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myotonia

Synonyms

Noun

1. tonicity

2. tonus, tone

Usage
Dialing Back Stiffness May Protect Muscles in Myotonic Dystrophy - University of Rochester
Muscle disease - Myotonic, Dystrophy, Congenital - Encyclopedia Britannica
Prospective Study of Video Hand Opening Time as a Quantitative Measurement of Myotonia in Patients With Myotonic Dystrophy Type 1 - Neurology® Journals
An Antibody–Oligonucleotide Conjugate for Myotonic Dystrophy Type 1 - The New England Journal of Medicine
Myotonia Drug Gets Green Light for Pediatric Patients in EU - Medscape
Reducing Muscle Stiffness Could Help Myotonic Dystrophy Patients - Bioengineer.org
Real-World Study Provides Support for Lamotrigine in Treating Non-Dystrophic Myotonias - NeurologyLive
Source of gastrointestinal problems in myotonic dystrophy - National Institutes of Health (NIH) | (.gov)
Undiagnosed Maternal Myotonic Dystrophy Type 1 Revealed by Congenital Myotonic Dystrophy in the Neonate - Cureus
The New England Journal of Medicine Publishes Results from Phase 1/2 MARINA® Trial of Delpacibart Etedesiran (del-desiran) for Treatment of Myotonic Dystrophy Type 1 - PR Newswire
Targeted long-read sequencing for high-resolution repeat profiling in myotonic dystrophy type 1 - Nature
Unlocking the Future of Paediatric Myotonia - EMJ
MDA 2026: Dyne therapy boosts strength, cognition in DM1 - Muscular Dystrophy News
Over-contracted gut muscles drive gastrointestinal symptoms in myotonic dystrophy - News-Medical
Toward Trial Readiness in Congenital Myotonic Dystrophy - Neurology® Journals
Role of Otolaryngology in Monitoring the Progression of Myotonic Dystrophy: A Case Report - Cureus
Biophysical and structural insights into the SCN4A E452K variant linked to myotonia and paramyotonia congenita - Nature
Myotonic dystrophy type 1: clinical diversity, molecular insights and therapeutic perspectives - Nature
Dyne hopes to bring new treatment for DM1 to US market in 2028 - Muscular Dystrophy News
Neonatal congenital myotonic dystrophy with DMPK gene expansion: clinical features and short-term outcomes - Frontiers
Toxic RNA drives progressive heart damage in myotonic dystrophy - News-Medical
MBNL loss of function in smooth muscle as a model for myotonic dystrophy associated gastrointestinal dysmotility - PNAS
Characterizing white matter hyperintensities in myotonic dystrophy type 1 through IVIM derived metrics - Nature
Discovery and characterization of Arthex Biotech’s ATX-01 for myotonic dystrophy type 1 - BioWorld News
2026 Grad Slam winner strives to understand sleep disruptions in myotonic dystrophy - Newsroom | UCLA
Therapeutic Promise and Mechanism of DYNE-101 to Treat Myotonic Dystrophy: Doug Kerr, MD, PhD - NeurologyLive
Researcher Reverse Myotonic Symptoms in Dystrophic Mice - Neurology Today
AMO-02 for myotonic dystrophy type 1 - Muscular Dystrophy News
Pearls and Oy-sters: Chronic Progressive External Ophthalmoplegia With Electrical Myotonia and Negative Initial Genetic Testing - Neurology® Journals
ARTHEx Biotech Delivers Multiple Presentations at IDMC-15 Highlighting Clinical Progress of ATX-01 and Mechanistic Insights for Myotonic Dystrophy Type 1 (DM1) and 2 (DM2) - PR Newswire
Antibody-Oligonucleotide Conjugate Shows Promise in Myotonic Dystrophy Type 1 - MedPage Today
PepGen Announces Presentations at the 15th International Myotonic Dystrophy Consortium Highlighting Clinical Data from the PGN-EDODM1 Program - Business Wire
Gene Therapy Fast Tracked for Non-Congenital Myotonic Dystrophy Type 1 - Neurology Advisor
Dyne Therapeutics Announces Completion of Enrollment in Registrational Expansion Cohort of ACHIEVE Trial of Z-Basivarsen for Myotonic Dystrophy Type 1 (DM1) - Yahoo Finance
