Results 31 to 40 of about 10,174 (206)

Screening of endocrine organ-specific humoral autoimmunity in 47,XXY Klinefelter's syndrome reveals a significant increase in diabetes-specific immunoreactivity in comparison with healthy control men. [PDF]

, 2015
The aim of this study was to evaluate the frequency of humoral endocrine organ-specific autoimmunity in 47,XXY Klinefelter’s syndrome (KS) by investigating the autoantibody profile specific to type 1 diabetes (T1DM), Addison’s disease (AD), Hashimoto ...
ANZUINI, Antonella, GIANFRILLI, DANIELE, GRANATO, SIMONA, LENZI, Andrea, PANIMOLLE, FRANCESCA, RADICIONI, Antonio, Semeraro, A, TIBERTI, Claudio   +7 more
core   +1 more source

Young boy with Addison’s disease

Sri Lanka Journal of Diabetes Endocrinology and Metabolism, 2021
No abstract ...
D. Karuppiah
doaj   +1 more source

A case report: retigabine induced oral mucosal dyspigmentation of the hard palate [PDF]

, 2015
Background Dyspigmentation of the oral mucosa has a multitude of aetiological causes. Retigabine, a new antiepileptic drug, has the potential side effect of inducing a blue/purple pigmentation of the oral mucosa in addition to the skin, lips, nails and ...
Beacher, Nicholas G., Brodie, Martin J., Goodall, Christine   +2 more
core   +1 more source

A case report: Addison disease caused by adrenal tuberculosis

Urology Case Reports, 2018
We report middle age man with skin hyperpigmentation oral and lip mucous membranes, general malaise and depression. Further examinations lead to adrenal insufficiency, Addison's disease.
Moh Adi Soedarso, K Hery Nugroho, K.A. Meira Dewi   +2 more
doaj   +1 more source

Type 1 Diabetes and Addison’s Disease: When the Diagnosis Is Suggested by the Continuous Glucose Monitoring System

Children, 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.
Francesco Vinci, Giuseppe d’Annunzio, Flavia Napoli, Marta Bassi, Carolina Montobbio, Giulia Ferrando, Nicola Minuto   +6 more
doaj   +1 more source

Premature ovarian failure and ovarian autoimmunity [PDF]

