Short-term prolactin administration causes expressible galactorrhea but does not affect bone turnover: pilot data for a new lactation agent

por Page-Wilson, Gabrielle, Smith, Patricia C, Welt, Corrine K
Publicado 2007

Ectopic ACTH Syndrome Emerging 5 Years after the Diagnosis of Neuroendocrine Tumor

por Liu, Minghao, Hamele-Bena, Diane, Ausiello, John, Page-Wilson, Gabrielle
Publicado 2019

Cushing Syndrome due to a Pancreatic Neuroendocrine Tumor Treated With Radiofrequency Ablation

por Gugger, Aristea Sideri, Fang, Jiali, Visrodia, Kavel H, Page-Wilson, Gabrielle
Publicado 2023

Digital Health Solutions for Indigenous Mental Well-Being

por Hensel, Jennifer M., Ellard, Katherine, Koltek, Mark, Wilson, Gabrielle, Sareen, Jitender
Publicado 2019

MON-282 Treatment of Hyperprolactinemia with Ropinirole: An Open-Label Dose Escalation Study

por Tsang, Amanda, Dimino, Cara, Khandji, Alexander G, Panigrahi, Sunil Kumar, Page-Wilson, Gabrielle
Publicado 2020

Assay-Specific Spurious ACTH Results Lead to Misdiagnosis, Unnecessary Testing, and Surgical Misadventure—A Case Series

por Greene, Loren Wissner, Geer, Eliza B, Page-Wilson, Gabrielle, Findling, James W, Raff, Hershel
Publicado 2019

Response to Letter to the Editor: “Assay-Specific Spurious ACTH Results Lead to Misdiagnosis, Unnecessary Testing, and Surgical Misadventure—A Case Series”

por Wissner Greene, Loren, Geer, Eliza B, Page-Wilson, Gabrielle, Findling, James W, Raff, Hershel
Publicado 2019

SAT623 Everolimus For Treatment-refractory Prolactinomas

por Lin, Andrew L, Geer, Eliza Brevoort, Page-Wilson, Gabrielle, Magge, Rajiv S, Young, Robert J, Tabar, Viviane
Publicado 2023

PMON123 Diagnostically Challenging Case of Cushing's Syndrome from a Pancreatic Neuroendocrine Tumor Treated with Radiofrequency Ablation

por Gugger, Aristea Sideri, Fang, Jiali, Virk, Renu, Ahmad, Umar, Sagredo, Jorge Ariazza, Visrodia, Kavel H, Wilson, Gabrielle Page
Publicado 2022

Evaluating the burden of endogenous Cushing’s syndrome using a web-based questionnaire and validated patient-reported outcome measures

por Page-Wilson, Gabrielle, Oak, Bhagyashree, Silber, Abigail, Okeyo, Janetricks, Ortiz, Nancy, O’Hara, Matthew, Moloney, Stephen, Geer, Eliza B.
Publicado 2023

Genetic Analysis of RAB39B in an Early-Onset Parkinson's Disease Cohort

por Gao, Yujing, Wilson, Gabrielle R., Salce, Nicholas, Romano, Alexandra, Mellick, George D., Stephenson, Sarah E. M., Lockhart, Paul J.
Publicado 2020

MON-309 Prevalence of Silent Corticotroph Adenomas in a Large Cohort of Nonfunctioning Pituitary Adenomas: Plasma Proopiomelanocortin(POMC) Levels and Response to Pasireotide LAR

por Reyes-Vidal, Carlos, Page-Wilson, Gabrielle, Bruce, Jeffrey N, Post, Kalmon D, Hickman, Richard, Panigrahi, Sunil Kumar, Jin, Zhezhen, Khandji, Alexander, White, Anne, Wardlaw, Sharon L, Freda, Pamela
Publicado 2020

Distribution of Parkinson’s disease associated RAB39B in mouse brain tissue

por Gao, Yujing, Wilson, Gabrielle R., Stephenson, Sarah E. M., Oulad-Abdelghani, Mustapha, Charlet-Berguerand, Nicolas, Bozaoglu, Kiymet, McLean, Catriona A., Thomas, Paul Q., Finkelstein, David I., Lockhart, Paul J.
Publicado 2020

Obesity is independently associated with septic shock, renal complications, and mortality in a multiracial patient cohort hospitalized with COVID-19

por Page-Wilson, Gabrielle, Arakawa, Rachel, Nemeth, Samantha, Bell, Fletcher, Girvin, Zachary, Tuohy, Mary-Claire, Lauring, Max, Laferrère, Blandine, Reyes-Soffer, Gissette, Natarajan, Karthik, Chen, RuiJun, Kurlansky, Paul, Korner, Judith
Publicado 2021

Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency

por Sim, Joe C H, White, Susan M, Fitzpatrick, Elizabeth, Wilson, Gabrielle R, Gillies, Greta, Pope, Kate, Mountford, Hayley S, Torring, Pernille M, McKee, Shane, Vulto-van Silfhout, Anneke T, Jhangiani, Shalini N, Muzny, Donna M, Leventer, Richard J, Delatycki, Martin B, Amor, David J, Lockhart, Paul J
Publicado 2014

Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype

por de Vos, Ivo J H M, Tao, Evelyn Yaqiong, Ong, Sheena Li Ming, Goggi, Julian L, Scerri, Thomas, Wilson, Gabrielle R, Low, Chernis Guai Mun, Wong, Arnette Shi Wei, Grussu, Dominic, Stegmann, Alexander P A, van Geel, Michel, Janssen, Renske, Amor, David J, Bahlo, Melanie, Dunn, Norris R, Carney, Thomas J, Lockhart, Paul J, Coull, Barry J, van Steensel, Maurice A M
Publicado 2018