Search Results - "Ballarin, José"
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Cystatin C estimated glomerular filtration rate to assess renal function in early stages of autosomal dominant polycystic kidney disease
Published in PloS one (27-03-2017)“…Height-adjusted total kidney volume (htTKV) is the best marker of disease progression in early autosomal dominant polycystic kidney disease (ADPKD) when renal…”
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2
Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population
Published in Scientific reports (10-01-2020)“…Chronic kidney disease (CKD) patients have many affected physiological pathways. Variations in the genes regulating these pathways might affect the incidence…”
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3
Pre-gestational counselling for women living with CKD: starting from the bright side
Published in Clinical kidney journal (01-05-2024)“…Pregnancy in women living with chronic kidney disease (CKD) was often discouraged due to the risk of adverse maternal–fetal outcomes and the progression of…”
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4
Renal volume and cardiovascular risk assessment in normotensive autosomal dominant polycystic kidney disease patients
Published in Medicine (Baltimore) (01-12-2016)“…Cardiovascular disease, closely related to an early appearance of hypertension, is the most common mortality cause among autosomal dominant polycystic kidney…”
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5
Ciclosporin-induced hypertension is associated with increased sodium transporter of the loop of Henle (NKCC2)
Published in Nephrology, dialysis, transplantation (01-10-2007)“…Background. Hypertension induced by cyclosporine is associated with renal sodium and water retention. Using immunoblotting of kidney homogenates, we…”
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Long-Term Outcomes of IgA Nephropathy Presenting with Minimal or No Proteinuria
Published in Journal of the American Society of Nephrology (01-10-2012)“…The long-term outcome of patients with IgA nephropathy who present with normal renal function, microscopic hematuria, and minimal or no proteinuria is not well…”
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Clinical Utility of Genetic Testing in Children and Adults with Steroid-Resistant Nephrotic Syndrome
Published in Clinical journal of the American Society of Nephrology (01-05-2011)“…The increasing number of podocyte-expressed genes implicated in steroid-resistant nephrotic syndrome (SRNS), the phenotypic variability, and the…”
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Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity
Published in European journal of human genetics : EJHG (01-09-2015)“…Genetic diagnosis of steroid-resistant nephrotic syndrome (SRNS) using Sanger sequencing is complicated by the high genetic heterogeneity and phenotypic…”
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Shepherds View of Large Carnivore Recovery in the Pyrenees, Spain
Published in Animals (Basel) (23-06-2023)“…The studied farms are small family businesses, and so, in more than half of the cases, their continuity is not guaranteed. Livestock management is typical of a…”
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10
HLA-DQA1 and PLA2R1 Polymorphisms and Risk of Idiopathic Membranous Nephropathy
Published in Clinical journal of the American Society of Nephrology (01-02-2014)“…Single nucleotide polymorphisms (SNPs) within HLA complex class II HLA-DQ α-chain 1 (HLA-DQA1) and M-type phospholipase A2 receptor (PLA2R1) genes were…”
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Clinical and Practical Use of Calcimimetics in Dialysis Patients With Secondary Hyperparathyroidism
Published in Clinical journal of the American Society of Nephrology (07-01-2016)“…CKD and CKD-related mineral and bone disorders (CKD-MBDs) are associated with high cardiovascular and mortality risks. In randomized clinical trials (RCTs), no…”
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12
From Inflammation to the Onset of Fibrosis through A2A Receptors in Kidneys from Deceased Donors
Published in International journal of molecular sciences (21-11-2020)“…Pretransplant graft inflammation could be involved in the worse prognosis of deceased donor (DD) kidney transplants. A2A adenosine receptor (A2AR) can…”
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Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome
Published in Journal of the American Society of Nephrology (01-07-2018)“…Steroid-sensitive nephrotic syndrome (SSNS) is a childhood disease with unclear pathophysiology and genetic architecture. We investigated the genomic basis of…”
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14
Urinary Proteome Analysis Identified Neprilysin and VCAM as Proteins Involved in Diabetic Nephropathy
Published in Journal of diabetes research (01-01-2018)“…Urinary proteome was analyzed and quantified by tandem mass tag (TMT) labeling followed by bioinformatics analysis to study diabetic nephropathy (DN)…”
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Contribution of the TTC21B gene to glomerular and cystic kidney diseases
Published in Nephrology, dialysis, transplantation (01-01-2017)“…The TTC21B gene was initially described as causative of nephronophthisis (NPHP). Recently, the homozygous TTC21B p.P209L mutation has been identified in…”
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Unfermented grape juice reduce genomic damage on patients undergoing hemodialysis
Published in Food and chemical toxicology (01-06-2016)“…Chronic kidney disease (CKD) patients in dialysis (HD) are considered to be submitted to a continuous oxidative stress. This stress can cause damage on DNA…”
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Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis
Published in Kidney international (01-12-2009)“…Mutations in the NPHS1 gene cause congenital nephrotic syndrome of the Finnish type presenting before the first 3 months of life. Recently, NPHS1 mutations…”
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Clinical Value of NPHS2 Analysis in Early- and Adult-Onset Steroid-Resistant Nephrotic Syndrome
Published in Clinical journal of the American Society of Nephrology (01-02-2011)“…To date, very few cases with adult-onset focal segmental glomerulosclerosis (FSGS) carrying NPHS2 variants have been described, all of them being compound…”
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Vitamin E-coated dialysis membranes reduce the levels of oxidative genetic damage in hemodialysis patients
Published in Mutation research (01-03-2017)“…•Use vitamine E-coated hemodialysis membranes decrease the oxidative damage.•Hemoglobin values increased with the use of vitamin E-coated membranes.•The use of…”
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Diagnosis of autosomal dominant polycystic kidney disease using efficient PKD1 and PKD2 targeted next‐generation sequencing
Published in Molecular genetics & genomic medicine (01-09-2014)“…Molecular diagnostics of autosomal dominant polycystic kidney disease (ADPKD) relies on mutation screening of PKD1 and PKD2, which is complicated by extensive…”
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