Channels :: FRELIP Discovery

Author: Lawson, David

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Progressive muscular dystrophy in childhood

Similar Items: Progressive muscular dystrophy in childhood

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Duchenne muscular dystrophy in South Africa : molecular aspects
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Genetic heterogeneity in South African facioscapulohumeral muscular dystrophy (FSHD) families
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Cellular effects of Coenzyme Q10 and resveratrol in the SJL/J dysferlinopathy mouse model
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Circulating microRNAs in neuromuscular disorders
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The effects of coenzyme Q10 and resveratrol treatment on the leukocyte counts and muscle morphology of SJL/J mice with dysferlinopathy : a qualitative microscopic investigation
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Die handhawings- en aanpassingsgedrag van gesinne wat 'n kind het met 'n lewensbedreigende siektetoestand : 'n opvoedkundig-kliniese ondersoek met spesiale verwysing na omvattende hulpverlening
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Analysis of The Demographics, Pathways to Diagnosis, Burden of Disease and Long-term Outcomes of Patients with Spinal Muscular Atrophy Managed at Red Cross War Memorial Children's Hospital
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A qualitative exploration into how South African gay men understand the influence of social media on their own and other gay men's desire for muscularity
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Systemic regeneration medicines for muscular dystrophy: progress and challenges in pro-regenerative drug development
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Medical Claim Costs of Facioscapulohumeral Muscular Dystrophy in the United States
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Skin cells as a tool in genetic diagnosis of Duchenne muscular dystrophy
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A Case of Childhood Lupus Anticoagulant-Hypoprothrombinemia Syndrome with Diagnostic and Therapeutic Insight
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Screen Exposure and Childhood Adiposity in Socially Vulnerable Settings: Cross-Sectional Study
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Development of a Duchenne Muscular Dystrophy Registry in South Africa to optimise care
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Duchenne muscular dystrophy : mutation profiling in view of the emerging gene-based therapies
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Gene Editing for Duchenne Muscular Dystrophy: From Experimental Models to Emerging Therapies
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A Hypothesized Therapeutic Role of (Z)-Endoxifen in Duchenne Muscular Dystrophy (DMD)
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MYH2 as a Potential Modifier of Clinical Severity in Facioscapulohumeral Muscular Dystrophy
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Atypical Presentation of Rapidly Progressive Guillain–Barré Syndrome With Dysautonomia in an Adolescent With Persistent Mycoplasma pneumoniae Infection: A Case Report
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Intellectual and behavioural functioning in boys with Duchenne Muscular Dystrophy : neuropsychological testing and correlation with genotype
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16 | Immunoproteasome inhibition positively impacts the gut-muscle axis in Duchenne muscular dystrophy
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29 | RNA-based combinatorial multi-target therapy for the treatment of Duchenne muscular dystrophy
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Direct AMPK Activation Confers Mutation‐Independent Therapeutic Benefit in Duchenne Muscular Dystrophy
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Downstream Pathways of Dystrophin Deficiency in Duchenne Muscular Dystrophy: Implications for Muscle Degeneration and Regeneration