, 1997
Premature ovarian failure (POF) is defined as a syndrome characterized by menopause before the age of 40 yr. The patients suffer from anovulation and hypoestrogenism.
A. Hoek, Aaltonen, Ahonen, Ahonen, Aiman, Allison, Allison, Alper, Alper, Alper, Anasti, Anasti, Atria, Austin, Austyn, Austyn, Austyn, Ayala, Baker, Bannatyne, Batchelor, Bateman, Baumann-Antczak, Behrman, Belvisi, Betterle, Betz, Biddison, Bierer, Biscotti, Blizzard, Block, Blumenfeld, Board, Bohmig, Borst, Bottazzo, Bottazzo, Bottazzo, Brenner, Brenner, Burton, Byrne, Cameron, Campbell, Caux, Chamberlin, Charlton, Chen, Chiauzzi, Colle, Collen, Collins, Cooper, Corenblum, Costoff, Coulam, Coulam, Coulam, Coulam, Coulam, Coulam, Coulam, Cowchock, Dahl, Damewood, Damjanovic, Damjanovic, Day, de Moraes-Ruehsen, de Moraes-Ruehsen, Dean, DeGroot, Dewhurst, Duignan, d’Andrea, Edmonds, Elder, Emperaire, Emperaire, Epplen, Escobar, Falk, Falk, Fitch, Fitzgerald, Flechner, Fraser, Fraser, Freudenthal, Friedman, Friedman Cl Gurgen-Varol, Furmaniak, Germain, Gloor, Golonka, Goodnow, Green, Greenberger, Greiner, Griffin Jr, H. A. Drexhage, Hanafusa, Harding, Hart, Hart, Hart, Heller, Hens, Herberman, Hill, Ho, Ho, Hoek, Hoek, Horning, Inaba, Irvine, Irvine, Ivanova, Iwatani, J. Schoemaker, Jackson, Jackson, Jankovic, Jansen, Jaroudi, Jaszmann, Jeppsson, Jia, Jin, Johnson, Jones, June, Kabel, Kamada, Kamperdijk, Kappler, Kaufman, Kiessling, Kim, Kimura, Kinch, Koninckx, Krailo, Krauss, Krawinkel, Kroemer, Krohn, Kuki, Labarbera, Lanier, Lanier, Le Floch, Leder, Leenen, Leibovich, Linsley, Lonsdale, Lou, Luborsky, Lundberg, Luo, Many, Marazuela, Marrack, Mathur, Mathur, Mattison, Maxson, McNatty, Meeker, Menon, Meuer, Mignot, Mignot, Milgrom, Miller, Miller, Miyake, Miyake, Mohler, Monaco, Moncayo, Moncayo, Moncayo-Naveda, Moore, Morahan, Morrison, Mosmann, Moss, Muechler, Mueller, Muir, Munoz, Munro Neville, Murphy, Myers, Nagler, Neefjes, Nelson, Nelson, Norton, Nossal, Oettgen, Panidis, Parker, Pekonen, Perussia, Philip, Pierce, Plunkett, Podack, Powrie, Prickett, Prinz, Pure, Quill, Rabinowe, Rabinowe, Rabinowe, Rebar, Rebar, Rhim, Rock, Romagnani, Royer, Rudensky AYu Preston-Hulburt, Russell, Sakaguchi, Sakaguchi, Sakaguchi, Sakaguchi, Schreiber, Schwartz, Scott, Seaman, Sedmak, Sele, Serreze, Shangold, Sharf, Shimizu, Singh, Skinner, Sluss, Smith, Smith, Smith, Smith, Song, Sotsiou, Starup, Starup, Steinman, Strominger, Suda, Taguchi, Taguchi, Taguchi, Tang, Tas, Teh, Teunissen, Theofilopoulos, Tilly, Todd, Tonegawa, Townsend, Trinchieri, Trunca, Tsirigotis, Tung, Turkington, Uibo, Uibo, Vakkila, Vallotton, van Dongen, van Ewijk, van Furth, van Voorhis, van Weissenbruch, Velloso, Villanueva, Volpe, Voorbij, Voorbij, Walfish, Walsh, Wardell, Warne Gl Fairley, Waxman, Weetman, Wheatcroft, Whitehead, Wick, Wick, Wick, Williamson, Winqvist, Winqvist, Winqvist, Witmer, Wolfe, Wolffenbuttel, Wood, Wright, Wulffraat, Yamakawa, Yen, Yoon, Yuan, Zarate, Zarate, Zourlas   +315 more
core   +3 more sources

Addison’s Disease Caused by Tuberculosis: Diagnostic and Therapeutic Difficulties

European Journal of Case Reports in Internal Medicine, 2018
Objectives: To demonstrate difficulties in diagnosing and treating Addison’s disease caused by tuberculosis. Materials and methods: We present a clinical case and review of the literature.
Sanne van Haren Noman, Hannah Visser, Alex Muller, Gijs Limonard   +3 more
doaj   +1 more source

AIRE variations in Addison's disease and autoimmune polyendocrine syndromes (APS):partial gene deletions contribute to APS I [PDF]

, 2008
Udgivelsesdato: MarAutoimmune Addison's disease (AAD) is often associated with other components in autoimmune polyendocrine syndromes (APS). Whereas APS I is caused by mutations in the AIRE gene, the susceptibility genes for AAD and APS II are unclear ...
Bruland, O, Bøe Wolff, A S, Husebye, E S, Johansson, S, Knappskog, P M, Løvås, K, Meager, A, Oftedal, B, Pedersen, Carsten   +8 more
core   +1 more source

A Challenging Case of Addison’s Disease [PDF]

Bengal Physician Journal, 2022
Addison’s disease (AD) or primary adrenocortical insufficiency results from hypofunction/dysfunction of an adrenal cortex with a decreased production of mineralocorticoids, glucocorticoids, and androgens, and with increased levels of adrenocorticotropic ...
S Arulrhaj, Arulprakash, Aarathykannan, Chandrakumar, Manikandan, Md Faizur Rahman   +5 more
doaj   +1 more source

Primary adrenal insufficiency in adults: 150 years after Addison [PDF]

, 2004
Thomas Addison first described, 150 years ago, a clinical syndrome characterized by salt-wasting and skin hyperpigmentation, associated with a destruction of the adrenal gland.
Alvarenga, Daniela B. de, Castro, Margaret de, Cunha, Andréa Aparecida, Elias, Lucila L.k., Kater, Claudio Elias, Moraes, Andréia M. de, Moreira, Ayrton C., Silva, Regina do Carmo   +7 more
core   +4 more sources