Zobrazeno 1 - 10
of 607
pro vyhledávání: '"Autoimmune polyendocrinopathy"'
Autor:
Thomas Clarke, Pan Du, Satyendra Kumar, Shinji L. Okitsu, Mark Schuette, Qi An, Jinyang Zhang, Evgeni Tzvetkov, Mark A. Jensen, Timothy B. Niewold, Elise M. N. Ferre, Julie Nardone, Michail S. Lionakis, Jaromir Vlach, Julie DeMartino, Andrew T. Bender
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Autoimmune diseases vary in the magnitude and diversity of autoantibody profiles, and these differences may be a consequence of different types of breaks in tolerance. Here, we compared the disparate autoimmune diseases autoimmune polyendocrinopathy
Externí odkaz:
https://doaj.org/article/e823a778e94642ba916ed495ae37f622
Autor:
Lea Regoršek Vrabec, Tina Leban, Katarina Trebušak Podkrajšek, Nataša Bratina, Sara Bertok, Alenka Pavlič, Magdalena Avbelj Stefanija
Publikováno v:
Slovenska pediatrija, Vol 27, Iss 1, Pp 9-14 (2020)
Autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy (APECED) is a rare monogenic disor- der caused by pathological genetic alterations in the AIRE gene, which encodes a protein autoimmune regulator, which is implicated in the regu
Externí odkaz:
https://doaj.org/article/56cb28d9be8245bc84c990d26ec3f848
Akademický článek
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Akademický článek
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Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Externí odkaz:
https://doaj.org/article/8ae9f39c38e1459481eefb5bf36d666e
Autor:
Inbal Halabi, Marie Noufi Barohom, Sarit Peleg, Phillippe Trougouboff, Ghadir Elias-Assad, Rhania Agbaria, Yardena Tenenbaum-Rakover
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a rare monogenic disorder, associated with endocrine deficiencies and non-endocrine involvement. Gastrointestinal (GI) manifestations appear in approximately 25% of patients a
Externí odkaz:
https://doaj.org/article/ee36ead201fa4fbcadc6d218d37db75b
Autor:
Go Kawano, Takaoki Yokochi, Ryuta Nishikomori, Yoriko Watanabe, Keizo Ohbu, Yukitoshi Takahashi, Haruo Shintaku, Toyojiro Matsuishi
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy is a rare autosomal recessive disorder caused by a mutation in the autoimmune regulator gene. Patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy typi
Externí odkaz:
https://doaj.org/article/eb7c93aa9feb480db7a8d71b896a734d
Publikováno v:
Iatreia, Vol 31, Iss 4, Pp 393-399 (2018)
Chronic mucocutaneous candidiasis is an infectious phenotype characterized by recurrent or persistent infections in the skin, nails and mucous membranes produced by Candida sp. This is secondary to any alteration in the antifungal immunity, in which
Externí odkaz:
https://doaj.org/article/1627c920b3c844d88990de40a727a3d3
Autor:
Elise M. N. Ferré, Michail S. Lionakis
Publikováno v:
Frontiers in Immunology, Vol 11 (2021)
Autoimmune-polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), a monogenic disorder caused by biallelic mutations in the AIRE gene, has historically been defined by the development of chronic mucocutaneous candidiasis together with autoimmu
Externí odkaz:
https://doaj.org/article/bffe29190f5841f6aa88c4fd91ab102f
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Objective: Immunological abnormalities, the resulting endocrinopathies and their treatments may impact bone health in patients with autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy (APECED, APS1). The aim of the present study was to
Externí odkaz:
https://doaj.org/article/55ea337c4821410cab547e40b76a2f0e