Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Barbara MolsKowalczewski"'
Autor:
Tejaswini Maganti, Shobha Mandal, Vineela Kasireddy, Subash Ghimire, Sushmita Khadka, Barbara MolsKowalczewski
Publikováno v:
Journal of Adolescent and Young Adult Oncology. 11:122-125
Adrenal cortical carcinoma is a rare and aggressive cancer with poor prognosis. Cases usually present with signs and symptoms of excessive hormone production. Hyperglycemia and Cushing syndrome are common, but tumor-associated hypoglycemia due to par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7ee549dd089bb8ee79697de2ccb1498
https://doi.org/10.1089/jayao.2020.0229
https://doi.org/10.1089/jayao.2020.0229
Publikováno v:
Journal of the Endocrine Society. 5:A986-A987
Background: Parathyroid carcinoma is an extremely rare endocrine malignancy with a prevalence of &It 1%. It is associated with hyperparathyroidism-jaw tumor syndrome (HJTS), multiple endocrine neoplasia (MEN) type 1 or 2A syndromes, secondary hyperpa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac894f6e0a3fb296763285bcc3b011f7
https://doi.org/10.1210/jendso/bvab048.2018
https://doi.org/10.1210/jendso/bvab048.2018
Publikováno v:
Journal of the Endocrine Society
Introduction: The SGLT-2 inhibitors (SGLT-2i) are a newer anti-diabetic drugs. Their use has tremendously increased due to their favorable profile but they are also the focus of attention because of their side effect of euglycemic diabetic ketoacidos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9babc0a0268282a65dd9954faed272c2
https://doi.org/10.1210/jendso/bvab048.777
https://doi.org/10.1210/jendso/bvab048.777
Publikováno v:
Journal of the Endocrine Society
Introduction: According to White et al., health literacy is defined as ‘the degree to which individuals can obtain, process, understand, and communicate about health-related information needed to make informed health decisions. Nearly 36 percent of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26e25278e9d263b40de207af552b52e9
https://doi.org/10.1210/jendso/bvab048.759
https://doi.org/10.1210/jendso/bvab048.759
Publikováno v:
Journal of the Endocrine Society
Introduction: Pseudohypoaldosteronism type II (PHA II) or Gordon Syndrome is a rare, autosomally inherited disease with unknown prevalence. It is caused by mutations in the WNK1, WNK4, CUL3, or KLHL3 gene. It is characterized by hypertension, hyperka
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3d8b3602f70aab64887717b4af38b44
http://europepmc.org/articles/PMC8089166
http://europepmc.org/articles/PMC8089166