目次
WordNet
- any pathology of the muscles that is not attributable to nerve dysfunction
UpToDate Contents
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- 1. 小児における外眼筋に影響するミオパチー myopathies affecting the extraocular muscles in children
- 2. 眼咽頭型、遠位型，および先天性筋ジストロフィー oculopharyngeal distal and congenital muscular dystrophies
- 3. 代謝性ミオパチーへのアプローチ approach to the metabolic myopathies
- 4. 全身性疾患のミオパシー myopathies of systemic disease
- 5. 眼瞼下垂症の概要 overview of ptosis
English Journal
- Eyelid surgery in ocular myopathies.
- Doherty M, Winterton R, Griffiths PG.SourceRoyal Victoria Infirmary , Newcastle upon Tyne , United Kingdom , and.
- Orbit (Amsterdam, Netherlands).Orbit.2013 Feb;32(1):12-5. doi: 10.3109/01676830.2012.736599.
- ABSTRACT Objective: To retrospectively analyse surgical outcome and complications in patients with ocular myopathy undergoing ptosis correction and to introduce preoperative prophylactic lower lid elevation in this group. Methods: The medical records of all ocular myopathy patients who had under
- PMID 23387448
- Optineurin is potentially associated with TDP-43 and involved in the pathogenesis of inclusion body myositis.
- Yamashita S, Kimura E, Tawara N, Sakaguchi H, Nakama T, Maeda Y, Hirano T, Uchino M, Ando Y.SourceDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto 860-8556, Japan.
- Neuropathology and applied neurobiology.Neuropathol Appl Neurobiol.2012 Aug 3. doi: 10.1111/j.1365-2990.2012.01297.x. [Epub ahead of print]
- Aims: Increasing evidences suggest a similarity in the pathophysiological mechanisms of neuronal cell death in amyotrophic lateral sclerosis (ALS) and myofibre degeneration in sporadic inclusion body myositis (sIBM). The aim of this study is to elucidate the involvement of ALS-causing proteins in th
- PMID 22860700
Japanese Journal
- Oculopharyngeal Muscular Dystrophy Associated with Dementia
- Mizoi Yoshikazu,Yamamoto Toshimasa,Minami Narihiro,Ohkuma Aya,Nonaka Ikuya,Nishino Ichizo,Tamura Naotoshi,Amano Takahiro,Araki Nobuo
- Internal Medicine 50(20), 2409-2412, 2011
- … We report genetically confirmed heterozygote oculopharyngeal muscular dystrophy (OPMD) accompanied by dementia, suggesting a possible causal association between OPMD and dementia. … In addition, the proband's younger brother exhibited myopathy and dementia. …
- NAID 130001087759
- Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy
- MINAMI N
- Neuromuscul Disord 11, 699-702, 2001
- NAID 30008308450
Related Links
- Two patients are described with distinctive clinical features including an insidious onset, slow progression, bilateral ptosis, weakness of facial muscles, dysphagia, muscle atrophy, and weakness with a distal distribution in the ...
- BioInfoBank Library :: Oculopharyngeal muscular dystrophy: a polyalanine myopathy. Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotes. Multi-system neurological disease is common in ...
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