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Scandinavian Journal of Immunology|May 26, 2007
Fc-gamma receptor polymorphisms are not associated with autoimmune Addison's diseaseA S B Wolff, K-M Myhr, C A Vedeler, et al.
BMC Medical Genetics|August 20, 2011
Genome-wide copy number variation (CNV) in patients with autoimmune Addison's diseaseIngeborg Brønstad, Anette S B Wolff, Kristian Løvås, et al.
BMC Bioinformatics|November 16, 2024
Rare copy number variant analysis in case-control studies using snp array data: a scalable and automated data analysis pipelineHaydee Artaza, Ksenia Lavrichenko, Anette S B Wolff, et al.
Clinical and Experimental Immunology|August 14, 2023
Regulatory T cells in autoimmune primary adrenal insufficiencyThea Sjøgren, Jan-Inge Bjune, Eystein S Husebye, et al.
FEBS Letters|April 13, 2023
Systemic interferon type I and B cell responses are impaired in autoimmune polyendocrine syndrome type 1Bergithe E Oftedal, Nicolas Delaleu, David Dolan, et al.
Scandinavian Journal of Immunology|May 27, 2010
Flow cytometry study of blood cell subtypes reflects autoimmune and inflammatory processes in autoimmune polyendocrine syndrome type IA S B Wolff, B E V Oftedal, K Kisand, et al.
Frontiers in Immunology|September 19, 2017
Altered Immune Activation and IL-23 Signaling in Response to Candida albicans in Autoimmune Polyendocrine Syndrome Type 1Øyvind Bruserud, Eirik Bratland, Alexander Hellesen, et al.
Scandinavian Journal of Immunology|April 1, 2025
Longitudinal Immune Profiling in Autoimmune Polyendocrine Syndrome Type 1Isil Kucuka, Dorsa Iraji, Sarah Braun, et al.
Endocrine Connections|August 15, 2015
Hypomagnesemia and functional hypoparathyroidism due to novel mutations in the Mg-channel TRPM6Marianne C Astor, Kristian Løvås, Anette S B Wolff, et al.
Endocrine Connections|March 28, 2014
Functional studies of novel CYP21A2 mutations detected in Norwegian patients with congenital adrenal hyperplasiaIngeborg Brønstad, Lars Breivik, Paal Methlie, et al.
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