September 2026
- Guidelines for Genetic Testing of Peripheral Nerve Disorders
- Respiratory Care Trajectory in Patients With Duchenne Muscular Dystrophy in the Advanced Stage: A Retrospective Single‐Center Study
- Construct Validity and Reliability of the OMNI Scale in Children and Adolescents With Neuromuscular Diseases
- Online Crowdfunding Campaigns for People Living With ALS Demonstrate Financial Burden and Unmet Needs
- High‐Resolution Ultrasound for Diagnosing Severity of Traumatic Peripheral Nerve Injuries‐in‐Continuity: A Systematic Review, Meta‐Analysis of Individual Participants' Data, and Illustrative Patient Series
- Traumatic Neuroma of a Bifid Digital Nerve of the Index Finger: Sonographic and Intraoperative Findings of a Rare Variation
- Capturing Financial Burden Concerns in an ALS Multidisciplinary Clinic
- Neuralgic Amyotrophy Following B‐Cell Maturation Antigen‐Directed CAR‐T Therapy
- Myasthenia Gravis and Thymoma
- “Abductor Sparing”: A New Selective Involvement in ALS
- Quantitative Assessment of Tongue Atrophy in Amyotrophic Lateral Sclerosis Using Transoral Tongue Ultrasonography (TOTU): A Retrospective Single‐Center Study
- Imaging of Facial Muscles in Facioscapulohumeral Muscular Dystrophy: An Exploratory Study Comparing Magnetic Resonance Imaging and Ultrasound
- Diagnostic Performance of the Strength‐Duration Test for Bedside Screening of Critical Illness Polyneuropathy and/or Myopathy: A Prospective, Cross‐Sectional Study
- Poor Prognostic Factors After Gastrostomy in Patients With Amyotrophic Lateral Sclerosis: A Two‐Center Retrospective Cohort Study
- AANEM News & Insights
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- Calendar of Events
- Clinical and Electrodiagnostic Characterization of Pediatric Triple A Syndrome: A Cohort of 17 Patients
- Beyond the Neurological Level of Injury: The Critical Role of Electrodiagnostics in Cervical Spinal Cord Injury
- Lumbosacral Plexopathy: A Single‐Center Review of Etiology, Clinical Presentation, Electrodiagnostic Findings, and Long‐Term Outcomes
- Myotonia: Recognition, Evaluation, and Differential Diagnosis
- Revisiting the Extrapolated Reference Values (E‐Ref) Estimation
- Issue Information
- Sensory Cortical Hyperexcitability in Amyotrophic Lateral Sclerosis Involves a Broad Hand Representation Within the Primary Somatosensory Cortex
- Addressing the Global Disparities in Access to Treatment in Spinal Muscular Atrophy
- Exploring the Value of Quantitative Muscle Ultrasound in Neuromuscular Junction Disorders: A Pilot Study
- Emergencies in Amyotrophic Lateral Sclerosis
- Efficacy of Neuromuscular Electrical Stimulation in Mitigating Muscle Mass Loss: A Systematic Review and Meta‐Analysis of Randomized Controlled Trials
- Serum Neurofilament Light Chain and GFAP in Amyotrophic Lateral Sclerosis on a Commercial ECLIA Platform
- Risk Factors for Exercise‐Associated Muscle Cramps: A Systematic Review With Meta‐Analysis
- Whole Body Phase Angle as a Promising Marker of Disease Severity in Facioscapulohumeral Muscular Dystrophy
- Priorities for Advancing Palliative Care for Amyotrophic Lateral Sclerosis: A Consensus Report From a Palliative Care for ALS Working Group in the United States
- Military Service and Survival Among Persons With ALS in the U.S. National ALS Registry, 2011–2023
- Postural Torticollis and Early‐Onset Scoliosis in Infants With SMA Identified Through Newborn Screening: Single Institution Experience
- Factors Affecting Disease Progression, Survival, and Caregiver Burden in United States Veterans at a Multidisciplinary Veterans Affairs ALS Center
- It's Virtually Here: Telemedicine, Virtual Care, and Neuromuscular Disease
- Early‐Onset Wild‐Type Transthyretin Amyloidosis Polyneuropathy
- An Encouragement to Broaden the Frame: Spiritual Care as a Complementary Perspective on Healthcare Professionals' Emotional Experiences in ALS
- Enabling Functional Independence: A Scoping Review of Upper Extremity Assistive Devices for Adults With Progressive Neuromuscular Diseases
- Coexisting Inflammatory and Hereditary Neuropathies: A Review
- Patient Communication Outside of Visits: Implications for Remote Monitoring and Digital Care Models in Myasthenia Gravis
- Urinary Dysfunction in Myasthenic Syndromes: A Scoping Review of Clinical Features and Treatment‐Related Associations
- Targeted Muscle Reinnervation for Intuitive Prosthetic Control
- Targeted Muscle Reinnervation for Management and Prevention of Symptomatic Neuroma
- Electrical Modalities in the Rehabilitation of Peripheral Nerve Injuries: State of the Literature and Current Clinical Applications
- Late‐Onset Myasthenia Gravis: An Increasingly Frequent Clinical Entity With Distinctive Challenges
- Optimization of the Cell‐Based Assay Methodology to Study Degradation of Acetylcholine Receptors (Antigenic Modulation) by Antibodies From Myasthenia Gravis Patients
- Clinical Characteristics and Treatment Management of Seronegative Myasthenia Gravis: A Systematic Review of the Literature
- Muscle‐Specific Kinase Signaling and Its Therapeutic Potential
- Review of Congenital Myasthenic Syndrome Caused by Pathogenic Variants in GFPT1