An unusual cause of “pink diaper” in an infant: Answers

by Amin, Rasheda, Eid, Loai, Edvardsson, Vidar O., Fairbanks, Lynette, Moudgil, Asha
Published in Pediatr Nephrol (2015)

An Unusual Cause of Pink Diaper in An Infant

by Amin, Rasheda, Eid, Loai, Edvardsson, Vidar O., Fairbanks, Lynette, Moudgil, Asha
Published in Pediatr Nephrol (2015)

Impact of nephrolithiasis on kidney function

by Sigurjonsdottir, Vaka K., Runolfsdottir, Hrafnhildur L., Indridason, Olafur S., Palsson, Runolfur, Edvardsson, Vidar O.
Published in BMC Nephrol (2015)

Long-term Renal Outcome of APRT Deficiency Presenting in Childhood

by Runolfsdottir, Hrafnhildur Linnet, Palsson, Runolfur, Agustsdottir, Inger M, Indridason, Olafur S, Edvardsson, Vidar O
Published in Pediatr Nephrol (2018)

[Image: see text] Comparison of Aneroid and Oscillometric Blood Pressure Measurements in Children

by Eliasdottir, Sigridur B., Steinthorsdottir, Sandra D., Indridason, Olafur S., Palsson, Runolfur, Edvardsson, Vidar O.
Published in J Clin Hypertens (Greenwich) (2013)

Kidney Disease in Adenine Phosphoribosyltransferase Deficiency

by Runolfsdottir, Hrafnhildur Linnet, Palsson, Runolfur, Sch. Agustsdottir, Inger M., Indridason, Olafur S., Edvardsson, Vidar O.
Published in Am J Kidney Dis (2015)

Prevalence of Hypertension in 9‐ to 10‐Year‐Old Icelandic School Children

by Steinthorsdottir, Sandra D., Eliasdottir, Sigridur B., Indridason, Olafur S., Agustsdottir, Inger M., Palsson, Runolfur, Edvardsson, Vidar O.
Published in J Clin Hypertens (Greenwich) (2011)

Hereditary Causes of Kidney Stones and Chronic Kidney Disease

by Edvardsson, Vidar O., Goldfarb, David S., Lieske, John C., Beara-Lasic, Lada, Anglani, Franca, Milliner, Dawn S., Palsson, Runolfur
Published 2013

Urinary 2,8-Dihydroxyadenine Excretion in Patients with APRT Deficiency, Carriers and Healthy Control Subjects

by Runolfsdottir, Hrafnhildur L., Palsson, Runolfur, Thorsteinsdottir, Unnur A., Indridason, Olafur S., Agustsdottir, Inger M. Sch., Oddsdottir, G. Steinunn, Thorsteinsdottir, Margret, Edvardsson, Vidar O.
Published in Mol Genet Metab (2019)

Kidney Transplant Outcomes in Patients with Adenine Phosphoribosyltransferase Deficiency

by Runolfsdottir, Hrafnhildur Linnet, Palsson, Runolfur, Agustsdottir, Inger M. Sch., Indridason, Olafur S., Li, Jennifer, Dao, Myriam, Knebelmann, Bertrand, Milliner, Dawn S., Edvardsson, Vidar O.
Published in Transplantation (2020)

Are conventional stone analysis techniques reliable for the identification of 2,8-dihydroxyadenine kidney stones? A case series

by Runolfsdottir, Hrafnhildur L., Lin, Tzu-Ling, Goldfarb, David S., Sayer, John A., Michael, Mini, Ketteridge, David, Rich, Peter R., Edvardsson, Vidar O., Palsson, Runolfur
Published in Urolithiasis (2020)

Comparison of the effect of allopurinol and febuxostat on urinary 2,8-dihydroxyadenine excretion in patients with APRT deficiency: a clinical trial

by Edvardsson, Vidar O, Runolfsdottir, Hrafnhildur L, Thorsteinsdottir, Unnur A, Agustsdottir, Inger M Sch, Oddsdottir, G Steinunn, Eiriksson, Finnur, Goldfarb, David S, Thorsteinsdottir, Margret, Palsson, Runolfur
Published in Eur J Intern Med (2017)

Quantitative UPLC–MS/MS assay of urinary 2,8-dihydroxyadenine for diagnosis and management of adenine phosphoribosyltransferase deficiency

by Thorsteinsdottir, Margret, Thorsteinsdottir, Unnur A., Eiriksson, Finnur F., Runolfsdottir, Hrafnhildur L., Agustsdottir, Inger M.Sch., Oddsdottir, Steinunn, Sigurdsson, Baldur B., Hardarson, Hordur K., Kamble, Nilesh R., Sigurdsson, Snorri Th., Edvardsson, Vidar O., Palsson, Runolfur
Published in J Chromatogr B Analyt Technol Biomed Life Sci (2016)

