Results 71 to 80 of about 4,373 (200)

Guillain‐Barré syndrome: a comprehensive review

open access: yesEuropean Journal of Neurology, Volume 31, Issue 8, August 2024.
Abstract Guillain‐Barré syndrome (GBS) is a potentially devastating yet treatable disorder. A classically postinfectious, immune‐mediated, monophasic polyradiculoneuropathy, it is the leading global cause of acquired neuromuscular paralysis. In most cases, the immunopathological process driving nerve injury is ill‐defined.
Roberto Bellanti, Simon Rinaldi
wiley   +1 more source

Clinical and functional studies of autoimmune disorders of neuromuscular transmission

open access: yes, 2015
Inherited and acquired disorders of the neuromuscular junction are an important cause of muscle weakness and fatigability. In this thesis I focus on the autoimmune disorders of neuromuscular transmission.
Spillane, J
core  

NMR‐based metabolomic investigation of dogs with acute flaccid paralysis due to tick paralysis

open access: yesVeterinary Medicine and Science, Volume 10, Issue 4, July 2024.
The NMR‐based serum metabolomics approach used in this study revealed distinct up‐regulated/down‐regulated expressions, presenting a promising avenue for research. It was observed that energy metabolism, particularly liver function, was impaired in dogs with tick paralysis.
Erdem Gülersoy   +4 more
wiley   +1 more source

Lambert-Eaton Myasthenic Syndrome Caused by Nivolumab in a Patient with Squamous Cell Lung Cancer

open access: yesCase Reports in Neurology, 2018
Lambert-Eaton myasthenic syndrome (LEMS) is a representative paraneoplastic neurological syndrome. Recently, nivolumab, an anti-programmed cell death 1 inhibitor, has been approved for advanced non-small-cell lung cancer. Careful attention should be paid
Yuki Nakatani   +5 more
doaj   +1 more source

Coexistence of myasthenia gravis and lichen planus: A case report and systematic review of related case reports from 1971 to 2024

open access: yesClinical Case Reports, Volume 12, Issue 6, June 2024.
Key Clinical Message The co‐occurrence of myasthenia gravis (MG) and lichen planus (LP) is a rare phenomenon, with only 13 cases reported in the English literature between 1971 and 2024. Patients with MG or LP, regardless of the thymoma status, require close monitoring for other autoimmune diseases.
Melika Jameie   +5 more
wiley   +1 more source

Lambert-Eaton Myasthenic Syndrome And The Eye

open access: yes, 2013
Wide ranges on the frequency of ophthalmic symptoms and signs in Lambert-Eaton Myasthenic Syndrome (LEMS) have led to mixed and occasionally contradictory messages on how frequenly the visual system is ...
Jeffery D. Young; Jacqueline A. Leavitt; David O. Hodge
core  

Idiopathic Lambert-Eaton myasthenic syndrome. Report of one case Síndrome miasteniforme de Lambert-Eaton idiopático [PDF]

open access: yes, 2006
Lambert-Eaton myasthenic syndrome (LEMS) is an autoinmune idiopathic or paraneoplastic syndrome producing antibodies agaisnt presynaptic voltage calcium channels.
Luis Pedraza, C.   +3 more
core  

Paraneoplastic neurological syndromes

open access: yesOrphanet Journal of Rare Diseases, 2007
Paraneoplastic neurological syndromes (PNS) can be defined as remote effects of cancer that are not caused by the tumor and its metastasis, or by infection, ischemia or metabolic disruptions.
Antoine Jean-Christophe   +1 more
doaj   +1 more source

Initial screening for neuronal autoantibodies and their putative impact on survival in patients with small‐cell lung cancer

open access: yesThoracic Cancer, Volume 15, Issue 17, Page 1350-1356, June 2024.
In a retrospective study, serum from patients with biopsy‐proven small‐cell lung cancer (SCLC) at the time of diagnosis was studied prior to treatment. The sera were analyzed for the presence of neuronal autoantibodies blinded to clinical status. The main finding was demonstration that neuronal autoantibodies were frequent at the time of diagnosis ...
Anne With Mikkelsen   +4 more
wiley   +1 more source

Patient perspectives on Lambert-Eaton myasthenic syndrome

open access: yes
To better understand what it\u27s like to live with Lambert-Eaton myasthenic syndrome (LEMS), we spoke to two individuals who have been living with non-tumor LEMS for years.
Randall, David P   +5 more
core   +1 more source

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