Results 91 to 100 of about 10,135 (204)

Treatment of Ocular Myasthenia Gravis

open access: yesAsia-Pacific Journal of Ophthalmology, 2019
Myasthenia gravis is a relatively common neuromuscular disorder, with ocular myasthenia gravis being a subset defined as myasthenia gravis limited to the orbicularis, levator, and extraocular muscles. Patients with ocular myasthenia gravis can have disabling diplopia or functional blindness from ptosis and in most cases treatment is required.
openaire   +2 more sources

Cognitive Communication, Voice and Swallowing Difficulties Experienced by Adults With Long‐COVID: A Scoping Review

open access: yesHealth Expectations, Volume 29, Issue 1, February 2026.
ABSTRACT Background Adults with Long‐COVID frequently experience impairments in cognitive‐communication, voice and swallowing, however, few comprehensive reviews of the existing literature has yet to be conducted to map the current research landscape.
Kathleen McTiernan   +2 more
wiley   +1 more source

بررسی وضعيت سرولوژيک و الکتروفيزيولوژيک بيماران مبتلا به مياستنی گراويس [PDF]

open access: yes, 2013
زمينه و هدف: مياستنی گراويس نوعی اختلال خود ايمنی است که به طور اساسي در اثر آنتی بادی‌های ضد رسپتور استيل کولين در محل اتصال عصب به عضله ايجاد شده و کاهش رسپتورهای مذکور سبب اختلال در انتقال نوروترانسميتر و خستگی و ضعف عضلانی می‌شود.
اميرزرگر, علی اکبر   +6 more
core  

AChR deficiency due to ε-subunit mutations: Two common mutations in the Netherlands [PDF]

open access: yes, 2009
Congenital myasthenic syndromes are a clinically and genetically heterogeneous group of hereditary disorders affecting neuromuscular transmission. We have identified mutations within the acetylcholine receptor (AChR) ε-subunit gene underlying congenital ...
Baets, M.H. (Marc) de   +9 more
core   +1 more source

Frontalis sling procedure for ocular myasthenia gravis

open access: yesClinical Ophthalmology, 2012
Shinichi Asamura1, Hirohiko Kakizaki2, Mitsuhiro Enjyo1, Takahiro Hashimoto1, Noritaka Isogai11Department of Plastic and Reconstructive Surgery, Kinki University School of Medicine, Osakasayama, Osaka, Japan; 2Department of Ophthalmology, Aichi Medical ...
Isogai N   +4 more
doaj  

An Atypical Case of Myasthenia Gravis: Purely Bulbar in a Young Male

open access: yesMcGill Journal of Medicine, 2020
Myasthenia Gravis (MG), an uncommon autoimmune syndrome caused by the failure of neuromuscular transmission, results from bind- ing of autoantibodies to proteins that are involved in signaling at the neuromuscular junction (1).
Muhammad Amer Saleem   +3 more
doaj  

Myasthenia Gravis Patients with Anti-MuSK Antibodies [PDF]

open access: yes, 2009
In myasthenia gravis (MG) patients without detectable anti-acetylcholine receptor (anti-AChR) antibody, referred to as seronegative myasthenia gravis patients, there is a variable proportion of patients with antibodies against the muscle-specific kinase (
Davorka Vranješ   +5 more
core   +1 more source

Episodic neurologic disorders: syndromes, genes, and mechanisms. [PDF]

open access: yes, 2013
Many neurologic diseases cause discrete episodic impairment in contrast with progressive deterioration. The symptoms of these episodic disorders exhibit striking variety.
Fu, Ying-Hui   +2 more
core   +2 more sources

Review Article : Neuromuscular causes of weakness in critically ill patients [PDF]

open access: yes, 2017
Multiple predisposing factors are responsible for the development of neuromuscular weakness in a critically ill patient. Thorough history and physical examination is paramount and should not be omitted despite that the majority of patients are ...
Govindarajan, Raghav, Katyal, Nakul
core   +1 more source

The Anti-Acetylcholine Receptor Antibody Test in Suspected Ocular Myasthenia Gravis

open access: yesJournal of Ophthalmology, 2014
Aim. To estimate the clinical significance of anti-acetylcholine receptor antibody (anti-AChR-Ab) levels in suspected ocular myasthenia gravis. Methods. In total, 144 patients complaining of fluctuating diplopia and ptosis were evaluated for serum levels
Jung Jin Lee   +2 more
doaj   +1 more source

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