Zobrazeno 1 - 10
of 1 429
pro vyhledávání: '"Fatigable weakness"'
Akademický článek
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Publikováno v:
Journal of Neuro-Ophthalmology. 27:41-44
A 25-year-old man with chronically progressive ptosis and bilateral ophthalmoplegia displayed fatigability and fluctuation of ptosis, an abnormal single-fiber electromyogram, and a markedly elevated acetylcholine receptor antibody level. Yet a muscle
Publikováno v:
Journal of Neuro-Ophthalmology; Mar2007, Vol. 27 Issue 1, p41-44, 4p
Autor:
Lucy Feng, Matthew Pitt, Adnan Y. Manzur, Caroline Sewry, M. Illingworth, E. Vorstman, R. Gunny, David Beeson, Francesco Muntoni, Stephanie Robb, Marion Main
Publikováno v:
Neuromuscular disorders : NMD. 24(8)
The spectrum of RYR1 mutation associated disease encompasses congenital myopathies, exercise induced rhabdomyolysis, malignant hyperthermia susceptibility and King-Denborough syndrome. We report the clinical phenotype of two siblings who presented in
Akademický článek
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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
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
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
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.
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