Consensus statement on the diagnosis, treatment and follow‐up of patients with primary adrenal insufficiency von Husebye, E. S., Allolio, B., Arlt, W., Badenhoop, K., Bensing, S., Betterle, C., Falorni, A., Gan, E. H., Hulting, A.‐L., Kasperlik‐Zaluska, A., Kämpe, O., Løvås, K., Meyer, G., Pearce, S. H.

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Risk of hip fracture in Addison’s disease: a population‐based cohort study von Björnsdottir, S., Sääf, M., Bensing, S., Kämpe, O., Michaëlsson, K., Ludvigsson, J. F.

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Clinical manifestations and management of patients with autoimmune polyendocrine syndrome type I von Husebye, E. S., Perheentupa, J., Rautemaa, R., Kämpe, O.

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Diabetes Mellitus in Elkhounds Is Associated with Diestrus and Pregnancy von Fall, T., Hedhammar, Å., Wallberg, A., Fall, N., Ahlgren, K.M., Hamlin, H.H., Lindblad-Toh, K., Andersson, G., Kämpe, O.

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Hypomorphic Rag1 mutations alter the preimmune repertoire at early stages of lymphoid development von Ott de Bruin, L.M., Bosticardo, M., Barbieri, A., Lin, S.G., Rowe, J.H., Poliani, P.L., Ching, K., Eriksson, D., Landegren, N., Kämpe, O., Manis, J.P., Notarangelo, L.D.

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Concordance Between ICD-10 Codes and Clinical Diagnosis of Hypoparathyroidism in Sweden von Kamal, Wafa, Bjornsdottir, Sigridur, Kampe, Olle, Lagerros, Ylva Trolle

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Early exposure to dogs and farm animals and the risk of childhood asthma von Fall, Tove, Lundholm, Cecilia, Örtqvist, Anne K, Fall, Katja, Fang, Fang, Hedhammar, Åke, Kämpe, Olle, Ingelsson, Erik, Almqvist, Catarina

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role of pleiotropy and linkage in genes affecting a sexual ornament and bone allocation in the chicken von Johnsson, M, Rubin, C.‐J, Höglund, A, Sahlqvist, A.‐S, Jonsson, K. B, Kerje, S, Ekwall, O, Kämpe, O, Andersson, L, Jensen, P, Wright, D

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Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome von Abolhassani, Hassan, Landegren, Nils, Bastard, Paul, Materna, Marie, Modaresi, Mohammadreza, Du, Likun, Aranda-Guillén, Maribel, Sardh, Fabian, Zuo, Fanglei, Zhang, Peng, Marcotte, Harold, Marr, Nico, Khan, Taushif, Ata, Manar, Al-Ali, Fatima, Pescarmona, Remi, Belot, Alexandre, Béziat, Vivien, Zhang, Qian, Casanova, Jean-Laurent, Kämpe, Olle, Zhang, Shen-Ying, Hammarström, Lennart, Pan-Hammarström, Qiang

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Brain activity during working memory in patients with autoimmune Addison’s disease von van't Westeinde, Annelies, Padilla, Nelly, Fletcher-Sandersjöö, Sara, Kämpe, Olle, Bensing, Sophie, Lajic Näreskog, Svetlana

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TSGA10 - A Target for Autoantibodies in Autoimmune Polyendocrine Syndrome Type 1 and Systemic Lupus Erythematosus von Smith, C.J.A, Oscarson, M, Rönnblom, L, Alimohammadi, M, Perheentupa, J, Husebye, E.S, Gustafsson, J, Nordmark, G, Meloni, A, Crock, P.A, Kämpe, O, Bensing, S

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Increased Resting-State Functional Connectivity in Patients With Autoimmune Addison Disease von van’t Westeinde, Annelies, Padilla, Nelly, Fletcher-Sandersjöö, Sara, Kämpe, Olle, Bensing, Sophie, Lajic, Svetlana

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Clues for early detection of autoimmune Addison's disease – myths and realities von Sævik, Å. B., Åkerman, A.‐K., Grønning, K., Nermoen, I., Valland, S. F., Finnes, T. E., Isaksson, M., Dahlqvist, P., Bergthorsdottir, R., Ekwall, O., Skov, J., Nedrebø, B. G., Hulting, A.‐L., Wahlberg, J., Svartberg, J., Höybye, C., Bleskestad, I. H., Jørgensen, A. P., Kämpe, O., Øksnes, M., Bensing, S., Husebye, E. S.

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Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease von Eriksson, D., Bianchi, M., Landegren, N., Nordin, J., Dalin, F., Mathioudaki, A., Eriksson, G. N., Hultin‐Rosenberg, L., Dahlqvist, J., Zetterqvist, H., Karlsson, Å., Hallgren, Å., Farias, F. H. G., Murén, E., Ahlgren, K. M., Lobell, A., Andersson, G., Tandre, K., Dahlqvist, S. R., Söderkvist, P., Rönnblom, L., Hulting, A.‐L., Wahlberg, J., Ekwall, O., Dahlqvist, P., Meadows, J. R. S., Bensing, S., Lindblad‐Toh, K., Kämpe, O., Pielberg, G. R.

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Is there a need for an emergency card in hypoparathyroidism? von Astor, M. C., Zhu, W., Björnsdottir, S., Bollerslev, J., Kämpe, O., Husebye, E. S.

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Risk of autoimmune diabetes in APECED: association with short alleles of the 5′insulin VNTR von Paquette, J, Varin, D S E, Hamelin, C E, Hallgren, Å, Kämpe, O, Carel, J-C, Perheentupa, J, Deal, C L

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Immune system adaptation during gender-affirming testosterone treatment von Lakshmikanth, Tadepally, Consiglio, Camila, Sardh, Fabian, Forlin, Rikard, Wang, Jun, Tan, Ziyang, Barcenilla, Hugo, Rodriguez, Lucie, Sugrue, Jamie, Noori, Peri, Ivanchenko, Margarita, Piñero Páez, Laura, Gonzalez, Laura, Habimana Mugabo, Constantin, Johnsson, Anette, Ryberg, Henrik, Hallgren, Åsa, Pou, Christian, Chen, Yang, Mikeš, Jaromír, James, Anna, Dahlqvist, Per, Wahlberg, Jeanette, Hagelin, Anders, Holmberg, Mats, Degerblad, Marie, Isaksson, Magnus, Duffy, Darragh, Kämpe, Olle, Landegren, Nils, Brodin, Petter

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Shared etiology of type 1 diabetes and Hashimoto’s thyroiditis: a population-based twin study von Skov, Jakob, Kuja-Halkola, Ralf, Magnusson, Patrik K E, Gudbjörnsdottir, Soffia, Kämpe, Olle, Bensing, Sophie

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Co-aggregation and heritability of organ-specific autoimmunity: a population-based twin study von Skov, Jakob, Eriksson, Daniel, Kuja-Halkola, Ralf, Höijer, Jonas, Gudbjörnsdottir, Soffia, Svensson, Ann-Marie, Magnusson, Patrik K E, Ludvigsson, Jonas F, Kämpe, Olle, Bensing, Sophie

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Introduction: Autoimmune polyendocrine syndrome type 1 (APS‐1): a rare monogenic disorder as a model to improve understanding of tolerance and autoimmunity von Kampe, O

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