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Pig models for Duchenne muscular dystrophy – from disease mechanisms to  validation of new diagnostic and therapeutic concepts - Neuromuscular  Disorders
Pig models for Duchenne muscular dystrophy – from disease mechanisms to validation of new diagnostic and therapeutic concepts - Neuromuscular Disorders

Frontiers | Adeno-Associated Virus (AAV)-Mediated Gene Therapy for Duchenne  Muscular Dystrophy: The Issue of Transgene Persistence
Frontiers | Adeno-Associated Virus (AAV)-Mediated Gene Therapy for Duchenne Muscular Dystrophy: The Issue of Transgene Persistence

PDF) Characterizing health state utilities associated with Duchenne  muscular dystrophy: a systematic review
PDF) Characterizing health state utilities associated with Duchenne muscular dystrophy: a systematic review

Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2  study - Komaki - 2020 - Annals of Clinical and Translational Neurology -  Wiley Online Library
Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 study - Komaki - 2020 - Annals of Clinical and Translational Neurology - Wiley Online Library

Prognostic indicators of disease progression in Duchenne muscular  dystrophy: A literature review and evidence synthesis | PLOS ONE
Prognostic indicators of disease progression in Duchenne muscular dystrophy: A literature review and evidence synthesis | PLOS ONE

PDF) Cost-Effectiveness Analysis of Diagnosis of Duchenne/Becker Muscular  Dystrophy in Colombia
PDF) Cost-Effectiveness Analysis of Diagnosis of Duchenne/Becker Muscular Dystrophy in Colombia

Consensus on the diagnosis, treatment and follow-up of patients with  Duchenne muscular dystrophy | Neurología (English Edition)
Consensus on the diagnosis, treatment and follow-up of patients with Duchenne muscular dystrophy | Neurología (English Edition)

CRISPR technologies for the treatment of Duchenne muscular dystrophy:  Molecular Therapy
CRISPR technologies for the treatment of Duchenne muscular dystrophy: Molecular Therapy

Cost of Illness in Patients with Duchenne Muscular Dystrophy in Portugal:  The COIDUCH Study | SpringerLink
Cost of Illness in Patients with Duchenne Muscular Dystrophy in Portugal: The COIDUCH Study | SpringerLink

PDF) Comparison of Long-term Ambulatory Function in Patients with Duchenne  Muscular Dystrophy Treated with Eteplirsen and Matched Natural History  Controls
PDF) Comparison of Long-term Ambulatory Function in Patients with Duchenne Muscular Dystrophy Treated with Eteplirsen and Matched Natural History Controls

DMD genotypes and loss of ambulation in the CINRG Duchenne Natural History  Study | Neurology
DMD genotypes and loss of ambulation in the CINRG Duchenne Natural History Study | Neurology

CRISPR applications for Duchenne muscular dystrophy: From animal models to  potential therapies - Chey - WIREs Mechanisms of Disease - Wiley Online  Library
CRISPR applications for Duchenne muscular dystrophy: From animal models to potential therapies - Chey - WIREs Mechanisms of Disease - Wiley Online Library

Pig models for Duchenne muscular dystrophy – from disease mechanisms to  validation of new diagnostic and therapeutic concepts - ScienceDirect
Pig models for Duchenne muscular dystrophy – from disease mechanisms to validation of new diagnostic and therapeutic concepts - ScienceDirect

Consensus on the diagnosis, treatment and follow-up of patients with  Duchenne muscular dystrophy | Neurología (English Edition)
Consensus on the diagnosis, treatment and follow-up of patients with Duchenne muscular dystrophy | Neurología (English Edition)

PDF) Genotype characterization and delayed loss of ambulation by  glucocorticoids in a large cohort of patients with Duchenne muscular  dystrophy
PDF) Genotype characterization and delayed loss of ambulation by glucocorticoids in a large cohort of patients with Duchenne muscular dystrophy

Genes | Free Full-Text | Current Outline of Exon Skipping Trials in Duchenne  Muscular Dystrophy | HTML
Genes | Free Full-Text | Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy | HTML

New variants, challenges and pitfalls in DMD genotyping: implications in  diagnosis, prognosis and therapy | Journal of Human Genetics
New variants, challenges and pitfalls in DMD genotyping: implications in diagnosis, prognosis and therapy | Journal of Human Genetics

Nutrients | Free Full-Text | Metabogenic and Nutriceutical Approaches to  Address Energy Dysregulation and Skeletal Muscle Wasting in Duchenne  Muscular Dystrophy | HTML
Nutrients | Free Full-Text | Metabogenic and Nutriceutical Approaches to Address Energy Dysregulation and Skeletal Muscle Wasting in Duchenne Muscular Dystrophy | HTML

Muscle membrane integrity in Duchenne muscular dystrophy: recent advances  in copolymer-based muscle membrane stabilizers | Skeletal Muscle | Full Text
Muscle membrane integrity in Duchenne muscular dystrophy: recent advances in copolymer-based muscle membrane stabilizers | Skeletal Muscle | Full Text

Vicious cycle of postural instability that leads to loss of ambulation... |  Download Scientific Diagram
Vicious cycle of postural instability that leads to loss of ambulation... | Download Scientific Diagram

A new era in the management of Duchenne muscular dystrophy - Korinthenberg  - 2019 - Developmental Medicine & Child Neurology - Wiley Online Library
A new era in the management of Duchenne muscular dystrophy - Korinthenberg - 2019 - Developmental Medicine & Child Neurology - Wiley Online Library

Structure-activity relationships of 2-pyrimidinecarbohydrazides as utrophin  modulators for the potential treatment of Duchenne muscular dystrophy -  ScienceDirect
Structure-activity relationships of 2-pyrimidinecarbohydrazides as utrophin modulators for the potential treatment of Duchenne muscular dystrophy - ScienceDirect

Peak functional ability and age at loss of ambulation in Duchenne muscular  dystrophy - Zambon - 2022 - Developmental Medicine & Child Neurology -  Wiley Online Library
Peak functional ability and age at loss of ambulation in Duchenne muscular dystrophy - Zambon - 2022 - Developmental Medicine & Child Neurology - Wiley Online Library