Results 51 to 60 of about 31,308 (159)

Coexistence of Pernicious Anemia and Myasthenia Gravis—A Rare Combination of Autoimmune Diseases in Taiwan

Journal of the Formosan Medical Association, 2006
About 5-10% of patients with myasthenia gravis concomitantly have other autoimmune diseases. However, the coexistence of myasthenia gravis and pernicious anemia is rare.
Kuo-Hsuan Chang, Rong-Kuo Lyu, Long-Sun Ro, Yih-Ru Wu, Chiung-Mei Chen   +4 more
doaj   +1 more source

Epilepsy and Myasthenia Gravis: A Case Series

Brain Sciences
The association between epilepsy and myasthenia gravis has rarely been reported, and when it has been reported, it has only been in a small case series.
Iñigo Oyarzun, Guillermo Hernández, Jacint Sala-Padró, Francisco Morandeira, Carlos Casasnovas, Mercè Falip   +5 more
doaj   +1 more source

Delayed diagnosis of distal myasthenia gravis: a case report

Journal of Medical Case Reports
Introduction Myasthenia gravis, which initially presents with prominent distal muscle weakness, is rare and is referred to as distal myasthenia gravis.
M. L. Cao, Y. X. Qin, N. Shao, C. Y. Zhang, L. L. Deng, X. R. Xu, Q. Liu, X. Yang   +7 more
doaj   +1 more source

Study on the clinical and electrophysiological characteristics of nerve function in myasthenia gravis patients in Vietnam

SAGE Open Medicine
Background: In Vietnam, there is limited research on the role of nerve conduction in myasthenia gravis and its association with clinical features. Objective: This study aims to describe the electrophysiological features in patients with myasthenia gravis.
Tho Kieu Anh Pham, Phuong Van Pham, Tung Dinh Le, Binh Thanh Nguyen, Trung Kien Nguyen, Tam Thai Thanh Tran, Sam Phan Hai Nguyen, Minh Van Le   +7 more
doaj   +1 more source

Myasthenia gravis: analysis of serum autoantibody reactivities to 1827 potential human autoantigens by protein macroarrays.

PLoS ONE, 2013
BackgroundMyasthenia gravis is a disorder of neuromuscular transmission associated with autoantibodies against the nicotinic acetylcholine receptor. We have previously developed a customized protein macroarray comprising 1827 potential human autoantigens,
Anne Becker, Nicole Ludwig, Andreas Keller, Björn Tackenberg, Christian Eienbröker, Wolfgang H Oertel, Klaus Fassbender, Eckart Meese, Klemens Ruprecht   +8 more
doaj   +1 more source

Successful use of sugammadex for caesarean section in a patient with myasthenia gravis

Revista Brasileira de Anestesiologia
Myasthenia gravis is an autoimmune disorder that is characterized by muscle weakness that fluctuates, worsening with exertion, and improving with rest. Diagnosis of myasthenia gravis is made following clinical and physical examination and is confirmed by
Lokman Soyoral, Ugur Goktas, Muhammed Bilal Cegin, Volkan Baydi   +3 more
doaj   +1 more source

Myasthenia Gravis [PDF]

BMJ, 1959
openaire   +3 more sources

Familial Autoimmune Myasthenia Gravis (Report Of 3 Cases)

Annals of Indian Academy of Neurology, 2003
Familial Autoimmune myasthenia gravis is rare, occurring in only about 1.3% cases of myasthenia gravis (MG). Here in we report a family with three family members affected by MG. Proband presented with generalised myasthenia where as the other two
Girija A. S, Madhukar M, John John K
doaj  

Myasthenia gravis with Castleman disease: A case report with review of literature

Indian Journal of Pathology and Microbiology
Myasthenia gravis is an autoimmune disorder caused by the formation of autoantibodies directed against the synapses of neuromuscular junction. It is most commonly associated with other non-thymomatous lesions. Castleman disease is one of them, which is a
Sujit Nandy, Debashis Bhattacharya, Somenath Kundu, Uttara Chatterjee   +3 more
doaj   +1 more source

Exosomes in Myasthenia Gravis-Review. [PDF]

Cells
Ejdys K, Mycko MP.
europepmc   +1 more source