Search Results - "Hermida Prieto, Manuel"
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Donor Polymorphisms in Genes Related to B-Cell Biology Associated With Antibody-Mediated Rejection After Heart Transplantation
Published in Circulation Journal (25-04-2018)“…Background:Heart transplantation (HT) is a well-established lifesaving treatment for endstage cardiac failure. Antibody-mediated rejection (AMR) represents one…”
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2
Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 Mutations in Sporadic Hypertrophic Cardiomyopathy
Published in Circulation Journal (2013)“…Background: Hypertrophic cardiomyopathy (HCM) is a clinically heterogeneous genetic heart disease characterized by left ventricular hypertrophy in the absence…”
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3
Mutational screening of phospholamban gene in hypertrophic and idiopathic dilated cardiomyopathy and functional study of the PLN -42 C>G mutation
Published in European journal of heart failure (01-01-2007)“…Background: Phospholamban is an endogenous sarcoplasmic reticulum calcium ATPase inhibitor with a regulatory effect on cardiac contraction/relaxation coupling…”
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4
lncRNA CDKN2B-AS1 is downregulated in patients with ventricular fibrillation in acute myocardial infarction
Published in PloS one (21-05-2024)“…Ventricular fibrillation (VF) in acute myocardial infarction (AMI) is the main cause of deaths occurring in the acute phase of an ischemic event. Although it…”
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5
Allogeneic adipose-derived mesenchymal stem cell therapy in dogs with refractory atopic dermatitis: clinical efficacy and safety
Published in Veterinary record (01-12-2018)“…Canine atopic dermatitis (AD) is a common skin disease with a 10–15 per cent prevalence. Current treatments vary in their efficacy and safety. The…”
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6
Analysis of the Association between Copy Number Variation and Ventricular Fibrillation in ST-Elevation Acute Myocardial Infarction
Published in International journal of molecular sciences (22-02-2024)“…Sudden cardiac death due to ventricular fibrillation (VF) during ST-elevation acute myocardial infarction (STEAMI) significantly contributes to…”
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7
Circulating miR-181a-5p as a new biomarker for acute cellular rejection in heart transplantation
Published in The Journal of heart and lung transplantation (01-10-2020)“…Acute cellular rejection (ACR) is a major complication in heart transplantation (HTx). Endomyocardial biopsy is the reference method for early detection of…”
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8
Prevalence of Fabry Disease in a Cohort of 508 Unrelated Patients With Hypertrophic Cardiomyopathy
Published in Journal of the American College of Cardiology (18-12-2007)“…Prevalence of Fabry Disease in a Cohort of 508 Unrelated Patients With Hypertrophic Cardiomyopathy Lorenzo Monserrat, Juan Ramón Gimeno-Blanes, Francisco…”
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Rare Variants in Genes of the Cholesterol Pathway Are Present in 60% of Patients with Acute Myocardial Infarction
Published in International journal of molecular sciences (17-12-2022)“…Acute myocardial infarction (AMI) is a pandemic in which conventional risk factors are inadequate to detect who is at risk early in the asymptomatic stage…”
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10
AGT haplotype in ITGA4 gene is related to antibody-mediated rejection in heart transplant patients
Published in PloS one (23-07-2019)“…One of the main problems involved in heart transplantation (HT) is antibody-mediated rejection (AMR). Many aspects of AMR are still unresolved, including its…”
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11
Preliminary Investigation on Efficacy and Safety of Substance P-Coated Stent for Promoting Re-Endothelialization: A Porcine Coronary Artery Restenosis Model
Published in Tissue engineering and regenerative medicine (01-01-2024)“…Current polymer-based drug-eluting stents (DESs) have fundamental issues about inflammation and delayed re-endothelializaton of the vessel wall. Substance-P…”
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12
The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans
Published in International journal of cardiology (19-11-2010)“…Abstract Background The R820W mutation in the MYBPC3 gene has been associated with the development of hypertrophic cardiomyopathy (HCM) in rag-doll cats, but…”
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13
Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy
Published in BMC medical genetics (30-04-2010)“…MyBPC3 mutations are amongst the most frequent causes of hypertrophic cardiomyopathy, however, its prevalence varies between populations. They have been…”
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14
Systemic Treatment of Immune-Mediated Keratoconjunctivitis Sicca with Allogeneic Stem Cells Improves the Schirmer Tear Test Score in a Canine Spontaneous Model of Disease
Published in Journal of clinical medicine (20-12-2021)“…Keratoconjunctivitis sicca (KCS) is characterized by ocular discomfort, conjunctival hyperaemia, and corneal scarring, causing reduced aqueous tear production…”
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15
LIGHT/BTLA polymorphisms and antibody-mediated-rejection after heart transplantation
Published in Oncotarget (09-11-2018)Get full text
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16
Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects
Published in European heart journal (01-08-2007)“…Aims The E101K mutation in the alpha-cardiac actin gene (ACTC) has been associated with apical hypertrophic cardiomyopathy (HCM). As prominent trabeculations…”
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Polymorphisms in genes related to the complement system and antibody-mediated cardiac allograft rejection
Published in The Journal of heart and lung transplantation (01-04-2018)“…Heart transplantation (HT) is a life-saving treatment for patients with end-stage heart failure. One of the main problems after HT is the humoral response…”
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18
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations
Published in The American journal of cardiology (01-07-2004)“…LMNA mutations have been associated with familial or sporadic dilated cardiomyopathy (DC), with or without conduction system disease. We studied the LMNA gene…”
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19
Insights into genotype-phenotype correlation in hypertrophic cardiomyopathy. Findings from 18 Spanish families with a single mutation in MYBPC3
Published in Heart (British Cardiac Society) (01-12-2010)“…Mutations in the cardiac myosin-binding protein C (MYBPC3) gene are frequently found as a cause of hypertrophic cardiomyopathy (HCM). However, only a few…”
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20
Macrophagic enhancement in optical coherence tomography imaging by means of superparamagnetic iron oxide nanoparticles
Published in Cardiology journal (31-10-2017)“…The ability of optical coherence tomography (OCT) to visualise macrophages in vivo in coronary arteries is still controversial. We hypothesise that imaging of…”
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