Type 3 autoimmune polyglandular syndrome (APS-3) or type 3 multiple autoimmune syndrome (MAS-3): an expanding galaxy von Betterle, C., Furmaniak, J., Sabbadin, C., Scaroni, C., Presotto, F.

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Epidemiology, pathogenesis, and diagnosis of Addison’s disease in adults von Betterle, C., Presotto, F., Furmaniak, J.

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Type 3 autoimmune polyglandular syndrome (APS-3) or type 3 multiple autoimmune syndrome (MAS-3): an expanding galaxy von Betterle, C., Furmaniak, J., Sabbadin, C., Scaroni, C., Presotto, F.

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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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Renin and electrolytes indicate the mineralocorticoid activity of fludrocortisone: a 6 year study in primary adrenal insufficiency von Ceccato, F., Torchio, M., Tizianel, I., Peleg Falb, M., Barbot, M., Sabbadin, C., Betterle, C., Scaroni, C.

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Correction to: A non-classical presentation of APECED in a family with heterozygous R203X AIRE gene mutation von Radetti, G., Puel, A., Franceschi, R., Longhi, S., Gallo, N., Betterle, C.

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Autoimmune polyglandular syndrome Type 2: the tip of an iceberg? von Betterle, C., Lazzarotto, F., Presotto, F.

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A non-classical presentation of APECED in a family with heterozygous R203X AIRE gene mutation von Radetti, G., Puel, A., Franceschi, R., Longhi, S., Gallo, N., Betterle, C.

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Autoimmune gastritis: histology phenotype and OLGA staging von Rugge, M., Fassan, M., Pizzi, M., Zorzetto, V., Maddalo, G., Realdon, S., De Bernard, M., Betterle, C., Cappellesso, R., Pennelli, G., de Boni, M., Farinati, F.

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Premature Ovarian Failure in Patients with Autoimmune Addison's Disease: Clinical, Genetic, and Immunological Evaluation von Reato, G, Morlin, L, Chen, S, Furmaniak, J, Smith, B. Rees, Masiero, S, Albergoni, M. P, Cervato, S, Zanchetta, R, Betterle, C

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Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients von Garelli, S., Dalla Costa, M., Sabbadin, C., Barollo, S., Rubin, B., Scarpa, R., Masiero, S., Fierabracci, A., Bizzarri, C., Crinò, A., Cappa, M., Valenzise, M., Meloni, A., De Bellis, A. M., Giordano, C., Presotto, F., Perniola, R., Capalbo, D., Salerno, M. C., Stigliano, A., Radetti, G., Camozzi, V., Greggio, N. A., Bogazzi, F., Chiodini, I., Pagotto, U., Black, S. K., Chen, S., Rees Smith, B., Furmaniak, J., Weber, G., Pigliaru, F., De Sanctis, L., Scaroni, C., Betterle, C.

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Anti-heart and anti-intercalated disk autoantibodies: evidence for autoimmunity in idiopathic recurrent acute pericarditis von Caforio, A L P, Brucato, A, Doria, A, Brambilla, G, Angelini, A, Ghirardello, A, Bottaro, S, Tona, F, Betterle, C, Daliento, L, Thiene, G, Iliceto, S

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Autoimmune polyendocrine syndrome type 1 (APECED) in the Indian population: case report and review of a series of 45 patients von Fierabracci, A., Arena, A., Toto, F., Gallo, N., Puel, A., Migaud, M., Kumar, M., Chengappa, K. G., Gulati, R., Negi, V. S., Betterle, C.

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Thymic hyperplasia in patients with Graves’ disease von Dalla Costa, M., Mangano, F. A., Betterle, C.

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Autoimmune Polyglandular Syndrome Type 1 von Betterle, C, Greggio, N. A, Volpato, M

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Clinical review 93: Autoimmune polyglandular syndrome type 1 von Betterle, C, Greggio, N A, Volpato, M

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Tryptophan Hydroxylase Autoantibodies as Markers of a Distinct Autoimmune Gastrointestinal Component of Autoimmune Polyendocrine Syndrome Type 1 von Scarpa, R, Alaggio, R, Norberto, L, Furmaniak, J, Chen, S, Smith, B. Rees, Masiero, S, Morlin, L, Plebani, M, De Luca, F, Salerno, M. C, Giordano, R, Radetti, G, Ghizzoni, L, Tonini, G, Farinati, F, Betterle, C

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Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy from the pediatric perspective von Capalbo, D., Improda, N., Esposito, A., De Martino, L., Barbieri, F., Betterle, C., Pignata, C., Salerno, M.

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Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts von Mitchell, Anna L, Macarthur, Katie D R, Gan, Earn H, Baggott, Lucy E, Wolff, Anette S B, Skinningsrud, Beate, Platt, Hazel, Short, Andrea, Lobell, Anna, Kämpe, Olle, Bensing, Sophie, Betterle, Corrado, Kasperlik-Zaluska, Anna, Zurawek, Magdalena, Fichna, Marta, Kockum, Ingrid, Nordling Eriksson, Gabriel, Ekwall, Olov, Wahlberg, Jeanette, Dahlqvist, Per, Hulting, Anna-Lena, Penna-Martinez, Marissa, Meyer, Gesine, Kahles, Heinrich, Badenhoop, Klaus, Hahner, Stephanie, Quinkler, Marcus, Falorni, Alberto, Phipps-Green, Amanda, Merriman, Tony R, Ollier, William, Cordell, Heather J, Undlien, Dag, Czarnocka, Barbara, Husebye, Eystein, Pearce, Simon H S

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Molecular background and genotype-phenotype correlation in autoimmune-polyendocrinopathy-candidiasis-ectodermal-distrophy patients from Campania and in their relatives von Capalbo, D., Mazza, C., Giordano, R., Improda, N., Arvat, E., Cervato, S., Morlin, L., Pignata, C., Betterle, C., Salerno, M.

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