Results 21 to 30 of about 4,323 (166)

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

Successful treatment of advanced lung adenocarcinoma complicated with Lambert‐Eaton myasthenic syndrome: A case report and literature review

Thoracic Cancer, 2020
Lambert‐Eaton myasthenic syndrome (LEMS) is a rare disease characterized by involvement of the neuromuscular junction. Most cases have an underlying malignancy, especially small‐cell lung cancer (SCLC), while adenocarcinoma is less common.
Aili Wang, Xin Zhang, Jiawen Yi, Min Zhu, Yuhui Zhang   +4 more
doaj   +1 more source

A first case association of Lambert-Eaton Myasthenic Syndrome and First Episode Psychosis: a case report [PDF]

Eur Psychiatry
Introduction: Lambert-Eaton Myasthenic Syndrome is an autoimmune neuromuscular junction disorder characterized by proximal weakness, autonomic dysfunction, and areflexia associated with antibodies against voltage-gated calcium channels.
Siopa C, Cordeiro C, Moura B.
europepmc   +2 more sources

Hypotension due to Chemotherapy in a Patient with Small Cell Lung Cancer and Lambert-Eaton Myasthenic Syndrome Undergoing Hemodialysis: A First Case Report

Case Reports in Oncology, 2012
We present the first case of small cell lung cancer with Lambert-Eaton myasthenic syndrome during hemodialysis (HD). A 72-year-old male patient receiving HD experienced progressive muscle weakness.
Taiji Kuwata, Hidetaka Uramoto, Tetsuro Baba, Fumihiro Tanaka   +3 more
doaj   +1 more source

Simultaneous paraneoplastic cerebellar degeneration, Lambert-Eaton syndrome and neuropathy associated with AGNA/anti-SOX1 and VGCC antibodies

Neurological Research and Practice, 2021
Anti-glial nuclear antibody (AGNA) is an onconeuroal antibody targeting the nuclei of Bergmann glia in the cerebellum and Anti-SRY-related HMG-box 1 (SOX1).
Jonas Feldheim, Cornelius Deuschl, Martin Glas, Christoph Kleinschnitz, Tim Hagenacker   +4 more
doaj   +1 more source

Stimulated single-fiber electromyography (sSFEMG) in Lambert-Eaton syndrome

Clinical Neurophysiology Practice, 2018
Objective: To report the clinical features and the neurophysiological approach of a patient with Lambert-Eaton myasthenic syndrome (LEMS), highlighting the diagnostic role of the stimulated single fiber electromyography (sSFEMG).
Vincenzo Todisco, Giovanni Cirillo, Rocco Capuano, Alessandro d'Ambrosio, Gioacchino Tedeschi, Antonio Gallo   +5 more
doaj   +1 more source

Paraneoplastic Mononeuritis Multiplex as a Presenting Feature of Adenocarcinoma of the Lung

Case Reports in Oncological Medicine, 2013
Paraneoplastic neurologic syndromes are observed in less than 0.1% of cancer patients. Neurologic syndromes in lung cancer include Lambert-Eaton myasthenic syndrome, polyneuropathy, cerebellar degeneration, and rarely mononeuritis multiplex. In this case,
Esra Ekiz, Abdullah Ozkok, Nazan Kader Ertugrul   +2 more
doaj   +1 more source

Tubular aggregates in autoimmune Lambert–Eaton myasthenic syndrome

, 2016
Tubular aggregates are accumulations of densely packed tubules in muscle fibers, occurring in distinct hereditary and acquired disorders. We present a patient with tubular aggregates and autoimmune Lambert–Eaton myasthenic syndrome.
Funk, F., Weis, J., Cordts, I., Weis, Joachim, Schulz, J.B., Funk, Fabian, Claeys, Kristl, Cordts, Isabell, Schulz, Jörg B., Claeys, Kristl G.   +9 more
core   +1 more source

Chimeric Antigen Receptor T‐Cells in Myasthenia Gravis: Advances, Safety Challenges, and Future Directions

Muscle &Nerve, Volume 73, Issue 6, Page 942-951, June 2026.
ABSTRACT This review examines the emerging application of chimeric antigen receptor (CAR) T‐cell therapy in myasthenia gravis (MG), with emphasis on safety, efficacy signals, and future therapeutic potential in treatment‐refractory disease. A comprehensive literature search was conducted across PubMed, medRxiv, bioRxiv, and Google Scholar for studies ...
Tobias Hegelmaier, Alexander Duscha, Christiane Desel, Sarah Stassen, Tim Krzemien, Ann‐Katrin Hennemann, Vaia Pappa, Aiden Haghikia   +7 more
wiley   +1 more source

Using Intravenous Inmunoglobulin in an Atypical Case of Lambert Eaton Síndrome.

Medisur, 2007
A 48 year-old hypertensive, smoker patient who started presenting a generalized weakness, pait instability,visual disorders and uncontrolled blood pressure is presented. At physical examination quadriparesis and weakness extraocular muscles were found. A
Erélido Hernández Valero, Osbert Rodríguez Miranda   +1 more
doaj   +2 more sources