocorticoids (DELOS): a double-blind randomised placebo-controlled phase 3 trial

Different bone health progression patterns and early-stage risk marker in glucocorticoid-treated ambulatory Duchenne muscular dystrophy

Cardiac and skeletal muscle effects in the randomized HOPE-Duchenne trial

Evaluation of effects of continued corticosteroid treatment on cardiac and pulmonary function in non‐ambulatory males with Duchenne muscular dystrophy from MD STARnet

One in five patients with Duchenne muscular dystrophy dies from other causes than cardiac or respiratory failure

Genetic therapies and respiratory outcomes in patients with neuromuscular disease

A phase 2 open-label study of the safety and efficacy of weekly dosing of ATL1102 in patients with non-ambulatory Duchenne muscular dystrophy and pharmacology in mdx mice

Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy

Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

Pilot study of a virtual weight management program for Duchenne muscular dystrophy

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