Results 21 to 30 of about 9,049,445 (318)

PRIMARY SUPRARENAL GLANDULAR TUBERCULOSIS MIMICKING A MALIGNANT TUMOR

Jurnal Urologi Indonesia, 2023
ABSTRAK Objective: Our case demonstrates effective tuberculosis-related Addison's disease care with laparoscopic adrenalectomy and anti-tuberculosis medication.
Hikmat Satria, Kurnia Penta Seputra, Basuki Bambang Purnomo   +2 more
doaj   +1 more source

The Croonian Lectures on Addison's Disease [PDF]

BMJ, 1875
Edward Headlam Greenhow
openalex   +13 more sources

Primary adrenal insufficiency - Addison's disease

Journal of Education, Health and Sport, 2022
Introduction and purpose Addison's syndrome is defined as primary adrenal insufficiency, the symptoms of which result from hormonal deficiencies: glucocorticosteroids, mineralocorticosteroids and androgens.
Jakub Metelski, Aleksandra Metelska, Dominika Sereda, Hubert Nieścior, Monika Szwed   +4 more
doaj   +1 more source

Addison's disease symptoms--a cross sectional study in urban South Africa. [PDF]

PLoS ONE, 2013
BACKGROUND: Addison's disease is a potentially life-threatening disorder, and prompt diagnosis, and introduction of steroid replacement has resulted in near normal life-expectancy.
Ian Louis Ross, Naomi S Levitt
doaj   +1 more source

Characterization of clinicopathologic and abdominal ultrasound findings in dogs with glucocorticoid deficient hypoadrenocorticism

Journal of Veterinary Internal Medicine, 2022
Background Clinical findings of glucocorticoid‐deficient hypoadrenocorticism (GDH) can overlap with other diseases, presenting a diagnostic challenge.
Krystle L. Reagan, Ehren McLarty, Stanley L. Marks, Jamie Sebastian, Jennifer McGill, Chen Gilor   +5 more
doaj   +1 more source

The effect of sodium valproate in Cushing's disease, Nelson's syndrome and Addison's disease [PDF]

, 1988
We investigated the effect of sodium valproate on plasma ACTH and serum cortisol concentrations in different pathological states of ACTH hypersecretion.
Allolio, B., Jaursch-Hancke, C., Kaulen, D., Reincke, Martin, Winkelmann, W.   +4 more
core   +1 more source

Levothyroxine sodium oral solution to control thyroid function in a patient with hypothyroidism and celiac disease

Clinical Case Reports, 2021
Implementing a gluten‐free diet and switching to the levothyroxine oral solution significantly improved malabsorptive and hypothyroid symptoms in a patient with hypothyroidism, Addison's disease, and celiac disease without the need to increase ...
Ernest Asamoah
doaj   +1 more source

Association between Antibodies to the MR 67,000 Isoform of Glutamate Decarboxylase (GAD) and Type 1 (Insulin-Dependent) Diabetes Mellitus with Coexisting Autoimmune Polyendocrine Syndrome Type II [PDF]

, 1994
By using an immunoprecipitation assay, we analysed reactivity of autoantibodies to human recombinant GAD65 and GAD67 in sera from patients with autoimmune polyendocrine syndrome Type II (APS II) with and without Type 1 (insulin-dependent) diabetes ...
Baekkeskov S., Banga J. P., Bernhard O. Boehm, Betterle C. F., Bjork E., Bottazzo G. F, Bottazzo G. F., Christie M. R., Genovese S., Hagopan W. A., Jochen Seissler, Karlsen A. E., Kawasaki E., Kim J., Ludwig Mauch, Mauch L., Muir A., Nadja Yassin, Richter W., Riley W. J., Sabine Bieg, Scherbaum W. A, Scherbaum W. A., Schmidli R TS, Seissler J., Solimena M., Tarn A. C., Ujihara N., Velloso L. A., Wagner R., Wagner R., Werner A. Scherbaum, Wolfgang Northemann   +32 more
core   +1 more source

Addison′s disease

Contemporary Clinical Dentistry, 2012
Addison's disease is a rare endocrinal disorder, with several oral and systemic manifestations. A variety of pathological processes may cause Addison's disease. Classically, hyperpigmentation is associated with the disease, and intraoral pigmentation is perceived as the initial sign and develops earlier than the dermatological pigmentation.
Soumya Brata Sarkar, Subrata Sarkar, Supratim Ghosh, Subhankar Bandyopadhyay   +3 more
openaire   +3 more sources

Addison's disease in a lady with hemoglobin H disease

Iraqi Journal of Hematology, 2022
Hemoglobin H (HbH) disease is alpha (α)-thalassemia characterized by the inactivation of three of four α-globin genes due to deletions with or without nondeletional α-thalassemia.
Nawshirwan Gafoor Rashid
doaj   +1 more source