Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Fatigable weakness"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Neurology. 95:933-938
A 40-year-old man presented with slowly progressive weakness and eyelid droopiness. His symptoms began in his early 30s as increased fatigue with exertion. In his mid 30s, he developed droopy eyelids without double vision. About 3 years before presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8058bb8c5eae524dc66118c6c35b196
https://doi.org/10.1212/wnl.0000000000010613
https://doi.org/10.1212/wnl.0000000000010613
Autor:
Varun O. Agrawal, Narendra Vaidya
Publikováno v:
International Journal of Orthopaedics Sciences. 6:682-686
Myasthenia Gravis leads to painless fatigable weakness of specific muscles in the body. It is often associated with comorbidities. A major surgery like total knee replacement in such a patient can lead to myasthenic crisis and many other complication
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85e81951f6fd28fdef89274c23757b96
https://doi.org/10.22271/ortho.2020.v6.i1l.1944
https://doi.org/10.22271/ortho.2020.v6.i1l.1944
Publikováno v:
Cureus
Oropharyngeal dysphagia is defined as the inability or difficulty to initiate swallowing. It has a wide array of etiologies including structural and neurologic diseases. Myasthenia gravis (MG) is a rare autoimmune condition caused by antibodies again
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dba0d3705112a879825e74d1ff811ee
https://doi.org/10.7759/cureus.16880
https://doi.org/10.7759/cureus.16880
Autor:
Brian D. Stephens, Min K. Kang
Publikováno v:
Neurology. 96:545-547
Congenital myasthenic syndrome (CMS) is an important diagnosis to consider in an adult with both fixed and fatigable weakness.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b85071eaa3d09a26fe51eb4638e8aba6
https://doi.org/10.1212/wnl.0000000000011287
https://doi.org/10.1212/wnl.0000000000011287
Autor:
Meabh O'Hare, Christopher T. Doughty
Publikováno v:
Seminars in Neurology. 39:749-760
Myasthenia gravis is an antibody-mediated autoimmune disorder of the post-synaptic neuromuscular junction resulting in fluctuating, fatigable weakness. Most patients first present with extraocular symptoms (diplopia and/or ptosis), and in 15% of case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::840588200ed7ecc096d9beb68f5f3cf3
https://doi.org/10.1055/s-0039-1700527
https://doi.org/10.1055/s-0039-1700527
Publikováno v:
Electrodiagnostic Medicine ISBN: 9783030749965
The neuromuscular junction (NMJ) may be considered simply a connection between the nerve and muscle fiber. However, it is a specialized synapse which includes complex structures such as the presynaptic nerve terminal, synaptic cleft and a postsynapti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e198e115e76bf93cb111aa565b5ff7cb
https://doi.org/10.1007/978-3-030-74997-2_10
https://doi.org/10.1007/978-3-030-74997-2_10
Publikováno v:
Neuroimmunology ISBN: 9783030618827
Myasthenia gravis and Lambert-Eaton myasthenic syndrome are two autoimmune disorders of the neuromuscular junction. Antibodies against components of the postsynaptic membrane, most commonly the acetylcholine receptor, cause myasthenia gravis. It pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27aa9b2e24661d9bf546b0af7ce4905b
https://doi.org/10.1007/978-3-030-61883-4_19
https://doi.org/10.1007/978-3-030-61883-4_19
Autor:
Cynthia Bodkin, Robert M. Pascuzzi
Publikováno v:
Neurologic clinics. 39(1)
Myasthenia gravis (MG) and Lambert-Eaton myasthenic syndrome (LEMS) are the most common disorders of neuromuscular transmission in clinical practice. Disorders of the neuromuscular junction (NMJ) are characterized by fluctuating and fatigable weaknes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16b24252bd724d9869150873e8e8ed42
https://pubmed.ncbi.nlm.nih.gov/33223079
https://pubmed.ncbi.nlm.nih.gov/33223079
Autor:
Judith Cossins, Shanika Nandasiri, Lalinka Herath, Susan Maxwell, Sunethra Senanayake, David Beeson, Inuka Kishara Gooneratne, Kamal Gunaratne, Thashi Chang, Richard D. Webster
Publikováno v:
Journal of neuromuscular diseases. 8(1)
Congenital myasthenic syndromes (CMS) result from genetic mutations that cause aberrations in structure and/or function of proteins involved in neuromuscular transmission. The slow-channel CMS (SCCMS) is an autosomal dominant postsynaptic defect caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e10dc8dfe13be1db504063ba94b427b
https://pubmed.ncbi.nlm.nih.gov/33216040
https://pubmed.ncbi.nlm.nih.gov/33216040