Channels - Progressive muscular dystrophy in childhood :: FRELIP Discovery

Similar Items: Progressive muscular dystrophy in childhood

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

Author: Lawson, David

Quick Look
Progressive muscular dystrophy in childhood

Author: Dubowitz, Victor

Quick Look
Progressive muscular dystrophy in childhood