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Viðar Örn Eðvarðsson - Prófessor

Mynd af gervimanni

–

Heilbrigðisvísindasvið

Viðar Örn Eðvarðsson

Prófessor

Aðsetur
LSH - Hringbraut
Sími
543-1000 og 563-1015
Tölvupóstur
voe [hjá] hi.is

Starfseining
Læknadeild

ORCID vefsíða
https://orcid.org/0000-0002-4204-9342
Rannsóknagátt – Viðar Örn Eðvarðsson

Útgefið efni

2024

Exploring the Genetic Risk of Childhood Daytime Urinary IncontinenceJournal of Urology
Diversity of kidney care referral pathways in national child health systems of 48 European countriesFrontiers in Pediatrics
Optimization and validation of a UPLC-MS/MS assay for simultaneous quantification of 2,8-dihydroxyadenine, adenine, allopurinol, oxypurinol and febuxostat in human plasmaJournal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences

2023

Simplification of home urine sampling for measurement of 2,8-dihydroxyadenine in patients with adenine phosphoribosyltransferase deficiency

2022

Kidney Transplantation in Small ChildrenTransplantation
Current kidney function parameters overestimate kidney tissue repair in reversible experimental kidney diseaseKidney International

2021

Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiencyEuropean Journal of Human Genetics
Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone DiseaseKidney International Reports
Urinary Stone Disease and Nephrocalcinosis
Identification of genetic loci associated with nocturnal enuresisThe Lancet Child and Adolescent Health

2020

Stone recurrence among childhood kidney stone formersUrolithiasis
Are conventional stone analysis techniques reliable for the identification of 2,8-dihydroxyadenine kidney stones? A case seriesUrolithiasis
Kidney transplant outcomes in patients with adenine phosphoribosyltransferase deficiencyTransplantation
Cellular and molecular mechanisms of kidney injury in 2,8-dihydroxyadenine nephropathyJournal of the American Society of Nephrology

2019

Adenine Phosphoribosyltransferase DeficiencyGeneReviews
Urinary 2,8-dihydroxyadenine excretion in patients with adenine phosphoribosyltransferase deficiency, carriers and healthy control subjectsMolecular Genetics and Metabolism
Genetics of common complex kidney stone diseaseUrolithiasis
Sequence variants associating with urinary biomarkersHuman Molecular Genetics
Long-term renal outcomes of APRT deficiency presenting in childhoodPediatric Nephrology
Association between timing of dialysis initiation and clinical outcomes in the paediatric populationNephrology Dialysis Transplantation

2018

Incidence of kidney stone disease in Icelandic children and adolescents from 1985 to 2013Pediatric Nephrology
Causes of Pediatric Kidney Failure, Treatment of Chronic Kidney Disease, and Timing of Transplantation
Comparison of the effect of allopurinol and febuxostat on urinary 2,8-dihydroxyadenine excretion in patients with Adenine phosphoribosyltransferase deficiency (APRTd)European Journal of Internal Medicine
Corrigendum to “Quantitative UPLC–MS/MS assay of urinary 2,8-dihydroxyadenine for diagnosis and management of adenine phosphoribosyltransferase deficiency” [J. Chromatogr. B 1036–1037 (2016) 170–177] (S1570023216308467) (10.1016/j.jchromb.2016.09.018))Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences

2017

Infants Requiring Maintenance DialysisAmerican Journal of Kidney Diseases

2016

Kidney Versus Combined Kidney and Liver Transplantation in Young People With Autosomal Recessive Polycystic Kidney DiseaseAmerican Journal of Kidney Diseases
Kidney disease in adenine phosphoribosyltransferase deficiencyAmerican Journal of Kidney Diseases
First detection of a carbapenemase-producing Enterobacteriaceae in IcelandJournal of Global Antimicrobial Resistance
An unusual cause of pink diapers in an infantPediatric Nephrology
An unusual cause of “pink diaper” in an infantPediatric Nephrology
Quantitative UPLC–MS/MS assay of urinary 2,8-dihydroxyadenine for diagnosis and management of adenine phosphoribosyltransferase deficiencyJournal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences
Gender Disparities in Access to Pediatric Renal Transplantation in EuropeAmerican Journal of Transplantation

2015

Phenotype-Genotype correlations and estimated carrier frequencies of primary hyperoxaluriaJournal of the American Society of Nephrology
Urolithiasis in children
Impact of nephrolithiasis on kidney functionBMC Nephrology
Common and rare variants associated with kidney stones and biochemical traitsNature Communications

2014

Recurrent 2,8-dihydroxyadenine nephropathyAmerican Journal of Transplantation
Evaluation and Management of Pediatric Stones

2013

ErratumKidney International
Hereditary causes of kidney stones and chronic kidney diseasePediatric Nephrology
The relationship between birth weight and blood pressure in childhoodAmerican Journal of Hypertension
Comparison of aneroid and oscillometric blood pressure measurements in childrenJournal of Clinical Hypertension
Í tilefni af alþjóðlega nýrnadeginum 2013Laeknabladid
Temporal trends in the incidence of kidney stone diseaseKidney International

2012

Birth weight and childhood blood pressureCurrent Hypertension Reports
Adenine Phosphoribosyltransferase DeficiencyGeneReviews
Genetic causes of kidney stones and kidney failureClinical Reviews in Bone and Mineral Metabolism

2011

Plasma n-3 and n-6 fatty acids and the incidence of atrial fibrillation following coronary artery bypass graft surgeryEuropean Journal of Clinical Investigation
Prevalence of hypertension in 9- to 10-year-old Icelandic school childrenJournal of Clinical Hypertension

2010

Blood pressure in children and target-organ damage later in lifePediatric Nephrology
Does treatment with n-3 polyunsaturated fatty acids prevent atrial fibrillation after open heart surgery?Europace
Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseasesPLoS Genetics

2009

Familiality of kidney stone disease in IcelandScandinavian Journal of Urology and Nephrology
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral densityNature Genetics

2006

Epidemiology of kidney stones in IcelandScandinavian Journal of Urology and Nephrology
Adenine phosphoribosyltransferase Deficiency and 2,8-dihydroxyadeninuria
Resolution of proteinuria in a patient with X-linked Alport syndrome treated with cyclosporineScandinavian Journal of Urology and Nephrology

2005

High incidence of kidney stones in Icelandic childrenPediatric Nephrology
Increased frequency of C4B*Q0 alleles in patients with Henoch-Schönlein purpuraScandinavian Journal of Immunology

2003

Ómega-3 fjölómettaðar fitusýrur : hlutverk í læknisfræðiLæknablaðið

2002

Henoch-Schönlein purpura : innlagnir á LSH 1984-2000Læknablaðið

2001

Clinical features and genotype of adenine phosphoribosyltransferase deficiency in IcelandAmerican Journal of Kidney Diseases

1996

Effective immunization against influenza in pediatric renal transplant recipientsClinical Transplantation

1995

Natural history and etiology of hyperuricemia following pediatric renal transplantationPediatric Nephrology
Successful living-related renal transplantation in an adolescent with Down syndromePediatric Nephrology

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