Dopamine agonist therapy for prolactinomas: do we need to rethink the place of surgery in prolactinoma management?

por De Sousa, Sunita M C
Publicado 2022

Pituitary hyperplasia: case series and literature review of an under-recognised and heterogeneous condition

por De Sousa, Sunita M C, Earls, Peter, McCormack, Ann I
Publicado 2015

Serum prolactin overestimation and risk of misdiagnosis

por De Sousa, Sunita M.C., Saleem, Mohamed, Rankin, Wayne, Torpy, David J.
Publicado 2019

Familial GATA6 mutation causing variably expressed diabetes mellitus and cardiac and renal abnormalities

por Du, Yang Timothy, Moore, Lynette, Poplawski, Nicola K, De Sousa, Sunita M C
Publicado 2019

Cabergoline-associated valvulopathy of the tricuspid valve in the treatment of prolactinoma

por Hayes, Annabelle G, Shirazi, Masoumeh G, Thiyagarajah, Anand, Torpy, David J, De Sousa, Sunita M C
Publicado 2022

CBG Montevideo: A Clinically Novel SERPINA6 Mutation Leading to Haploinsufficiency of Corticosteroid-binding Globulin

por Meyer, Emily Jane, Spangenberg, Lucía, Ramírez, Maria José, De Sousa, Sunita Maria Christina, Raggio, Victor, Torpy, David James
Publicado 2021

Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome

por De Sousa, Sunita M. C., Kassahn, Karin S., McIntyre, Liam C., Chong, Chan-Eng, Scott, Hamish S., Torpy, David J.
Publicado 2016

A putative role for the aryl hydrocarbon receptor (AHR) gene in a patient with cyclical Cushing’s disease

por De Sousa, Sunita M. C., Manavis, Jim, Feng, Jinghua, Wang, Paul, Schreiber, Andreas W., Scott, Hamish S., Torpy, David J.
Publicado 2020

MON-LB48 The Genomic Landscape of Sporadic Thyrotrophinomas

por shen, Angeline, Wang, Paul, De Sousa, Sunita M C, Torpy, David J, Scott, Hamish, King, James, Colman, Peter Grahame, Yates, Christopher James
Publicado 2020

MEN4, the MEN1 Mimicker: A Case Series of three Phenotypically Heterogenous Patients With Unique CDKN1B Mutations

por Seabrook, Amanda, Wijewardene, Ayanthi, De Sousa, Sunita, Wong, Tang, Sheriff, Nisa, Gill, Anthony J, Iyer, Rakesh, Field, Michael, Luxford, Catherine, Clifton-Bligh, Roderick, McCormack, Ann, Tucker, Katherine
Publicado 2022

OR34-6 A Novel Mechanism of SDH-Deficient Tumorigenesis and Implications for Genetic Testing in Patients with Pheochromocytoma-Paraganglioma

por De Sousa, Sunita M.C., Toubia, John, Feng, Jingua, Wang, Paul, Hardy, Tristan S.E., Babic, Milena, Geoghegan, Joel, Hall, Rachel, Scott, Grist, Rawlings, Lesley, Schreiber, Andreas, Luxford, Catherine, Clifton-Bligh, Roderick, Poplawski, Nicola, Scott, Hamish, Torpy, David
Publicado 2019

The clinical and genetic features of hereditary pancreatitis in South Australia

por Wu, Denghao, Bampton, Tristan J, Scott, Hamish S, Brown, Alex, Kassahn, Karin, Drogemuller, Christopher, De Sousa, Sunita MC, Moore, David, Ha, Thuong, Chen, John WC, Khurana, Sanjeev, Torpy, David J, Radford, Toni, Couper, Richard, Palmer, Lyle, Coates, P Toby
Publicado 2022

Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas

por De Sousa, Sunita M C, Toubia, John, Hardy, Tristan S E, Feng, Jinghua, Wang, Paul, Schreiber, Andreas W, Geoghegan, Joel, Hall, Rachel, Rawlings, Lesley, Buckland, Michael, Luxford, Catherine, Novos, Talia, Clifton-Bligh, Roderick J, Poplawski, Nicola K, Scott, Hamish S, Torpy, David J
Publicado 2020

Development and validation of a targeted gene sequencing panel for application to disparate cancers

por McCabe, Mark J., Gauthier, Marie-Emilie A., Chan, Chia-Ling, Thompson, Tanya J., De Sousa, Sunita M.C., Puttick, Clare, Grady, John P., Gayevskiy, Velimir, Tao, Jiang, Ying, Kevin, Cipponi, Arcadi, Deng, Niantao, Swarbrick, Alex, Thomas, Melissa L., Lord, Reginald V., Johns, Amber L., Kohonen-Corish, Maija, O’Toole, Sandra A., Clark, Jonathan, Mueller, Simon A., Gupta, Ruta, McCormack, Ann I., Dinger, Marcel E., Cowley, Mark J.
Publicado 2019