Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Roxanne Merkel"'
Autor:
Cristiane J. Gomes-Lima, Sungyoung Auh, Shilpa Thakur, Marina Zemskova, Craig Cochran, Roxanne Merkel, Armando C. Filie, Mark Raffeld, Snehal B. Patel, Liqiang Xi, Leonard Wartofsky, Kenneth D. Burman, Joanna Klubo-Gwiezdzinska
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Background: Thyroid ultrasound (US), fine needle aspiration biopsy (FNAB), and molecular testing have been widely used to stratify the risk of malignancy in thyroid nodules. The goal of this study was to investigate a novel diagnostic approach for cy
Externí odkaz:
https://doaj.org/article/feeaec14157a41b7ac321e789207b2e8
Autor:
Shirisha Avadhanula, Monica C. Skarulis, Asma Azam, Susanne Neumann, Meryl Waldman, Craig Cochran, Joanna Klubo-Gwiezdzinska, Katherine A Araque, Sriram Gubbi, Marvin C. Gershengorn, Peter D. Burbelo, Roxanne Merkel
Publikováno v:
Ann Intern Med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd77dd67f954cf4f92c744258ef9070c
https://europepmc.org/articles/PMC9473454/
https://europepmc.org/articles/PMC9473454/
Autor:
Apostolos Gaitanidis, Dhaval Patel, Pavel Nockel, Electron Kebebew, Naris Nilubol, Mustapha El Lakis, Roxanne Merkel, Karel Pacak, Tamara Prodanov
Publikováno v:
Ann Surg
BACKGROUND: Fluorodeoxyglucose ((18)F-FDG) positron emission tomography/computed tomography (PET/CT) imaging is recommended in patients with metastatic pheochromocytoma (PC) and paraganglioma (PGL). There are no data on whether routine preoperative (
Autor:
James Welch, Lee S. Weinstein, Roxanne Merkel, Electron Kebebew, Pavel Nockel, Dhaval Patel, Naris Nilubol, Bin Guan, William F. Simonds, Sunita K. Agarwal, Stephen J. Marx, Mustapha El Lakis, Apostolos Gaitanidis, Amit Tirosh
Publikováno v:
Journal of the American College of Surgeons. 226:933-938
Background Approximately 10% of patients with primary hyperparathyroidism (PHPT) have hereditary disease. Hereditary PHPT may be syndromic (MEN1, 2, and 4 and hyperparathyroidism-jaw tumor syndrome) or non-syndromic (familial isolated PHPT). There ar
Autor:
Roxanne Merkel, Naris Nilubol, Pavel Nockel, Karel Pacak, Tamara Prodanov, Mustapha El Lakis, Lily Yang, Apostolos Gaitanidis, Dhaval Patel, Electron Kebebew
Publikováno v:
Surgery. 163:191-196
Background Our knowledge of the susceptibility genes for pheochromocytomas/paragangliomas has increased; however, data on its impact on surgical decision-making has not been described. The aim of this study was to determine the effect of routine preo
Autor:
James Welch, Robert T. Jensen, Vaishali I. Parekh, Jenny E Blau, Sunita K. Agarwal, William F. Simonds, Adel Mandl, Roxanne Merkel, Lee S. Weinstein, Zahraa Abdul Sater, Jaydira Del Rivero, David S. Schrump, Craig Cochran, Gayathri Veeraraghavan
Publikováno v:
Journal of the Endocrine Society
Patients with the multiple endocrine neoplasia 1 (MEN1) syndrome develop various tumors during their lifetime. One of the rare manifestations observed in MEN1 patients is thymic neuroendocrine tumor (Th-NET) or thymic carcinoid, which is a major caus
Autor:
Lee S. Weinstein, Naris Nilubol, William F. Simonds, Roxanne Merkel, Karel Pacak, Craig Cochran, Abhishek Jha, Sunita K. Agarwal, James Welch, Jenny E Blau, Adel Mandl, Corina Millo, Aisha Tepede
Publikováno v:
Journal of the Endocrine Society
18F-FDOPA PET/CT accurately identifies pheochromocytoma in 70-year-old male with MEN1 Background: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant inherited disorder that causes tumors most often in the parathyroid, pancreas, and p
Autor:
Lee S. Weinstein, Stephen A. Wank, Aisha Tepede, James Welch, Craig Cochran, Dhaval Patel, Naris Nilubol, Roxanne Merkel, Adel Mandl, Sunita K. Agarwal, Jaydira Del Rivero, William F. Simonds, Sheila Kumar, Jenny E Blau, Corina Millo, Rashika Bansal
Publikováno v:
Journal of the Endocrine Society
BACKGROUND: Gastric neuroendocrine tumors (carcinoid) associated with Zollinger Ellison Syndrome (ZES) induced hypergastrinemia in Multiple Endocrine Neoplasia type 1 (MEN1) occur in 15-50% of patients and are generally thought to be benign. Here we
Autor:
Phillip Gorden, William F. Simonds, Craig Cochran, James Welch, Naris Nilubol, Jenny E Blau, Megan Startzell, Miho Itatani, Adel Mandl, Sunita K. Agarwal, Diala El-Maouche, Samira Sadowski Veuthey, Lee S. Weinstein, Richard Chang, Amit Tirosh, Roxanne Merkel, Aisha Tepede
Publikováno v:
Journal of the Endocrine Society
Background: Further characterization of insulinomas from MEN1 patients versus sporadic cases may help elucidate pathophysiological differences and improve future diagnostic algorithms. Methods A retrospective analysis of all patients with insulinoma
Autor:
Armando C. Filie, Sungyoung Auh, Snehal Patel, Joanna Klubo-Gwiezdzinska, Liqiang Xi, Mark Raffeld, Roxanne Merkel, Craig Cochran, Kenneth D. Burman, Marina S. Zemskova, Cristiane Jeyce Gomes-Lima, Shilpa Thakur
Publikováno v:
Journal of the Endocrine Society
Background Thyroid ultrasound (US) and US-guided fine needle aspiration biopsy (FNAB) have been widely used to stratify the risk of malignancy in thyroid nodules (TN). Cytology material characterized as category III and IV by the Bethesda System for