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[DOC File]Rheumatology 2002
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My laboratory takes genetic and cell biology approaches to understand how intracellular transport processes are affected in neurodegenerative diseases, focusing primarily on Drosophila models of motor neuron and peripheral nerve diseases.
is myositis hereditary

[DOC File]tom's res - Neuroscience
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In keeping with the IIM, proximal muscles tend to be more severely affected. Distal muscle involvement, such as the deep flexors of fingers and deep extensors of the foot are more commonly seen in inclusion body myositis and neurodegenerative condition such as …
what causes inclusion body myositis

[DOC File]Neuromuscular Questions - Residency
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On the basis of well defined clinical, demographic, histologic and immunopathological criteria, the inflammatory myopathies can be classified into three major groups: polymyositis (PM), dermatomyositis (DM), and inclusion body myositis (IBM). General Clinical Features. The incidence of PM, DM, and IBM is approximately 1 in 100,000.
body inclusion myopathy

[DOCX File]www.research.manchester.ac.uk
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Revised May 2009. Ataxia Clinic: Monday afternoons. Referrals: The Ataxia Clinic provides comprehensive diagnostic evaluation and management of patients with postural and movement disorders, with emphasis upon cerebellar disturbances, including the hereditary spinocerebellar ataxias, sporadic olivopontocerebellar atrophy, multiple system atrophy and Friedreich's ataxia.
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Sporadic Inclusion Body Myositis | The Myositis Association
The following can be seen in Inclusion Body Myositis except: Distal upper extremetiy weakness. Occurs more frequently in younger patients. Muscle biopsy shows inflammatory changes and deposition of amyloid. EMG shows diffuse irritability and fibrillation potentials. In HNPP the genetic defect is found on which chromosome?
sporadic inclusion body myositis

[DOCX File]Title: Statin Induced Autoimmune Myopathy
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Clinically they are sub-classified as dermatomyositis (DM), polymyositis (PM), inclusion body myositis (IBM), and increasingly recognised immune-mediated necrotizing myopathy (IMNM). IIM are thought to be complex genetic diseases, initiated by immune activation following specific environmental events in genetically predisposed individuals.
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Hereditary inclusion body myositis