Heart Failure Clinics
IF
3.18
Papers
869
Papers 914
1 page of 92 pages (914 results)
Newest
#1Michele Lioncino (Seconda Università degli Studi di Napoli)H-Index: 3
#2Emanuele Monda (Seconda Università degli Studi di Napoli)H-Index: 9
Last. Barbara D’Onofrio (Seconda Università degli Studi di Napoli)
view all 18 authors...
Transthyretin cardiac amyloidosis (ATTR-CA) is a systemic disorder resulting from the extracellular deposition of amyloid fibrils of misfolded transthyretin protein in the heart. ATTR-CA is a life-threatening disease, which can be caused by progressive deposition of wild type transthyretin (wtATTR) or by aggregation of an inherited mutated variant of transthyretin (mATTR). mATTR Is a rare condition transmitted in an autosomal dominant manner with incomplete penetrance, causing heterogenous pheno...
Source
#1Michael Würdinger (UZH: University of Zurich)H-Index: 3
#2Victoria L. Cammann (UZH: University of Zurich)H-Index: 15
Last. Christian Templin (UZH: University of Zurich)H-Index: 39
view all 4 authors...
Spontaneous coronary artery dissection is an infrequent cause of acute coronary syndrome with comparable clinical features. Previously considered a rare disease, recent scientific interest has revealed spontaneous coronary artery dissection as an important differential diagnosis of acute coronary syndrome, especially in young women, during pregnancy or postpartum, and in patients with fibromuscular dysplasia or other arteriopathies. However, there remain many uncertainties regarding pathophysiol...
Source
#1Emanuele Monda (Seconda Università degli Studi di Napoli)H-Index: 9
#2Michele Lioncino (Seconda Università degli Studi di Napoli)H-Index: 3
Last. Nunzia Borrelli (Seconda Università degli Studi di Napoli)H-Index: 1
view all 19 authors...
"Sudden unexplained death (SUD) is a tragic event for both the family and community, particularly when it occurs in young individuals. Sudden cardiac death (SCD) represents the leading form of SUD and is defined as an unexpected event without an obvious extracardiac cause, occurring within 1 hour after the onset of symptoms. In children, the main causes of SCD are inherited cardiac disorders, whereas coronary artery diseases (congenital or acquired), congenital heart diseases, and myocarditis ar...
Source
#1Adelaide Fusco (Seconda Università degli Studi di Napoli)H-Index: 4
#2Alfredo Mauriello (Seconda Università degli Studi di Napoli)H-Index: 1
view all 19 authors...
The inherited connective tissue disorders (Marfan syndrome, Loeys-Dietz syndrome [LDS], and Ehlers-Danlos syndrome [EDS]) involve connective tissue of various organ systems. These pathologies share many common features, nonetheless compared to Marfan syndrome, LDS' cardiovascular manifestations tend to be more severe. In contrast, no association is reported between LDS and the presence of ectopia lentis. The EDS are currently classified into thirteen subtypes. There is substantial symptoms overl...
Source
#1Giuseppe Limongelli (Seconda Università degli Studi di Napoli)H-Index: 58
#2Emanuele Monda (Seconda Università degli Studi di Napoli)H-Index: 9
Last. Eduardo BossoneH-Index: 77
view all 4 authors...
Source
#1Marta Rubino (Seconda Università degli Studi di Napoli)H-Index: 8
#2Emanuele Monda (Seconda Università degli Studi di Napoli)H-Index: 9
view all 20 authors...
Fabry disease (FD, OMIM 301500) is an X-linked lysosomal storage disease caused by pathogenic variants in the GLA gene. Cardiac involvement is common in FD and is responsible for impaired quality of life and premature death. The classic cardiac involvement is a nonobstructive form of hypertrophic cardiomyopathy, usually manifesting as concentric left ventricular hypertrophy, with subsequent arrhythmogenic intramural fibrosis. Treatment of patients with FD should be directed to prevent the diseas...
Source
#1Ioannis Protonotarios (University Hospital Southampton NHS Foundation Trust)
#2Angeliki Asimaki (St. George's University)
Last. Adalena TsatsopoulouH-Index: 23
view all 5 authors...
Naxos disease is a recessively inherited pattern of arrhythmogenic cardiomyopathy with palmoplantar keratoderma and woolly hair. The causative mutation identified in plakoglobin protein gene indicated a potential role of the desmosomal protein complex as culprit for cardiomyopathy. In the context of a family, the early evident cutaneous features may serve as a clinical screening tool to spot arrhythmogenic cardiomyopathy in subclinical stage. "Myocarditis-like episodes" may step up the disease e...
Source
#1Giuseppe LimongelliH-Index: 58
#2Emanuele MondaH-Index: 9
Last. Eduardo BossoneH-Index: 77
view all 4 authors...
Source
#1Giuseppe Palmiero (Leonardo)
#2Erica Vetrano (Leonardo)
Last. Laura Capodicasa (Leonardo)
view all 20 authors...
Cardiac amyloidosis is an infiltrative disorder caused by transthyretin or immunoglobulin free light-chain deposition, which determines clinical disease with similar phenotype but different time course, prognosis and therapy. Multimodality imaging is the cornerstone for disease diagnosis and management. Multimodality imaging has revolutionized the approach to the disease favoring its awareness and simplifying its diagnosis, especially in ATTR cardiac amyloidosis. This describes the different ima...
Source
#1Annapaola Cirillo (Seconda Università degli Studi di Napoli)H-Index: 6
#2Michele Lioncino (Seconda Università degli Studi di Napoli)H-Index: 3
Last. Augusto Esposito (Seconda Università degli Studi di Napoli)H-Index: 8
view all 20 authors...
DiGeorge syndrome (DGS), also known as "22q11.2 deletion syndrome" (22q11DS) (MIM # 192430 # 188400), is a genetic disorder caused by hemizygous microdeletion of the long arm of chromosome 22. In the last decades, the introduction of fluorescence in situ hybridization assays, and in selected cases the use of multiplex ligation-dependent probe amplification, has allowed the detection of chromosomal microdeletions that could not be previously identified using standard karyotype analysis. The aim o...
Source
12345678910
Top fields of study
This website uses cookies.
We use cookies to improve your online experience. By continuing to use our website we assume you agree to the placement of these cookies.
To learn more, you can find in our Privacy Policy.