Search Results - Runolfsdottir, Hrafnhildur L
- Showing 1 - 8 results of 8
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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 2019Text -
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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 2020Text -
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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 2017Text -
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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 2016Text -
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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 2018Text -
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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 2021Text -
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Monoclonal gammopathy of undetermined significance and COVID-19: a population-based cohort study by Rognvaldsson, Saemundur, Eythorsson, Elias, Thorsteinsdottir, Sigrun, Vidarsson, Brynjar, Onundarson, Pall Torfi, Agnarsson, Bjarni A., Sigurdardottir, Margret, Thorsteinsdóttir, Ingunn, Olafsson, Isleifur, Runolfsdottir, Hrafnhildur L., Helgason, Dadi, Emilsdottir, Arna R., Agustsson, Arnar S., Bjornsson, Aron H., Kristjansdottir, Gudrun, Thordardottir, Asdis Rosa, Indridason, Olafur Skuli, Jonsson, Asbjorn, Gislason, Gauti Kjartan, Olafsson, Andri, Steingrimsdottir, Hlif, Kampanis, Petros, Hultcrantz, Malin, Durie, Brian G. M., Harding, Stephen, Landgren, Ola, Palsson, Runolfur, Love, Thorvarður Jon, Kristinsson, Sigurdur Yngvi
Published 2021Text