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Advances in the Unmet Needs of Myotonic Dystrophy Type 1 (DM1)
Addressing the Unmet Needs of Myotonic Dystrophy Type 1 (DM1)
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Addressing DMD Time to Diagnosis: Microlearning for Pediatricians & Primary Care
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Evolutions in the Management of DMD: Treatment Implications for the Present and Future
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Conference Updates in DMD and LGMD (WMS and MDA)
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Fall 2023 Neuromuscular Conference Updates
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GLP-1 RAs: Real-World Patient-Care Strategies for Type 2 Diabetes
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Limb-Girdle Muscular Dystrophy EXPLORE Module
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Understanding Lysosomal Storage Disorders: From Newborn Screening to Treatments
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Growing Importance of Newborn Screening in DMD
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The Immune Response in DMD Gene Therapies
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New Data from Gene Therapy Clinical Trials in DMD
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Changing the Phenotype of DMD
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LGMD: Mutation-specific Nomenclature
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LGMD Symptomatology
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LGMD Mutations and Disease Types
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Tests and Outcomes - DMD
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Genes, Exons, and the Pathophysiology of DMD
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The Natural History of DMD
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MDA Conference Coverage
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Rheumatic Learning: Next Steps for Mr. S's Established RA
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Rheumatic Learning: Next Steps for Mrs. J's Early RA
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Rheumatic Learning: How Can You Help Jeff With His Psoriatic Arthritis?
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Rheumatic Learning: How can you help Andrea with her Psoriatic Arthritis?
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WMS Conference Coverage on DMD and LGMD: Experts Reporting From the Field
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Conference Coverage on DMD & LGMD
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Understanding Lysosomal Storage Disorders
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Applying Principles of Pain Management
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Patient Case: Osteoarthritis (OA) of the Knee
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Patient Case: Lower Back Pain
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A Practical Guide to Rehabilitation in Multiple Sclerosis: 2nd Edition
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Shedding Light on Jane’s ILD Diagnosis
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Gene Therapy for SMA: An Emerging Treatment Option for a Devastating Disease
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SMA: Data, Insights and Practice
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From Bench to Bedside: Gene Therapy Approaches for Rare Diseases
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What’s New in Spinal Muscular Atrophy? Reporting from Dallas
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SMA Updates from Los Angeles
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Updates in SMA and Gene Therapy from Arlington, VA
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Targeting B-cells in Primary Progressive MS (PPMS)
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Comorbidities and Selection of DMTs
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The Gut Microbiota in MS
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Vitamin D: Modifiable Risk Factor and its Role in the Management of Patients with MS
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A 30 y/o Female w/2-year History of Shoulder Weakness and Elevated AST and ALT
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32 y/o Male w/Progressive Weakness, Dilated Cardiomyopathy & Respiratory...
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A 60 y/o Male w/4-year History Of Shoulder Weakness
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Addressing Common Barriers to Adherence
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Approach to Genetic Testing in Myopathies
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Molecular Diagnosis of Limb-Girdle Muscle Weakness

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