Evidence mapPaperPMID 41762439Full record

ReviewJournal of neural transmission (Vienna, Austria : 1996)2026

Myopathies in clinical care: a focus on treatable causes.

Genevieve C Uy, Raymond Rosales, Satish Khadilkar

Abstract readReview
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In one paragraph

Review in Journal of neural transmission (Vienna, Austria : 1996), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Genevieve C Uy *Department of Neuromuscular Research, National Center of Neurology and Psychiatry, Ogawahigashi-cho, Kodaira, Tokyo, 187-8551, Japan. gengucciuy@gmail.com.
Raymond Rosales *The Center for Neurodiagnostic and Therapeutic Services, Metropolitan Medical Center, 1357 G. Masangkay St., 1003, Sta. Cruz, Manila, Philippines.
Satish KhadilkarDepartment of Neurology, Bombay Hospital Institute of Medical Sciences, 12 Vitthaldas Thackersey Marg, New Marine Lines, Marine Lines, Mumbai, Maharashtra, 400020, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myopathies are a group of disorders that affect the skeletal muscles, manifesting as weakness, fatigue, or pain. Generally, they are classified as acquired or inherited. It is important to note that while most acquired myopathies are treatable, in the advent of targeted molecular and gene-based therapy, some inherited forms now have effective therapeutic options. These myopathies can be classified based on their underlying causes, including infections, autoimmune disorders leading to muscle inflammation, metabolic abnormalities within muscle cells, skeletal muscle channel dysfunctions, critical illness myopathy, and inherited conditions such as muscular dystrophies. In this review, we first present a clinical approach to neuromuscular diseases and subsequently place specific emphasis on myopathies, particularly those with established or emerging treatment options.

Indexed as

Gene therapyImmunotherapyInflammatory myositisMetabolic myopathiesMuscle channelopathiesMuscular dystrophiesMyopathiesNeuromuscular disorders

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.