Pages that link to "Q47347094"
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The following pages link to Cardiac involvement in a large kindred with myotonic dystrophy. Quantitative assessment and relation to size of CTG repeat expansion (Q47347094):
Displaying 29 items.
- Elevation of RNA-binding protein CUGBP1 is an early event in an inducible heart-specific mouse model of myotonic dystrophy (Q24670706) (← links)
- Muscle wasting in myotonic dystrophies: a model of premature aging (Q26798784) (← links)
- Does cytosine-thymine-guanine (CTG) expansion size predict cardiac events and electrocardiographic progression in myotonic dystrophy? (Q28353993) (← links)
- Identification of genes in toxicity pathways of trinucleotide-repeat RNA in C. elegans (Q30586121) (← links)
- Cytoplasmic CUG RNA foci are insufficient to elicit key DM1 features (Q30855205) (← links)
- Heart-specific overexpression of CUGBP1 reproduces functional and molecular abnormalities of myotonic dystrophy type 1. (Q33697703) (← links)
- Clinical and genetic heterogeneity in myotonic dystrophies (Q34096504) (← links)
- Loss of muscleblind-like 1 results in cardiac pathology and persistence of embryonic splice isoforms (Q34466715) (← links)
- Clinical Predictors of Conduction Disease Progression in Type I Myotonic Muscular Dystrophy (Q34561092) (← links)
- Cardiac involvement in Steinert myotonic dystrophy: Moroccan experience, about 18 cases (Q35714784) (← links)
- Assessment of cardiac involvement in myotonic muscular dystrophy by T1 mapping on magnetic resonance imaging (Q36282231) (← links)
- Structural myocardial involvement in adult patients with type 1 myotonic dystrophy (Q36868793) (← links)
- Prolonged Corrected QT Interval in Patients with Myotonic Dystrophy Type 1. (Q37043348) (← links)
- Muscleblind-like 3 deficit results in a spectrum of age-associated pathologies observed in myotonic dystrophy (Q39533050) (← links)
- Pacing for conduction disturbances in Steinert's disease: a new indication for biventricular ICD? (Q41867041) (← links)
- Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophy (Q47210873) (← links)
- Female patient with proximal myotonic myopathy and ventricular tachycardia (Q51328075) (← links)
- Characterization of cardiac conduction system abnormalities in mice with targeted disruption of Six5 gene. (Q52547985) (← links)
- Dissecting Pathogenetic Mechanisms and Therapeutic Strategies in Models of Myotonic Dystrophy Type 1 (Q60950065) (← links)
- Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats (Q71788855) (← links)
- Myocardial tissue velocity reduction is correlated with clinical neurologic severity in myotonic dystrophy (Q73668681) (← links)
- Cardiac abnormalities and cytosine-thymineguanine trinucleotide repeats in myotonic dystrophy (Q73739637) (← links)
- Hypertrophic cardiomyopathy in congenital myotonic dystrophy (Q74551801) (← links)
- Myotonic dystrophy associated with QT prolongation and torsade de pointes (Q74588297) (← links)
- Molecular basis of neuromuscular diseases (Q77810812) (← links)
- Increased mortality with left ventricular systolic dysfunction and heart failure in adults with myotonic dystrophy type 1 (Q82828485) (← links)
- Evaluation of biventricular functions with tissue Doppler imaging in patients with myotonic dystrophy (Q83198168) (← links)
- Aberrant Expression of a Non-muscle RBFOX2 Isoform Triggers Cardiac Conduction Defects in Myotonic Dystrophy (Q89936495) (← links)
- [Cardiac involvement in Steinert's myotonic dystrophy] (Q94466042) (← links)