S Borsari
Overview
Explore the profile of S Borsari including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
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Articles
40
Citations
314
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Recent Articles
1.
Spadafora M, Megna A, Lippolis N, Cavicchi M, Borsari S, Piana S, et al.
J Eur Acad Dermatol Venereol
. 2024 Apr;
39(1):109-116.
PMID: 38572809
Background: Differential diagnosis of amelanotic/hypomelanotic melanoma among solitary flat pink lesions is challenging, due to limited clinical and dermoscopic clues. Dermoscopy and reflectance confocal microscopy assessments improve diagnostic accuracy, but...
2.
Brancatella A, Cappellani D, Pierotti L, Dinoi E, Sardella C, Borsari S, et al.
J Endocrinol Invest
. 2024 Feb;
47(9):2305-2312.
PMID: 38329607
Purpose: The screening test to suspect infantile hypercalcemia-1 (HCINF1) is the measure of 25(OH)D/24,25(OH)D ratio at mass spectroscopy (MS). When the ratio is > 80, the gold standard for the...
3.
Dinoi E, Pierotti L, Mazoni L, Citro F, Della Valentina S, Sardella C, et al.
J Endocrinol Invest
. 2023 Aug;
47(2):469-478.
PMID: 37561279
Purpose: Hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome, also known as Barakat syndrome, is a rare autosomal dominant disease characterized by the triad of hypoparathyroidism, deafness, and renal abnormalities. The...
4.
Saponaro F, Alfi G, Cetani F, Matrone A, Mazoni L, Apicella M, et al.
J Endocrinol Invest
. 2022 Jun;
45(10):1909-1918.
PMID: 35751804
Purpose: Hypoparathyroidism (HypoPT) is a rare endocrine disease and conventional therapy is based on calcium and vitamin D analogues. Conventional therapy does not restore calcium homeostasis and patients complain with...
5.
Lai M, Muscianese M, Piana S, Chester J, Borsari S, Paolino G, et al.
J Eur Acad Dermatol Venereol
. 2022 May;
36(9):1524-1540.
PMID: 35536546
Cutaneous adnexal tumours (ATs) encompass a variegated group of hamartomas and benign or malignant tumours, originating from the hair follicle, sebaceous, eccrine or apocrine glands that may simulate other cutaneous...
6.
Mazoni L, Matrone A, Apicella M, Saponaro F, Borsari S, Pardi E, et al.
J Endocrinol Invest
. 2021 Oct;
45(3):573-582.
PMID: 34637114
Purpose: Conventional therapy (calcium and activated vitamin D) does not restore calcium homeostasis in patients with chronic hypoparathyroidism (HypoPT) and is associated with renal complications and reduced quality of life...
7.
Borsari S, Peccerillo F, Pampena R, Lai M, Spadafora M, Moscarella E, et al.
J Eur Acad Dermatol Venereol
. 2020 May;
34(12):2802-2808.
PMID: 32402129
Background: Melanocytic lesions with eccentric hyperpigmentation (EH), even though without other dermatoscopic features of melanoma, are often excised. Objective: Aiming to understand whether the EH in a pigmented lesion is...
8.
Saponaro F, Cetani F, Mazoni L, Apicella M, Di Giulio M, Carlucci F, et al.
J Endocrinol Invest
. 2019 Dec;
43(5):677-682.
PMID: 31873910
Context: The latest guidelines of the 4th International Workshop on Asymptomatic Primary Hyperparathyroidism (aPHPT) reintroduced hypercalciuria (i.e. urinary calcium > 400 mg/day) as criterion for surgery. However, the value of...
9.
Cetani F, Pardi E, Aretini P, Saponaro F, Borsari S, Mazoni L, et al.
J Endocrinol Invest
. 2019 Sep;
43(3):399.
PMID: 31559585
Unfortunately, the 13th author name has been published incorrectly in the original publication.
10.
Cetani F, Pardi E, Aretini P, Saponaro F, Borsari S, Mazoni L, et al.
J Endocrinol Invest
. 2019 Sep;
43(2):231-245.
PMID: 31486992
Purpose: Familial isolated hyperparathyroidism (FIHP) is a rare inherited disease accounting for 1% of all cases of primary hyperparathyroidism (PHPT). It is genetically heterogeneous being associated with mutations in different...