Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hans K. Ghayee DO"'
Autor:
Sherin Elsa Mathews MD, Jessica Castellanos-Diaz MD, Ashok Srihari MD, Sushma Kadiyala MD, Julio Leey-Casella MD, Hans K. Ghayee DO, Amie Ogunsakin MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 9 (2021)
A 67-year-old male was admitted with shortness of breath and diarrhea. His COVID-19 polymerase chain reaction test was positive, and he was found to be in acute heart failure. Troponin levels were elevated, echocardiogram showed ejection fraction of
Externí odkaz:
https://doaj.org/article/0419a366c3c441169eea7afb3019f161
Expression of Key Androgen-Activating Enzymes in Ovarian Steroid Cell Tumor, Not Otherwise Specified
Autor:
Evana Valenzuela Scheker MD, Amita Kathuria MD, Ashwini Esnakula MD, Hironobu Sasano MD, Yuto Yamazaki MD, Sergei Tevosian PhD, Richard J. Auchus MD, PhD, Hans K. Ghayee DO, Gauri Dhir MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 8 (2020)
To characterize the expression of steroidogenic enzymes implicated in the development of ovarian steroid cell tumors, not otherwise specified (SCT-NOS). We present 4 ovarian SCT-NOS evaluated by immunohistochemical staining of steroidogenic enzymes a
Externí odkaz:
https://doaj.org/article/706de87157df4deb9b3cd5771ad07233
Autor:
Christopher A. Newton MD, Eleni Sheehan MSN, ARNP, Kathleen Wyne MD, PhD, Kenneth Cusi MD, Julio Leey MD, MSc, Hans K. Ghayee DO
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 5 (2017)
Objective: To illustrate how steroid replacement in adrenal insufficiency can influence the development of hypoglycemia in a patient with type 1 diabetes mellitus (T1D). Methods: We describe the case of a 36-year-old female patient with T1D and Addis
Externí odkaz:
https://doaj.org/article/7642f788f5cd48bfaa6c5d8ecd9f277f
Publikováno v:
AACE Clinical Case Reports, Vol 7, Iss 1, Pp 72-74 (2021)
Objectives: The evaluation of an adrenal mass is challenging. We present the case of a 33-year-old pregnant woman who was found to have an adrenal incidentaloma. Four months after the initial imaging, the mass vanished. Methods: We described the case
Externí odkaz:
https://doaj.org/article/64c39df7b2664a77a7fcd87181329dcf
Autor:
Sushma Kadiyala, MD, Yasmin Khan, MD, Valeria de Miguel, MD, Megan N. Frone, MS, CGC, Fiemu Nwariaku, MD, Jennifer Rabaglia, MD, Stacey Woodruff, MD, Elizabeth E. King, MD, Sumitha S. Hathiramani, MD, Karel Pacak, MD, PhD, Hans K. Ghayee, DO
Publikováno v:
AACE Clinical Case Reports, Vol 4, Iss 3, Pp 186-190 (2018)
ABSTRACT: Objective: Succinate dehydrogenase complex, subunit D (SDHD) gene mutations are most commonly associated with head and neck paragangliomas. We describe a pair of cases with early-onset, bilateral pheochromocytoma (PCC) and paraganglioma (PG
Externí odkaz:
https://doaj.org/article/4ac371901afa45da87f4511af3b8ed48
Autor:
Awais Masood, MD, Anna Tumyan, MD, Daniel R. Nussenzveig, MD, PhD, Dara N. Wakefield, MD, Diana Barb, MD, Hans K. Ghayee, DO, Naim M. Maalouf, MD
Publikováno v:
AACE Clinical Case Reports, Vol 3, Iss 4, Pp 307-312 (2017)
ABSTRACT: Objective: Adrenal lymphoma is a rare and aggressive form of non-Hodgkin lymphoma (NHL). We report 2 cases of adrenal lymphoma: one with typical symptoms of adrenal insufficiency, the other with the unusual presentation of symptomatic hyper
Externí odkaz:
https://doaj.org/article/f55309eeedd04fe292a1c09e61c03634