M F Faienza
Overview
Explore the profile of M F Faienza including associated specialties, affiliations and a list of published articles.
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Articles
32
Citations
259
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Recent Articles
1.
Aversa T, De Sanctis L, Faienza M, Gambineri A, Balducci A, DAprile R, et al.
J Endocrinol Invest
. 2024 Feb;
47(7):1585-1598.
PMID: 38376731
Purpose: Transition from pediatric to adult care is associated with significant challenges in patients with Turner syndrome (TS). The objective of the TRansition Age Management In Turner syndrome in Italy...
2.
Aiello F, Palumbo S, Cirillo G, Tornese G, Fava D, Wasniewska M, et al.
J Endocrinol Invest
. 2023 Dec;
47(6):1477-1485.
PMID: 38112911
Purpose: MKNR3 is a paternally expressed gene whose mutations are the main cause of central precocious puberty (CPP). Protein circulating levels can be easily measured, as demonstrated in idiopathic CPP...
3.
Faienza M, Brunetti G, Fintini D, Grugni G, Wasniewska M, Crino A, et al.
J Endocrinol Invest
. 2023 Mar;
46(9):1901-1909.
PMID: 36917420
Purpose/methods: Prader-Willi syndrome (PWS) is a rare genetic disorder displaying different clinical features, including obesity and bone impairment. LIGHT/TNFSF14 is a cytokine produced by immune cells affecting both fat and...
4.
Panfili F, Convertino A, Grugni G, Mazzitelli L, Bocchini S, Crino A, et al.
J Endocrinol Invest
. 2023 Jan;
46(7):1397-1406.
PMID: 36708456
Purpose: 25OHD levels in patients with Prader-Willi Syndrome (PWS), the most frequent cause of genetic obesity with a peculiar fat mass distribution, are still debated. Insulin resistance (IR), Body Mass...
5.
Palumbo S, Cirillo G, Sanchez G, Aiello F, Fachin A, Baldo F, et al.
J Endocrinol Invest
. 2022 Dec;
46(6):1233-1240.
PMID: 36577869
Purpose: We aimed to investigate a cohort of female and male patients with idiopathic central precocious puberty (CPP), negative for Makorin Ring Finger Protein 3 (MKRN3) defect, by molecular screening...
6.
Di Bonito P, Licenziati M, Corica D, Wasniewska M, Di Sessa A, Miraglia Del Giudice E, et al.
J Endocrinol Invest
. 2022 May;
45(9):1719-1727.
PMID: 35579861
Purpose: To assess the prevalence of pre-diabetes phenotypes, i.e., impaired fasting glucose (IFG), impaired glucose tolerance (IGT), increased HbA1c (IA1c), and their association with metabolic profile and atherogenic lipid profile...
7.
Chiarito M, Piacente L, Chaoul N, Pontrelli P, DAmato G, Grandone A, et al.
J Endocrinol Invest
. 2022 Mar;
45(6):1255-1263.
PMID: 35237949
Purpose: Girls affected with Turner syndrome (TS) present with low bone mineral density (BMD) and osteopenia/osteoporosis. Thus, they have an increased risk to develop fractures compared to normal population. The...
8.
Faienza M, Brunetti G, Grugni G, Fintini D, Convertino A, Pignataro P, et al.
J Endocrinol Invest
. 2021 Mar;
44(10):2261-2271.
PMID: 33656700
Background: Prader-Willi syndrome (PWS) is associated to distinctive clinical symptoms, including obesity, cognitive and behavioral disorders, and bone impairment. Irisin is a myokine that acts on several target organs including...
9.
Stefania D, Clodoveo M, Cariello M, DAmato G, Franchini C, Faienza M, et al.
Crit Rev Food Sci Nutr
. 2020 May;
61(11):1804-1826.
PMID: 32436425
Obesity represents one of the most important public health challenges of the 21st century and is characterized by a multifactorial etiology in which environmental, behavioral, metabolic, and genetic factors work...
10.
Faienza M, Baldinotti F, Marrocco G, Tyutyusheva N, Peroni D, Baroncelli G, et al.
J Endocrinol Invest
. 2020 Apr;
43(12):1711-1716.
PMID: 32297288
Background: Deficiency of 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) is a rare autosomal recessive 46,XY disorder of sex development (DSD). It is due to pathogenetic variants in the HSD17B3 gene. Mutated...