Miles of Hope: A year-long ride for Myotonic Dystrophy awareness - News 9
Lupin Announces Launch of Orphan Drug NaMuscla® in Germany and the UK for the Treatment of Myotonia in Non-Dystrophic Myotonic Disorders - Lupin | Press Release - lupin.com
ARTHEx Biotech Granted FDA Fast Track Designation for ATX-01 for the Treatment of Myotonic Dystrophy Type 1 (DM1) - PR Newswire
U.S. FDA Grants Mexiletine Orphan Drug Designation - lupin.com
Dyne Therapeutics Announces Initiation of Phase 3 HARMONIA - GlobeNewswire
Structure-based RNA could lead to treatment for neuromuscular disorders - Medical Xpress
FDA Grants Fast Track Designation to SAR446268 Gene Therapy for Non-Congenital Myotonic Dystrophy Type 1 - Vera Health
FDA curtails Pepgen’s Freedom2 operate in DM1 - BioWorld News
DM1 gene therapy trial seeks patients ages 10-50 - Muscular Dystrophy News
Design Therapeutics begins DM1 trial for DT-818, aims at genetic cause - Stock Titan
Landmarks light up green for Myotonic Dystrophy Awareness Day - WRGB
Del-desiran for myotonic dystrophy type 1 - Muscular Dystrophy News
Dyne commences Phase III HARMONIA trial for DM1 therapy - Clinical Trials Arena
PepGen slumps as FDA places hold on lead drug - pharmaphorum
Experimental DM1 drug hits key trial milestone, Dyne eyes 2028 US launch - Stock Titan
Pearls & Oy-sters: Severe Myotonic Crisis Resembling Malignant Hyperthermia - Neurology® Journals
AMO Pharma Reports Long-Term Safety Data from REACHCDM-X Study of AMO-02 in Treatment of Congenital Myotonic Dystrophy Type 1 - PR Newswire
CUHK scientists reveal a new mechanism by which myotonic dystrophy type 1 damages the nervous system - CUHK Communications and Public Relations Office
Severe Adult-Onset Non-Dystrophic Myotonia With Apnea and Laryngospasm Due to Digenic Inheritance of SCN4A and CLCN1 Variants - Neurology® Journals
Three cases of pregnancies complicated with myotonic dystrophy type 1 - obgyn.onlinelibrary.wiley.com
Lupin Gets EMA Approval to Expand NaMuscla Use for Children with Rare Muscle Disorder - Medical Dialogues
Fight, Flight, Or Fall Over: Meet The Myotonic Goat - IFLScience
Dyne Therapeutics Reports Significant One-Year Clinical Data for Zeleciment Basivarsen in Patients with Myotonic Dystrophy Type 1 - Quiver Quantitative
Dyne Therapeutics Initiates Phase 3 HARMONIA Trial to Evaluate Efficacy of Z-Basivarsen in Myotonic Dystrophy Type 1 - Quiver Quantitative
News - New research could unlock ways to treat myotonic dystrophy - University of Nottingham
Correction of Clcn1 alternative splicing reverses muscle fiber type transition in mice with myotonic dystrophy - Nature
Idiopathic generalized epilepsy in a family with SCN4A‐related myotonia - Talarico - 2024 - Epilepsia Open - Wiley Online Library
Consensus-based care recommendations for adults with myotonic dystrophy type 2 - Neurology® Journals
Hypokalaemic periodic paralysis and myotonia in a patient with homozygous mutation p.R1451L in Na - Nature
Myotonic dystrophy: GABA receptors implicated in sleepiness, via mouse model - Emory News
Myotonia Congenita: Clinical Characteristic and Mutation Spectrum of CLCN1 in Chinese Patients - Frontiers
Anaesthesia for Paramyotonia Congenita: A Narrative Review - Cureus
Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation - Nature
Case report: A CLCN1 complex variant mutation in exon 15 in a mixed-breed dog with hereditary myotonia - Frontiers
A large intragenic deletion in the CLCN1 gene causes Hereditary Myotonia in pigs - Nature
MDA 2024: Myotonic dystrophy type 1 reverses with AOC 1001 treatment - Muscular Dystrophy News
Calcium Channel Blockers Key to Reversing Myotonic Dystrophy Muscle Weakness, Study Finds - University of Rochester
Here’s the bizarre truth about ‘fainting goats’ - The Indian Express
Late-Onset Proximal Myotonic Myopathy (PROMM): A Rare Presentation in an Adult - Cureus
