Trajectories of motor function in children with Duchenne muscular dystrophy: A longitudinal study on a Colombian population

Effect of Different Corticosteroid Dosing Regimens on Clinical Outcomes in Boys With Duchenne Muscular Dystrophy

(2022) Michela Guglieri et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Walking alone milestone combined reading-frame rule improves early prediction of Duchenne muscular dystrophy

(2022) Yan-li Ma et al.   Frontiers in Pediatrics

Longitudinal motor function in proximal versus distal DMD pathogenic variants

(2021) Mathula Thangarajh et al.   MUSCLE & NERVE

Implementation of Motor Function Measure score percentile curves - Predicting motor function loss in Duchenne muscular dystrophy

(2021) Patricia Hafner et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

The impact of genotype on outcomes in individuals with Duchenne muscular dystrophy: A systematic review

(2021) Shelagh M. Szabo et al.   MUSCLE & NERVE

Genetic modifiers of respiratory function in Duchenne muscular dystrophy

(2020) Luca Bello et al.   Annals of Clinical and Translational Neurology

Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis

(2020) Salvatore Crisafulli et al.   Orphanet Journal of Rare Diseases

Natural History of Steroid-Treated Young Boys With Duchenne Muscular Dystrophy Using the NSAA, 100m, and Timed Functional Tests

(2020) Natalie F. Miller et al.   PEDIATRIC NEUROLOGY

Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

(2019) Claudia Brogna et al.   PLoS One

Muscular dystrophies

(2019) Eugenio Mercuri et al.   LANCET

DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtype

(2018) Richard T. Wang et al.   HUMAN MUTATION

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

(2018) David J Birnkrant et al.   LANCET NEUROLOGY

Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management

(2018) David J Birnkrant et al.   LANCET NEUROLOGY

Rehabilitation Management of the Patient With Duchenne Muscular Dystrophy

(2018) Laura E. Case et al.   PEDIATRICS

Comparison of the phenotypes of patients harboring in-frame deletions starting at exon 45 in the Duchenne muscular dystrophy gene indicates potential for the development of exon skipping therapy

(2016) Akinori Nakamura et al.   JOURNAL OF HUMAN GENETICS

DMDgenotypes and loss of ambulation in the CINRG Duchenne Natural History Study

(2016) Luca Bello et al.   NEUROLOGY

Challenges of clinical trial design for DMD

(2015) Valeria Ricotti et al.   NEUROMUSCULAR DISORDERS

Motor Function Measure: Validation of a Short Form for Young Children With Neuromuscular Diseases

(2013) Capucine de Lattre et al.   ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION

Evidence-based path to newborn screening for duchenne muscular dystrophy

(2012) Jerry R. Mendell et al.   ANNALS OF NEUROLOGY

Motor assessment in patients with Duchenne muscular dystrophy

(2012) Gabriela Palhares Campolina Diniz et al.   ARQUIVOS DE NEURO-PSIQUIATRIA

Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function Measure

(2009) CAROLE VUILLEROT et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY