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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)

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)

Fall 2023 Neuromuscular Conference Updates

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

Growing Importance of Newborn Screening in DMD

The Immune Response in DMD Gene Therapies

New Data from Gene Therapy Clinical Trials in DMD

Changing the Phenotype of DMD

LGMD: Mutation-specific Nomenclature

LGMD Symptomatology

LGMD Mutations and Disease Types

Tests and Outcomes - DMD

Genes, Exons, and the Pathophysiology of DMD

The Natural History of DMD

MDA Conference Coverage

Rheumatic Learning: Next Steps for Mr. S's Established RA

Rheumatic Learning: Next Steps for Mrs. J's Early RA

Rheumatic Learning: How Can You Help Jeff With His Psoriatic Arthritis?

Rheumatic Learning: How can you help Andrea with her Psoriatic Arthritis?

WMS Conference Coverage on DMD and LGMD: Experts Reporting From the Field

Conference Coverage on DMD & LGMD

Understanding Lysosomal Storage Disorders

Applying Principles of Pain Management

Patient Case: Osteoarthritis (OA) of the Knee

Patient Case: Lower Back Pain

A Practical Guide to Rehabilitation in Multiple Sclerosis: 2nd Edition

Shedding Light on Jane’s ILD Diagnosis

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Gene Therapy for SMA: An Emerging Treatment Option for a Devastating Disease

SMA: Data, Insights and Practice

From Bench to Bedside: Gene Therapy Approaches for Rare Diseases

What’s New in Spinal Muscular Atrophy? Reporting from Dallas

SMA Updates from Los Angeles

Updates in SMA and Gene Therapy from Arlington, VA

Targeting B-cells in Primary Progressive MS (PPMS)

Comorbidities and Selection of DMTs

The Gut Microbiota in MS

Vitamin D: Modifiable Risk Factor and its Role in the Management of Patients with MS

A 30 y/o Female w/2-year History of Shoulder Weakness and Elevated AST and ALT

32 y/o Male w/Progressive Weakness, Dilated Cardiomyopathy & Respiratory...

A 60 y/o Male w/4-year History Of Shoulder Weakness

Addressing Common Barriers to Adherence

Approach to Genetic Testing in Myopathies

Molecular Diagnosis of Limb-Girdle Muscle Weakness