ArticleFrontiers in neurology2020
Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in
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Article in Frontiers in neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 38% of its field
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
8 citing papers in PubMed, 12 citations in OpenAlex.
- Review
- Voltage-gated sodium channels in the nervous system: Molecular physiology to therapeutic interventions.Neural regeneration research · 2026Article
- Idiopathic generalized epilepsy in a family with SCN4A-related myotonia.Epilepsia open · 2024Article
- Functional effects of drugs and toxins interacting with NaFrontiers in pharmacology · 2024Review
- A c.1775C > T Point Mutation of Sodium Channel Alfa Subunit Gene (SCN4A) in a Three-Generation Sardinian Family with Sodium Channel Myotonia.Journal of neuromuscular diseases · 2024Article
- Muscle channelopathies: A review.Annals of the Child Neurology Society · 2023Review
- p.Asn1180Ile mutation of SCN4A gene in an Italian family with myopathy and myotonic syndrome.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021Article
- Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for Therapy.Cells · 2021Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
31 authors at 16 institutions in 1 country.
Lorenzo MaggiNeuroimmunology and Neuromuscular Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Raffaella BrugnoniNeuroimmunology and Neuromuscular Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Eleonora CanioniNeuroimmunology and Neuromuscular Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Paola ToninSection of Clinical Neurology, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Veronica SalettiDevelopmental Neurology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Patrizia SolaClinica Neurologica, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Stefano Cotti PiccinelliUnit of Neurology, Center for Neuromuscular Diseases, ASST Spedali Civili and University of Brescia, Brescia, Italy.
Lara ColleoniNeuroimmunology and Neuromuscular Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Paola FerrignoSC Neurologia e Stroke Unit, Azienda Ospedaliera Brotzu, Cagliari, Italy.
Antonella PiniChild Neurology and Psychiatry Unit, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Riccardo MassonDevelopmental Neurology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Fiore ManganelliDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples "Federico II", Naples, Italy.
Daniele LiettiPediatric Unit, Ospedale Valduce, Como, Italy.
Liliana VercelliDepartment of Neurosciences Rita Levi Montalcini, University of Turin, Turin, Italy.
Giulia RicciDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Claudio BrunoCenter of Translational and Experimental Myology, Istituto Giannina Gaslini, Genova, Italy.
Giorgio TascaUnità Operativa Complessa di Neurologia, Dipartimento di Scienze Dell'Invecchiamento, Neurologiche, Ortopediche e della Testa-Collo, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Antonio PizzutiFondazione IRCCS Casa Sollievo della Sofferenza, Laboratory of Medical Genetics, San Giovanni Rotondo, Italy.
Alessandro PadovaniUnit of Neurology, Center for Neuromuscular Diseases, ASST Spedali Civili and University of Brescia, Brescia, Italy.
Carlo FuscoDipartimento Materno-Infantile, S.C. Neuropsichiatria Infantile, Presidio Ospedaliero Provinciale Santa Maria Nuova, IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Elena PegoraroDepartment of Neurosciences, University of Padova, Padova, Italy.
Lucia RuggieroDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples "Federico II", Naples, Italy.
Sabrina RavagliaEmergency Neurology, IRCCS Mondino Foundation, Pavia, Italy.
Gabriele SicilianoDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Lucia MorandiNeuroimmunology and Neuromuscular Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Raffaele DubbiosoDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples "Federico II", Naples, Italy.
Tiziana MonginiDepartment of Neurosciences Rita Levi Montalcini, University of Turin, Turin, Italy.
Massimiliano FilostoUnit of Neurology, Center for Neuromuscular Diseases, ASST Spedali Civili and University of Brescia, Brescia, Italy.
Irene TramacereResearch and Clinical Development Department, Scientific Directorate, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Renato MantegazzaNeuroimmunology and Neuromuscular Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Pia BernasconiNeuroimmunology and Neuromuscular Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Fondazione IRCCS Istituto Neurologico Carlo Besta · ITUniversity of Brescia · ITUniversity of Naples Federico II · ITUniversity of Pisa · ITUniversity of Turin · ITAzienda Ospedaliera G. Brotzu · ITFondazione Istituto Neurologico Nazionale Casimiro Mondino · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITIstituto delle Scienze Neurologiche di Bologna · ITIstituto Giannina Gaslini · ITOspedale Valduce · ITPoliclinico di Modena · ITPresidio Ospedaliero · ITSapienza University of Rome · ITUniversity of Padua · ITUniversity of Verona · IT
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
channelopathiesmyotoniaperiodic paralysisSCN4A gene mutationSNELvoltage-gated sodium channel NaV1.4
Identifiers
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Registered trials
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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.