Výsledky vyhledávání - Runolfsdottir, Hrafnhildur L
- Zobrazuji výsledky 1 - 8 z 8
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Urinary 2,8-Dihydroxyadenine Excretion in Patients with APRT Deficiency, Carriers and Healthy Control Subjects Autor Runolfsdottir, Hrafnhildur L., Palsson, Runolfur, Thorsteinsdottir, Unnur A., Indridason, Olafur S., Agustsdottir, Inger M. Sch., Oddsdottir, G. Steinunn, Thorsteinsdottir, Margret, Edvardsson, Vidar O.
Vydáno 2019Text -
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Are conventional stone analysis techniques reliable for the identification of 2,8-dihydroxyadenine kidney stones? A case series Autor Runolfsdottir, Hrafnhildur L., Lin, Tzu-Ling, Goldfarb, David S., Sayer, John A., Michael, Mini, Ketteridge, David, Rich, Peter R., Edvardsson, Vidar O., Palsson, Runolfur
Vydáno 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 Autor 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
Vydáno 2017Text -
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Quantitative UPLC–MS/MS assay of urinary 2,8-dihydroxyadenine for diagnosis and management of adenine phosphoribosyltransferase deficiency Autor 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
Vydáno 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... Autor 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
Vydáno 2018Text -
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Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency Autor 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
Vydáno 2021Text -
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Monoclonal gammopathy of undetermined significance and COVID-19: a population-based cohort study Autor 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
Vydáno 2021Text