Raffaella Di Mase
Overview
Explore the profile of Raffaella Di Mase including associated specialties, affiliations and a list of published articles.
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25
Citations
230
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Recent Articles
1.
Capalbo D, Esposito A, Gaeta V, Lorello P, Vasaturo S, Di Mase R, et al.
Front Endocrinol (Lausanne)
. 2024 Oct;
15:1411774.
PMID: 39351530
Primary adrenal insufficiency (PAI) is a rare medical condition, characterized by a deficiency in adrenal hormones. Although rare, PAI is a life-threatening disease requiring prompt recognition and treatment. However, symptoms...
2.
Rivera Romero O, Chae H, Faienza M, Vergani E, Cheon C, Di Mase R, et al.
Front Endocrinol (Lausanne)
. 2024 Jul;
15:1419667.
PMID: 39050564
Introduction: To analyse the perspectives of healthcare professionals (HCPs) regarding the acceptance of digital health solutions for growth hormone (GH) deficiency care. This study identified factors impacting HCPs' intent to...
3.
Cassio A, Marescotti G, Aversa T, Salerno M, Tornese G, Stancampiano M, et al.
J Clin Endocrinol Metab
. 2024 Feb;
109(8):2061-2070.
PMID: 38308814
Context: There are only a few nationwide studies on boys with central precocious puberty (CPP) and the last Italian study is a case series of 45 boys that dates back...
4.
Di Mase R
Recenti Prog Med
. 2023 Nov;
114(12):3e-5e.
PMID: 38031864
When properly treated, congenital hypothyroidism (CH) allows normal growth. We describe the case of a girl followed-up for CH diagnosed upon newborn screening, with good adherence to L-T4 therapy, who...
5.
Santamaria F, Scandurra C, Mezzalira S, Bochicchio V, Salerno M, Di Mase R, et al.
Horm Res Paediatr
. 2023 Sep;
97(3):254-260.
PMID: 37748459
Introduction: The aim of this study was to evaluate (i) the knowledge about different dimensions of sexual identity in a group of family pediatricians and (ii) the efficacy of a...
6.
Improda N, Moracas C, Raso G, Valente V, Crisci G, Lorello P, et al.
Horm Res Paediatr
. 2023 Jun;
97(2):140-147.
PMID: 37290420
Introduction: Growth hormone deficiency (GHD) may be associated with subtle cardiovascular abnormalities, reversible upon starting GH treatment. Data on vascular morphology and function in GHD children are scanty and inconclusive....
7.
Esposito A, Vigone M, Polizzi M, Wasniewska M, Cassio A, Mussa A, et al.
Front Endocrinol (Lausanne)
. 2022 Sep;
13:923448.
PMID: 36133316
Objectives: We designed a multicentre open prospective randomized trial to evaluate the risk-benefit profile of two different initial treatment schemes with levothyroxine (L-T4), 10-12.5 μg/kg/day vs 12.6-15 μg/kg/day, on growth...
8.
Zucchini S, Di Iorgi N, Pozzobon G, Pedicelli S, Parpagnoli M, Driul D, et al.
J Clin Endocrinol Metab
. 2021 Oct;
107(3):e1020-e1031.
PMID: 34718649
Context: Nationwide data on children diagnosed with craniopharyngioma (CP) are not available in Italy. Objective: This work aimed to identify patients' characteristics, type of surgical approach, complications and recurrences, number...
9.
Vigone M, Ortolano R, Vincenzi G, Pozzi C, Ratti M, Assirelli V, et al.
Eur J Endocrinol
. 2021 Oct;
186(1):45-52.
PMID: 34714772
Objective: Oral solution and tablet formulations of levothyroxine (L-T4) are both used in the treatment of congenital hypothyroidism (CH). However, few studies and with a limited follow-up period have been...
10.
Aiello F, Cirillo G, Cassio A, Di Mase R, Tornese G, Umano G, et al.
Ital J Pediatr
. 2021 Jan;
47(1):5.
PMID: 33413516
Background: Prokineticin receptor 2 (PROKR2) loss of function mutations have been described as cause of hypogonadotropic hypogonadism. In 2017, a first case of central precocious puberty (CPP) caused by PROKR2...