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Cardiogenetics, Vol. 12, Pages 270-275: Could the BGN Gene Be Pathogenic with Spontaneous Coronary Artery Dissection (SCAD) and Fibromuscular Dysplasia (FMD)?
Cardiogenetics, Vol. 12, Pages 270-275: Could the BGN Gene Be Pathogenic with Spontaneous Coronary Artery Dissection (SCAD) and Fibromuscular Dysplasia (FMD)?
BACKGROUND. Spontaneous coronary artery dissection (SCAD) is a cause of myocardial infarction, especially in younger women...
Cardiogenetics, Vol. 12, Pages 261-269: Moderately Prolonged QTc in Computer-Assessed ECG, Random Variation or Significant Risk Factor? A Literature Review
Cardiogenetics, Vol. 12, Pages 261-269: Moderately Prolonged QTc in Computer-Assessed ECG, Random Variation or Significant Risk Factor? A Literature Review
Most ECGs in European hospitals are recorded with equipment giving computer measured intervals and interpretation of the r...
Cardiogenetics, Vol. 12, Pages 253-260: Screening Method for 22q11 Deletion Syndrome Involving the Use of TaqMan qPCR for TBX1 in Patients with Conotruncal Congenital Heart Disease
Cardiogenetics, Vol. 12, Pages 253-260: Screening Method for 22q11 Deletion Syndrome Involving the Use of TaqMan qPCR for TBX1 in Patients with Conotruncal Congenital Heart Disease
22q11.2 deletion syndrome is a phenotypic spectrum that encompasses DiGeorge syndrome (OMIM: 188400) and velocardiofacial ...
Cardiogenetics, Vol. 12, Pages 246-252: Recurrent Episodes of Acute Myocardial Infarction Secondary to Paradoxical Coronary Artery Embolism
Cardiogenetics, Vol. 12, Pages 246-252: Recurrent Episodes of Acute Myocardial Infarction Secondary to Paradoxical Coronary Artery Embolism
Coronary artery embolism is a rare cause of acute myocardial infarction, attributed to approximately 10% of all paradoxica...
Cardiogenetics, Vol. 12, Pages 235-245: Association of GSTT1, GSTM1 and GSTP1 (Ile105Val) mRNA Expression with Cardiometabolic Risk Parameters in Women with Breast Cancer and Comorbidities
Cardiogenetics, Vol. 12, Pages 235-245: Association of GSTT1, GSTM1 and GSTP1 (Ile105Val) mRNA Expression with Cardiometabolic Risk Parameters in Women with Breast Cancer and Comorbidities
Breast cancer (BC) and cardiometabolic diseases share a multifactorial and modifiable etiology, modulated by complex molec...
Cardiogenetics, Vol. 12, Pages 218-234: Studying Epigenetics of Cardiovascular Diseases on Chip Guide
Cardiogenetics, Vol. 12, Pages 218-234: Studying Epigenetics of Cardiovascular Diseases on Chip Guide
Epigenetics is defined as the study of inheritable changes in the gene expressions and phenotypes that occurs without alte...
Cardiogenetics, Vol. 12, Pages 212-217: Identification of Single-Nucleotide Polymorphisms in ZNF469 in a Patient with Aortoiliac Aneurysmal Disease
Cardiogenetics, Vol. 12, Pages 212-217: Identification of Single-Nucleotide Polymorphisms in ZNF469 in a Patient with Aortoiliac Aneurysmal Disease
Thoracic aortic aneurysms and dissections often have inter-related pathologies that are increasingly recognized to have a ...
Cardiogenetics, Vol. 12, Pages 206-211: Clinical Exome Sequencing Revealed a De Novo FLNC Mutation in a Child with Restrictive Cardiomyopathy
Cardiogenetics, Vol. 12, Pages 206-211: Clinical Exome Sequencing Revealed a De Novo FLNC Mutation in a Child with Restrictive Cardiomyopathy
Restrictive cardiomyopathy (RCM) is a rare disease of the myocardium caused by mutations in several genes including TNNT2,...
Cardiogenetics, Vol. 12, Pages 185-197: Modified Body Mass Index as a Novel Nutritional and Prognostic Marker in Patients with Cardiac Amyloidosis
Cardiogenetics, Vol. 12, Pages 185-197: Modified Body Mass Index as a Novel Nutritional and Prognostic Marker in Patients with Cardiac Amyloidosis
The nutritional assessment is gaining clinical relevance since cardiac cachexia and malnutrition are emerging as novel mar...
