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Muscles and connective tissue
Myotonic dystrophy
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Publications (1019)
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Life expectancy and causes of death in patients with Myotonic Dystrophy Type 2. (2024/11/01) ♡
- Hypogammaglobulinemia and infection risk in myotonic dystrophy type 1. (2024/11/01) ♡
- Calcium handling abnormalities increase arrhythmia susceptibility in DMSXL myotonic dystrophy type 1 mice. (2024/11/01) ♡
- Latent factors underlying the symptoms of adult-onset myotonic dystrophy type 1 during the clinical course. (2024/11/01) ♡
- The COVID-19 Pandemic and Its Influence on Patients With Myotonic Dystrophy Type 1: Lessons Learned. (2024/11/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. [Metabolic dysfunctions in type I myotonic dystrophy: A potential therapeutic target]. (2024/11/01) ♡
- International collaboration to improve knowledge on myotonic dystrophy type 2. (2024/11/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Hereditary Neuromuscular Disorders in Reproductive Medicine. (2024/10/30) ♡
- Spiny mice are primed but fail to regenerate volumetric skeletal muscle loss injuries. (2024/10/29) ♡
- MBNL splicing factors regulate the microtranscriptome of skeletal muscles. (2024/10/28) ♡
- Cancer Risk in Patients With Muscular Dystrophy and Myotonic Dystrophy: A Register-Based Cohort Study. (2024/10/22) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Altered drug metabolism and increased susceptibility to fatty liver disease in a mouse model of myotonic dystrophy. (2024/10/21) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. The Gut Microbiota Involvement in the Panorama of Muscular Dystrophy Pathogenesis. (2024/10/21) ♡
- Quantum Chemical Characterization of Rotamerism in Thio-Michael Additions for Targeted Covalent Inhibitors. (2024/10/14) ♡
- AntimiR treatment corrects myotonic dystrophy primary cell defects across several CTG repeat expansions with a dual mechanism of action. (2024/10/11) ♡
- [Application of triplet-primer PCR technology for the genetic testing and prenatal diagnosis of patients with Myotonic dystrophy type 1]. (2024/10/10) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Rescue of Scn5a mis-splicing does not improve the structural and functional heart defects of a DM1 heart mouse model. (2024/10/07) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Longitudinal Course of Myotonic Dystrophy Type 1 With Gait Training Using a Hybrid Assistive Limb: A Case Report. (2024/10/07) ♡
- Fetal Brain MRI Findings in Myotonic Dystrophy and Considerations for Prenatal Genetic Testing. (2024/10/04) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Late-onset myopathies. (2024/10/01) ♡
- Comprehensive four-year disease progression assessment of myotonic dystrophy type 1. (2024/10/01) ♡
- Molecular Pathology of Myotonic Dystrophy Type 1 in Iceland. (2024/10/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. [Beyond premature apnea pauses: congenital myotonic dystrophy type 1]. (2024/10/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. An Autopsy Case of Myotonic Dystrophy Type 1 With Pancreatic Intraductal Papillary Mucinous Neoplasm. (2024/09/26) ♡
- CTG repeat length underlying cardiac events and sudden death in myotonic dystrophy type 1. (2024/09/18) ♡
- Survival in myotonic dystrophy type 1: a long time follow up-study with special reference to gastrointestinal symptoms. (2024/09/17) ♡
- Ameliorated cellular hallmarks of myotonic dystrophy in hybrid myotubes from patient and unaffected donor cells. (2024/09/15) ♡
- Association between Reported Sleep Disorders and Behavioral Issues in Children with Myotonic Dystrophy Type 1-Results from a Retrospective Analysis in Italy. (2024/09/14) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Alternative splicing dysregulation across tissue and therapeutic approaches in a mouse model of myotonic dystrophy type 1. (2024/09/13) ♡
- Effect of exercise training on clinical and physiological variables in adults with myotonic dystrophy type 1: A systematic review protocol. (2024/09/12) ♡
- The Study of the Inheritance Mechanisms of Myotonic Dystrophy Type 1 (DM1) in Families from the Republic of North Ossetia-Alania. (2024/09/09) ♡
- Investigation of Glucose Metabolism by Continuous Glucose Monitoring and Validation of Dipeptidyl Peptidase 4 Inhibitor Use in Patients with Myotonic Dystrophy Type 1. (2024/09/05) ♡
- Clinical and genetic evaluation of hereditary myopathies in an adult Saudi cohort. (2024/09/04) ♡
- Computational identification and molecular dynamics simulation of potential circularRNA derived peptide from gene expression profile of Rheumatoid arthritis, Alzheimer's disease, and Atrial fibrillation. (2024/09/01) ♡
- Population-based incidence rates of 15 neuromuscular disorders: a nationwide capture-recapture study in the Netherlands. (2024/09/01) ♡
- Myotonic Dystrophy Type 1 With Cerebellar Ataxia and Cerebellar Atrophy. (2024/09/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Common Characteristics Between Frailty and Myotonic Dystrophy Type 1: A Narrative Review. (2024/08/29) ♡
- NMR structures and magnetic force spectroscopy studies of small molecules binding to models of an RNA CAG repeat expansion. (2024/08/21) ♡
- Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024/08/20) ♡
- Characterization of the neuropathic pain component contributing to myalgia in patients with myotonic dystrophy type 1 and 2. (2024/08/13) ♡
- Hereditary sensory autonomic neuropathy type VI in the age of genetic testing. (2024/08/11) ♡
- In Myotonic Dystrophy Type 1 Head Repositioning Errors Suggest Impaired Cervical Proprioception. (2024/08/09) ♡
- Ventricular stimulation in patients with myotonic dystrophy type 1 may not predict future ventricular arrhythmias. (2024/08/09) ♡
- Psychosocial functioning in patients with altered facial expression: a scoping review in five neurological diseases. (2024/08/01) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Msi2 enhances muscle dysfunction in a myotonic dystrophy type 1 mouse model. (2024/08/01) ♡
- Developing small Cas9 hybrids using molecular modeling. (2024/07/26) ♡
- A Five-Year Review of Newborn Screening for Spinal Muscular Atrophy in the State of Utah: Lessons Learned. (2024/07/22) ♡
- Resolving the chromatin impact of mosaic variants with targeted Fiber-seq. (2024/07/13) ♡
- RNA mis-splicing in children with myotonic dystrophy is associated with physical function. (2024/07/03) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Excessive daytime sleepiness in myotonic dystrophy: a narrative review. (2024/07/01) ♡
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