Search Results - "Davì, M. V."
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1
Bone histomorphometry in acromegaly patients with fragility vertebral fractures
Published in Pituitary (01-02-2018)“…Context The high risk of vertebral fractures (VFs) in acromegaly patients despite normal bone mineral density (BMD) is well known. The reasons for this…”
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2
Gender-related differences in patients with carcinoid syndrome: new insights from an Italian multicenter cohort study
Published in Journal of endocrinological investigation (01-04-2024)“…Background The incidence of neuroendocrine neoplasm (NEN) and related carcinoid syndrome (CaS) has increased markedly in recent decades, and women appear to be…”
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3
Natural history of gastro-entero-pancreatic and thoracic neuroendocrine tumors. Data from a large prospective and retrospective Italian Epidemiological study: THE NET MANAGEMENT STUDY
Published in Journal of endocrinological investigation (01-10-2012)“…Background: The few epidemiological data available in literature on neuroendocrine tumors (NET) are mainly based on Registry databases, missing therefore…”
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4
Prevalence of AIP mutations in a large series of sporadic Italian acromegalic patients and evaluation of CDKN1B status in acromegalic patients with multiple endocrine neoplasia
Published in European journal of endocrinology (01-09-2010)“…BackgroundGermline mutations in the aryl hydrocarbon receptor-interacting protein (AIP) gene and the p27KIP1 encoding gene CDKN1B have been associated with two…”
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5
Autoimmune hypoglycaemia caused by alpha-lipoic acid: a rare condition in Caucasian patients
Published in Endocrinology, diabetes & metabolism case reports (11-12-2018)“…Summary Insulin autoimmune syndrome (IAS), a rare cause of autoimmune hyperinsulinaemic hypoglycaemia, is relatively well known in Japan. The incidence in…”
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6
Rare diseases in clinical endocrinology: a taxonomic classification system
Published in Journal of endocrinological investigation (01-02-2015)“…Purpose Rare endocrine–metabolic diseases (REMD) represent an important area in the field of medicine and pharmacology. The rare diseases of interest to…”
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Is Laparoscopic CME Right Hemicolectomy an Optimal Indication for NET of the Right Colon and Terminal Ileum?
Published in Journal of gastrointestinal surgery (2021)“…Purpose Since lymphadenectomy is crucial in midgut neuroendocrine tumor (NET) surgery, we adopted laparoscopic CME right hemicolectomy (LRH-CME) for the…”
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Clinico–pathological features, treatments and survival of malignant insulinomas: a multicenter study
Published in European journal of endocrinology (01-04-2020)“…Introduction Management of malignant insulinomas is challenging due to the need to control both hypoglycaemic syndrome and tumor growth. Literature data is…”
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Hyperinsulinemic hypoglycemia associated with ectopic Cushing’s syndrome due to a pancreatic endocrine tumor in a Type 2 diabetes mellitus patient: Clinical implications of a rare association
Published in Journal of endocrinological investigation (01-03-2011)“…Background : The coexistence of insulin and ACTH hypersecretion in the same patient is extremely rare. A diabetic patient with a pancreatic endocrine tumor…”
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10
Carcinoid crisis induced by receptor radionuclide therapy with 90Y-DOTATOC in a case of liver metastases from bronchial neuroendocrine tumor (atypical carcinoid)
Published in Journal of endocrinological investigation (01-06-2006)“…SS receptors are overexpressed in many tumors, mainly of neuroendocrine origin, thus enabling the treatment with SS analogs. The clinical experience of…”
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11
The treatment of hyperinsulinemic hypoglycaemia in adults: an update
Published in Journal of endocrinological investigation (01-01-2017)“…Background Treatment of hyperinsulinemic hypoglycaemia (HH) is challenging due to the rarity of this condition and the difficulty of differential diagnosis…”
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12
Long-term quiescence of ectopic Cushing's syndrome caused by pulmonary neuroendocrine tumor (typical carcinoid) and tumorlets: spontaneous remission or therapeutic effect of bromocriptine?
Published in Journal of endocrinological investigation (01-04-2006)“…In 1990, a 55-yr-old woman was admitted to the Medical Department of our hospital for severe hypercortisolism complicated by secondary diabetes mellitus and…”
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13
Presentation, diagnostic features and glucose handling in a monocentric series of insulinomas
Published in Journal of endocrinological investigation (01-10-2013)“…Background: New aspects have emerged in the clinical and diagnostic scenarios of insulinoma: current guidelines have lowered the diagnostic insulin threshold…”
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14
Hyperinsulinemic hypoglycemia associated with ectopic Cushing's syndrome due to a pancreatic endocrine tumor in a Type 2 diabetes mellitus patient: clinical implications of a rare association
Published in Journal of endocrinological investigation (01-03-2011)“…BACKGROUNDThe coexistence of insulin and ACTH hypersecretion in the same patient is extremely rare. A diabetic patient with a pancreatic endocrine tumor (PET)…”
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15
Clinical presentation, genotype–phenotype correlations, and outcome of pancreatic neuroendocrine tumors in Von Hippel–Lindau syndrome
Published in Endocrine (01-10-2021)“…Purpose Data regarding the clinical management and follow-up of pancreatic neuroendocrine tumors (PanNETs) associated with Von Hippel–Lindau (VHL) syndrome are…”
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16
An unusual case of adrenal failure due to isolated metastases of breast cancer
Published in Journal of endocrinological investigation (01-07-1996)“…We describe a patient affected by adrenal insufficiency due to metastases of breast cancer. Adrenal involvement became clinically evident 20 years after…”
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17
Effect of deflazacort on growth hormone response to insulin tolerance test
Published in Hormone and metabolic research (01-07-1992)“…Deflazacort (DF) has been claimed to be provided with a reduced distribution into the central nervous system, therefore it is conceivable that this…”
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18
Assessment of the awareness and management of sleep apnea syndrome in acromegaly. The COM.E.TA (Comorbidities Evaluation and Treatment in Acromegaly) Italian Study Group
Published in Journal of endocrinological investigation (2011)“…In 2007 the Italian COM.E.T.A. (COMorbidities Evaluation and Treatment in Acromegaly) study group started to assess the application in a clinical setting of…”
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19
Heterogeneity of nuclear DNA pattern and its relationship with cell cycle activity parameters in multinodular goitre
Published in Clinical endocrinology (Oxford) (01-06-1997)“…OBJECTIVE Recent studies suggest that the malignancy rate in multinodular goitre is not significantly different from that observed in solitary nodules and that…”
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Cushing's disease associated with empty sella: a clinical case treated for years with ketoconazole
Published in Annali italiani di medicina interna (01-10-1996)“…Cushing's disease and empty sella without evidence of pituitary adenoma are rarely observed. To our knowledge, there is very little documentation on long-term…”
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