Results 11 to 20 of about 3,664 (121)

Lambert-Eaton myasthenic syndrome [PDF]

Canadian Medical Association Journal, 2006
What's your call? ![Figure][1] Figure. A 72-year-old female smoker presented with morning fatigue, discrete left ptosis and absent reflexes in lower limbs. Top panel: Electromyogram showing evoked motor response of abductor of the fifth finger after stimulation of the left ulnar ...
Monique, D'Amour, Gilles, Gariepy, Joseph, Braidy   +2 more
openaire   +3 more sources

Lambert-Eaton Myasthenic Syndrome [PDF]

Neurologic 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, Shin J, Oh, Mazen M, Dimachkie, Richard J, Barohn   +3 more
openaire   +2 more sources

An unusual case of delayed recovery from spinal anesthesia in a patient with Lambert-Eaton myasthenic syndrome—a case report

Ain Shams Journal of Anesthesiology, 2023
Background The Lambert-Eaton myasthenic syndrome (LEMS) is a rare disorder characterized by proximal muscle weakness and autonomic dysfunction due to involvement of the neuromuscular junction A case of delayed unilateral recovery from spinal anesthesia ...
Souvik Mukherjee, Vaishali Waindeskar, Kiran Molli, Akhil Kuttan Koovakattil   +3 more
doaj   +1 more source

Atypical Presentation of Seronegative Paraneoplastic Lambert–Eaton Myasthenic Syndrome with Cerebellar Ataxia [PDF]

Annals of Indian Academy of Neurology
Shalesh Rohatgi, Siddharth Nimal, Satish Nirhale, Prajwal Rao, Pravin Naphade, Prashant Dubey, Advait Gitay, Pranit Khandait, Khusboo Hatekar, Salil Gundewar   +9 more
doaj   +2 more sources

Electrophysiological evaluation of the neuromuscular junction: a brief review

Arquivos de Neuro-Psiquiatria, 2023
The nerve terminal and muscle membrane compose the neuromuscular junction. After opening the voltage-gated calcium channels, action potentials from the motor axons provoke a cascade for the acetylcholine release from synaptic vesicles to the synaptic ...
João Aris Kouyoumdjian, Eduardo de Paula Estephan   +1 more
doaj   +1 more source

LAMBERT-EATON MYASTHENIC SYNDROME

Vestnik, 2022
Миастенический Синдром Ламберта-Итона (МСЛИ) - это нервно-мышечное заболевание, характеризующееся образованием антител к потенциалзависимым кальциевым каналам (ПЗКК), триггером которых является опухолевый процесс (чаще всего мелкоклеточный рак легких) или как первичный аутоиммунный процесс.
M A, Hernández, A A, Köhler, M, Marrodán, A, Lautre, P, Brand, M, Nogués, F, Barroso   +6 more
openaire   +3 more sources

Congenital Lambert-Eaton myasthenic syndrome [PDF]

Electroencephalography and Clinical Neurophysiology, 1985
A 4 year old girl had been hypotonic and areflexic since birth with delayed milestones in motor development. Repetitive stimulation at high rates performed at 3 years elicited an incremental response typical of the Lambert-Eaton Syndrome.
B, Bady, G, Chauplannaz, H, Carrier
openaire   +2 more sources

Lambert-Eaton myasthenic syndrome against the background of thyroid cancer: a clinical case [PDF]

Клиническая практика
BACKGROUND: Lambert–Eaton myasthenic syndrome (G73.1 according to ICD-10) is a rare autoimmune disease associated with a presynaptic impairment of neuromuscular transmission due to the production of antibodies to voltage-gated calcium channels.
Elena V. Khozhenko, Elena S. Kiparisova, Iraida V. Larina, Alexandra L. Vaulicheva, Sergey S. Grigoriev, Elvira S. Mavlyudova   +5 more
doaj   +1 more source

Lung adenocarcinoma with Lambert–Eaton myasthenic syndrome indicated by voltage-gated calcium channel: a case report

Journal of Medical Case Reports, 2012
Introduction Lambert–Eaton myasthenic syndrome is a rare disorder and it is known as a paraneoplastic neurological syndrome. Small cell lung cancer often accompanies this syndrome.
Arai Hiromasa, Inui Kenji, Hashimoto Kazuki, Kan-o Kazuki, Nishii Teppei, Kishida Hitaru, Okudela Koji, Tsuboi Masahiro, Nozawa Akinori, Kaneko Takeshi, Masuda Munetaka   +10 more
doaj   +1 more source

Lambert-Eaton myasthenic syndrome as a cause of persistent neuromuscular weakness after a mediastinoscopic biopsy -A case report- [PDF]

Korean Journal of Anesthesiology, 2010
There are many causes of prolonged postoperative muscle weakness, including drugs, residual anesthetics, cerebrovascular events, electrolyte imbalance, hypothermia, and neuromuscular disease.
Cheol Jin Lee, Se Hun Lim, Chee Mahn Shin, Young Jae Kim, Young Kyun Choe, Soon Ho Cheong, Kun Moo Lee, Jeong Han Lee, Young Hwan Kim, Kwang Rae Cho, Sang Eun Lee, Jong Suk Bae   +11 more
doaj   +1 more source