Diagnosis and study of rare heart diseases: multimodality - hypertrophic cardiomyopathy

Jaime Andrés Torres-Matiz; José Julián Carvajal-Rivera

doi:10.1016/j.rccar.2019.05.001

Diagnosis and study of rare heart diseases: multimodality - hypertrophic cardiomyopathy

Título traducido de la contribución: Diagnóstico y estudio de cardiopatías infrecuentes: multimodalidad – miocardiopatía hipertrófica: multimodality - hypertrophic cardiomyopathy

Jaime Andrés Torres-Matiz, José Julián Carvajal-Rivera

Producción científica: Contribución a una revista › Artículo de Investigación › revisión exhaustiva

Resumen

Abstract Hypertrophic cardiomyopathy is a genetic disorder, characterised by left ventricular hypertrophy not explained by secondary causes, including non-dilated ventricle and preserved or augmented ejection fraction.1 Histologically, hypertrophic cardiac myocytes are observed that are disorganised, losing parallel alignment due to random orientation, and separated by wide areas of fibrosis.

Título traducido de la contribución	Diagnóstico y estudio de cardiopatías infrecuentes: multimodalidad – miocardiopatía hipertrófica: multimodality - hypertrophic cardiomyopathy
Idioma original	Inglés
Páginas (desde-hasta)	46-53
Número de páginas	8
Publicación	Revista Colombiana de Cardiologia
Volumen	26
DOI	https://doi.org/10.1016/j.rccar.2019.05.001
Estado	Publicada - jul. 2019
Publicado de forma externa	Sí

Áreas temáticas de ASJC Scopus

Cardiología y medicina cardiovascular

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

Acceder al documento

10.1016/j.rccar.2019.05.001

Otros archivos y enlaces

Citar esto

@article{3f8b8e692c5c4701a9ca2cce2a3399b8,

title = "Diagnosis and study of rare heart diseases: multimodality - hypertrophic cardiomyopathy",

abstract = "Abstract Hypertrophic cardiomyopathy is a genetic disorder, characterised by left ventricular hypertrophy not explained by secondary causes, including non-dilated ventricle and preserved or augmented ejection fraction.1 Histologically, hypertrophic cardiac myocytes are observed that are disorganised, losing parallel alignment due to random orientation, and separated by wide areas of fibrosis.",

author = "Torres-Matiz, {Jaime Andr{\'e}s} and Carvajal-Rivera, {Jos{\'e} Juli{\'a}n}",

year = "2019",

month = jul,

doi = "10.1016/j.rccar.2019.05.001",

language = "Ingl{\'e}s",

volume = "26",

pages = "46--53",

journal = "Revista Colombiana de Cardiologia",

issn = "0120-5633",

publisher = "Sociedad Colombiana de Cardiologia y Cirugia Cardiovascular",

}

TY - JOUR

T1 - Diagnosis and study of rare heart diseases: multimodality - hypertrophic cardiomyopathy

AU - Torres-Matiz, Jaime Andrés

AU - Carvajal-Rivera, José Julián

PY - 2019/7

Y1 - 2019/7

N2 - Abstract Hypertrophic cardiomyopathy is a genetic disorder, characterised by left ventricular hypertrophy not explained by secondary causes, including non-dilated ventricle and preserved or augmented ejection fraction.1 Histologically, hypertrophic cardiac myocytes are observed that are disorganised, losing parallel alignment due to random orientation, and separated by wide areas of fibrosis.

AB - Abstract Hypertrophic cardiomyopathy is a genetic disorder, characterised by left ventricular hypertrophy not explained by secondary causes, including non-dilated ventricle and preserved or augmented ejection fraction.1 Histologically, hypertrophic cardiac myocytes are observed that are disorganised, losing parallel alignment due to random orientation, and separated by wide areas of fibrosis.

UR - http://www.scopus.com/inward/record.url?scp=85067971313&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85067971313&partnerID=8YFLogxK

U2 - 10.1016/j.rccar.2019.05.001

DO - 10.1016/j.rccar.2019.05.001

M3 - Artículo de Investigación

AN - SCOPUS:85067971313

SN - 0120-5633

VL - 26

SP - 46

EP - 53

JO - Revista Colombiana de Cardiologia

JF - Revista Colombiana de Cardiologia

ER -