Cardiogenetics, Vol. 12, Pages 170-184: Left Ventricular Non-Compaction Spectrum in Adults and Children: From a Morphological Trait to a Structural Muscular Disease
Cardiogenetics, Vol. 12, Pages 170-184: Left Ventricular Non-Compaction Spectrum in Adults and Children: From a Morphological Trait to a Structural Muscular Disease
Left ventricular non-compaction (LVNC) is an extremely heterogeneous disorder with a highly variable clinical presentation...
Cardiogenetics, Vol. 12, Pages 142-169: Clinical Phenotypes of Cardiovascular and Heart Failure Diseases Can Be Reversed? The Holistic Principle of Systems Biology in Multifaceted Heart Diseases
Cardiogenetics, Vol. 12, Pages 142-169: Clinical Phenotypes of Cardiovascular and Heart Failure Diseases Can Be Reversed? The Holistic Principle of Systems Biology in Multifaceted Heart Diseases
Recent advances in cardiology and biological sciences have improved quality of life in patients with complex cardiovascula...
Cardiogenetics, Vol. 12, Pages 133-141: Pancarditis as the Clinical Presentation of Eosinophilic Granulomatosis with Polyangiitis: A Multimodality Approach to Diagnosis
Cardiogenetics, Vol. 12, Pages 133-141: Pancarditis as the Clinical Presentation of Eosinophilic Granulomatosis with Polyangiitis: A Multimodality Approach to Diagnosis
Eosinophilic pancarditis (EP) is a rare, often unrecognized condition caused by endomyocardial infiltration of eosinophil ...
Cardiogenetics, Vol. 12, Pages 122-132: MYH7 Genotype–Phenotype Correlation in a Cohort of Finnish Patients
Cardiogenetics, Vol. 12, Pages 122-132: MYH7 Genotype–Phenotype Correlation in a Cohort of Finnish Patients
Cardiomyopathies (CMPs) are a heterogeneous group of diseases, frequently genetic, affecting the heart muscle. The symptom...
Cardiogenetics, Vol. 12, Pages 112-121: Clinical and Molecular Characteristics of Patients with PLN R14del Cardiomyopathy: State-of-the-Art Review
Cardiogenetics, Vol. 12, Pages 112-121: Clinical and Molecular Characteristics of Patients with PLN R14del Cardiomyopathy: State-of-the-Art Review
The deletion of the arginine 14 codon (R14del) in the phospholamban (PLN) gene is a rare cause of arrhythmogenic cardiomyo...
Cardiogenetics, Vol. 12, Pages 102-108: Diagnosis of Fabry Disease in a Patient with a Surgically Repaired Congenital Heart Defect: When Clinical History and Genetics Make the Difference
Cardiogenetics, Vol. 12, Pages 102-108: Diagnosis of Fabry Disease in a Patient with a Surgically Repaired Congenital Heart Defect: When Clinical History and Genetics Make the Difference
Fabry disease (FD) is a multiorgan disease, which can potentially affect any organ or tissue, with the heart, kidneys, and...
Cardiogenetics, Vol. 12, Pages 90-101: Genetic Diagnostics Contribute to the Risk Stratification for Major Arrhythmic Events in Pediatric Patients with Long QT Syndrome Type 1–3
Cardiogenetics, Vol. 12, Pages 90-101: Genetic Diagnostics Contribute to the Risk Stratification for Major Arrhythmic Events in Pediatric Patients with Long QT Syndrome Type 1–3
Long QT syndrome (LQTS) is an inherited arrhythmic disorder associated with sudden cardiac death (SCD). This study aimed t...
Cardiogenetics, Vol. 12, Pages 80-88: Pharmacogenomics of Pediatric Cardiac Arrest: Cisplatin Treatment Worsened by a Ryanodine Receptor 2 Gene Mutation
Cardiogenetics, Vol. 12, Pages 80-88: Pharmacogenomics of Pediatric Cardiac Arrest: Cisplatin Treatment Worsened by a Ryanodine Receptor 2 Gene Mutation
In thelast few decades, the roles of cardio-oncology and cardiovascular geneticsgained more and more attention in research...
Cardiogenetics, Vol. 12, Pages 49-62: The Roles of Platelet-Activating Factor and Magnesium in Pathophysiology of Hypertension, Atherogenesis, Cardiovascular Disease, Stroke and Aging
Cardiogenetics, Vol. 12, Pages 49-62: The Roles of Platelet-Activating Factor and Magnesium in Pathophysiology of Hypertension, Atherogenesis, Cardiovascular Disease, Stroke and Aging
Hypertension and atherosclerosis are debilitating diseases that affect millions each year. Long-term consequences include ...
Cardiogenetics, Vol. 12, Pages 63-79: Genetics of Heritable Thoracic Aortic Disease
Cardiogenetics, Vol. 12, Pages 63-79: Genetics of Heritable Thoracic Aortic Disease
Genetic testing plays an increasing diagnostic and prognostic role in the management of patients with heritable thoracic a...
