Related references
Note: Only part of the references are listed.JCS/JHFS 2018 Guideline on the Diagnosis and Treatment of Cardiomyopathies
Hiroaki Kitaoka et al.
CIRCULATION JOURNAL (2021)
Native T1 and Extracellular Volume in Transthyretin Amyloidosis
Ana Martinez-Naharro et al.
JACC-CARDIOVASCULAR IMAGING (2019)
Myocardial T1 and ECV Measurement Underlying Concepts and Technical Considerations
Austin A. Robinson et al.
JACC-CARDIOVASCULAR IMAGING (2019)
Myocardial perfusion reserve quantified by cardiac magnetic resonance imaging is associated with late gadolinium enhancement in hypertrophic cardiomyopathy
Daisuke Tezuka et al.
HEART AND VESSELS (2018)
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Ray E. Hershberger et al.
GENETICS IN MEDICINE (2018)
Genetic background of Japanese patients with pediatric hypertrophic and restrictive cardiomyopathy
Takeharu Hayashi et al.
JOURNAL OF HUMAN GENETICS (2018)
Hypertrophic Cardiomyopathy Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy
Ali J. Marian et al.
CIRCULATION RESEARCH (2017)
Classification, Epidemiology, and Global Burden of Cardiomyopathies
William J. McKenna et al.
CIRCULATION RESEARCH (2017)
A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism
Abdelaziz Beqqali et al.
CARDIOVASCULAR RESEARCH (2016)
How Hypertrophic Cardiomyopathy Became a Contemporary Treatable Genetic Disease With Low Mortality Shaped by 50 Years of Clinical Research and Practice
Barry J. Maron et al.
JAMA CARDIOLOGY (2016)
Atlas of the clinical genetics of human dilated cardiomyopathy
Jan Haas et al.
EUROPEAN HEART JOURNAL (2015)
Whole Exome Sequencing Identifies a Causal RBM20 Mutation in a Large Pedigree With Familial Dilated Cardiomyopathy
Quinn S. Wells et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2013)
Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy
Katharine M. Brauch et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2009)