"
Severe Ectopic Cushing’s Syndrome Due to ACTH-Secreting Pheochromocytoma"
written by Aurelio Negro, Enrica Manicardi, Chiara Grasselli, Massimiliano Babini, Rosaria Santi, Valeria Pugni, Lucia Spaggiari, Elena Tagliavini,
published by
International Journal of Clinical Medicine,
Vol.4 No.4, 2013
has been cited by the following article(s):
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[1]
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Ectopic ACTH- and/or CRH-Producing Pheochromocytomas
The Journal of Clinical Endocrinology & Metabolism,
2021
DOI:10.1210/clinem/dgaa488
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[2]
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Case Report: Irreversible Watery Diarrhea, Severe Metabolic Acidosis, Hypokalemia and Achloridria Syndrome Related to Vasoactive Intestinal Peptide Secreting Malignant Pheochromocytoma
Frontiers in Endocrinology,
2021
DOI:10.3389/fendo.2021.652045
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[3]
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Concurrent heterozygous Von-Hippel–Lindau and transmembrane-protein-127 gene mutation causing an erythropoietin-secreting pheochromocytoma in a normotensive patient with severe erythrocytosis
Journal of Hypertension,
2020
DOI:10.1097/HJH.0000000000002253
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[4]
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Concurrent heterozygous Von-Hippel–Lindau and transmembrane-protein-127 gene mutation causing an erythropoietin-secreting pheochromocytoma in a normotensive patient with severe erythrocytosis
Journal of Hypertension,
2020
DOI:10.1097/HJH.0000000000002253
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[5]
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Severe Cushing Syndrome Due to an ACTH-Producing Pheochromocytoma: A Case Presentation and Review of the Literature
Journal of the Endocrine Society,
2018
DOI:10.1210/js.2018-00086
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[6]
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Bowel perforation complicating an ACTH-secreting phaeochromocytoma
Endocrinology, Diabetes & Metabolism Case Reports,
2016
DOI:10.1530/EDM-16-0061
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