Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms
about
Congenital and childhood myotonic dystrophy: Current aspects of disease and future directionsModel organisms in the fight against muscular dystrophy: lessons from drosophila and ZebrafishIdentification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotypeHow Research on Human Progeroid and Antigeroid Syndromes Can Contribute to the Longevity Dividend InitiativeFunctional KCa1.1 channels are crucial for regulating the proliferation, migration and differentiation of human primary skeletal myoblastsExpanded CCUG repeat RNA expression in Drosophila heart and muscle trigger Myotonic Dystrophy type 1-like phenotypes and activate autophagocytosis genes.Marathoning with myotonic dystrophy type 2 (proximal myotonic myopathy) and leukopenia.The UK Myotonic Dystrophy Patient Registry: facilitating and accelerating clinical researchEffects on murine behavior and lifespan of selectively decreasing expression of mutant huntingtin allele by supt4h knockdownLinking RNA Dysfunction and Neurodegeneration in Amyotrophic Lateral Sclerosis.ClC-1 chloride channels: state-of-the-art research and future challenges.Reconstructing the Rasch-Built Myotonic Dystrophy Type 1 Activity and Participation Scale"I Know that You Know that I Know": Neural Substrates Associated with Social Cognition Deficits in DM1 Patients.A Molecular Signature of Myalgia in Myotonic Dystrophy 2Brain MRI abnormalities in the adult form of myotonic dystrophy type 1: A longitudinal case series studyCan long-term thiamine treatment improve the clinical outcomes of myotonic dystrophy type 1?RNA Transcription and Maturation in Skeletal Muscle Cells are Similarly Impaired in Myotonic Dystrophy and Sarcopenia: The Ultrastructural Evidence.Hypo- and Hyper-Assembly Diseases of RNA-Protein Complexes.Genome Editing of Monogenic Neuromuscular Diseases: A Systematic Review.Can Human Pluripotent Stem Cell-Derived Cardiomyocytes Advance Understanding of Muscular Dystrophies?Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular Mechanism.Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects.Spatially and temporally regulating translation via mRNA-binding proteins in cellular and neuronal function.Dystrophia myotonica type 1 presenting with dysarthria: A case report and literature review.Splicing of human chloride channel 1.Receptor and post-receptor abnormalities contribute to insulin resistance in myotonic dystrophy type 1 and type 2 skeletal muscle.Brain Connectomics' Modification to Clarify Motor and Nonmotor Features of Myotonic Dystrophy Type 1.Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1.Gastrobronchial fistula following minimally invasive esophagectomy for esophageal cancer in a patient with myotonic dystrophy: Case report.CRISPR/Cas9-Mediated Deletion of CTG Expansions Recovers Normal Phenotype in Myogenic Cells Derived from Myotonic Dystrophy 1 Patients.Circulating Irisin Is Reduced in Male Patients with Type 1 and Type 2 Myotonic Dystrophies.An engineered RNA binding protein with improved splicing regulation.Risk of skin cancer among patients with myotonic dystrophy type 1 based on primary care physician data from the U.K. Clinical Practice Research Datalink.Duchenne and Becker Muscular Dystrophies: A Review of Animal Models, Clinical End Points, and Biomarker Quantification.MBNL expression in autoregulatory feedback loops.Sarcolemmal excitability in the myotonic dystrophies.Forensic Considerations in Cases of Myotonic Dystrophy at Autopsy.Electromechanical delays during a fatiguing exercise and recovery in patients with myotonic dystrophy type 1.Speech characteristics in the congenital and childhood-onset forms of myotonic dystrophy type 1.Electrophysiological and histopathological findings of muscular disease suspected as myotonic dystrophy in a Shiba dog.
P2860
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P2860
Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms
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2015 nî lūn-bûn
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2015 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Myotonic dystrophies: An updat ...... and molecular pathomechanisms
@ast
Myotonic dystrophies: An updat ...... and molecular pathomechanisms
@en
Myotonic dystrophies: An updat ...... and molecular pathomechanisms
@nl
type
label
Myotonic dystrophies: An updat ...... and molecular pathomechanisms
@ast
Myotonic dystrophies: An updat ...... and molecular pathomechanisms
@en
Myotonic dystrophies: An updat ...... and molecular pathomechanisms
@nl
prefLabel
Myotonic dystrophies: An updat ...... and molecular pathomechanisms
@ast
Myotonic dystrophies: An updat ...... and molecular pathomechanisms
@en
Myotonic dystrophies: An updat ...... and molecular pathomechanisms
@nl
P3181
P1476
Myotonic dystrophies: An updat ...... and molecular pathomechanisms
@en
P2093
Rosanna Cardani
P304
P3181
P356
10.1016/J.BBADIS.2014.05.019
P407
P577
2015-04-01T00:00:00Z