Results 11 to 20 of about 1,009 (150)

Miocardiopatía hipertrófica septal, la gran simuladora

open access: yesArchivos Peruanos de Cardiología y Cirugía Cardiovascular, 2021
La miocardiopatía hipertrófica es la enfermedad miocárdica más frecuente de carácter genético (60-70%) causada por mutaciones en uno de varios genes del sarcómero que codifican componentes del aparato contráctil del corazón.
Santiago Forero, Nelson Leandro Moreno
doaj   +1 more source

Beware of regression of electrocardiographic abnormalities on detraining – It may not always mean ‘athlete's heart’

open access: yesRevista Portuguesa de Cardiologia, 2021
Hypertrophic cardiomyopathy is one of the main causes of sudden cardiac death in young athletes. Differentiating between this pathological condition and ‘athlete's heart’ can be quite challenging, warranting a thorough clinical and imaging assessment ...
José Pedro Marques   +2 more
doaj   +1 more source

Miocardiopatía Hipertrófica

open access: yesRevista Clínica de la Escuela de Medicina UCR-HSJD, 2020
La Miocardiopatía Hipertrófica (MCH) es actualmente una de las afecciones cardiacas hereditarias más prevalentes. Es definida como una enfermedad del músculo cardiaco adquirida como un rasgo autosómico dominante con expresión variable, causada por ...
Johanna Vindas Porras
doaj   +1 more source

Miocardiopatia de Takotsubo e suas variáveis: uma revisão integrativa [PDF]

open access: yes, 2021
In post-modern society, changes in people's lifestyle have triggered both professional and personal problems. In this context, encouraging the biopsychosocial look at the patient, there is a concern to research more about Takotsubo Cardiomyopathy.
Antero da Silva, Marcelo   +7 more
core   +5 more sources

An unusual ST-segment elevation: Apical hypertrophic cardiomyopathy shows the ace up its sleeve

open access: yesRevista Portuguesa de Cardiologia, 2013
Apical hypertrophic cardiomyopathy is part of the broad clinical and morphologic spectrum of hypertrophic cardiomyopathy. We report a patient with electrocardiographic abnormalities in whom acute coronary syndrome was excluded and apical hypertrophic ...
Francesco de Santis   +5 more
doaj   +1 more source

Rastreo de familiares de una paciente con miocardiopatía hipertrófica obstructiva

open access: yesRevista Colombiana de Cardiología, 2018
Introducción: La miocardiopatía hipertrófica familiar es la modalidad hereditaria autosómica dominante de la miocardiopatía hipertrófica, de penetrancia incompleta y expresión variable.
Eliza Kaori Uenishi   +3 more
doaj   +1 more source

Serum NT pro-BNP: relation to systolic and diastolic function in cardiomyopathies and pericardiopathies [PDF]

open access: yes, 2008
FUNDAMENTO: O NT pro-BNP é marcador de disfunção sistólica e diastólica. OBJETIVO: Determinar os níveis de NT pro-BNP em pacientes com cardiopatia chagásica, hipertrófica, restritiva e afecções pericárdicas, e sua relação com medidas ecocardiográficas de
ARTEAGA, Edmundo   +8 more
core   +2 more sources

Síndrome Leopard e miocardiopatia hipertrófica: uma associação relacionada à morte súbita Síndrome leopard y miocardiopatía hipertrófica: una asociación relacionada a la muerte súbita Leopard syndrome and hypertrophic cardiomyopathy: an association related to sudden death

open access: yesArquivos Brasileiros de Cardiologia, 2009
Relatamos a rara associação entre síndrome Leopard e miocardiopatia hipertrófica em mulher de 27 anos, pouco sintomática, que veio para estratificação e prevenção de risco de morte súbita.
Murillo de Oliveira Antunes   +3 more
doaj   +1 more source

Cardiac Anderson-Fabry disease: Lessons from a 25-year-follow up

open access: yesRevista Portuguesa de Cardiologia, 2014
Sarcomeric hypertrophic cardiomyopathy (HCM) is the most common genetic cause of unexplained left ventricular hypertrophy and has no specific treatment. Anderson-Fabry disease (AFD) is rare and usually multisystemic, but occasionally expresses clinically
Dulce Brito   +4 more
doaj   +1 more source

Report of the first Brazilian infantile Pompe disease patient to be treated with recombinant human acid alpha-glucosidase [PDF]

open access: yes, 2008
Objetivo: Relatar o primeiro caso de forma infantil da doença de Pompe tratado no Brasil. Descrição: Trata-se de doença de depósito lisossomal que se caracteriza por defeitos da enzima alfa-glicosidase ácida, com acúmulo intracelular de glicogênio ...
BERDITCHEVISKY, Célia R.   +2 more
core   +2 more sources

Home - About - Disclaimer - Privacy