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Mario Perotti

Explore the profile of Mario Perotti including associated specialties, affiliations and a list of published articles. Areas
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Articles 26
Citations 316
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Recent Articles
1.
Ornaghi S, Fernicola F, Marelli E, Perotti M, Di Gennaro F, Cameroni I, et al.
Gynecol Endocrinol . 2023 Jul; 39(1):2234492. PMID: 37486308
Unilateral non-hemorrhagic adrenal infarction (NHAI) is a very uncommon cause of acute abdomen in pregnancy. Diagnosis is highly challenging due to its rarity, heterogeneity of clinical presentation, and inconclusiveness of...
2.
Fiorini G, Cortinovis I, Corrao G, Franchi M, Pincelli A, Perotti M, et al.
Int J Environ Res Public Health . 2020 Nov; 17(21). PMID: 33167380
Type 2 diabetes is increasingly recognized as a spectrum of metabolic disorders sharing chronic hyperglycaemia. In Europe, the continually growing number of migrants from developing countries could affect diabetes phenotypes....
3.
Pincelli A, Perotti M, Massariello F, Gatti A, Calella D, Cimino V, et al.
Curr Aging Sci . 2018 Dec; 11(3):195-200. PMID: 30520387
Introduction: Doege-Potter Syndrome (DPS) is a rare but life-threatening paraneoplastic syndrome, characterized by Non-Islet Cell Tumor-Induced Hypoglycemia (NICTH) secondary to a Solitary Fibrous Tumor (SFT), which secretes an incompletely processed...
4.
Rigamonti A, Bini S, Rocco M, Giardini V, Massimini D, Crippa M, et al.
Endocrine . 2016 Mar; 55(1):113-123. PMID: 27022941
Although different hypotheses have been proposed, the underlying mechanism(s) of the weight loss induced by laparoscopic sleeve gastrectomy (LSG) is still unknown. The aim of this study was to determine...
5.
Manzoni M, Roversi G, Di Bella C, Pincelli A, Cimino V, Perotti M, et al.
Histopathology . 2015 Sep; 68(6):866-74. PMID: 26334919
Aims: The correct identification of solid cell nests (SCNs) is an important issue in thyroid pathology because of the spectrum of differential diagnoses of this type of lesion. Methods And...
6.
Crippa M, Bestetti I, Perotti M, Castronovo C, Tabano S, Picinelli C, et al.
BMC Med Genet . 2014 Jun; 15:52. PMID: 24886451
Background: Trichorhinophalangeal syndrome (TRPS) is a rare autosomal dominant genetic disorder characterised by distinctive craniofacial and skeletal abnormalities. TRPS is generally associated with mutations in the TRPS1 gene at 8q23.3...
7.
Brambilla G, Perotti M, Perra S, DellOro R, Grassi G, Pincelli A
J Nephrol . 2013 Mar; 26(3):594-8. PMID: 23475471
Background: We describe a 79-year-old man with biochemical and radiological features of Gitelman syndrome: hypokalemia, hypomagnesemia, hyperreninemic hyperaldosteronism in absence of secondary hyperaldosteronism causes, and chondrocalcinosis.
 Methods And Results: The...
8.
Rigamonti A, Sartorio A, Bonomo S, Giunta M, Grassi G, Perotti M, et al.
Metabolism . 2012 Jul; 61(12):1797-802. PMID: 22784430
Objective: Changes in circulating levels of many adipocyte-derived peptides, including adipokines such as adiponectin, leptin and tumor necrosis factor alpha (TNF-α), have been reported in obesity (OB). Somatostatin (SRIF) inhibits...
9.
Perotti M, Caumo A, Brunani A, Cambiaghi N, Casati M, Scacchi M, et al.
Clin Endocrinol (Oxf) . 2012 Apr; 77(5):721-7. PMID: 22519803
Objective: Adult growth hormone deficiency (GHD) has detrimental effects on metabolic profile, leading to an increased cardiovascular mortality and morbidity. Above all, disturbance in postprandial triglyceride metabolism is of major...
10.
Pincelli A, Masera N, Tavecchia L, Perotti M, Perra S, Mariani R, et al.
Pediatr Endocrinol Rev . 2011 Jun; 8 Suppl 2:284-9. PMID: 21705979
Endocrine complications in Β-thalassemia represent a prominent cause of morbidity. Above all, dysfunction of GH-IGF-1 axis is of a major concern because of its pathogenic role on cardiac and bone...