Results 11 to 20 of about 6,688 (239)

Lambert-Eaton Myasthenic Syndrome [PDF]

open access: yesNeurologic Clinics, 2018
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 generated against the P/Q-type voltage-gated calcium channels present on presynaptic nerve terminals and ...
Vita G, Kesner   +3 more
openaire   +4 more sources

Presynaptic Paraneoplastic Disorders of the Neuromuscular Junction: An Update [PDF]

open access: yesBrain Sciences, 2021
The neuromuscular junction (NMJ) is the target of a variety of immune-mediated disorders, usually classified as presynaptic and postsynaptic, according to the site of the antigenic target and consequently of the neuromuscular transmission alteration ...
Maria Pia Giannoccaro   +2 more
doaj   +3 more sources

Late onset cerebellar ataxia syndrome after non-paraneoplastic Lambert-Eaton myasthenic syndrome: a case study [PDF]

open access: yesBMC Neurology
This is an unusual case of voltage gated calcium channel (VGCC) antibodies leading to two distinct and chronologically separated neurologic syndromes without the presence of an underlying neoplasm.
David P. Randall, Matthew C. Randall
doaj   +2 more sources

Efficacy of durvalumab plus chemotherapy in small-cell lung cancer with Lambert-Eaton myasthenic syndrome [PDF]

open access: yesRespiratory Medicine Case Reports
Lambert-Eaton myasthenic syndrome (LEMS) is a rare disease but is often associated with small-cell lung cancer (SCLC). We discuss the case of a 65-year-old man diagnosed with SCLC-LEMS and treated with carboplatin, etoposide, and durvalumab.
Naoya Ishibashi   +7 more
doaj   +2 more sources

The Case of a 28‐Year‐Old Man With Gradually Progressive Proximal Leg Weakness

open access: yesAnnals of Clinical and Translational Neurology
This is a case of a 28‐year‐old man who presented with a 6‐month history of gradually progressive proximal leg weakness and pain that worsened on exercise and was relieved by rest. He had no symptoms in his upper limbs.
Melody T. Asukile   +3 more
doaj   +2 more sources

A rare case of concomitant Lambert-Eaton myasthenic syndrome and syndrome of inappropriate antidiuretic hormone secretion in a patient with small cell lung carcinoma. [PDF]

open access: yesRespir Med Case Rep, 2023
Small cell lung carcinoma (SCLC) is a neuroendocrine carcinoma with a poor prognosis and is a common cause of paraneoplastic syndromes. Paraneoplastic syndromes are characterized by neurological and endocrinological problems in patients with malignancy ...
Oda Y   +9 more
europepmc   +3 more sources

Relapse of both small cell lung cancer and Lambert–Eaton myasthenic syndrome after a 13-year disease-free survival period [PDF]

open access: goldChinese Journal of Cancer, 2016
Lambert–Eaton myasthenic syndrome (LEMS) is a paraneoplastic syndrome and only 3% of small cell lung carcinoma (SCLC) patients have LEMS. Moreover, the recurrence of SCLC after a disease-free survival (DFS) of more than 10 years is rare.
Fumio Asano   +10 more
doaj   +2 more sources

Burden of disease in Lambert-Eaton myasthenic syndrome: taking the patient's perspective. [PDF]

open access: yesJ Neurol
Background: Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmune-mediated neuromuscular disorder leading to muscle weakness, autonomic dysregulation and hyporeflexia. Psychosocial well-being is affected. Previously, we assessed burden of disease for
Lehnerer S   +8 more
europepmc   +3 more sources

Lambert-Eaton myasthenic syndromes [PDF]

open access: bronzeJournal of the Neurological Sciences, 2019
K. El Salem
openalex   +2 more sources

Home - About - Disclaimer - Privacy