Myopathies, Nemaline

Known as: Myopathy, Rod Body, Nemaline Rod Disease, Myopathy, Rod 
A group of inherited congenital myopathic conditions characterized clinically by weakness, hypotonia, and prominent hypoplasia of proximal muscles… (More)
National Institutes of Health

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Highly Cited
2002
Highly Cited
2002
Nemaline myopathy is a clinically and genetically heterogeneous muscle disorder. In the nebulin gene we have detected a number of… (More)
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Highly Cited
2002
Highly Cited
2002
OBJECTIVE To describe the use of large-scale gene expression profiles to distinguish broad categories of myopathy and subtypes of… (More)
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Review
2001
Review
2001
We report 143 Australian and North American cases of primary nemaline myopathy. As classified by the European Neuromuscular… (More)
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Review
2001
Review
2001
The term nemaline myopathy (NM) encompasses a heterogeneous group of disorders of primary skeletal muscle weakness characterized… (More)
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Highly Cited
2000
Highly Cited
2000
The nemaline myopathies are characterized by weakness and eosinophilic, rodlike (nemaline) inclusions in muscle fibers. Amish… (More)
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Review
2000
Review
2000
Animal and plant uncoupling protein (UCP) homologues form a subfamily of mitochondrial carriers that are evolutionarily related… (More)
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Highly Cited
1999
Highly Cited
1999
Muscle contraction results from the force generated between the thin filament protein actin and the thick filament protein myosin… (More)
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Highly Cited
1999
Highly Cited
1999
The congenital nemaline myopathies are rare hereditary muscle disorders characterized by the presence in the muscle fibers of… (More)
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Highly Cited
1995
Highly Cited
1995
screen of the microscope. Between 150 to 300 nerve fibers were analyzed per cross section. 13. C. F. Eldridge, M. Bartlett, R. P… (More)
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Highly Cited
1995
Highly Cited
1995
Nemaline myopathies are diseases characterized by the presence in muscle fibres of pathognomonic rod bodies. These are composed… (More)
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