myotonic dystrophy - Robuta Search

https://epub.ub.uni-muenchen.de/65100/ Consensus-based care recommendations for adults with myotonic dystrophy type 1 care recommendations for adults myotonic dystrophy consensus based https://commondataelements.ninds.nih.gov/Myotonic%20Muscular%20Dystrophy Myotonic Dystrophy | NINDS CDE myotonic dystrophy ninds cde https://disorders.eyes.arizona.edu/references/retinal-changes-myotonic-dystrophy-clinical-and-follow-evaluation Retinal changes in myotonic dystrophy. Clinical and follow-up evaluation | Hereditary Ocular... myotonic dystrophy https://disorders.eyes.arizona.edu/disorders/myotonic-dystrophy-2 Myotonic Dystrophy 2 | Hereditary Ocular Diseases myotonic dystrophy hereditary ocular diseases https://www.frontiersin.org/journals/neurology/articles/10.3389/fneur.2019.00681/full Frontiers | Two Adult Siblings With Myotonic Dystrophy Type 1 With Different Phenotypes Presenting... Myotonic dystrophy type 1 (DM1) is an autosomal dominant disease characterized by progressive muscle weakness and myotonia along with multiple organ system i... adult siblings myotonic dystrophy https://www.mdpi.com/2077-0383/12/5/1947 Echocardiographic Features of Cardiac Involvement in Myotonic Dystrophy 1: Prevalence and... Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy in adults. Cardiac involvement is reported in 80% of cases and includes conduction... myotonic dystrophy features cardiac involvement https://rarediseases.info.nih.gov/diseases/9134/congenital-myotonic-dystrophy Congenital myotonic dystrophy | About the Disease | GARD Find symptoms and other information about Congenital myotonic dystrophy. about the disease myotonic dystrophy congenital gard https://disorders.eyes.arizona.edu/references/segregation-distortion-myotonic-dystrophy Segregation distortion in myotonic dystrophy | Hereditary Ocular Diseases myotonic dystrophy segregation distortion hereditary ocular https://prism.northwestern.edu/records/02k3s-dev10 Myotonic Dystrophy: Severity and Maternal Age myotonic dystrophy severity maternal age https://my.clevelandclinic.org/health/diseases/24516-myotonic-dystrophy-dm Myotonic Dystrophy: What It Is, Symptoms, Types & Treatment Myotonic dystrophy (DM) is an inherited condition that mainly causes progressive muscle loss, weakness and myotonia. It can also affect other parts of your... what it is myotonic dystrophy symptoms types treatment https://experts.colorado.edu/display/meshid_C10.668.491.175.500.500 Neuromuscular Diseases - Myotonic Dystrophy | CU Experts | CU Boulder neuromuscular diseases myotonic dystrophy experts boulder https://nigms.nih.gov/image-gallery/3573 Myotonic dystrophy type 2 genetic defect | National Institute of General Medical Sciences myotonic dystrophy https://www.ideals.illinois.edu/items/116320 Relating structure and function: Discovery of novel inhibitors of myotonic dystrophy | IDEALS myotonic dystrophy relating structure function discovery https://theses.gla.ac.uk/76136/ Understanding Somatic Mosaicism in Myotonic Dystrophy Type 1 - Enlighten Theses myotonic dystrophy understanding somatic type enlighten https://www.urmc.rochester.edu/neurology/national-registry/research Research Studies - National Registry for Myotonic Dystrophy (DM) and Facioscapulohumeral Dystrophy... research studies national registry myotonic dystrophy dm https://sciencedaily.com/releases/2022/09/220929132646.htm Myotonic dystrophy: GABA receptors implicated in sleepiness, via mouse model | ScienceDaily People with the inherited disorder myotonic dystrophy (DM) often experience excessive daytime sleepiness and fatigue, as well as altered responses to... myotonic dystrophy mouse model gaba receptors implicated https://pubmed.ncbi.nlm.nih.gov/29789616/ rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type... Myotonic dystrophy type 1 and type 