que se leu este artigo
array:22 [ "pii" => "S0870255123002779" "issn" => "08702551" "doi" => "10.1016/j.repc.2023.05.006" "estado" => "S300" "fechaPublicacion" => "2023-10-01" "aid" => "2211" "copyrightAnyo" => "2023" "documento" => "simple-article" "crossmark" => 1 "subdocumento" => "dis" "cita" => "Rev Port Cardiol. 2023;42:845-6" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "itemSiguiente" => array:18 [ "pii" => "S0870255123003050" "issn" => "08702551" "doi" => "10.1016/j.repc.2023.01.028" "estado" => "S300" "fechaPublicacion" => "2023-10-01" "aid" => "2218" "copyright" => "Sociedade Portuguesa de Cardiologia" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Rev Port Cardiol. 2023;42:847-55" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original Article</span>" "titulo" => "Intracardiac echocardiography-guided left atrial appendage occlusion: The path to independence" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "pt" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "847" "paginaFinal" => "855" ] ] "titulosAlternativos" => array:1 [ "pt" => array:1 [ "titulo" => "Encerramento de apêndice auricular esquerdo guiado por ecocardiograma intracardíaco: o caminho para a independência" ] ] "contieneResumen" => array:2 [ "en" => true "pt" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1848 "Ancho" => 2341 "Tamanyo" => 403253 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Pre-procedural cardiac computed angiography scan to assess left atrial appendage morphology and dimensions.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "André Grazina, António Fiarresga, Ruben Ramos, José Viegas, Isabel Cardoso, Bárbara Lacerda Teixeira, Lídia de Sousa, Duarte Cacela, Rui Cruz Ferreira" "autores" => array:9 [ 0 => array:2 [ "nombre" => "André" "apellidos" => "Grazina" ] 1 => array:2 [ "nombre" => "António" "apellidos" => "Fiarresga" ] 2 => array:2 [ "nombre" => "Ruben" "apellidos" => "Ramos" ] 3 => array:2 [ "nombre" => "José" "apellidos" => "Viegas" ] 4 => array:2 [ "nombre" => "Isabel" "apellidos" => "Cardoso" ] 5 => array:2 [ "nombre" => "Bárbara" "apellidos" => "Lacerda Teixeira" ] 6 => array:2 [ "nombre" => "Lídia" "apellidos" => "de Sousa" ] 7 => array:2 [ "nombre" => "Duarte" "apellidos" => "Cacela" ] 8 => array:2 [ "nombre" => "Rui Cruz" "apellidos" => "Ferreira" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0870255123003050?idApp=UINPBA00004E" "url" => "/08702551/0000004200000010/v1_202310030529/S0870255123003050/v1_202310030529/en/main.assets" ] "itemAnterior" => array:18 [ "pii" => "S0870255123002767" "issn" => "08702551" "doi" => "10.1016/j.repc.2023.03.017" "estado" => "S300" "fechaPublicacion" => "2023-10-01" "aid" => "2213" "copyright" => "Sociedade Portuguesa de Cardiologia" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Rev Port Cardiol. 2023;42:835-43" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original Article</span>" "titulo" => "Analysis of <span class="elsevierStyleItalic">KLF7</span> and <span class="elsevierStyleItalic">KLF5</span> transcription factors gene variants in coronary artery disease" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "pt" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "835" "paginaFinal" => "843" ] ] "titulosAlternativos" => array:1 [ "pt" => array:1 [ "titulo" => "Análise das variantes dos genes dos fatores de transcrição <span class="elsevierStyleItalic">KLF7</span> e <span class="elsevierStyleItalic">KLF</span>5 na doença arterial coronária" ] ] "contieneResumen" => array:2 [ "en" => true "pt" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1066 "Ancho" => 987 "Tamanyo" => 198154 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">KLF7</span> rs2302870 genotyping by Tetra Primer ARMS-PCR. The ladder is 100 bp. Pair band of 325 and 211 bp belongs to the wild (AA) genotype, pair band of 325 and 169 bp homozygote mutant (GG), three band of 325, 211 and 169 bp heterozygote mutant (AG).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Vahid Akbari Kordkheyli, Arash Poursheikhani, Seyed Hasan Sharobandi, Sayed Mostafa Hosseini" "autores" => array:4 [ 0 => array:2 [ "nombre" => "Vahid" "apellidos" => "Akbari Kordkheyli" ] 1 => array:2 [ "nombre" => "Arash" "apellidos" => "Poursheikhani" ] 2 => array:2 [ "nombre" => "Seyed Hasan" "apellidos" => "Sharobandi" ] 3 => array:2 [ "nombre" => "Sayed Mostafa" "apellidos" => "Hosseini" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0870255123002767?idApp=UINPBA00004E" "url" => "/08702551/0000004200000010/v1_202310030529/S0870255123002767/v1_202310030529/en/main.assets" ] "en" => array:12 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Editorial comment</span>" "titulo" => "Genetics in coronary artery disease" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "845" "paginaFinal" => "846" ] ] "autores" => array:1 [ 0 => array:3 [ "autoresLista" => "Ilda Patrícia Ribeiro" "autores" => array:1 [ 0 => array:4 [ "nombre" => "Ilda Patrícia" "apellidos" => "Ribeiro" "email" => array:1 [ 0 => "ildaribeiro.patricia@gmail.com" ] "referencia" => array:4 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] 2 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] 3 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">d</span>" "identificador" => "aff0020" ] ] ] ] "afiliaciones" => array:4 [ 0 => array:3 [ "entidad" => "Cytogenetics and Genomics Laboratory, Institute of Cellular and Molecular Biology, Faculty of Medicine, University of Coimbra, Coimbra, Portugal" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "University of Coimbra, Coimbra Institute for Clinical and Biomedical Research (iCBR) and Center of Investigation on Environment Genetics and Oncobiology (CIMAGO), Faculty of Medicine, Coimbra, Portugal" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "University of Coimbra, Center for Innovative Biomedicine and Biotechnology (CIBB), Coimbra, Portugal" "etiqueta" => "c" "identificador" => "aff0015" ] 3 => array:3 [ "entidad" => "Clinical Academic Center of Coimbra (CACC), Coimbra, Portugal" "etiqueta" => "d" "identificador" => "aff0020" ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "A genética na doença coronária" ] ] "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Worldwide, coronary artery disease (CAD) is predicted to remain the leading cause of death, posing a significant socioeconomic burden.<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> Preventing and managing this disease is a major challenge due to its multifactorial nature. CAD appears to be caused by the interaction of environmental risk factors and multiple predisposing genes. However, the complex etiology of CAD has not been fully clarified to date. Several conventional risk factors, such as hypertension, hyperlipidemia, diabetes, family history and smoking are linked to CAD.<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> Other factors, such as lipoprotein (a), homocysteine, higher oxidative stress, low levels of antioxidants, being sedentary and leading a stressful lifestyle are also thought to play a key role in the development of the disease.<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> Identifying the causative factors for CAD development and/or progression is challenging due to its etiologic heterogeneity.</p><p id="par0010" class="elsevierStylePara elsevierViewall">The standard treatment for CAD can be medical, surgical or a combination of both according to the extent, severity, and clinical presentation of the disease.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> Nowadays, technological and scientific progress has led to the development of novel therapeutic approaches, such as stem cells, nanotechnology, robotic surgery, three-dimensional printing and drugs.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> Some of these strategies already have evidence supporting their clinical use, while others are still in an experimental stage.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">Since we live in the era of Big Data, MultiOmics technologies and artificial intelligence, the future for characterizing the genetic architecture of CAD and developing novel therapeutic options looks promising. The development of massive parallel sequencing technology, also known as next-generation-sequencing technology has ushered in a new era in genetic information, opening unexplored avenues in genomic medicine and ultimately advancing precision medicine with a huge growth in available genetic tests. The explosion of knowledge of how genomic variations in an individual's DNA can affect disease and health because of the Human Genome Project has meant we are now witnessing new discoveries in genetic cardiovascular disease; patient management has changed substantially over the last decade.</p><p id="par0020" class="elsevierStylePara elsevierViewall">Several studies using high-throughput sequencing methods have addressed single nucleotide polymorphisms (SNPs) with cardiovascular disease.<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">4</span></a> Genome-wide association studies (GWAS) have identified about 208 susceptibility loci for CAD.<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">5,6</span></a> Several studies have focused on the association of variants at the GWAS loci with CAD in specific populations. Despite the lack of consistency in the association patterns of these genes/loci across the populations, 11q23.3 and 9p21.3 chromosomal regions are the most frequently CAD-associated loci reported. Tcheandjieu et al.<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> reported a GWAS of CAD with cohorts of Caucasian, Black, and Hispanic individuals from the Million Veteran Program, identifying 95 novel loci, including the first nine to be identified on the X-chromosome, and reporting near equivalent heritability of CAD across multiple ancestral groups.</p><p id="par0025" class="elsevierStylePara elsevierViewall">In the current issue of the Journal, Kordkheyli et al.