Kết quả tìm kiếm - Torpy, David
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A case of Aromatase deficiency due to a novel CYP19A1 mutation Bằng Gagliardi, Lucia, Scott, Hamish S, Feng, Jinghua, Torpy, David J
Được phát hành 2014Text -
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The epidemiology of primary and secondary adrenal malignancies and associated adrenal insufficiency in hospitalised patients: an analysis of hospital admission data, NSW, Australia Bằng Lubomski, Anna, Falhammar, Henrik, Torpy, David J., Rushworth, R. Louise
Được phát hành 2021Text -
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Genetic Testing in Endocrinology Bằng De Sousa, Sunita MC, Hardy, Tristan SE, Scott, Hamish S, Torpy, David J
Được phát hành 2018Text -
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Serum prolactin overestimation and risk of misdiagnosis Bằng De Sousa, Sunita M.C., Saleem, Mohamed, Rankin, Wayne, Torpy, David J.
Được phát hành 2019Text -
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Ambulatory intravenous insulin and islet cell transplantation to treat severe type III insulin hypersensitivity in a patient with type 1 diabetes mellitus Bằng Clarke, Brigette, Loudovaris, Tom, Radford, Toni, Drogemuller, Chris, Coates, Patrick Toby, Torpy, David
Được phát hành 2020Text -
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Adrenal crises in adolescents and young adults Bằng Rushworth, R. Louise, Chrisp, Georgina L., Bownes, Suzannah, Torpy, David J., Falhammar, Henrik
Được phát hành 2022Text -
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Systematic Review: adrenal insufficiency secondary to swallowed topical corticosteroids in eosinophilic oesophagitis Bằng Philpott, Hamish, Dougherty, Michael K., Reed, Craig C., Caldwell, Marie, Kirk, Deepa, Torpy, David J., Dellon, Evan S.
Được phát hành 2018Text -
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MON-457 One in Five Patients Develop Multiple Hormone Deficiencies Following Radiotherapy for Acromegaly or Cushing's Disease Bằng Shen, Angeline, Yates, Christopher, Phillips, Liza, Torpy, Helena, Torpy, Rachel, Das, Sourav, King, James, Torpy, David, Colman, Peter
Được phát hành 2019Text -
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CBG Montevideo: A Clinically Novel SERPINA6 Mutation Leading to Haploinsufficiency of Corticosteroid-binding Globulin Bằng Meyer, Emily Jane, Spangenberg, Lucía, Ramírez, Maria José, De Sousa, Sunita Maria Christina, Raggio, Victor, Torpy, David James
Được phát hành 2021Text -
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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 Bằng De Sousa, Sunita M. C., Kassahn, Karin S., McIntyre, Liam C., Chong, Chan-Eng, Scott, Hamish S., Torpy, David J.
Được phát hành 2016Text -
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