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miopatia nemalinowa · Vinony

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Autosomal recessive disorders
miopatia nemalinowa

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EntityQ1507379· pop 12· linked from 120 articles

miopatia nemalinowa

Also known as nemaline rod myopathy, rod myopathy, nemaline body disease, NEM, NM

choroba genetyczna powodowana przez mutacje genu NEB, który koduje nebulinę

Research

1,179 papers

Sporadic Late-Onset Nemaline Myopathy: Current Landscape.Current neurology and neuroscience reports · 2023
Pediatric Nemaline Myopathy: A Systematic Review Using Individual Patient Data.Journal of child neurology · 2022
Recent advances in nemaline myopathy.Neuromuscular disorders : NMD · 2021
Sarcomere Dysfunction in Nemaline Myopathy.Journal of neuromuscular diseases · 2017
[Sporadic Late Onset Nemaline Myopathy].Brain and nerve = Shinkei kenkyu no shinpo · 2025

Wikidata facts

Image: Congenital nemaline myopathy.jpg

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Connections

myotonia congenita

epidermolysis bullosa simplex

Categories

Autosomal recessive disorders Myoneural junction and neuromuscular diseases Rare diseases

Sources

wikipedia.externallinksexternallink

exact match

www.orpha.net/ORDO/Orphanet_607

Commons category

Nemaline myopathy

Sources (6)

wikidata.org
registry.identifiers.org
platform.opentargets.org
en.wikipedia.org
docs.openalex.org
web.archive.org

via Wikidata · CC0

neurology

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digital object identifier

International Standard Serial Number

magnetic resonance imaging

International Statistical Classification of Diseases and Related Health Problems

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What links here120 pages

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facioscapulohumeral muscular dystrophy

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