Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Robert Galagan"'
Publikováno v:
Journal of the Endocrine Society. 6:A538-A539
Background Pituitary adenomas co-secreting GH, Prolactin and ACTH are rare. Clinical Case A 38-year-old male with a past medical history of depression and type 2 diabetes mellitus was seen in the endocrinology clinic for an evaluation of acromegaly.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b90a9a88d21a073019068740efdc16b5
https://doi.org/10.1210/jendso/bvac150.1120
https://doi.org/10.1210/jendso/bvac150.1120
Publikováno v:
Diabetes. 71
Introduction: Tacrolimus is effective immunosuppressant in posttransplant patients. It inhibits calcineurin and prevents T cell activation. Post-transplantation diabetes mellitus (PTDM) is a well-established adverse effect of tacrolimus. We report th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::378da25165ab2d173cece5d829471576
https://doi.org/10.2337/db22-194-lb
https://doi.org/10.2337/db22-194-lb
Publikováno v:
Journal of the Endocrine Society
Background: Thyroid-stimulating hormone (TSH) secreting tumors (TSHoma) account for 0.5-2% of all pituitary adenomas with a prevalence of 1-2 cases per million, indicating that TSHomas are very rare. The majority of TSHomas solely secrete TSH however
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b620cc9b290dbc92ee3e818ea924629
http://europepmc.org/articles/PMC7208713
http://europepmc.org/articles/PMC7208713
Publikováno v:
Journal of the Endocrine Society
Background: Congenital adrenal hyperplasia (CAH) is a group of rare inherited autosomal recessive disorders characterized by a deficiency of various enzymes participating in steroid hormone synthesis. It occurs in 1 in 5000 to 1 in 15000 births. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71f7baa9be6f562cc11c67a5e7b9b221
https://doi.org/10.1210/jendso/bvaa046.1943
https://doi.org/10.1210/jendso/bvaa046.1943
Publikováno v:
Journal of the Endocrine Society
Background: Multiple Endocrine Neoplasia Type 2A (MEN 2A) is a genetic syndrome in which the patient is susceptible to the development of: 1. medullary thyroid carcinoma, 2. pheochromocytoma, and 3. parathyroid adenomas or hyperplasia. Our objective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57b0a863b97785ce9e2fe363901bdb80
http://europepmc.org/articles/PMC8089189
http://europepmc.org/articles/PMC8089189
Autor:
Robert Galagan, Tien-Hao Lee
Publikováno v:
Journal of the Endocrine Society
Background: Adrenocortical carcinoma is a rare disease which may be complicated by co-secretion of multiple steroid hormones. Clinical Case: A 53- year-old female was discovered to have 1 cm left and 1.7 cm right adrenal nodules by Chest CT scan in 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7cc5c913a2b766cdff24e71abd686ad
http://europepmc.org/articles/PMC8090326
http://europepmc.org/articles/PMC8090326