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Intranuclear Rod Myopathy

Known as: Intranuclear Nemaline Rod Myopathy, Nemaline Myopathy with Exclusively Intranuclear Rods 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2017
0120042017

Related topics

Related topics

1 relation

Broader (1)

Myopathies, Nemaline

Related mentions per year

Related mentions per year

1956-2018
1960198020002020
Intranuclear Rod Myopathy
Myopathies, Nemaline

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy.
Nemaline myopathy (NM) is a common form of congenital nondystrophic skeletal muscle disease characterized by muscular weakness of… (More)
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2016
2016
The Effects of Disease Models of Nuclear Actin Polymerization on the Nucleus
Actin plays a crucial role in regulating multiple processes within the nucleus, including transcription and chromatin… (More)
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2015
2015
Hypoxic ischemic encephalopathy in a case of intranuclear rod myopathy without any prenatal sentinel event.
Intranuclear rod myopathy (IRM), a variant of nemaline myopathy, is characterized by the presence of nemaline bodies in myonuclei… (More)
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2007
2007
Mechanisms underlying intranuclear rod formation.
Specific mutations within the alpha-skeletal actin gene (ACTA1) result in intranuclear rod myopathy (IRM), characterized by rod… (More)
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Review
2004
Review
2004
Congenital myopathies: diseases of the actin cytoskeleton.
Congenital myopathies are clinical and genetic heterogeneous disorders characterized by skeletal muscle weakness ranging in… (More)
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