Zobrazeno 1 - 10
of 70
pro vyhledávání: '"schmidt's syndrome"'
Publikováno v:
Avicenna Journal of Medicine, Vol 14, Iss 02, Pp 130-133 (2024)
Schmidt's syndrome, or autoimmune polyendocrine syndrome type 2 (APS-2), is an uncommon disorder characterized by the co-occurrence of autoimmune thyroiditis and adrenalitis. APS-2 is defined as a combination of Addison's disease, autoimmune thyroid
Externí odkaz:
https://doaj.org/article/d4d026fca9784a0fb0aa557a4346fecc
Autor:
Marta Arrigoni, Paolo Cavarzere, Lara Nicolussi Principe, Rossella Gaudino, Franco Antoniazzi
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-6 (2023)
Abstract Background Primary adrenal insufficiency (PAI) in childhood is a life-threatening disease most commonly due to impaired steroidogenesis. Differently from adulthood, autoimmune adrenalitis is a rare condition amongst PAI’s main aetiologies
Externí odkaz:
https://doaj.org/article/79e35ada31084c258c8063d220d22382
Publikováno v:
Caspian Journal of Internal Medicine, Vol 12, Iss Supplement 2, Pp 392-396 (2021)
Background: Schmidt’s syndrome (SS) is a rare endocrine disorder (14-20:1000000), which consists of autoimmune thyroiditis (AIT) and autoimmune Addison’s disease (aAD), and usually occurs in young adults. Here, we report a unique case of late-ons
Externí odkaz:
https://doaj.org/article/c4f433396d944a61ae5c891201574cf3
Autor:
L.V. Shkala
Publikováno v:
Mìžnarodnij Endokrinologìčnij Žurnal, Vol 16, Iss 8, Pp 713-720 (2020)
Background. Autoimmune polyglandular syndrome type 2 is the most common. The development and course of Schmidt’s syndrome is of interest, which requires a comprehensive diagnosis due to the combination of several autoimmune endocrinopathies, and ra
Externí odkaz:
https://doaj.org/article/bf24c6a3a97344a6b166e2c3e9503578
Akademický článek
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Autor:
Francesco Vinci, Giuseppe d’Annunzio, Flavia Napoli, Marta Bassi, Carolina Montobbio, Giulia Ferrando, Nicola Minuto
Publikováno v:
Children, Vol 8, Iss 8, p 702 (2021)
Our objective is to emphasize the important role of continuous glucose monitoring (CGM) in suggesting adrenal insufficiency in patients affected by type 1 diabetes. We describe an adolescent girl with type 1 diabetes and subsequent latent Addison’s
Externí odkaz:
https://doaj.org/article/c7c5860e36494866b3de7cd4a7ee85c0
Publikováno v:
Caspian Journal of Internal Medicine, Vol 12, Iss Supplement 2, Pp 392-396 (2021)
Caspian Journal of Internal Medicine
Caspian Journal of Internal Medicine
Background: Schmidt’s syndrome (SS) is a rare endocrine disorder (14-20:1000000), which consists of autoimmune thyroiditis (AIT) and autoimmune Addison’s disease (aAD), and usually occurs in young adults. Here, we report a unique case of late-ons
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
L.V. Shkala
Publikováno v:
INTERNATIONAL JOURNAL OF ENDOCRINOLOGY (Ukraine); Vol. 16 No. 8 (2020); 713-720
Международный эндокринологический журнал-Mìžnarodnij endokrinologìčnij žurnal; Том 16 № 8 (2020); 713-720
Міжнародний ендокринологічний журнал-Mìžnarodnij endokrinologìčnij žurnal; Том 16 № 8 (2020); 713-720
Международный эндокринологический журнал-Mìžnarodnij endokrinologìčnij žurnal; Том 16 № 8 (2020); 713-720
Міжнародний ендокринологічний журнал-Mìžnarodnij endokrinologìčnij žurnal; Том 16 № 8 (2020); 713-720
Background. Autoimmune polyglandular syndrome type 2 is the most common. The development and course of Schmidt’s syndrome is of interest, which requires a comprehensive diagnosis due to the combination of several autoimmune endocrinopathies, and ra
Autor:
Carolina Montobbio, Francesco Vinci, Marta Bassi, Giulia Ferrando, Giuseppe d'Annunzio, Nicola Minuto, Flavia Napoli
Publikováno v:
Children
Children, Vol 8, Iss 702, p 702 (2021)
Children, Vol 8, Iss 702, p 702 (2021)
Our objective is to emphasize the important role of continuous glucose monitoring (CGM) in suggesting adrenal insufficiency in patients affected by type 1 diabetes. We describe an adolescent girl with type 1 diabetes and subsequent latent Addison’s