Corrigendum to “Quantitative UPLC–MS/MS assay of urinary 2,8-dihydroxyadenine for diagnosis and management of adenine phosphoribosyltransferase deficiency” [J. Chromatogr. B 1036–1...

by Thorsteinsdottir, Margret, Thorsteinsdottir, Unnur A., Eiriksson, Finnur F., Runolfsdottir, Hrafnhildur L., Agustsdottir, Inger M.Sch., Oddsdottir, Steinunn, Sigurdsson, Baldur B., Hardarson, Hordur K., Kamble, Nilesh R., Sigurdsson, Snorri Th., Edvardsson, Vidar O., Palsson, Runolfur
Published in J Chromatogr B Analyt Technol Biomed Life Sci (2018)

Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency

by Runolfsdottir, Hrafnhildur L., Sayer, John A., Indridason, Olafur S., Edvardsson, Vidar O., Jensson, Brynjar O., Arnadottir, Gudny A., Gudjonsson, Sigurjon A., Fridriksdottir, Run, Katrinardottir, Hildigunnur, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari, Palsson, Runolfur
Published in Eur J Hum Genet (2021)

Recurrent 2,8-dihydroxyadenine nephropathy: a rare but preventable cause of renal allograft failure

by Zaidan, Mohamad, Palsson, Runolfur, Gall, Emilie Cornec-Le, Garstka, Antoine, Maggiore, Umberto, Deteix, Patrice, Battista, Michele, Gagné, Eve-Reine, Ceballos-Picot, Irène, Van Huyen, Jean-Paul Duong, Legendre, Christophe, Daudon, Michel, Edvardsson, Vidar O., Knebelmann, Bertrand
Published in Am J Transplant (2014)

Common and rare variants associated with kidney stones and biochemical traits

by Oddsson, Asmundur, Sulem, Patrick, Helgason, Hannes, Edvardsson, Vidar O., Thorleifsson, Gudmar, Sveinbjörnsson, Gardar, Haraldsdottir, Eik, Eyjolfsson, Gudmundur I., Sigurdardottir, Olof, Olafsson, Isleifur, Masson, Gisli, Holm, Hilma, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Indridason, Olafur S., Palsson, Runolfur, Stefansson, Kari
Published in Nat Commun (2015)

Cellular and Molecular Mechanisms of Kidney Injury in 2,8-Dihydroxyadenine Nephropathy

by Klinkhammer, Barbara Mara, Djudjaj, Sonja, Kunter, Uta, Palsson, Runolfur, Edvardsson, Vidar Orn, Wiech, Thorsten, Thorsteinsdottir, Margret, Hardarson, Sverrir, Foresto-Neto, Orestes, Mulay, Shrikant R., Moeller, Marcus Johannes, Jahnen-Dechent, Wilhelm, Floege, Jürgen, Anders, Hans-Joachim, Boor, Peter
Published in J Am Soc Nephrol (2020)

Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

by Gudbjartsson, Daniel F., Holm, Hilma, Indridason, Olafur S., Thorleifsson, Gudmar, Edvardsson, Vidar, Sulem, Patrick, de Vegt, Femmie, d'Ancona, Frank C. H., den Heijer, Martin, Franzson, Leifur, Rafnar, Thorunn, Kristjansson, Kristleifur, Bjornsdottir, Unnur S., Eyjolfsson, Gudmundur I., Kiemeney, Lambertus A., Kong, Augustine, Palsson, Runolfur, Thorsteinsdottir, Unnur, Stefansson, Kari
Published 2010

Correction: Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

by Gudbjartsson, Daniel F., Holm, Hilma, Indridason, Olafur S., Thorleifsson, Gudmar, Edvardsson, Vidar, Sulem, Patrick, de Vegt, Femmie, d'Ancona, Frank C. H., den Heijer, Martin, Wetzels, Jack F. M., Franzson, Leifur, Rafnar, Thorunn, Kristjansson, Kristleifur, Bjornsdottir, Unnur S., Eyjolfsson, Gudmundur I., Kiemeney, Lambertus A., Kong, Augustine, Palsson, Runolfur, Thorsteinsdottir, Unnur, Stefansson, Kari
Published 2010