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1982 2
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1993 7
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2007 12
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360 results

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Page 1
Lambert-Eaton Myasthenic Syndrome.
Kesner VG, Oh SJ, Dimachkie MM, Barohn RJ. Kesner VG, et al. Neurol Clin. 2018 May;36(2):379-394. doi: 10.1016/j.ncl.2018.01.008. Neurol Clin. 2018. PMID: 29655456 Free PMC article. Review.
Lambert-Eaton myasthenic syndrome is a paraneoplastic or primary autoimmune neuromuscular junction disorder characterized by proximal weakness, autonomic dysfunction and ariflexia. The characteristic symptoms are thought to be caused by antibodies gene
Lambert-Eaton myasthenic syndrome is a paraneoplastic or primary autoimmune neuromuscular junction disorder char
Update in the Management of Myasthenia Gravis and Lambert-Eaton Myasthenic Syndrome.
Bodkin C, Pascuzzi RM. Bodkin C, et al. Neurol Clin. 2021 Feb;39(1):133-146. doi: 10.1016/j.ncl.2020.09.007. Epub 2020 Nov 7. Neurol Clin. 2021. PMID: 33223079 Review.
Myasthenia gravis (MG) and Lambert-Eaton myasthenic syndrome (LEMS) are the most common disorders of neuromuscular transmission in clinical practice. ...
Myasthenia gravis (MG) and Lambert-Eaton myasthenic syndrome (LEMS) are the most common disorders of neuromuscul …
Epidemiology, diagnostics, and biomarkers of autoimmune neuromuscular junction disorders.
Punga AR, Maddison P, Heckmann JM, Guptill JT, Evoli A. Punga AR, et al. Lancet Neurol. 2022 Feb;21(2):176-188. doi: 10.1016/S1474-4422(21)00297-0. Lancet Neurol. 2022. PMID: 35065040 Review.
Muscle-specific tyrosine kinase antibody-positive myasthenia gravis and Lambert-Eaton myasthenic syndrome are about 20 times less common. ...For prognostic purposes, determining whether the disease is paraneoplastic is of great importance, as myastheni …
Muscle-specific tyrosine kinase antibody-positive myasthenia gravis and Lambert-Eaton myasthenic syndrome are ab …
Neuromuscular Diseases.
Morrison BM. Morrison BM. Semin Neurol. 2016 Oct;36(5):409-418. doi: 10.1055/s-0036-1586263. Epub 2016 Sep 23. Semin Neurol. 2016. PMID: 27704495 Review.
., chronic inflammatory demyelinating polyradiculoneuropathy), neuromuscular junction (i.e., myasthenia gravis or Lambert-Eaton myasthenic syndrome), muscle (i.e., inflammatory myopathy or muscular dystrophy), or any combination of these sites. ...
., chronic inflammatory demyelinating polyradiculoneuropathy), neuromuscular junction (i.e., myasthenia gravis or Lambert-Eaton
Foodborne Botulism: Clinical Diagnosis and Medical Treatment.
Lonati D, Schicchi A, Crevani M, Buscaglia E, Scaravaggi G, Maida F, Cirronis M, Petrolini VM, Locatelli CA. Lonati D, et al. Toxins (Basel). 2020 Aug 7;12(8):509. doi: 10.3390/toxins12080509. Toxins (Basel). 2020. PMID: 32784744 Free PMC article. Review.
The most know typical clinical syndrome of botulism refers to the foodborne form. All different forms are characterized by the same symptoms, caused by toxin-induced neuromuscular paralysis. ...Foodborne botulism intoxication is often underdiagnosed; the initial symptoms c …
The most know typical clinical syndrome of botulism refers to the foodborne form. All different forms are characterized by the same s …
Lambert-Eaton Myasthenic Syndrome and Botulism.
Raja SM. Raja SM. Continuum (Minneap Minn). 2022 Dec 1;28(6):1596-1614. doi: 10.1212/CON.0000000000001205. Continuum (Minneap Minn). 2022. PMID: 36537971 Review.
PURPOSE OF REVIEW: This article reviews the pathophysiology, epidemiology, clinical features, diagnosis, and treatment of Lambert-Eaton myasthenic syndrome (LEMS) and botulism, presynaptic disorders of neuromuscular transmission in which rapid diagnosi …
PURPOSE OF REVIEW: This article reviews the pathophysiology, epidemiology, clinical features, diagnosis, and treatment of Lambert- …
Updated consensus statement: Intravenous immunoglobulin in the treatment of neuromuscular disorders report of the AANEM ad hoc committee.
Tavee J, Brannagan TH 3rd, Lenihan MW, Muppidi S, Kellermeyer L, D Donofrio P; AANEM. Tavee J, et al. Muscle Nerve. 2023 Oct;68(4):356-374. doi: 10.1002/mus.27922. Epub 2023 Jul 11. Muscle Nerve. 2023. PMID: 37432872 Review.
Based on Class I evidence, IVIG is recommended in the treatment of chronic inflammatory demyelinating polyneuropathy, Guillain-Barre Syndrome (GBS) in adults, multifocal motor neuropathy, dermatomyositis, stiff-person syndrome and myasthenia gravis exacerbations but …
Based on Class I evidence, IVIG is recommended in the treatment of chronic inflammatory demyelinating polyneuropathy, Guillain-Barre Synd
Lambert-Eaton myasthenic syndrome.
Lipka AF, Verschuuren JJGM. Lipka AF, et al. Handb Clin Neurol. 2024;200:307-325. doi: 10.1016/B978-0-12-823912-4.00012-8. Handb Clin Neurol. 2024. PMID: 38494285 Review.
Lambert-Eaton myasthenic syndrome (LEMS) is a rare autoimmune disease characterized by proximal muscle weakness, loss of tendon reflexes, and autonomic dysfunction. ...
Lambert-Eaton myasthenic syndrome (LEMS) is a rare autoimmune disease characterized by proximal muscle weakness,
Lambert-Eaton myasthenic syndrome - diagnosis, pathogenesis and therapy.
Hülsbrink R, Hashemolhosseini S. Hülsbrink R, et al. Clin Neurophysiol. 2014 Dec;125(12):2328-36. doi: 10.1016/j.clinph.2014.06.031. Epub 2014 Jul 4. Clin Neurophysiol. 2014. PMID: 25065299 Review.
Lambert-Eaton myasthenic syndrome (LEMS) describes a rare human autoimmune disorder of the neuromuscular junction (NMJ). ...
Lambert-Eaton myasthenic syndrome (LEMS) describes a rare human autoimmune disorder of the neuromuscular junctio
Synaptic Pathophysiology and Treatment of Lambert-Eaton Myasthenic Syndrome.
Tarr TB, Wipf P, Meriney SD. Tarr TB, et al. Mol Neurobiol. 2015 Aug;52(1):456-63. doi: 10.1007/s12035-014-8887-2. Epub 2014 Sep 9. Mol Neurobiol. 2015. PMID: 25195700 Free PMC article. Review.
Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmune disease that disrupts the normally reliable neurotransmission at the neuromuscular junction (NMJ). ...
Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmune disease that disrupts the normally reliable neurotrans
360 results