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Glucocorticoid excess and COVID-19 disease

Reviews in endocrine & metabolic disorders, 2021-12, Vol.22 (4), p.703-714

2021

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A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype

Endocrine, 2017-03, Vol.55 (3), p.959-968

2017

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Combination therapy for Cushing’s disease: effectiveness of two schedules of treatment. Should we start with cabergoline or ketoconazole?

Pituitary, 2014-04, Vol.17 (2), p.109-117

2014

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Long-term treatment of Cushing’s disease with pasireotide: 5-year results from an open-label extension study of a Phase III trial

Endocrine, 2017-07, Vol.57 (1), p.156-165

2017

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Analysis of GPR101 and AIP genes mutations in acromegaly: a multicentric study

Endocrine, 2016-12, Vol.54 (3), p.762-767

2016

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Perioperative multidisciplinary management of endoscopic transsphenoidal surgery for sellar lesions: practical suggestions from the Padova model

Neurosurgical review, 2020-08, Vol.43 (4), p.1109-1116

2020

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Pasireotide treatment reduces cardiometabolic risk in Cushing’s disease patients: an Italian, multicenter study

Endocrine, 2018-07, Vol.61 (1), p.118-124

2018

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The role of an acute pasireotide suppression test in predicting response to treatment in patients with Cushing’s disease: findings from a pilot study

Endocrine, 2015-09, Vol.50 (1), p.154-161

2015

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Venous thromboembolism in patients with Cushing’s syndrome: need of a careful investigation of the prothrombotic risk profile

Pituitary, 2013-06, Vol.16 (2), p.175-181

2013

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Pituitary Society Delphi Survey: An international perspective on endocrine management of patients undergoing transsphenoidal surgery for pituitary adenomas

Pituitary, 2022-02, Vol.25 (1), p.64-73

2022

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Thrombin generation in Cushing’s Syndrome: do the conventional clotting indices tell the whole truth?

Pituitary, 2014-02, Vol.17 (1), p.68-75

2014

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Treatment of skeletal impairment in patients with endogenous hypercortisolism: when and how?

Osteoporosis international, 2014-02, Vol.25 (2), p.441-446

2014

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Cyclic Cushing's syndrome: an overview

Pituitary, 2004-12, Vol.7 (4), p.203-207

2004

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Retinal abnormalities associated with a mutation of the nucleotide 683 in von Hippel-Lindau disease

Graefe's archive for clinical and experimental ophthalmology, 2000-07, Vol.238 (7), p.615-620

2000

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A community-based study of incidence, risk factors and outcome of transient ischaemic attacks in Umbria, Italy : the SEPIVAC study

Journal of neurology, 1991-04, Vol.238 (2), p.87-90

1991

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Prognostic value of the dense middle cerebral artery sign in patients with acute ischemic stroke

Italian journal of neurological sciences, 1991-02, Vol.12 (1), p.45-47

1991

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HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency

Human genetics, 1981-01, Vol.58 (3), p.331-337

1981

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Glucocorticoid excess and COVID-19 disease

A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype

Combination therapy for Cushing’s disease: effectiveness of two schedules of treatment. Should we start with cabergoline or ketoconazole?

Long-term treatment of Cushing’s disease with pasireotide: 5-year results from an open-label extension study of a Phase III trial

Analysis of GPR101 and AIP genes mutations in acromegaly: a multicentric study

Perioperative multidisciplinary management of endoscopic transsphenoidal surgery for sellar lesions: practical suggestions from the Padova model

Pasireotide treatment reduces cardiometabolic risk in Cushing’s disease patients: an Italian, multicenter study

The role of an acute pasireotide suppression test in predicting response to treatment in patients with Cushing’s disease: findings from a pilot study

Venous thromboembolism in patients with Cushing’s syndrome: need of a careful investigation of the prothrombotic risk profile

Pituitary Society Delphi Survey: An international perspective on endocrine management of patients undergoing transsphenoidal surgery for pituitary adenomas

Thrombin generation in Cushing’s Syndrome: do the conventional clotting indices tell the whole truth?

Treatment of skeletal impairment in patients with endogenous hypercortisolism: when and how?

Cyclic Cushing's syndrome: an overview

Retinal abnormalities associated with a mutation of the nucleotide 683 in von Hippel-Lindau disease

A community-based study of incidence, risk factors and outcome of transient ischaemic attacks in Umbria, Italy : the SEPIVAC study

Prognostic value of the dense middle cerebral artery sign in patients with acute ischemic stroke

HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency

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