Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional …

DJ Birnkrant, K Bushby, CM Bann, SD Apkon… - The Lancet …, 2018 - thelancet.com
Since the publication of the Duchenne muscular dystrophy (DMD) care considerations in
2010, multidisciplinary care of this severe, progressive neuromuscular disease has evolved …

Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the …

DJ Birnkrant, K Bushby, CM Bann, SD Apkon… - The Lancet …, 2018 - thelancet.com
Improvements in the function, quality of life, and longevity of patients with Duchenne
muscular dystrophy (DMD) have been achieved through a multidisciplinary approach to …

Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy

JW McGreevy, CH Hakim… - Disease models & …, 2015 - journals.biologists.com
Duchenne muscular dystrophy (DMD) is a progressive muscle-wasting disorder. It is caused
by loss-of-function mutations in the dystrophin gene. Currently, there is no cure. A highly …

Muscular dystrophies

E Mercuri, F Muntoni - The Lancet, 2013 - thelancet.com
Muscular dystrophies are a heterogeneous group of inherited disorders that share similar
clinical features and dystrophic changes on muscle biopsy. An improved understanding of …

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

V Ricotti, WPL Mandy, M Scoto, M Pane… - … Medicine & Child …, 2016 - Wiley Online Library
Aim Duchenne muscular dystrophy (DMD) is associated with neuropsychiatric disorders.
The aim of the study was to characterize the DMD neuropsychiatric profile fully and to …

[HTML][HTML] Dystrophin Dp71 and the neuropathophysiology of Duchenne muscular dystrophy

M Naidoo, K Anthony - Molecular Neurobiology, 2020 - Springer
Duchenne muscular dystrophy (DMD) is caused by frameshift mutations in the DMD gene
that prevent the body-wide translation of its protein product, dystrophin. Besides a severe …

Cognitive and neurobehavioral profile in boys with Duchenne muscular dystrophy

R Banihani, S Smile, G Yoon, A Dupuis… - Journal of child …, 2015 - journals.sagepub.com
Duchenne muscular dystrophy is a progressive neuromuscular condition that has a high rate
of cognitive and learning disabilities as well as neurobehavioral disorders, some of which …

Current and emerging treatment strategies for Duchenne muscular dystrophy

JK Mah - Neuropsychiatric disease and treatment, 2016 - Taylor & Francis
Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy in
childhood. It is caused by mutations of the DMD gene, leading to progressive muscle …

Current and emerging therapies for Duchenne muscular dystrophy and spinal muscular atrophy

M Iftikhar, J Frey, MJ Shohan, S Malek… - Pharmacology & …, 2021 - Elsevier
Many neuromuscular diseases are genetically inherited or caused by mutations in motor
function proteins. Two of the most prevalent neuromuscular diseases are Duchenne …

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

A Veerapandiyan, KR Wagner, S Apkon… - Muscle & …, 2020 - Wiley Online Library
Abstract The coronavirus disease 2019 (COVID‐19) pandemic has resulted in the
reorganization of health‐care settings affecting clinical care delivery to patients with …