<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> investigated the potential correlation between <span class="elsevierStyleItalic">KLF5</span> (rs3812852) and <span class="elsevierStyleItalic">KLF7</span> (rs2302870) SNPs with the risk of CAD in the Iranian population. It is known that Krüppel-like factors are DNA-binding proteins belonging to the family of zinc-finger transcription factors that can regulate gene expression linked to numerous biological processes, such as cell growth, differentiation, and death, as well as the development and maintenance of specialized tissues, under both physiological and pathological conditions.<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> KLFs are also known to be involved in regulating several key processes of cardiovascular diseases, including inflammation, oxidative stress, and cell proliferation.</p><p id="par0030" class="elsevierStylePara elsevierViewall">Kordkheyli et al.’s study has shed new light on the molecular pathogenesis of CAD by identifying the <span class="elsevierStyleItalic">KLF7</span> gene as a candidate for CAD susceptibility, while also suggesting that the <span class="elsevierStyleItalic">KLF5</span> SNP is unlikely to influence CAD risk.</p><p id="par0035" class="elsevierStylePara elsevierViewall">The authors acknowledge that more functional studies are needed to fully understand the molecular mechanisms underlying the pathogenesis of CAD and to clarify the precise correlation of other polymorphisms in <span class="elsevierStyleItalic">KLF5</span> and <span class="elsevierStyleItalic">KLF7</span> with the CAD risk across different populations.</p><p id="par0040" class="elsevierStylePara elsevierViewall">Currently, there is still much to learn about the role of KLFs in the risk of cardiac diseases, as well as the potential contribution of these proteins as therapeutic targets.</p><p id="par0045" class="elsevierStylePara elsevierViewall">As a final remark, CAD, a disorder with complex inheritance pattern, should be analyzed at different biological levels. Therefore, it is also important to understand the epigenetic mechanisms that regulate the expression of these genes. The advancement in molecular technology allows for a thorough characterization of cardiac diseases at different omic levels (e.g. genomics, transcriptomics, proteomics, epigenomics, metabolomics, etc.), empowers physicians to treat these diseases based on each patient's unique profile by understanding the individual differences and characteristics, including specific genotypes, of patients with similar clinical presentations, thereby enhancing risk stratification, diagnosis, and therapeutic decision-making.<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a></p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of interest</span><p id="par0050" class="elsevierStylePara elsevierViewall">The author has no conflicts of interest to declare.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0005" "titulo" => "Conflicts of interest" ] 1 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0015" "bibliografiaReferencia" => array:10 [ 0 => array:3 [ "identificador" => "bib0055" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Projections of global mortality and burden of disease from 2002 to 2030" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "C.D. Mathers" 1 => "D. Loncar" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1371/journal.pmed.0030442" "Revista" => array:5 [ "tituloSerie" => "PLoS Med" "fecha" => "2006" "volumen" => "3" "paginaInicial" => "e442" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/17132052" "web" => "Medline" ] ] ] ] ] ] ] ] 1 => array:3 [ "identificador" => "bib0060" "etiqueta" => "2" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Molecular studies on coronary artery disease – a review" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "A.S. Simon" 1 => "T. Vijayakumar" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1007/s12291-013-0303-6" "Revista" => array:6 [ "tituloSerie" => "Indian J Clin Biochem" "fecha" => "2013" "volumen" => "28" "paginaInicial" => "215" "paginaFinal" => "226" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/24426215" "web" => "Medline" ] ] ] ] ] ] ] ] 2 => array:3 [ "identificador" => "bib0065" "etiqueta" => "3" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Recent advances in treatment of coronary artery disease: role of science and technology" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "E. Kandaswamy" 1 => "L. Zuo" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.3390/ijms19020424" "Revista" => array:5 [ "tituloSerie" => "Int J Mol Sci" "fecha" => "2018" "volumen" => "19" "paginaInicial" => "424" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/29385089" "web" => "Medline" ] ] ] ] ] ] ] ] 3 => array:3 [ "identificador" => "bib0070" "etiqueta" => "4" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "A decade of genome-wide association studies for coronary artery disease: the challenges ahead" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:3 [ 0 => "J. Erdmann" 1 => "T. Kessler" 