Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Jawairia Shakil"'
Autor:
Maleeha Zahid, MD, Shalini Koshy, MD, Jawairia Shakil, MD, Helmi S. Khadra, MD, Luan D. Truong, MD, Archana R. Sadhu, MD
Publikováno v:
AACE Clinical Case Reports, Vol 10, Iss 2, Pp 41-44 (2024)
Background/Objective: Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumors. Here, we report an unusual case of synchronous PPGL in an asymptomatic patient with tuberous sclerosis complex (TSC). Case Report: A 49-year-old woman wit
Externí odkaz:
https://doaj.org/article/4102822fe8ed47a1a10e5fc19b0ed174
Publikováno v:
Case Reports in Endocrinology, Vol 2020 (2020)
We report the case of a woman with a sporadic medullary thyroid carcinoma. Genomic analysis found that her tumor did not contain any common RET mutations but did harbor a BRAF V600E mutation. Only one other well-confirmed example of the BRAF V600E mu
Externí odkaz:
https://doaj.org/article/77766fe6c5de4f43bae91a7c9de3eb04
Autor:
Samaneh Dowlatshahi, Bhargavi Patham, Jawairia Shakil, Maleeha Zahid, Priya Arunchalam, Abhishek Kansara, Archana R. Sadhu
Publikováno v:
Diabetes Spectrum. 35:420-426
Insulin remains the mainstay of treatment for inpatient hyperglycemia in the United States and Canada. However, some other countries commonly use noninsulin agents such as metformin and sulfonylureas, and several trials have demonstrated the efficacy
Publikováno v:
Methodist DeBakey Cardiovascular Journal. 18:62-72
Sodium-glucose transport protein 2 inhibitors, commonly referred to as SGLT2i, are a group of prescription pharmaceuticals that are approved by the United States Food and Drug Administration for use with diet and exercise to lower blood glucose in ad
Autor:
Maleeha Zahid, Jawairia Shakil
Publikováno v:
Endocrine Practice. 29:S44-S45
Publikováno v:
Endocrine Practice. 29:S38-S39
Autor:
Faiza Mubeen, Jawairia Shakil
Publikováno v:
Endocrine Practice. 29:S50-S51
Publikováno v:
JCEM Case Reports. 1
Clinical syndromes involving multiple endocrine glands have been well recognized for over a century. Multiple reports describing hereditary multiple endocrine neoplasia (MEN) syndromes involving pituitary, parathyroid, and pancreatic neuroendocrine t
Publikováno v:
Endocrine Practice. 29:S39
Autor:
Maleeha Zahid, Jawairia Shakil
Publikováno v:
Journal of the Endocrine Society. 6:A539-A539
Introduction The clinical manifestations of pituitary apoplexy (PA) are highly variable and are caused by a rapid increase in the size of intrasellar contents, leading to an increase in intrasellar pressure. Headache, visual disturbances, cranial ner