Results 181 to 190 of about 105,547 (226)

Addison's disease.

open access: yesSouth African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 2003
openaire   +1 more source

Addison's disease

The Lancet, 2005
Kristian, Løvås, Eystein S, Husebye
openaire   +4 more sources

Autoimmune Addison's disease

Best Practice & Research Clinical Endocrinology & Metabolism, 2020
Primary adrenal insufficiency (PAI) occurs in 1/5000-1/7000 individuals in the general population. Autoimmune Addison's disease (AAD) is the major cause of PAI and is a major component of autoimmune polyendocrine syndrome type 1 (APS1) and type 2 (APS2). Presence of 21-hydroxylase autoantibodies (21OHAb) identifies subjects with ongoing clinical or pre-
Serena, Saverino, Alberto, Falorni
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Autoimmune Addison's disease

La Presse Médicale, 2012
Addison's disease is a rare autoimmune disorder. In the developed world, autoimmune adrenalitis is the commonest cause of primary adrenal insufficiency, where the majority of patients have circulating antibodies against the key steroidogenic enzyme 21-hydroxylase.
Catherine, Napier, Simon H S, Pearce
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Autoimmune Addison’s Disease

2010
Primary adrenocortical insufficiency, or Addison's disease (AD), results from an adrenal cortex hypofunction/dysfunction with a deficient production of glucocorticoids, mineralocorticoids and androgens, and with high levels of both ACTH and plasma renin activity.
BETTERLE, CORRADO, MORLIN L.
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Tuberculous Addison's disease

Postgraduate Medicine, 1991
Addison's disease is a possible diagnosis in any patient who presents with weakness, weight loss, hyperpigmentation, hyponatremia, and hypotension. Laboratory findings, including depressed levels of cortisol and aldosterone, help to confirm the diagnosis. Computed tomography may reveal adrenal calcification and abnormal-sized adrenal glands.
openaire   +2 more sources

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