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Association of ANRIL gene polymorphisms with major adverse cardiovascular events in hemodialysis patients

Clinica chimica acta, 2017-03, Vol.466, p.61-67

2017

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Corrigendum to ‘Association of ANRIL gene polymorphisms with major adverse cardiovascular events in hemodialysis patients’ [Clinica Chimica Acta (2017) 61–67]

Clinica chimica acta, 2017-08, Vol.471, p.94-94

2017

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Pre-metrological variation of immunological quantities

Scandinavian journal of clinical and laboratory investigation, 2008, Vol.68 (5), p.431-432

2008

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Déficit de testosterona como factor de riesgo de fractura de cadera en hombres de edad avanzada

Actas urologicas españolas, 2013-03, Vol.37 (3), p.142-146

2013

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Data on genotypic distribution and linkage disequilibrium of several ANRIL polymorphisms in hemodialysis patients

Data in brief, 2017-04, Vol.11 (C), p.221-224

2017

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Testosterone-deficiency as a risk factor for hip fracture in elderly men

Actas urológicas españolas (English ed.), 2013-03, Vol.37 (3), p.142-146

2013

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Reference values assessment in a Mediterranean population for small dense low-density lipoprotein concentration isolated by an optimized precipitation method

Vascular health and risk management, 2017-01, Vol.13, p.201-207

2017

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ANRIL as a genetic marker for cardiovascular events in renal transplant patients

Clinica chimica acta, 2019-06, Vol.493, p.S184-S185

2019

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Lack of randomness of internal quality control data: An alert for the in vitro diagnostic industry

Scandinavian journal of clinical and laboratory investigation, 2007, Vol.67 (2), p.253-255

2007

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Relationship between five genetic variants and the variability of hypertriglyceridemia

Atherosclerosis, 2020-12, Vol.315, p.e188-e188

2020

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Genetic contribution in statin treatment response: Cholesterol LDL and NonHDL targets achievement and changes in the lipid profile

Clinica chimica acta, 2019-06, Vol.493, p.S641-S642

2019

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Diagnostic accuracy of a novel predictive model for ischemic events based on small dense LDL-cholesterol concentration (SDLDL-C) and lipid characterization by NMR

Clinica chimica acta, 2019-06, Vol.493, p.S81-S82

2019

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Genetic polymorphisms of hypertriglyceridemia and asymptomatic atherosclerosis in women with Systemic Lupus Erythematosus: A case-control study

Atherosclerosis, 2022-08, Vol.355, p.234

2022

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Testosterone-deficiency as a risk factor for hip fracture in eldery men

Actas urologicas españolas, 2013-03, Vol.37 (3), p.142-146

2013

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Rapid detection of HLA-B51 by real-time polymerase chain reaction and high-resolution melting analysis

Tissue antigens, 2015-08, Vol.86 (2), p.139-142

2015

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Prevalence of risk alleles of polygenic hypertriglyceridemia and association with maximum triglyceride serum concentration on southern Barcelona metropolitan area population

Atherosclerosis, 2018-08, Vol.275, p.e184-e184

2018

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Survival in type 2 diabetic patients in dialysis and the number of risk alleles in polymorphisms of the renin-angiotensin system genes

Clinical biochemistry, 2009, Vol.42 (1), p.5-11

2009

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Thyroid function in adults patients undergoing cardiac surgery: A pilot study

Clinical nutrition ESPEN, 2020-12, Vol.40, p.506-507

2020

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Comment on: Brentuximab vedotin-related neuropathy in a patient with Gilbert syndrome: Do mutations of UGT1A1 gene affect brentuximab toxicity?

Pediatric blood & cancer, 2023-11, Vol.70 (11), p.e30527-e30527

2023

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KIF6 gene as a pharmacogenetic marker for lipid-lowering effect in statin treatment

PloS one, 2018-10, Vol.13 (10), p.e0205430-e0205430

2018

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Precipitated sdLDL: An easy method to estimate LDL particle size

Journal of clinical laboratory analysis, 2020-07, Vol.34 (7), p.e23282-n/a

2020

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ANRIL as a genetic marker for cardiovascular events in renal transplant patients – an observational follow‐up cohort study

Transplant international, 2018-09, Vol.31 (9), p.1018-1027

2018

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Influence of 6 genetic variants on the efficacy of statins in patients with dyslipidemia

Journal of clinical laboratory analysis, 2018-10, Vol.32 (8), p.e22566-n/a

2018

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Genetic contribution to lipid target achievement with statin therapy: a prospective study

The pharmacogenomics journal, 2020-06, Vol.20 (3), p.494-504

2020

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Foreign influence and welfare

Journal of international economics, 2011-07, Vol.84 (2), p.135-148

2011

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Association of ANRIL gene polymorphisms with major adverse cardiovascular events in hemodialysis patients

Corrigendum to ‘Association of ANRIL gene polymorphisms with major adverse cardiovascular events in hemodialysis patients’ [Clinica Chimica Acta (2017) 61–67]

Pre-metrological variation of immunological quantities

Déficit de testosterona como factor de riesgo de fractura de cadera en hombres de edad avanzada

Data on genotypic distribution and linkage disequilibrium of several ANRIL polymorphisms in hemodialysis patients

Testosterone-deficiency as a risk factor for hip fracture in elderly men

Reference values assessment in a Mediterranean population for small dense low-density lipoprotein concentration isolated by an optimized precipitation method

ANRIL as a genetic marker for cardiovascular events in renal transplant patients

Lack of randomness of internal quality control data: An alert for the in vitro diagnostic industry

Relationship between five genetic variants and the variability of hypertriglyceridemia

Genetic contribution in statin treatment response: Cholesterol LDL and NonHDL targets achievement and changes in the lipid profile

Diagnostic accuracy of a novel predictive model for ischemic events based on small dense LDL-cholesterol concentration (SDLDL-C) and lipid characterization by NMR

Genetic polymorphisms of hypertriglyceridemia and asymptomatic atherosclerosis in women with Systemic Lupus Erythematosus: A case-control study

Testosterone-deficiency as a risk factor for hip fracture in eldery men

Rapid detection of HLA-B51 by real-time polymerase chain reaction and high-resolution melting analysis

Prevalence of risk alleles of polygenic hypertriglyceridemia and association with maximum triglyceride serum concentration on southern Barcelona metropolitan area population

Survival in type 2 diabetic patients in dialysis and the number of risk alleles in polymorphisms of the renin-angiotensin system genes

Thyroid function in adults patients undergoing cardiac surgery: A pilot study

Comment on: Brentuximab vedotin-related neuropathy in a patient with Gilbert syndrome: Do mutations of UGT1A1 gene affect brentuximab toxicity?

KIF6 gene as a pharmacogenetic marker for lipid-lowering effect in statin treatment

Precipitated sdLDL: An easy method to estimate LDL particle size

ANRIL as a genetic marker for cardiovascular events in renal transplant patients – an observational follow‐up cohort study

Influence of 6 genetic variants on the efficacy of statins in patients with dyslipidemia

Genetic contribution to lipid target achievement with statin therapy: a prospective study

Foreign influence and welfare

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