Cardiogenetics, Vol. 12, Pages 1-11: Transthyretin Gene Variants and Associated Phenotypes in Danish Patients with Amyloid Cardiomyopathy
Cardiogenetics, Vol. 12, Pages 1-11: Transthyretin Gene Variants and Associated Phenotypes in Danish Patients with Amyloid Cardiomyopathy
Genotyping divides transthyretin cardiac amyloidosis (ATTR-CA) in hereditary (ATTRv) and wild type (ATTRwt) forms. This st...
Cardiogenetics, Vol. 12, Pages 24-36: Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (DSP)
Cardiogenetics, Vol. 12, Pages 24-36: Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (DSP)
Background: Variants in the desmoplakin (DSP) gene have been recognized in association with the pathogenesis of arrhythmog...
Cardiogenetics, Vol. 12, Pages 12-23: Nanoparticle-Based Modification of the DNA Methylome: A Therapeutic Tool for Atherosclerosis?
Cardiogenetics, Vol. 12, Pages 12-23: Nanoparticle-Based Modification of the DNA Methylome: A Therapeutic Tool for Atherosclerosis?
Cardiovascular epigenomics is a relatively young field of research, yet it is providing novel insights into gene regulatio...
Cardiogenetics, Vol. 11, Pages 263-289: Pathogenesis, Diagnosis and Risk Stratification in Arrhythmogenic Cardiomyopathy
Cardiogenetics, Vol. 11, Pages 263-289: Pathogenesis, Diagnosis and Risk Stratification in Arrhythmogenic Cardiomyopathy
Arrhythmogenic cardiomyopathy (ACM) is a genetically determined myocardial disease associated with sudden cardiac death (S...
Cardiogenetics, Vol. 11, Pages 255-262: Understanding the Function of a Locus Using the Knowledge Available at Single-Nucleotide Polymorphisms
Cardiogenetics, Vol. 11, Pages 255-262: Understanding the Function of a Locus Using the Knowledge Available at Single-Nucleotide Polymorphisms
Understanding the function of a locus is an issue in molecular biology. Although numerous molecular data have been generat...
Cardiogenetics, Vol. 11, Pages 31-38: Overlapping Phenotype of Cardiomyopathy in a Patient with Double Mutation: A Case Report
Cardiogenetics, Vol. 11, Pages 31-38: Overlapping Phenotype of Cardiomyopathy in a Patient with Double Mutation: A Case Report
Hypertrophic cardiomyopathy and left ventricular noncompaction commonly occur as separate disorders with distinct clinical...
Cardiogenetics, Vol. 11, Pages 39-49: Cardiac Involvement in Autosomal Dominant Polycystic Kidney Disease
Cardiogenetics, Vol. 11, Pages 39-49: Cardiac Involvement in Autosomal Dominant Polycystic Kidney Disease
Cardiovascular disorders are the main complication in autosomal dominant polycystic kidney disease (ADPKD). contributing t...
Cardiogenetics, Vol. 11, Pages 50-67: Constraints in Clinical Cardiology and Personalized Medicine: Interrelated Concepts in Clinical Cardiology
Cardiogenetics, Vol. 11, Pages 50-67: Constraints in Clinical Cardiology and Personalized Medicine: Interrelated Concepts in Clinical Cardiology
Systems biology is established as an integrative computational analysis methodology with practical and theoretical applica...
Cardiogenetics, Vol. 11, Pages 68-72: Genetic Diagnosis in Sudden Cardiac Death: The Crucial Role of Multidisciplinary Care
Cardiogenetics, Vol. 11, Pages 68-72: Genetic Diagnosis in Sudden Cardiac Death: The Crucial Role of Multidisciplinary Care
Sudden death, especially at a young age, may be caused by an underlying genetic cause. Hereditary conditions with an incre...
Cardiogenetics, Vol. 11, Pages 230-254: MicroRNAs: From Junk RNA to Life Regulators and Their Role in Cardiovascular Disease
Cardiogenetics, Vol. 11, Pages 230-254: MicroRNAs: From Junk RNA to Life Regulators and Their Role in Cardiovascular Disease
MicroRNAs (miRNAs) are single-stranded small non-coding RNA (18–25 nucleotides) that until a few years ago were ...
Cardiogenetics, Vol. 11, Pages 219-229: Arrhythmogenic Cardiomyopathy—Further Insight into the Clinical Spectrum of Desmoplakin Disease
Cardiogenetics, Vol. 11, Pages 219-229: Arrhythmogenic Cardiomyopathy—Further Insight into the Clinical Spectrum of Desmoplakin Disease
Arrhythmogenic cardiomyopathy is a familial heart muscle disease characterized by structural, electrical, and pathological...
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