ReviewIranian journal of neurology2016
Myotonic disorders: A review article.
Review in Iranian journal of neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
What it found
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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
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Who cites it
15 citing papers in PubMed, 31 citations in OpenAlex.
- Navigating gastrointestinal challenges in genetic myopathies: Diagnostic insights and future directions.World journal of methodology · 2025Article
- Special electromyographic features in a child with paramyotonia congenita: A case report and review of literature.World journal of clinical cases · 2024Article
- DILEMMAS ABOUT THE SELECTION OF ANESTHESIA FOR ELECTIVE CESAREAN SECTION IN PREGNANT WOMEN WITH MYOTONIC DYSTROPHY TYPE 2 AND SUSPECTED von WILLEBRAND DISEASE: A CASE REPORT.Acta clinica Croatica · 2023Article
- Pain and Motor Function in Myotonic Dystrophy Type 1: A Cross-Sectional Study.International journal of environmental research and public health · 2023Article
- [Rare diseases in the differential diagnosis of myalgia].Der Nervenarzt · 2022Article
- [Rare diseases in the differential diagnosis of myalgia].Schmerz (Berlin, Germany) · 2022Article
- Article
- A case of paramyotonia congenita in pregnancy.Obstetric medicine · 2020Article
- Myotonic disorders and pregnancy.Obstetric medicine · 2020Review
- Article
- Summary of Selected Healthcare Encounters among a Selection of Patients with Myotonic Muscular Dystrophy.Southern medical journal · 2019Article
- Clinical implication of maximal voluntary ventilation in myotonic muscular dystrophy.Medicine · 2019Observational
- 30-day all-cause readmission rates among a cohort of individuals with rare conditions.Disability and health journal · 2019Article
- Electrophysiological and histopathological findings of muscular disease suspected as myotonic dystrophy in a Shiba dog.The Journal of veterinary medical science · 2018Article
- An Unusual Case of Hybrid Odontogenic Tumor in Type 1 Myotonic Dystrophy Patient.International journal of applied & basic medical researchArticle
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 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The myotonic disorders are a heterogeneous group of genetically determined diseases that are unified by the presence of myotonia, which is defined as failure of muscle relaxation after activation. The presentation of these disorders can range from asymptomatic electrical myotonia, as seen in some forms of myotonia congenita (MC), to severe disability with muscle weakness, cardiac conduction defects, and other systemic features as in myotonic dystrophy type I (DM1). In this review, we describe the clinical features and pathophysiology of the different myotonic disorders, their laboratory and electrophysiologic findings and briefly review the currently available treatments.
Indexed as
Identifiers
27141276PMC4852070W2226574669What 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.