Zobrazeno 1 - 10
of 523
pro vyhledávání: '"RAMON BRUGADA"'
Autor:
Lenises de Paula van der Steld, Mario de Seixas Rocha, Ana Marice Teixeira Ladeia, Humberto Lago Livramento, Gervásio Batista Campos, Francisco Carlos da Costa Darrieux, Oscar Campuzano, Ramon Brugada
Publikováno v:
Einstein (São Paulo), Vol 22 (2024)
ABSTRACT Objective This study aimed to provide a long-term follow-up of PRKAG2 syndrome and describe the new phenotypic aspects of the condition. PRKAG2 syndrome is a rare autosomal-dominant glycogen storage disease characterized by cardiac hypertrop
Externí odkaz:
https://doaj.org/article/b477a0c0b169440da04a9db30e553c04
Autor:
Josep Iglesies-Grau, Ana Garcia-Alvarez, Belén Oliva, Guiomar Mendieta, Inés García-Lunar, José J. Fuster, Ana Devesa, Cristina Pérez-Herreras, Antonio Fernández-Ortiz, Ramon Brugada, Borja Ibanez, Rodrigo Fernandez-Jimenez, Valentin Fuster
Publikováno v:
Cardiovascular Diabetology, Vol 22, Iss 1, Pp 1-12 (2023)
Abstract Background Elevated glycated hemoglobin (HbA1c) is associated with a higher burden of subclinical atherosclerosis (SA). However, the association with SA of earlier insulin resistance markers is poorly understood. The study assessed the assoc
Externí odkaz:
https://doaj.org/article/5db9bdcc44bd4b539910b57632c81aff
Autor:
Fernando Bonet, Oscar Campuzano, José Córdoba-Caballero, Mireia Alcalde, Georgia Sarquella-Brugada, Aitana Braza-Boïls, Ramon Brugada, Francisco Hernández-Torres, Maribel Quezada-Feijoo, Monica Ramos, Alipio Mangas, Juan A. G. Ranea, Rocío Toro
Publikováno v:
Biomedicines, Vol 12, Iss 8, p 1807 (2024)
Arrhythmogenic cardiomyopathy is an inherited entity characterized by irregular cell–cell adhesion, cardiomyocyte death and fibro-fatty replacement of ventricular myocytes, leading to malignant ventricular arrythmias, contractile dysfunction and su
Externí odkaz:
https://doaj.org/article/945d2dc181984d7480a2a40bb22752e5
Autor:
Anna Fernandez-Falgueras, Monica Coll, Anna Iglesias, Coloma Tiron, Oscar Campuzano, Ramon Brugada
Publikováno v:
PLoS ONE, Vol 19, Iss 5, p e0297914 (2024)
Inherited cardiovascular diseases are rare diseases that are difficult to diagnose by non-expert professionals. Genetic analyses play a key role in the diagnosis of these diseases, in which the identification of a pathogenic genetic variant is often
Externí odkaz:
https://doaj.org/article/8d0f7a2faeb94c2782f017309a271ac0
Autor:
Muzamil Khawaja, Yusuf Kamran Qadeer, Rehma Siddiqui, Mihail G. Chelu, Noppawit Aiumtrakul, June K. Pickett, Ramon Brugada, Josep Brugada, Pedro Brugada, Chayakrit Krittanawong
Publikováno v:
Cardiogenetics, Vol 13, Iss 2, Pp 61-74 (2023)
Brugada syndrome (BrS) is an inherited cardiac channelopathy with variable expressivity that can lead to sudden cardiac arrest (SCA). Studies worldwide suggest that BrS and Brugada pattern (BrP) have low prevalences in general. However, studies also
Externí odkaz:
https://doaj.org/article/f35abb2b1ab44e51a31061ba694370c1
Autor:
Rebecca Martínez-Moreno, Alexandra Pérez-Serra, Elisabet Selga, David Carreras, Begoña Aran, Bernd Kuebler, Fabiana S. Scornik, Guillermo J. Pérez, Ramon Brugada
Publikováno v:
Stem Cell Research, Vol 73, Iss , Pp 103239- (2023)
Tissue-specific cells differentiated from patient-derived human induced pluripotent stem cells (hiPSC) are a relevant cellular model to study several diseases. We obtained a hiPSC line from skin fibroblasts of a patient affected by familial atrial fi
Externí odkaz:
https://doaj.org/article/a5a6383660434068bac6b7654e908c00
Autor:
Sergio Moral, MD, PhD, Sandra Martinez-Ballart, MD, Esther Ballesteros, MD, Ramon Brugada, MD, PhD
Publikováno v:
JACC: Case Reports, Vol 28, Iss , Pp 102085- (2023)
Intramyocardial dissecting hematoma (IDH), in the setting of an acute coronary syndrome, is a rare type of cardiac rupture. However, the best treatment for IDH in each clinical scenario is not clearly defined. We present a case in which the best appr
Externí odkaz:
https://doaj.org/article/d7f5d630c4fe4270b2c515d36841d5a9
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Externí odkaz:
https://doaj.org/article/d5680f758e40413b8fc59441a02ec858
Severe Aortic Stenosis Associated with Other Valve Diseases: Open Surgery or Percutaneous Treatment?
Publikováno v:
Reviews in Cardiovascular Medicine, Vol 25, Iss 3, p 99 (2024)
Treatment decisions in the context of severe aortic stenosis (AS) associated with other valvular heart diseases (VHDs) have become a major challenge in recent years. Transcatheter aortic valve replacement (TAVR) in AS has increased significantly in y
Externí odkaz:
https://doaj.org/article/0f9f0ff519bb49679de2ac03d9c60b87
Publikováno v:
Reviews in Cardiovascular Medicine, Vol 25, Iss 2, p 40 (2024)
Valvulopathies are among the most common cardiovascular diseases, significantly increasing morbidity and mortality. While many valvular heart diseases are acquired later in life, an important genetic component has been described, particularly in mitr
Externí odkaz:
https://doaj.org/article/90ff7725638d4235bc2c09af0f6890ca