Upper limb disease evolution in exon 53 skipping eligible patients with Duchenne muscular dystrophy
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DOI: 10.1002/acn3.51417
Abstract: To understand the natural disease upper limb progression over 3 years of ambulatory and non‐ambulatory patients with Duchenne muscular dystrophy (DMD) using functional assessments and quantitative magnetic resonance imaging (MRI) and to exploratively identify prognostic… read more here.
Keywords: patients duchenne; muscular dystrophy; disease; upper limb ... See more keywords
The association between cardiac involvement and long‐term clinical outcomes in patients with Duchenne muscular dystrophy
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DOI: 10.1002/ehf2.13970
Abstract: Despite advances in contemporary cardiopulmonary therapies, cardiomyopathy remains the leading cause of death in patients with Duchenne muscular dystrophy (DMD). Also, the long‐term clinical outcomes of patients with DMD and cardiomyopathy is unknown. This study… read more here.
Keywords: long term; clinical outcomes; duchenne muscular; patients duchenne ... See more keywords
Letter Regarding: “Evaluation of Early Left Ventricular Dysfunction in Patients with Duchenne Muscular Dystrophy Using Two-Dimensional Speckle Tracking Echocardiography and Tissue Doppler Imaging,” Cho et al., Pediatric Cardiology ePub July 2018
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DOI: 10.1007/s00246-018-1983-8
Abstract: With interest I read the article “Evaluation of Early Left Ventricular Dysfunction in Patients with Duchenne Muscular Dystrophy Using Two-Dimensional Speckle Tracking Echocardiography and Tissue Doppler Imaging,” by Cho et al. [1]. In the manuscript,… read more here.
Keywords: patients duchenne; cardiology; dysfunction; muscular dystrophy ... See more keywords
Influence of β2 adrenergic receptor genotype on longitudinal measures of forced vital capacity in patients with Duchenne muscular dystrophy
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DOI: 10.1016/j.nmd.2021.12.006
Abstract: The progression of decline in forced vital capacity as percent predicated (FVC%p) is a strong indicator of worsening prognosis in patients with Duchenne muscular dystrophy (DMD). Evidence suggests that ß2 adrenergic (ADRB2) receptors may play… read more here.
Keywords: muscular dystrophy; genotype longitudinal; patients duchenne; vital capacity ... See more keywords
Perioperative complications of scoliosis surgery in patients with Duchenne muscular dystrophy and spinal muscular atrophy, focussing on wound healing disorders
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DOI: 10.1080/00207454.2016.1196688
Abstract: Purpose: Patients with Duchenne muscular dystrophy (DMD) or spinal muscular atrophy (SMA), both neuromuscular diseases, sustain spinal scoliosis in the course of their disease. To reduce the concomitant major morbidity and to improve their quality… read more here.
Keywords: surgery; patients duchenne; spinal muscular; muscular dystrophy ... See more keywords