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Myofibrillar Myopathy

Known as: Myofibrillar Myopathies, Myofibrillar changes 
An inherited or sporadic disorder affecting the skeletal muscles.
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
AIMS To report the clinical, pathological and genetic findings in a group of patients with a previously not described phenotype… Expand
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Highly Cited
2010
Highly Cited
2010
Myofibrillar myopathies are a heterogeneous group of neuromuscular disorders characterized by disintegration of myofibrils. The… Expand
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Highly Cited
2008
Highly Cited
2008
Objective:To compare muscle imaging findings in different subtypes of myofibrillar myopathies (MFM) in order to identify… Expand
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Review
2007
Review
2007
Mutations in the filamin C gene (FLNC) cause a myofibrillar myopathy (MFM), morphologically characterized by focal myofibrillar… Expand
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Highly Cited
2005
Highly Cited
2005
Myofibrillar myopathy (MFM) is a human disease that is characterized by focal myofibrillar destruction and pathological… Expand
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Highly Cited
2005
Highly Cited
2005
The role of cardiac myosin binding protein-C (cMyBP-C) phosphorylation in cardiac physiology or pathophysiology is unclear. To… Expand
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Highly Cited
2004
Highly Cited
2004
BACKGROUND AND OBJECTIVE The term myofibrillar myopathy (MFM) is a noncommittal term for a pathologic pattern of myofibrillar… Expand
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Highly Cited
2003
Highly Cited
2003
We here report the second and third mutations in alphaB-crystallin causing myofibrillar myopathy. Two patients had adult-onset… Expand
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Highly Cited
1997
Highly Cited
1997
Hypertrophic cardiomyopathy (HCM), the most common cause of sudden death in the young, is an autosomal dominant disease… Expand
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Highly Cited
1987
Highly Cited
1987
Five healthy untrained young male subjects were studied before, immediately after, and 10 days after a 45-min bout of eccentric… Expand
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