Sporadic inclusion body myositis misdiagnosed as idiopathic granulomatous myositis
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference9 articles.
1. Inclusion body myositis and sarcoid myopathy: coincidental occurrence or associated diseases;Sanmaneechai;Neuromuscul Disord,2015
2. Seropositivity for NT5c1A antibody in sporadic inclusion body myositis predicts more severe motor, bulbar and respiratory involvement;Goyal;J Neurol Neurosurg Psychiatry,2015
3. A retrospective cohort study identifying the principal pathological features useful in the diagnosis of inclusion body myositis;Brady;BMJ open,2014
4. Clinical correlates of granulomas in muscle;Mozaffar;J Neurol,1998
5. Clinical assessment determines the diagnosis of inclusion body myositis independently of pathological features;Brady;J Neurol Neurosurg Psychiatry,2013
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