Rare Cardiovascular Diseases, An Issue of Heart Failure Clinics
- 1st Edition, Volume 18-1 - November 22, 2021
- Imprint: Elsevier
- Editors: Giuseppe Limongelli, Eduardo Bossone
- Language: English
- Hardback ISBN:9 7 8 - 0 - 3 2 3 - 9 1 9 8 7 - 6
- eBook ISBN:9 7 8 - 0 - 3 2 3 - 9 1 9 8 8 - 3
In this issue of Heart Failure Clinics, Guest Editors Giuseppe Limongelli and Eduardo Bossone bring their considerable expertise to the topic of rare cardiovascular diseases. To… Read more
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In this issue of Heart Failure Clinics, Guest Editors Giuseppe Limongelli and Eduardo Bossone bring their considerable expertise to the topic of rare cardiovascular diseases. Top experts in the field cover key topics such as coronary artery dissection, genetics in congenital heart disease, HCM in Rasopathies, and more.
- Provides in-depth, clinical reviews on Rare Cardiovascular Diseases, providing actionable insights for clinical practice.
- Presents the latest information on this timely, focused topic under the leadership of experienced editors in the field; Authors synthesize and distill the latest research and practice guidelines to create these timely topic-based reviews.
- Contains 17 relevant, practice-oriented topics including The influence of genotype on the phenotype, clinical course, and risk of adverse events in children with Hypertrophic cardiomyopathy; Unravelling the genetic background in heritable and non-heritable BAV: a long roadmap; The risk of sudden unexpected cardiac death in children: epidemiology, clinical causes, and prevention; The renal involvement in patients with storage and infiltrative cardiomyopathies; and more.
The Influence of Genotype on the Phenotype, Clinical Course, and Risk of Adverse Events in Children with Hypertrophic Cardiomyopathy
The Risk of Sudden Death in Children with Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and Management
Diagnosis and Management of Cardiovascular Involvement in Friedreich Ataxia
Diagnosis and Management of Cardiovascular Involvement in Fabry Disease
Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options
The Role of New Imaging Technologies in the Diagnosis of Cardiac Amyloidosis
Cardiovascular Involvement in Transthyretin Cardiac Amyloidosis
Clinical and Molecular Aspects of Naxos Disease
The Arrhythmic Phenotype in Cardiomyopathy
The Risk of Sudden Unexpected Cardiac Death in Children: Epidemiology, Clinical Causes, and Prevention
Epidemiology, Pathogenesis, and Clinical Course of Takotsubo Syndrome
Genetics in Congenital Heart Diseases: Unraveling the Link Between Cardiac Morphogenesis, Heart Muscle Disease, and Electrical Disorders
Clinical Manifestations of 22q11.2 Deletion Syndrome
The Heart Muscle and Valve Involvement in Marfan Syndrome, Loeys-Dietz Syndromes, and Collagenopathies
New Frontiers in the Treatment of Homozygous Familial Hypercholesterolemia
Spontaneous Coronary Artery Dissection: A Rare Event?
The Risk of Sudden Death in Children with Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and Management
Diagnosis and Management of Cardiovascular Involvement in Friedreich Ataxia
Diagnosis and Management of Cardiovascular Involvement in Fabry Disease
Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options
The Role of New Imaging Technologies in the Diagnosis of Cardiac Amyloidosis
Cardiovascular Involvement in Transthyretin Cardiac Amyloidosis
Clinical and Molecular Aspects of Naxos Disease
The Arrhythmic Phenotype in Cardiomyopathy
The Risk of Sudden Unexpected Cardiac Death in Children: Epidemiology, Clinical Causes, and Prevention
Epidemiology, Pathogenesis, and Clinical Course of Takotsubo Syndrome
Genetics in Congenital Heart Diseases: Unraveling the Link Between Cardiac Morphogenesis, Heart Muscle Disease, and Electrical Disorders
Clinical Manifestations of 22q11.2 Deletion Syndrome
The Heart Muscle and Valve Involvement in Marfan Syndrome, Loeys-Dietz Syndromes, and Collagenopathies
New Frontiers in the Treatment of Homozygous Familial Hypercholesterolemia
Spontaneous Coronary Artery Dissection: A Rare Event?
- Edition: 1
- Volume: 18-1
- Published: November 22, 2021
- Imprint: Elsevier
- Language: English
GL
Giuseppe Limongelli
Affiliations and expertise
University of Campania “Luigi Vanvitelli” Monaldi Hospital,EB
Eduardo Bossone
Prof. Bossone MD, PhD, FCCP, FESC, FACC graduated with honors in Medicine and Surgery from the University of Naples "Federico II". He is specialist in cardiology, respiratory diseases and PhD in cardiovascular sciences. He is a fellow of the European Society of Cardiology, American College of Chest Physician, American College of Cardiology and Adjunct Professor at the Cardiology Fellowship Program and International PhD Program in Cardiovascular Pathophysiology and Therapeutics, University of Naples. In 2006 for his scientific merits, he was awarded the title of scholar of the Italian Society of Cardiology.
Affiliations and expertise
Director Cardiology Division University of Salerno, Amalfi Coast Hospital, Lauro-Avellino, Italy