Data from: The demanding grey zone: sport indices by cardiac magnetic resonance imaging differentiate hypertrophic cardiomyopathy from

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关键词：

sport indices;hypertrophic cardiomyopathy;cardiac magnetic resonance;athlete's heart

DOI：

doi:10.5061/dryad.7947gd0

摘要：

ng cardiac magnetic resonance (CMR) quantification method to differentiate physiological hypertrophy and hypertrophic cardiomyopathy based on a large population of highly trained

dilated cardiomyopathy

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关键词：

Heart failure;Cardiovascular imaging;magnetic resonance imaging

DOI：

doi:10.5061/dryad.4j12q

摘要：

ients with non-ischaemic dilated cardiomyopathy (NIDCM). Design: Prospective observational study. Setting: Single centre, tertiary care hospital. Participants: 6 outpat

Data from: Cardiac dysfunction in Duchenne muscular dystrophy is less frequent in patients with mutations in the dystrophin Dp116 coding region tha

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关键词：

Duchenne muscular dystrophy;Humans

DOI：

doi:10.5061/dryad.2m614

摘要：

ause of mutations in the DMD gene. Although DMD is characterized by fatal progressive muscle wasting, cardiomyopathy is the most important nonmuscle symptom

Data from: Cardiac and skeletal muscle effects in the randomized HOPE-Duchenne trial

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Cardiomyopathy;January 2016 to August 2017;Cell therapy;Skeletal muscle function;Duchenne muscular dystrophy;Performance of Upper Limb

DOI：

doi:10.5061/dryad.7651036

摘要：

ients with Duchenne muscular dystrophy (DMD). Methods: The Halt Cardiomyopathy Progression (HOPE)-Duchenne trial is a phase I/II, randomized, controlled, open-label trial (NCT02485938

Data from: Expression profiling of human pluripotent stem cell-derived cardiomyocytes exposed to doxorubicin—integration and visualization of multi

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关键词：

cardiomyocytes;toxicity;multi-omics data;proteomics;human pluripotent stem cells;doxorubicin

DOI：

doi:10.5061/dryad.g335f

摘要：

ng the most cardiotoxic therapeutic drugs presently on the market. Chemotherapeutic-induced cardiomyopathy is one of the leading causes of di

Data from: Chorea, psychosis, acanthocytosis, and prolonged survival associated with ELAC2 mutations

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关键词：

Mitochondrial disorders;Chorea;ELAC2;genetics;Movement Disorders

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doi:10.5061/dryad.j6s420k

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e hypertrophic cardiomyopathy, delayed psychomotor development, and usually death during childhood. Only 20 families have been reported with this syndrome. Neither

Data from: Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations

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关键词：

LMNA Mutations;Computer-Assisted Image Analysis;Nuclear Envelope;fluorescence microscopy;Dilated Cardiomyopathy

DOI：

doi:10.5061/dryad.sr595

摘要：

Nuclear shape defects are a distinguishing characteristic in laminopathies, cancers, and other pathologies. Correlating these defects to the symptoms