2 (DM1, DM2) are caused by expansions of CTG and CCTG repeats, respectively. RNAs containing expanded CUG or CCUG repeats... https://iris.cnr.it/handle/20.500.14243/127660 CTG repeat number in the nonaffected allele of myotonic dystrophy patients is not critical for... https://www.news-medical.net/news/20260403/Toxic-RNA-drives-progressive-heart-damage-in-myotonic-dystrophy.aspx Toxic RNA drives progressive heart damage in myotonic dystrophy Apr 4, 2026 - Myotonic dystrophy type 1 (DM1) is the most common cause of adult-onset muscular dystrophy, a genetic disorder that leads to muscle weakness and wasting, but... toxic rna drives progressive heart https://pubmed.ncbi.nlm.nih.gov/23807151/ Diagnostic odyssey of patients with myotonic dystrophy The onset and symptoms of the myotonic dystrophies are diverse, complicating their diagnoses and limiting a comprehensive approach to their clinical care. This... diagnostic odyssey patients dystrophy https://ltu.diva-portal.org/smash/record.jsf?faces-redirect=true&language=sv&searchType=SIMPLE&query=&af=%5B%5D&aq=%5B%5B%5D%5D&aq2=%5B%5B%5D%5D&aqe=%5B%5D&pid=diva2%3A977335&noOfRows=50&sortOrder=author_sort_asc&sortOrder2=title_sort_asc&onlyFullText=false&sf=all Echocardiographic features of myotonic dystrophy features dystrophy https://mcb.illinois.edu/news/2025-12-04/researchers-uncover-molecular-basis-mitochondrial-dysfunction-myotonic-dystrophy Researchers uncover the molecular basis of mitochondrial dysfunction in myotonic dystrophy type 1 |... Myotonic Dystrophy type 1, also known as DM1, is a genetic disorder that causes progressive muscle weakness, delayed muscle relaxation, and cardiac issues that... https://pubmed.ncbi.nlm.nih.gov/35328504/ Blood Transcriptome Profiling Links Immunity to Disease Severity in Myotonic Dystrophy Type 1 (DM1) The blood transcriptome was examined in relation to disease severity in type I myotonic dystrophy (DM1) patients who participated in the Observational... https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2019.00649/full Frontiers | Global Increase in Circular RNA Levels in Myotonic Dystrophy Splicing aberrations induced as a consequence of the sequestration of MBNL splicing factors on the DMPK transcript, which contains expanded CUG repeats, pres... circular rna frontiers global increase levels https://cordis.europa.eu/project/id/875615/it New food for special medical purposes to nutritionally manage Myotonic Dystrophy type 1 |... Myotonic Dystrophy type 1 (DM1) is the most common and multisystemic neuromuscular rare disease affecting 1 million people worldwide, 100,000 EU citizens, who... https://experts.arizona.edu/en/publications/cloning-and-chromosomal-location-of-a-novel-member-of-the-myotoni/ Cloning and chromosomal location of a novel member of the myotonic dystrophy family of protein... https://neuromuscular.wustl.edu/musdist/pe-eom.html Myopathies without EOM Weakness: Facioscapulohumeral + Myotonic Dystrophy without eom weakness dystrophy https://scholars.uky.edu/en/publications/spin-label-study-of-erythrocyte-membrane-fluidity-in-myotonic-and/ Spin label study of erythrocyte membrane fluidity in myotonic and Duchenne muscular dystrophy and... https://www.ideals.illinois.edu/items/93082 Design, synthesis, and biological activities of small molecules that target myotonic dystrophy |... https://www.urmc.rochester.edu/neurology/national-registry/about-us/help How You Can Help - About the Registry - National Registry for Myotonic Dystrophy (DM) and... how you can help about the registry https://pubmed.ncbi.nlm.nih.gov/2419758/ Expression of apamin receptor in muscles of patients with myotonic muscular dystrophy Myotonic muscular dystrophy, or Steinert disease, is a dominantly inherited disease of muscle which occurs with a frequency of between 1 in 18,000 and 1 in... expression receptor