ReviewNeurologic clinics2014
Distal myopathies.
Review in Neurologic clinics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
11 citing papers in PubMed, 32 citations in OpenAlex.
- Integrative Approaches to Myopathies and Muscular Dystrophies: Molecular Mechanisms, Diagnostics, and Future Therapies.International journal of molecular sciences · 2025Review
- Revisiting the compound muscle action potential (CMAP).Clinical neurophysiology practice · 2024Review
- Why so low? An unusual case of myositis in a child.Pediatric rheumatology online journal · 2023Article
- Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022Article
- A new dysferlin gene mutation in a Portuguese family with Miyoshi myopathy.BMJ case reports · 2021Article
- Diagnosis of Cardiac Abnormalities in Muscular Dystrophies.Medicina (Kaunas, Lithuania) · 2021Review
- Diagnostic yield of exome sequencing in myopathies: Experience of a Slovenian tertiary centre.PloS one · 2021Article
- Slowly progressive distal muscle weakness: neuropathy or myopathy?BMJ case reports · 2019Article
- Non-linear growth trends of toe flexor muscle strength among children, adolescents, and young adults: a cross-sectional study.European journal of applied physiology · 2018Article
- GNE missense mutation in recessive familial amyotrophic lateral sclerosis.Neurogenetics · 2017Article
- Whole Exome Sequencing Identifies Atypical Welander Distal Myopathy in Patient.Journal of clinical neuromuscular disease · 2017Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
In this article, distal myopathy syndromes are discussed. A discussion of the more traditional distal myopathies is followed by discussion of the myofibrillar myopathies. Other clinically and genetically distinctive distal myopathy syndromes usually based on single or smaller family cohorts are reviewed. Other neuromuscular disorders that are important to recognize are also considered, because they show prominent distal limb weakness.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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 OpenQuestion graph.