المؤلفون: F. Bogazzi, Giorgio Radetti, Mariacarolina Salerno, B. Rees Smith, Stefano Masiero, L. de Sanctis, F. Presotto, Carla Giordano, Roberto Perniola, Valentina Camozzi, C. Betterle, Carla Scaroni, Antonella Meloni, Sarah Black, Francesca Pigliaru, Chiara Sabbadin, Alessandra Fierabracci, Carla Bizzarri, Marco Cappa, Garvin Weber, Donatella Capalbo, Susi Barollo, Jadwiga Furmaniak, Mariella Valenzise, Antonio Stigliano, A. Crinò, N. A. Greggio, Riccardo Scarpa, Silvia Garelli, Uberto Pagotto, M. Dalla Costa, A. De Bellis, Iacopo Chiodini, Shu Chen, Beatrice Rubin

المساهمون: Garelli, S., Dalla Costa, M., Sabbadin, C., Barollo, S., Rubin, B., Scarpa, R., Masiero, S., Fierabracci, A., Bizzarri, C., Crino, A., Cappa, M., Valenzise, M., Meloni, A., De Bellis, A. M., Giordano, C., Presotto, F., Perniola, R., Capalbo, D., Salerno, M., 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., Garelli S., Dalla Costa M., Sabbadin C., Barollo S., Rubin B., Scarpa R., Masiero S., Fierabracci A., Bizzarri C., Crino 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., 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

المصدر: Journal of Endocrinological Investigation

مصطلحات موضوعية: Male, Transcription Factor, Endocrinology, Diabetes and Metabolism, Autoimmune hepatitis, Gene mutation, Gastroenterology, Chronic mucocutaneous candidiasis, Endocrinology, Addison Disease, Autoimmune Polyglandular Syndrome type 1 (APS-1), Prevalence, Medicine, Polyendocrinopathies, Autoimmune, Candidiasis, Chronic Mucocutaneou, Addison’s disease, AIRE gene mutations, Autoimmune Polyglandular Syndrome type 1 (APS-1), Autoimmune-poly-endocrine-candidiasis-ectodermal-dystrophy (APECED), Chronic hypoparathyroidism, Chronic mucocutaneous candidiasis, Interferon autoantibodies, Candidiasis, Chronic Mucocutaneous, AIRE gene mutations, Addison’s disease, autoimmune polyglandular syndrome type 1 (APS-1), autoimmune-poly-endocrine-candidiasis-ectodermal-dystrophy (APECED), chronic hypoparathyroidism, chronic mucocutaneous candidiasis, interferon autoantibodies, Autoimmune regulator, Autoantibodie, Italy, Interferon autoantibodie, Addison's disease, Interferon Type I, Original Article, Female, Chronic hypoparathyroidism, Human, Adult, medicine.medical_specialty, Autoimmune Gastritis, Hypoparathyroidism, Internal medicine, Interferon autoantibodies, Humans, Mortality, Autoantibodies, Autoimmune-poly-endocrine-candidiasis-ectodermal-dystrophy (APECED), business.industry, Chronic mucocutaneous candidiasi, AIRE gene mutation, Autoantibody, medicine.disease, Autoimmune polyendocrine syndrome type 1, Mutation, business, Transcription Factors

وصف الملف: ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b5fd2c7ee684fd4d65c71851e2fdb32Test
http://hdl.handle.net/11568/1123121Test

المؤلفون: Miao Chen, Jing Ruan, Xianyong Jiang, Xuan Wang

المصدر: BMC Medical Genomics
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-5 (2021)

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, lcsh:Internal medicine, lcsh:QH426-470, Acquired Pure Red Cell Aplasia, Pure red cell aplasia, Case Report, Red-Cell Aplasia, Pure, urologic and male genital diseases, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Humans, Large granular lymphocytic leukaemia, lcsh:RC31-1245, Genetics (clinical), Bronchiectasis, business.industry, AIRE gene mutation, medicine.disease, Premature ovarian failure, Leukemia, Large Granular Lymphocytic, lcsh:Genetics, 030104 developmental biology, Autoimmune polyendocrine syndrome type 1, Hypoparathyroidism, 030220 oncology & carcinogenesis, Mutation, Immunology, Female, business, Glucocorticoid, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56fc4aab097a98459b690e42ed378cb5Test
http://europepmc.org/articles/PMC7814426Test

المؤلفون: Ayşe Derya Buluş, Pascale Saugier Veber, Handan Akil, Soner Keskin, Nesibe Andiran

المصدر: Journal of Clinical Ophthalmology and Research, Vol 4, Iss 1, Pp 37-39 (2016)

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, genetic structures, 03 medical and health sciences, Atrophy, autoimmune polyendocrine syndrome, lcsh:Ophthalmology, Retinitis pigmentosa, Medicine, Chronic mucocutaneous candidiasis, Adrenocortical Insufficiency, business.industry, AIRE gene mutation, medicine.disease, Autoimmune regulator, Dermatology, eye diseases, 030104 developmental biology, Autoimmune polyendocrine syndrome type 1, Hypoparathyroidism, cataract, lcsh:RE1-994, Autoimmune polyendocrine syndrome, Immunology, sense organs, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc0a953085b819c205ebd84ed3480b56Test
https://doi.org/10.4103/2320-3897.174414Test