Chronic endoplasmic reticulum stress in myotonic dystrophy type 2 promotes autoimmunity via mitochondrial DNA release - Nature
PepGen’s stock up 120% on DM1 trial success - Clinical Trials Arena
Teaching Video NeuroImages: Lid lag sign and diplopia in paramyotonia congenita - Neurology® Journals
Use of HSALR female mice as a model for the study of myotonic dystrophy type I | Lab Animal - Nature
Ultrasound-enhanced delivery of Morpholino with Bubble liposomes ameliorates the myotonia of myotonic dystrophy model mice - Nature
[8-K] PepGen Inc. Reports Material Event - Stock Titan
Establishment of quantitative and consistent in vitro skeletal muscle pathological models of myotonic dystrophy type 1 using patient-derived iPSCs - Nature
New Grants Support Research on Myotonic Dystrophy and ALS in the Berglund Lab - University at Albany
Dosage effect of multiple genes accounts for multisystem disorder of myotonic dystrophy type 1 - Nature
Commonly used drug could transform treatment of rare muscle disorder - UCL | University College London
Teaching Video NeuroImages: Cold-induced eyelid myotonia - Neurology® Journals
Opioid use may be associated with postoperative complications in myotonic dystrophy type 1 with high-grade muscular impairment - Nature
A large cohort of myotonia congenita probands: novel mutations and a high-frequency mutation region in exons 4 and 5 of the CLCN1 gene - Nature
Analysis of human urinary extracellular vesicles reveals disordered renal metabolism in myotonic dystrophy type 1 - Nature
Electrical Alternance in a Patient With Type 1 Myotonic Dystrophy: What Diagnosis? - American Heart Association Journals
Discovery and Treatment of Action Potential-Independent Myotonia in Hyperkalemic Periodic Paralysis - Wiley Online Library
Lupin Secures EMA Approval to Expand NaMuscla for Pediatric Use - scanx.trade
SCN4A as modifier gene in patients with myotonic dystrophy type 2 - Nature
Hyperadrenocorticoid (Cushing) myopathy, stiff gait, dog - MSD Veterinary Manual
Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9 - Science | AAAS
HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy - PNAS
Expert heart advice for rare genetic muscle disorder - www.heart.org
Myotonia of the Tongue - The New England Journal of Medicine
Molecular genetics of myotonic dystrophy and the evolution of therapeutic approaches | Journal of Human Genetics - Nature
FORCE platform overcomes barriers of oligonucleotide delivery to muscle and corrects myotonic dystrophy features in preclinical models | Communications Medicine - Nature
Increased Muscleblind levels by chloroquine treatment improve myotonic dystrophy type 1 phenotypes in in vitro and in vivo models - PNAS
International Myotonic Dystrophy Awareness Day Declared for September 15, 2021 - Muscular Dystrophy Association
Foreign Language Equivalents
Foreign Language Equivalents of 'myotonia'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
myotonoa,   motonia,   ymotonia,   mytoonia,   myotoonia,   muotonia,   myotnia,   myotonua,   myotomia,   myyotonia,   myotnoia,   myotpnia,   myitonia,   myotinia,   myotoni,   myotoina,   mmyotonia,   mtotonia,   yotonia,   myotoniaa,   myoronia,   nyotonia,   myotonnia,   mytonia,   myotonis,   myotoia,   myotobia,   myotona,   moytonia,   myottonia,   ,yotonia,   myoyonia,   myootnia,   myotoniia,   myptonia,   myootonia,   myotonai,   myoonia
Words Starting with Letter - 'A'
a a battery a billion
a bit a bit much a capella singing
a cappella singing a couple of a few
a fortiori a good deal a great deal
a horizon a hundred a hundred and one
a hundred thousand a hundred times a kempis
a la carte a la mode a level
a little a lot a million
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