Search Results - "Zampetti, Benedetta"

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  1. 1

    Bilateral inferior petrosal sinus sampling by Zampetti, Benedetta, Grossrubatscher, Erika, Dalino Ciaramella, Paolo, Boccardi, Edoardo, Loli, Paola

    Published in Endocrine Connections (01-07-2016)
    “…Simultaneous bilateral inferior petrosal sinus sampling (BIPSS) plays a crucial role in the diagnostic work-up of Cushing’s syndrome. It is the most accurate…”
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    Journal Article
  2. 2

    Case Report: Opposite Tumoral and Hormonal Responses to Low-dose Pasireotide in Cushing's Disease by Serban, Andreea Liliana, Zampetti, Benedetta, Saladino, Andrea, Favero, Vittoria, Chiodini, Iacopo, Cozzi, Renato

    “…Pasireotide is a multireceptor somatostatin analogue approved for the treatment of patients with Cushing's disease (CD) who are ineligible or poor candidates…”
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    Journal Article
  3. 3

    Updated and New Perspectives on Diagnosis, Prognosis, and Therapy of Malignant Pheochromocytoma/Paraganglioma by Parenti, Gabriele, Zampetti, Benedetta, Rapizzi, Elena, Ercolino, Tonino, Giachè, Valentino, Mannelli, Massimo

    Published in Journal of Oncology (01-01-2012)
    “…Malignant pheochromocytomas/paragangliomas are rare tumors with a poor prognosis. Malignancy is diagnosed by the development of metastases as evidenced by…”
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    Journal Article
  4. 4

    Clinical Management of Acromegaly: Therapeutic Frontiers and New Perspectives for Somatostatin Receptor Ligands (SRLs) by Brunetti, Alessandro, Antonini, Simone, Saladino, Andrea, Lavezzi, Elisabetta, Zampetti, Benedetta, Cozzi, Renato

    Published in Medicina (Kaunas, Lithuania) (13-06-2022)
    “…Somatostatin receptor ligands (SRLs) represent a true milestone in the medical therapy for acromegaly. The first-generation SRLs (FG-SRLs), octreotide and…”
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    Journal Article
  5. 5

    Efficacy of pasireotide LAR for acromegaly: a prolonged real-world monocentric study by Favero, Vittoria, Zampetti, Benedetta, Carioni, Emanuela I, Dalino Ciaramella, Paolo, Grossrubatscher, Erika, Dallabonzana, Daniela, Chiodini, Iacopo, Cozzi, Renato

    Published in Frontiers in endocrinology (Lausanne) (01-02-2024)
    “…Acromegaly is caused by excessive growth hormone (GH) and insulin-like growth factor 1 (IGF1). Medical therapy plays a role as a treatment option for…”
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    Journal Article
  6. 6

    A Tale of Two Hypersecreting Adrenal Neoplasms in the Heartland of COVID-19 Pandemic, Lombardy, Italy by Zampetti, Benedetta, Attanasio, Roberto, Carioni, Emanuela, Dallabonzana, Daniela, Pauna, Iuliana, Boniardi, Marco, Cozzi, Renato

    Published in Case reports in endocrinology (18-02-2022)
    “…In this study, we report the management, in Lombardy, Italy, of one patient with Cushing’s syndrome due to adrenal adenoma and another one with…”
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    Journal Article
  7. 7

    Osilodrostat in Cushing’s disease: the management of its efficacy and the pitfalls of post-surgical results by Antonini, Simone, Brunetti, Alessandro, Zampetti, Benedetta, Boeris, Davide, Saladino, Andrea, Cesare Cozzi, Renato

    “…Summary Osilodrostat is a novel, orally administered cortisol synthesis inhibitor, approved in 2020 by the European Medicines Agency (EMA) for the treatment of…”
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    Journal Article
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    ACTH Stimulation Test for the Diagnosis of Secondary Adrenal Insufficiency: Light and Shadow by Birtolo, Maria Francesca, Antonini, Simone, Saladino, Andrea, Zampetti, Benedetta, Lavezzi, Elisabetta, Chiodini, Iacopo, Mazziotti, Gherardo, Lania, Andrea G A, Cozzi, Renato

    Published in Biomedicines (01-03-2023)
    “…Secondary Adrenal Insufficiency (SAI) is a condition characterized by inappropriately low ACTH secretion due to a disease or injury to the hypothalamus or the…”
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    Journal Article
  10. 10

    Hyponatremia after anticoagulant treatment: a rare cause of adrenal failure by Zampetti, Benedetta, Attanasio, Roberto, Cozzi, Renato

    “…Summary A 69-year-old male was admitted for severe hyponatremia disclosed after an accidental fall. He was anticoagulated from 2 months after the implantation…”
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    Journal Article
  11. 11

    Effective long-term temozolomide rechallenge in a macroprolactinoma by Zampetti, Benedetta, Simonetti, Giorgia, Attanasio, Roberto, Silvani, Antonio, Cozzi, Renato

    “…Summary We describe the 20-year course of a 63-year-old male with a macroprolactinoma that acquired resistance to treatment and aggressive behavior after a…”
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    Journal Article
  12. 12

    Six controversial issues on subclinical Cushing’s syndrome by Chiodini, Iacopo, Albani, Adriana, Ambrogio, Alberto Giacinto, Campo, Michela, De Martino, Maria Cristina, Marcelli, Giorgia, Morelli, Valentina, Zampetti, Benedetta, Colao, Annamaria, Pivonello, Rosario

    Published in Endocrine (01-05-2017)
    “…Subclinical Cushing’s syndrome is a condition of hypercortisolism in the absence of signs specific of overt cortisol excess, and it is associated with an…”
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    Journal Article
  13. 13

    False Positive of 68 Ga-DOTATATE PET-CT in a Paraganglioma by Zampetti, Benedetta, Attanasio, Roberto, Boniardi, Marco, Cozzi, Renato

    “…Functional imaging with Ga-DOTATATE PET-CT is widely employed to detect both primary and metastatic pheochromocytomas and paragangliomas (PGL), but its results…”
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    Effectiveness of low‐dose pasireotide in a patient with Cushing's disease: antiproliferative effect and predictivity of a short pasireotide suppression test by Grossrubatscher, Erika, Zampetti, Benedetta, Dalino Ciaramella, Paolo, Doneda, Paola, Loli, Paola

    Published in Clinical case reports (01-08-2015)
    “…Key Clinical Message This case shows efficacy of low‐dose pasireotide in biochemical and clinical control of severe hypercortisolism and in tumor volume…”
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    Journal Article
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    Succinate Dehydrogenase Subunit B Mutations Modify Human Neuroblastoma Cell Metabolism and Proliferation by Rapizzi, Elena, Ercolino, Tonino, Fucci, Rossella, Zampetti, Benedetta, Felici, Roberta, Guasti, Daniele, Morandi, Andrea, Giannoni, Elisa, Giaché, Valentino, Bani, Daniele, Chiarugi, Alberto, Mannelli, Massimo

    Published in Hormones & cancer (01-06-2014)
    “…Paragangliomas (PGLs) are rare neuroendocrine tumours. About 30–40 % of these tumours are mutated in one of the different susceptibility genes, including those…”
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    Journal Article
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