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Updated: Feb 28, 2026

Antigenic Liposomes for Generation of Disease-specific Antibodies
Published on: October 25, 2018
[Seronegative nonparaneoplastic Lambert-Eaton myasthenic syndrome]
A G Sanadze1, D V Sidnev2, D A Tumurov3
1Pirogov Russian National Medical Research University, Moscow, Russia; Moscow City Health Department, Moscow Myasthenia Center, SFHI Municipal Clinical Hospital #51, Moscow, Russia; Moscow Research and Clinical Center for Neuropsychiatry, Moscow, Russia.
This study highlights two Lambert-Eaton myasthenic syndrome (LEMS) cases lacking typical autoantibodies. Despite this, clinical and electrophysiological findings confirmed LEMS, responding effectively to glucocorticoid treatment, suggesting an autoimmune basis.
Area of Science:
- Neurology
- Immunology
- Clinical Medicine
Background:
- Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmune disorder affecting neuromuscular transmission.
- Diagnosis typically relies on detecting P/Q type voltage-gated calcium channel autoantibodies.
- Atypical presentations without these specific autoantibodies pose diagnostic challenges.
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