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Myasthenia gravis Lambert-Eaton overlap syndrome

Muscle & nerve, 2016-01, Vol.53 (1), p.20-26

Oh, Shin J.

2016

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Perry Syndrome: A Distinctive Type of TDP-43 Proteinopathy

Journal of neuropathology and experimental neurology, 2017-08, Vol.76 (8), p.676-682

2017

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Transforming Growth Factor Beta (TGF-β) Is a Muscle Biomarker of Disease Progression in ALS and Correlates with Smad Expression

PloS one, 2015-09, Vol.10 (9), p.e0138425-e0138425

2015

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3,4-Diaminopyridine is more effective than placebo in a randomized, double-blind, cross-over drug study in LEMS

Muscle & nerve, 2009-11, Vol.40 (5), p.795-800

2009

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Assessment of the compound muscle action potential amplitude return time between exercises or tests in the repetitive nerve stimulation test for Lambert‐Eaton myasthenic syndrome

Muscle & nerve, 2020-12, Vol.62 (6), p.742-745

Oh, Shin J.

2020

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Distal spinal and bulbar muscular atrophy caused by dynactin mutation

Annals of neurology, 2005-05, Vol.57 (5), p.687-694

2005

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Chronic inflammatory axonal polyneuropathy

Journal of neurology, neurosurgery and psychiatry, 2020-11, Vol.91 (11), p.1175-1180

2020

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Ten-second exercise is superior to 30-second exercise for post-exercise facilitation in diagnosing Lambert-Eaton myasthenic syndrome

Muscle & nerve, 2008-05, Vol.37 (5), p.572-575

2008

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Ocular LEMS or MLOS

Muscle & nerve, 2016-11, Vol.54 (5), p.981-982

2016

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Diagnostic markers of axonal degeneration and demyelination in sensory nerve conduction

Muscle & nerve, 2016-06, Vol.53 (6), p.866-871

2016

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Distinguishing Features of the Repetitive Nerve Stimulation Test Between Lambert-Eaton Myasthenic Syndrome and Myasthenia Gravis, 50-Year Reappraisal

Journal of clinical neuromuscular disease, 2017-12, Vol.19 (2), p.66-75

Oh, Shin J

2017

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Single-fiber electromyography in sporadic inclusion body myopathy

Clinical neurophysiology, 2007-07, Vol.118 (7), p.1563-1568

2007

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Statins may aggravate myasthenia gravis

Muscle & nerve, 2008-09, Vol.38 (3), p.1101-1107

2008

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On-nerve needle nerve conduction study in the sural nerve: A new technique for evaluation of peripheral neuropathy

Clinical neurophysiology, 2015-09, Vol.126 (9), p.1811-1816

2015

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Diagnostic value of the near‐nerve needle sensory nerve conduction in sensory inflammatory demyelinating polyneuropathy

Muscle & nerve, 2018-03, Vol.57 (3), p.414-418

2018

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Single-fiber EMG and clinical correlation in Lambert-Eaton myasthenic syndrome

Muscle & nerve, 2013-05, Vol.47 (5), p.664-667

2013

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Electrophysiological differences in seropositive and seronegative Lambert-Eaton myasthenic syndrome

Muscle & nerve, 2007-02, Vol.35 (2), p.178-183

2007

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Amifampridine phosphate (Firdapse®) is effective and safe in a phase 3 clinical trial in LEMS

Muscle & nerve, 2016-05, Vol.53 (5), p.717-725

2016

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Repetitive nerve stimulation of facial muscles in musk antibody-positive myasthenia gravis

Muscle & nerve, 2006-04, Vol.33 (4), p.500-504

2006

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Anti-Hu antibody neuropathy: a clinical, electrophysiological, and pathological study

Clinical neurophysiology, 2005, Vol.116 (1), p.28-34

2005

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Asymptomatic vasculitic neuropathy

Muscle & nerve, 2015-07, Vol.52 (1), p.34-38

2015

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Post-exercise exhaustion in Lambert–Eaton myasthenic syndrome

Clinical neurophysiology, 2014-02, Vol.125 (2), p.411-414

2014

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Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

Nature (London), 2000-08, Vol.406 (6798), p.906-910

2000

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A patient diagnosed with Mg at onset and Lems 20 years later

Muscle & nerve, 2013-11, Vol.48 (5), p.841-842

2013

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Interdigital nerve conduction study of the foot for an early detection of diabetic sensory polyneuropathy

Clinical neurophysiology, 2003-05, Vol.114 (5), p.894-897

2003

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Myasthenia gravis Lambert-Eaton overlap syndrome

Perry Syndrome: A Distinctive Type of TDP-43 Proteinopathy

Transforming Growth Factor Beta (TGF-β) Is a Muscle Biomarker of Disease Progression in ALS and Correlates with Smad Expression

3,4-Diaminopyridine is more effective than placebo in a randomized, double-blind, cross-over drug study in LEMS

Assessment of the compound muscle action potential amplitude return time between exercises or tests in the repetitive nerve stimulation test for Lambert‐Eaton myasthenic syndrome

Distal spinal and bulbar muscular atrophy caused by dynactin mutation

Chronic inflammatory axonal polyneuropathy

Ten-second exercise is superior to 30-second exercise for post-exercise facilitation in diagnosing Lambert-Eaton myasthenic syndrome

Ocular LEMS or MLOS

Diagnostic markers of axonal degeneration and demyelination in sensory nerve conduction

Distinguishing Features of the Repetitive Nerve Stimulation Test Between Lambert-Eaton Myasthenic Syndrome and Myasthenia Gravis, 50-Year Reappraisal

Single-fiber electromyography in sporadic inclusion body myopathy

Statins may aggravate myasthenia gravis

On-nerve needle nerve conduction study in the sural nerve: A new technique for evaluation of peripheral neuropathy

Diagnostic value of the near‐nerve needle sensory nerve conduction in sensory inflammatory demyelinating polyneuropathy

Single-fiber EMG and clinical correlation in Lambert-Eaton myasthenic syndrome

Electrophysiological differences in seropositive and seronegative Lambert-Eaton myasthenic syndrome

Amifampridine phosphate (Firdapse®) is effective and safe in a phase 3 clinical trial in LEMS

Repetitive nerve stimulation of facial muscles in musk antibody-positive myasthenia gravis

Anti-Hu antibody neuropathy: a clinical, electrophysiological, and pathological study

Asymptomatic vasculitic neuropathy

Post-exercise exhaustion in Lambert–Eaton myasthenic syndrome

Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

A patient diagnosed with Mg at onset and Lems 20 years later

Interdigital nerve conduction study of the foot for an early detection of diabetic sensory polyneuropathy

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