Cargando…

Chromosome Y Haplogroup R Was Associated with the Risk of Premature Myocardial Infarction with ST-Elevation: Data from the CholeSTEMI Registry

Cardiovascular disease (CVD) is the leading cause of death worldwide, with coronary artery disease (CAD) being one of its main manifestations. Both environmental and genetic factors are widely known to be related to CAD, such as smoking, diabetes mellitus, dyslipidemia, and a family history of CAD....

Descripción completa

Detalles Bibliográficos
Autores principales:	Lorca, Rebeca, Aparicio, Andrea, Salgado, María, Álvarez-Velasco, Rut, Pascual, Isaac, Gomez, Juan, Vazquez-Coto, Daniel, Garcia-Lago, Claudia, Velázquez-Cuervo, Lucinda, Cuesta-Llavona, Elías, Avanzas, Pablo, Coto, Eliecer
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10381015/ https://www.ncbi.nlm.nih.gov/pubmed/37510926 http://dx.doi.org/10.3390/jcm12144812

Ejemplares similares

Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry
por: Lorca, Rebeca, et al.
Publicado: (2020)

Mitochondrial Heteroplasmy as a Marker for Premature Coronary Artery Disease: Analysis of the Poly-C Tract of the Control Region Sequence
por: Lorca, Rebeca, et al.
Publicado: (2023)

Common mitochondrial haplogroups as modifiers of the onset-age for critical COVID-19
por: Vázquez-Coto, Daniel, et al.
Publicado: (2022)

Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients
por: Salgado, María, et al.
Publicado: (2023)

Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia
por: Aparicio, Andrea, et al.
Publicado: (2023)

Premature STEMI in Men and Women: Current Clinical Features and Improvements in Management and Prognosis
por: Lorca, Rebeca, et al.
Publicado: (2021)

The IFIH1/MDA5 rs1990760 Gene Variant (946Thr) Differentiates Early- vs. Late-Onset Skin Disease and Increases the Risk of Arthritis in a Spanish Cohort of Psoriasis
por: Coto-Segura, Pablo, et al.
Publicado: (2023)

Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome
por: Lorca, Rebeca, et al.
Publicado: (2020)

Characterization of Left Ventricular Non-Compaction Cardiomyopathy
por: Lorca, Rebeca, et al.
Publicado: (2020)

The Renin–Angiotensin–Aldosterone System and Coronavirus Disease 2019
por: Coto, Eliecer, et al.
Publicado: (2021)

Gene Variant in the NF-κB Pathway Inhibitor NFKBIA Distinguishes Patients with Psoriatic Arthritis within the Spectrum of Psoriatic Disease
por: Coto-Segura, Pablo, et al.
Publicado: (2019)

Association of the Genetic Variation in the Long Non-Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy
por: Cuesta-Llavona, Elías, et al.
Publicado: (2022)

Genetic variants in the NF-κB signaling pathway (NFKB1, NFKBIA, NFKBIZ) and risk of critical outcome among COVID-19 patients
por: Camblor, Daniel G., et al.
Publicado: (2022)

Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy
por: Rodríguez Junquera, Manuel, et al.
Publicado: (2022)

The FCGR2A rs1801274 polymorphism was associated with the risk of death among COVID-19 patients
por: López-Martínez, Rocío, et al.
Publicado: (2022)

Relatos choles = albilbä tyi lakty'añ.
Publicado: (1995)

KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort
por: Lorca, Rebeca, et al.
Publicado: (2022)

Observed and Expected Survival in Men and Women after Suffering a STEMI
por: Pascual, Isaac, et al.
Publicado: (2020)

Daphnis et Cholé La valse /
por: Ravel, Maurice, 1875-1937
Publicado: (1993)

Genetic Variants of the NF-κB Pathway: Unraveling the Genetic Architecture of Psoriatic Disease
por: Queiro, Rubén, et al.
Publicado: (2021)

Frailty Assessment in a Cohort of Elderly Patients with Severe Symptomatic Aortic Stenosis: Insights from the FRailty Evaluation in Severe Aortic Stenosis (FRESAS) Registry
por: Solla-Suárez, Pablo, et al.
Publicado: (2021)

Capillary electrophoresis of PCR fragments with 5´-labelled primers for testing the SARS-Cov-2
por: Gómez, Juan, et al.
Publicado: (2020)

AN EXPERIMENTAL STUDY OF THE EFFECT OF CHOLE-CYSTGASTROSTOMY ON GASTRIC ACIDITY
por: Grey, Ernest G.
Publicado: (1916)

Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome
por: Gómez, Juan, et al.
Publicado: (2020)

Bilineal inheritance of type 1 autosomal dominant polycystic kidney disease (ADPKD) and recurrent fetal loss
por: Peces, Ramón, et al.
Publicado: (2008)

Mutation analysis of the LCE3B/LCE3C genes in Psoriasis
por: Coto, Eliecer, et al.
Publicado: (2010)

Practical applicability of the STAMCO and ChOLE classification in cholesteatoma care
por: ten Tije, Fleur A., et al.
Publicado: (2020)

Association between the interferon-induced transmembrane protein 3 gene (IFITM3) rs34481144 / rs12252 haplotypes and COVID-19
por: Cuesta-Llavona, Elías, et al.
Publicado: (2021)

Long term follow up of percutaneous treatment for degenerated Mitroflow prosthesis with self-expanding transcatheter aortic valve implantation
por: Pascual, Isaac, et al.
Publicado: (2020)

Assessing the Prognostic Value of the ChOLE Classification in Predicting the Severity of Acquired Cholesteatoma
por: Eggink, Maura C., et al.
Publicado: (2022)

Efecto Citogenético del herbicida Paraquat ( Gramoxone) en células Meristematicas de la Raíz de Vicia faba :
por: Xiguil Coto, Domingo Pascual
Publicado: (1997)

Los choles de Tila y su mundo =Jiñi ch'olubü tyi Tila yik'oty imelbalob tyi pañümil : tradición oral
por: Pérez Chacón, José L.
Publicado: (1993)

Age-dependent effect of the IFIH1/MDA5 gene variants on the risk of critical COVID-19
por: Muñiz-Banciella, María G., et al.
Publicado: (2022)

Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: a case report
por: Mejia-Gaviria, Natalia, et al.
Publicado: (2010)

DNA genotyping of the ABO gene showed a significant association of the A-group (A1/A2 variants) with severe COVID-19.
por: Gómez, Juan, et al.
Publicado: (2021)

Mapping the ChOLE classification to hearing outcomes and disease-specific health-related quality of life
por: Weiss, Nora M., et al.
Publicado: (2020)

Evaluating hearing outcome, recidivism and complications in cholesteatoma surgery using the ChOLE classification system
por: Bächinger, David, et al.
Publicado: (2020)

IGHG3 hinge length variation was associated with the risk of critical disease and death in a Spanish COVID-19 cohort
por: López-Martínez, Rocío, et al.
Publicado: (2022)

A single-nucleotide polymorphism in the human p27(kip1 )gene (-838C>A) affects basal promoter activity and the risk of myocardial infarction
por: González, Pelayo, et al.
Publicado: (2004)

NKG2D and its ligands: active factors in the outcome of solid organ transplantation?
por: Suárez-Álvarez, Beatriz, et al.
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_4dui322meeo7u76lgqucirnh1p