Results 71 to 80 of about 4,606 (191)

Modulation of mechanosensitive genes during embryonic aortic arch development

Developmental Dynamics, Volume 254, Issue 3, Page 222-239, March 2025.
Abstract Background Early embryonic aortic arches (AA) are a dynamic vascular structures that are in the process of shaping into the great arteries of cardiovascular system. Previously, a time‐lapsed mechanosensitive gene expression map was established for AA subject to altered mechanical loads in the avian embryo. To validate this map, we investigated
Hummaira Banu Siddiqui, Tansu Golcez, Merve Çelik, Börteçine Sevgin, Mervenur Çoban, İlke Süder, Özen Kaya, Nesrin Özören, Kerem Pekkan   +8 more
wiley   +1 more source

A rare presentation of spontaneous ventricular tachycardia in young adult

Heart India, 2017
Arrhythmogenic right ventricular dysplasia (ARVD) is a common cause of sudden cardiac death in young adults. It is a disease that has a wide spectrum of presentation.
Ram Narayan, Mansoor C Abdulla, Jemshad Alungal   +2 more
doaj   +1 more source

Incidental Findings Identified by Prenatal Microarray Analysis and Consensus Reporting Criteria of the Catalan Public Health Network XIGENICS

Prenatal Diagnosis, Volume 45, Issue 3, Page 326-347, March 2025.
ABSTRACT Objective The study aimed to evaluate the frequency of pathogenic copy number variants (CNVs) classified as incidental findings (IFs) in prenatal diagnosis and to develop consensus recommendations for standardizing their reporting across six centers within the Catalan public health system (XIGENICS network).
Irene Mademont‐Soler, Neus Castells‐Sarret, Adela Cisneros, Laura Foj, Clara Benavent‐Bofill, Mar Xunclà, Marina Viñas‐Jornet, Andrea Ros, Natalia Rey, Ignacio Blanco, Ricard López‐Ortega, María Obón, Alberto Plaja   +12 more
wiley   +1 more source

Arrhythmogenic Right Ventricular Cardiomyopathy in Children: A Systematic Review

Diagnostics
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited disease characterized by the progressive replacement of the normal myocardium by fibroadipocytic tissue.
Stefana Maria Moisa, Elena Lia Spoiala, Eliza Cinteza, Radu Vatasescu, Lacramioara Ionela Butnariu, Crischentian Brinza, Alexandru Burlacu   +6 more
doaj   +1 more source

Kocher-Debre-Semelaigne syndrome with arrhythmogenic right ventricular cardiomyopathy: A hitherto unrecognized association

Indian Journal of Endocrinology and Metabolism, 2012
Kocher-Debre-Semelaigne (KDS) syndrome is a rare form of hypothyroid myopathy, with associated hypertrophy of muscles. Although cardiac manifestations of hypothyroidism are well known, reports of cardiac involvement in KDS have only described the ...
Nagaraja Moorthy, Sudeep Kumar, Preeti Dabadghao, Aditya Kapoor   +3 more
doaj   +1 more source

[Arrhythmogenic right ventricular dysplasia].

Arquivos brasileiros de cardiologia, 1992
To evaluate the clinical findings and complementary investigation to support the diagnosis of arrhythmogenic right ventricular dysplasia.Six males with a mean age of 40 years old with episodes of sustained ventricular tachycardia with left bundle branch block pattern.
I G, Maia, R, Sá, R, Bassan, P, Alves, J C, Ribeiros, L H, Loyola, F E, Cruz Filho, A, Valverde, L, Belém   +8 more
openaire   +2 more sources

An atypical case report of an arrhythmogenic cardiomyopathy in a 70-years-old patient with suggestive left ventricular signs

Radiology Case Reports
Arrhythmogenic dysplasia of the right ventricule (ARVC), actually known as arrhythmogenic cardiomyopathy (ACM) is a rare genetic condition caused by the replacement of the normal right ventricular myocardium with fibrofatty tissue.
ikram Tahani, MD, oumayma Hattab, MD, Nabila ismaili, PhD, Noha el ouafi, PhD   +3 more
doaj   +1 more source

Naxos disease: from the origin to today

Orphanet Journal of Rare Diseases, 2018
Naxos disease, first described by Dr. Nikos Protonotarios and colleagues on the island of Naxos, Greece, is a special form of arrhythmogenic right ventricular dysplasia (ARVD).
Guo-Liang Li, Ardan M. Saguner, Guy H. Fontaine   +2 more
doaj   +1 more source

Varied Presentation of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C): A Case Series. [PDF]

Cureus, 2023
Mishra D, Shankar O, Aggarwal V.
europepmc   +1 more source

Arrhythmogenic Right Ventricular Dysplasia (ARVD) With Protein Plakophilin-2 Mutation. [PDF]

Cureus, 2022
Riasat M, Khan A, Meghrajani V, Gaikwad M, Gill R.   +4 more
europepmc   +1 more source