Results 1 to 10 of about 6,688 (239)

Myasthenia Gravis and Lambert-Eaton Myasthenic Syndrome: New Developments in Diagnosis and Treatment [PDF]

Neuropsychiatric Disease and Treatment, 2022
Robert M Pascuzzi, Cynthia L Bodkin Indiana University School of Medicine, Indiana University Health, Indianapolis, IN, USACorrespondence: Robert M Pascuzzi, Indiana University School of Medicine, Indiana University Health, Indianapolis, IN, 46202, USA ...
Pascuzzi RM, Bodkin CL
doaj   +4 more sources

Nationwide survey of Lambert-Eaton myasthenic syndrome in Japan [PDF]

BMJ Neurology Open, 2022
Background There was no nationwide epidemiological study of Lambert-Eaton myasthenic syndrome (LEMS) in Japan; therefore, we conducted a nationwide survey.Methods For the first survey, we sent survey sheets to randomly selected medical departments (n ...
Yutaka Furukawa, Satoshi Kuwabara, Nagato Kuriyama, Yoshiko Nomura, Yasunari Sakai, Makoto Matsui, Yosikazu Nakamura, Hiroyuki Murai, Yumi Adachi, Hiroaki Yoshikawa, Kazuo Iwasa   +10 more
doaj   +4 more sources

Congenital Lambert-Eaton myasthenic syndrome. [PDF]

Electroencephalography and Clinical Neurophysiology, 1987
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, Howard Carrier
openalex   +4 more sources

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   +3 more sources

Lambert-Eaton Myasthenic Syndrome

BMJ Case Reports
Lambert-Eaton myasthenic syndrome is a disorder of neuromuscular transmission in which an autoantibody is directed against the pre-synaptic calcium channel. It presents with proximal limb weakness, greater in the legs, with or without peripheral and autonomic neuropathy. Bulbar involvement is rare and fatigueability is not a feature.
Jayarangaiah A, Lui F, Theetha Kariyanna P.   +2 more
europepmc   +12 more sources

Lambert‐Eaton myasthenic syndrome with primary thymic marginal zone B‐cell lymphoma: A case report [PDF]

Respirology Case Reports, 2023
Lambert‐Eaton myasthenic syndrome (LEMS) is an autoimmune paraneoplastic syndrome with proximal muscle weakness, that often complicates small cell lung cancer.
Toshihiko Soma, Akira Matsumoto, Tsuyoshi Shoji, Hiromichi Katakura   +3 more
doaj   +2 more sources

Spontaneous regression of small cell lung cancer associated with Lambert-Eaton Myasthenic Syndrome: Case report [PDF]

Radiology Case Reports, 2023
Spontaneous regression (SR) of cancer is very rare, especially of small cell lung cancer (SCLC). Recently, an association of paraneoplastic neurological syndrome (PNS) has been reported as a cause of SR of cancer, and onconeural antibodies are a possible
Michimi Otani, MD, Miki Nishimori, MD, PhD, Hitomi Iwasa, MD, PhD, Mamiko Iwamura, MD, Takayasu Izumi, MD, Kosuke Nakaji, MD, Noriko Nitta, MD, Kana Miyatake, MD, Rika Yoshimatsu, MD, PhD, Tomoaki Yamanishi, MD, Tomohiro Matsumoto, MD, PhD, Yasushi Osaki, MD, PhD, Noriko Wada, MD, Makoto Toi, MD, PhD, Marino Yamamoto, MD, PhD, Yu Nakatani, MD, Tetsuya Kubota, MD, PhD, Takuji Yamagami, MD, PhD   +17 more
doaj   +2 more sources

062 Pembrolizumab induced lambert-eaton myasthenic syndrome [PDF]

BMJ Neurology Open, 2021
Rob Zielinski, Rami Haddad, Jasmine Ashhurst   +2 more
doaj   +2 more sources

Lambert–Eaton myasthenic syndrome presenting with occult mediastinal small cell carcinoma and positivity for anti-CV2/CRMP5 and anti-SOX1 antibodies: a case report [PDF]

BMC Neurology
Background Lambert-Eaton myasthenic syndrome (LEMS) is a rare autoimmune neuromuscular disorder characterized by proximal muscle weakness, autonomic dysfunction and hyporeflexia.
Anna Wang, He Li, Dewen Li, Kangfeng Wang, Lijuan Zhang   +4 more
doaj   +2 more sources

Lambert-Eaton myasthenic syndrome: report of two cases [PDF]

Arquivos de Neuro-Psiquiatria, 1998
Two cases of Lambert-Eaton myasthenic syndrome, in female patients whose neoplasm investigation was negative, are reported. Repetitive stimulation of ulnar nerve showed an incremental response (+187% and +198%).
ROSANA H. SCOLA, FÁBIO M. IWAMOTO, CÁSSIO S. RAMOS, ANGELA M. SANDERSON, DIEGO LOPARDO, ALESSANDRA CANTARELLI, MARCELO WATANABE, WALTER HORTA, LINEU CESAR WERNECK   +8 more
doaj   +3 more sources