2 => "L. Munoz Venegas" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1093/cvr/cvy084" "Revista" => array:6 [ "tituloSerie" => "Cardiovasc Res" "fecha" => "2018" "volumen" => "114" "paginaInicial" => "1241" "paginaFinal" => "1257" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/29617720" "web" => "Medline" ] ] ] ] ] ] ] ] 4 => array:3 [ "identificador" => "bib0075" "etiqueta" => "5" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Identification of 64 novel genetic loci provides an expanded view on the genetic architecture of coronary artery disease" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "P. van der Harst" 1 => "N. Verweij" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1161/CIRCRESAHA.117.312086" "Revista" => array:6 [ "tituloSerie" => "Circ Res" "fecha" => "2018" "volumen" => "122" "paginaInicial" => "433" "paginaFinal" => "443" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/29212778" "web" => "Medline" ] ] ] ] ] ] ] ] 5 => array:3 [ "identificador" => "bib0080" "etiqueta" => "6" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:3 [ 0 => "S. Koyama" 1 => "K. Ito" 2 => "C. Terao" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1038/s41588-020-0705-3" "Revista" => array:6 [ "tituloSerie" => "Nat Genet" "fecha" => "2020" "volumen" => "52" "paginaInicial" => "1169" "paginaFinal" => "1177" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/33020668" "web" => "Medline" ] ] ] ] ] ] ] ] 6 => array:3 [ "identificador" => "bib0085" "etiqueta" => "7" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Large-scale genome-wide association study of coronary artery disease in genetically diverse populations" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:3 [ 0 => "C. Tcheandjieu" 1 => "X. Zhu" 2 => "A.T. Hilliard" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1038/s41591-022-01891-3" "Revista" => array:6 [ "tituloSerie" => "Nat Med" "fecha" => "2022" "volumen" => "28" "paginaInicial" => "1679" "paginaFinal" => "1692" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/35915156" "web" => "Medline" ] ] ] ] ] ] ] ] 7 => array:3 [ "identificador" => "bib0090" "etiqueta" => "8" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Analysis of KLF7 and KLF5 transcription factors genes variants in coronary artery disease" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:3 [ 0 => "V.A. Kordkheyli" 1 => "A. Poursheikhani" 2 => "S.H. Sharobandi" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "Rev Port Cardiol" "fecha" => "2023" "volumen" => "42" "paginaInicial" => "835" "paginaFinal" => "843" ] ] ] ] ] ] 8 => array:3 [ "identificador" => "bib0095" "etiqueta" => "9" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Krüppel-like factors in cancer" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "M.-P. Tetreault" 1 => "Y. Yang" 2 => "J.P. Katz" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1038/nrc3582" "Revista" => array:7 [ "tituloSerie" => "Nat Rev Cancer" "fecha" => "2013" "volumen" => "13" "paginaInicial" => "701" "paginaFinal" => "713" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/24060862" "web" => "Medline" ] ] "itemHostRev" => array:3 [ "pii" => "S1474442214701449" "estado" => "S300" "issn" => "14744422" ] ] ] ] ] ] ] 9 => array:3 [ "identificador" => "bib0100" "etiqueta" => "10" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Precision medicine and the future of cardiovascular diseases: a clinically oriented comprehensive review" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:3 [ 0 => "Y. Sethi" 1 => "N. Patel" 2 => "N. Kaka" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.3390/jcm12051799" "Revista" => array:5 [ "tituloSerie" => "J Clin Med" "fecha" => "2023" "volumen" => "12" "paginaInicial" => "1799" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/36902588" "web" => "Medline" ] ] ] ] ] ] ] ] ] ] ] ] ] "idiomaDefecto" => "en" "url" => "/08702551/0000004200000010/v1_202310030529/S0870255123002779/v1_202310030529/en/main.assets" "Apartado" => array:4 [ "identificador" => "93359" "tipo" => "SECCION" "pt" => array:2 [ "titulo" => "Original articles" "idiomaDefecto" => true ] "idiomaDefecto" => "pt" ] "PDF" => "https://static.elsevier.es/multimedia/08702551/0000004200000010/v1_202310030529/S0870255123002779/v1_202310030529/en/main.pdf?idApp=UINPBA00004E&text.app=https://revportcardiol.org/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0870255123002779?idApp=UINPBA00004E" ]
Ano/Mês | Html | Total | |
---|---|---|---|
2024 Novembro | 11 | 10 | 21 |
2024 Outubro | 54 | 35 | 89 |
2024 Setembro | 55 | 31 | 86 |
2024 Agosto | 52 | 45 | 97 |
2024 Julho | 38 | 39 | 77 |
2024 Junho | 42 | 34 | 76 |
2024 Maio | 40 | 39 | 79 |
2024 Abril | 27 | 23 | 50 |
2024 Maro | 38 | 23 | 61 |
2024 Fevereiro | 29 | 30 | 59 |
2024 Janeiro | 24 | 27 | 51 |
2023 Dezembro | 25 | 23 | 48 |
2023 Novembro | 60 | 56 | 116 |
2023 Outubro | 144 | 72 | 216 |
2023 Setembro | 22 | 17 | 39 |
2023 Agosto | 18 | 11 | 29 |
2023 Julho | 35 | 29 | 64 |
2023 Junho | 47 | 37 | 84 |
2023 Maio | 0 | 2 | 2 |