Results 141 to 150 of about 4,323 (166)

Lambert-Eaton Myasthenic Syndrome Complicated by Anti-GABA_B Receptor Encephalitis. [PDF]

Intern Med
Yamada K, Yaguchi H, Ishikawa K, Tanaka D, Oshima Y, Mizushima K, Uwatoko H, Shirai S, Takahashi-Iwata I, Matsushima M, Tanaka K, Yabe I.   +11 more
europepmc   +1 more source

A Unique Case of Non-paraneoplastic Lambert-Eaton Myasthenic Syndrome Treated With Subcutaneous Immunoglobulin: A Case Report and Review of Literature. [PDF]

Cureus
Park SK, Taylor MG.
europepmc   +1 more source

Independence in activities of daily living was achieved using aerobic exercise without overwork weakness during rehabilitation: a case report of Lambert-Eaton myasthenic syndrome. [PDF]

J Phys Ther Sci
Harayama E, Goto K, Yamauchi K.
europepmc   +1 more source

Long-term Follow-up, Quality of Life, and Survival of Patients With Lambert-Eaton Myasthenic Syndrome. [PDF]

Neurology, 2021
europepmc   +1 more source

3,4-diaminopyridine for the treatment of Lambert–Eaton myasthenic syndrome

Expert Review of Clinical Immunology, 2010
The Lambert Eaton myasthenic syndrome (LEMS) is an autoimmune disease in which antibodies against voltage-gated calcium channels inhibit cholinergic neurotransmission LEMS is clinically characterized by muscle weakness and autonomic dysfunction 3 4 ...
Paul W Wirtz, Maarten J Titulaer, Jan J G M Verschuuren   +2 more
exaly   +2 more sources

A close look at autoimmune muscle disorders: association of Lambert–Eaton myasthenic syndrome with dermatomyositis

Scandinavian Journal of Rheumatology, 2004
Dermatomyositis/ polymyositis (DM/PM) and Lambert- Eaton myasthenic syndrome (LEMS) are two autoimmune disorders that have very rarely been reported to occur together in the same patient.
Rotraut Mössner
exaly   +2 more sources

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Congenital Myasthenic Syndrome From a Single Center: Phenotypic and Genotypic features

Journal of Child Neurology, 2021
Partha S Ghosh
exaly