Rare Cardiovascular Diseases, An Issue of Heart Failure Clinics

The Influence of Genotype on the Phenotype, Clinical Course, and Risk of Adverse Events in Children with Hypertrophic Cardiomyopathy<br>The Risk of Sudden Death in Children with Hypertrophic Cardiomyopathy<br>Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and Management<br>Diagnosis and Management of Cardiovascular Involvement in Friedreich Ataxia<br>Diagnosis and Management of Cardiovascular Involvement in Fabry Disease<br>Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options<br>The Role of New Imaging Technologies in the Diagnosis of Cardiac Amyloidosis<br>Cardiovascular Involvement in Transthyretin Cardiac Amyloidosis<br>Clinical and Molecular Aspects of Naxos Disease<br>The Arrhythmic Phenotype in Cardiomyopathy<br>The Risk of Sudden Unexpected Cardiac Death in Children: Epidemiology, Clinical Causes, and Prevention<br>Epidemiology, Pathogenesis, and Clinical Course of Takotsubo Syndrome<br>Genetics in Congenital Heart Diseases: Unraveling the Link Between Cardiac Morphogenesis, Heart Muscle Disease, and Electrical Disorders<br>Clinical Manifestations of 22q11.2 Deletion Syndrome<br>The Heart Muscle and Valve Involvement in Marfan Syndrome, Loeys-Dietz Syndromes, and Collagenopathies<br>New Frontiers in the Treatment of Homozygous Familial Hypercholesterolemia<br>Spontaneous Coronary Artery Dissection: A Rare Event?