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

Translated title of the contribution: Diagnosis and study of rare heart diseases: multimodality - hypertrophic cardiomyopathy

Jaime Andrés Torres-Matiz, José Julián Carvajal-Rivera

Research output: Contribution to journal › Research Article › peer-review

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.

Translated title of the contribution	Diagnosis and study of rare heart diseases: multimodality - hypertrophic cardiomyopathy
Original language	English
Pages (from-to)	46-53
Number of pages	8
Journal	Revista Colombiana de Cardiologia
Volume	26
DOIs	https://doi.org/10.1016/j.rccar.2019.05.001
State	Published - Jul 2019
Externally published	Yes

All Science Journal Classification (ASJC) codes

Cardiology and Cardiovascular Medicine

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1016/j.rccar.2019.05.001

Cite this

@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 -

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

Abstract

All Science Journal Classification (ASJC) codes

UN SDGs

Access to Document

Other files and links

Cite this