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 …

Connective tissue growth factor: Role in trabecular meshwork remodeling and intraocular pressure lowering

MDS Hassan, N Razali, AS Abu Bakar… - Experimental …, 2023 - journals.sagepub.com
Connective tissue growth factor (CTGF) is a distinct signaling molecule modulating many
physiological and pathophysiological processes. This protein is upregulated in numerous …

Clinical management of Duchenne muscular dystrophy: the state of the art

S Messina, GL Vita - Neurological Sciences, 2018 - Springer
Introduction Duchenne muscular dystrophy (DMD) is a devastating, progressive
neuromuscular disorder for which there is no cure. As the dystrophin gene is located on the …

[HTML][HTML] Left ventricular deformation and myocardial fibrosis in pediatric patients with Duchenne muscular dystrophy

TP Kerstens, WM van Everdingen, J Habets… - International Journal of …, 2023 - Elsevier
Background Left ventricular (LV) strain and rotation are emerging functional markers for
early detection of LV dysfunction and have been associated with the burden of myocardial …

[HTML][HTML] Development of Duchenne Video Assessment scorecards to evaluate ease of movement among those with Duchenne muscular dystrophy

MG Contesse, LP Lowes, MK White, L Dalle Pazze… - PloS one, 2022 - journals.plos.org
Background Patients with Duchenne muscular dystrophy (DMD) adopt compensatory
movement patterns as muscles weaken. The Duchenne Video Assessment (DVA) measures …

[HTML][HTML] Evaluation of pro-regenerative and anti-inflammatory effects of isolecanoric acid in the muscle: Potential treatment of Duchenne Muscular Dystrophy

L Matias-Valiente, C Sanchez-Fernandez… - Biomedicine & …, 2024 - Elsevier
Duchenne muscular dystrophy (DMD) is a devastating degenerative disease of skeletal
muscles caused by loss of dystrophin, a key protein that maintains muscle integrity, which …

[HTML][HTML] Morpholino oligomer-induced dystrophin isoforms to map the functional domains in the dystrophin protein

D Li, AM Adams, RD Johnsen, S Fletcher… - … Therapy-Nucleic Acids, 2020 - cell.com
Dystrophin plays a crucial role in maintaining sarcolemma stability during muscle
contractions, and mutations that prevent the expression of a functional protein cause …

Cardiopulmonary phenotypic discordance is common in Duchenne muscular dystrophy

JB Jin, JC Carter, DW Sheehan… - Pediatric …, 2019 - Wiley Online Library
Objective To determine the prevalence of discordant cardiopulmonary function among
patients with Duchenne muscular dystrophy (DMD) in our clinic. Methods Retrospective …

Left ventricular end-diastolic diameter and cardiac mortality in duchenne muscular dystrophy

K Segawa, N Sugawara, K Maruo… - Neuropsychiatric …, 2020 - Taylor & Francis
Purpose This study aimed to examine weather left ventricular end-diastolic diameter (LVDd)
could predict mortality from heart failure in patients with Duchenne muscular dystrophy …

[HTML][HTML] A modified diet does not ameliorate muscle pathology in a mouse model for Duchenne muscular dystrophy

IEC Verhaart, D van de Vijver… - Plos one, 2019 - journals.plos.org
Duchenne muscular dystrophy (DMD) is caused by a lack of dystrophin protein. Next to
direct effects on the muscles, this has also metabolic consequences. The influence of …