Idiopathic lumbosacral neuropathy: a cause of persistent leg pain

Mexiletine is an effective antimyotonia treatment in myotonic dystrophy type 1.

Neurology·2010

Incidence and mortality rates of myasthenia gravis and myasthenic crisis in US hospitals.

Neurology·2009

Distal myasthenia gravis with a decrement, an increment, and denervation.

Journal of clinical neuromuscular disease·2008

Inflammatory myopathy in hemiatrophy resulting from linear scleroderma.

Journal of clinical neuromuscular disease·2008

Painful small-fiber neuropathy in Sjogren syndrome.

Neurology·2005

Quantitative analysis of the "warm-up" phenomenon in myotonic dystrophy type 1.

Muscle & nerve·2005

The Two-Dimensional Framework of Nerve Injury.

Muscle & nerve·2026

Assessment of Lectin Staining Biomarkers for GNE Myopathy Gene Therapy.

Muscle & nerve·2026

Reduced Phrenic CMAP Amplitudes in Obesity Despite Preserved Diaphragm Ultrasound Measures.

Muscle & nerve·2026

Reference Electrode Position Affects Compound Muscle Action Potential Amplitude in Ulnar Nerve Conduction Studies Recorded From the First Dorsal Interosseous Muscle.

Muscle & nerve·2026

Sociodemographic and Clinical Profile of Adult Males With Duchenne Muscular Dystrophy.

Muscle & nerve·2026

Clinical Outcomes and Treatment Efficacy in Juvenile Myasthenia Gravis: A Retrospective Review From a Single Center.

Muscle & nerve·2026

Interventions for post-stroke cognitive impairment: a systematic review of neuroplastic mechanisms, comparative efficacy, and multimodal approaches.

Frontiers in neuroscience·2026

Na V 1.7-dependent peripheral sensitization drives chronic pain in Parkinson's disease.

bioRxiv : the preprint server for biology·2026

Proteomic profiling across early postnatal development of midbrain dopamine axons innervating the dorsal striatum.

bioRxiv : the preprint server for biology·2026

Intrasegmental and propriospinal pre-phrenic interneuron circuitry in intact CNS and following cervical spinal cord injury.

bioRxiv : the preprint server for biology·2026

Related Experiment Videos

Idiopathic lumbosacral neuropathy: a cause of persistent leg pain

Related Concept Videos

Mexiletine is an effective antimyotonia treatment in myotonic dystrophy type 1.

Incidence and mortality rates of myasthenia gravis and myasthenic crisis in US hospitals.

Distal myasthenia gravis with a decrement, an increment, and denervation.

Inflammatory myopathy in hemiatrophy resulting from linear scleroderma.

Painful small-fiber neuropathy in Sjogren syndrome.

Quantitative analysis of the "warm-up" phenomenon in myotonic dystrophy type 1.

The Two-Dimensional Framework of Nerve Injury.

Assessment of Lectin Staining Biomarkers for GNE Myopathy Gene Therapy.

Reduced Phrenic CMAP Amplitudes in Obesity Despite Preserved Diaphragm Ultrasound Measures.

Reference Electrode Position Affects Compound Muscle Action Potential Amplitude in Ulnar Nerve Conduction Studies Recorded From the First Dorsal Interosseous Muscle.

Sociodemographic and Clinical Profile of Adult Males With Duchenne Muscular Dystrophy.

Clinical Outcomes and Treatment Efficacy in Juvenile Myasthenia Gravis: A Retrospective Review From a Single Center.

Interventions for post-stroke cognitive impairment: a systematic review of neuroplastic mechanisms, comparative efficacy, and multimodal approaches.

Na V 1.7-dependent peripheral sensitization drives chronic pain in Parkinson's disease.

Proteomic profiling across early postnatal development of midbrain dopamine axons innervating the dorsal striatum.

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Idiopathic lumbosacral neuropathy: a cause of persistent leg pain

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