Mariacarolina Salerno
Overview
Explore the profile of Mariacarolina Salerno including associated specialties, affiliations and a list of published articles.
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137
Citations
1876
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Recent Articles
1.
Capalbo D, Moracas C, Guazzarotti L, Baronio F, Stancampiano M, Ortolano R, et al.
J Clin Endocrinol Metab
. 2025 Feb;
PMID: 39919031
Context: There has been concern about a potential increase in the incidence or severity of Coronavirus Disease 2019 (COVID-19) in individuals with adrenal insufficiency (AI). Data on the course of...
2.
Ferrigno R, Salerno M, Savage M
Front Endocrinol (Lausanne)
. 2024 Dec;
15:1512883.
PMID: 39726847
No abstract available.
3.
Valerio G, Di Bonito P, Calcaterra V, Cherubini V, Corica D, de Sanctis L, et al.
Ital J Pediatr
. 2024 Oct;
50(1):205.
PMID: 39380079
Despite the implementation of preventive measures to counteract the obesity epidemics, the prevalence of childhood obesity is still alarming all over the world. Childhood obesity is the most common risk...
4.
Improda N, Chioma L, Capalbo D, Bizzarri C, Salerno M
J Endocrinol Invest
. 2024 Oct;
48(1):37-52.
PMID: 39352628
Purpose: Glucocorticoids (GCs) are commonly used for several acute and chronic pediatric diseases. However, chronic treatment may result in hypothalamic-pituitary-adrenal axis (HPA) dysfunction. Glucocorticoid-induced adrenal insufficiency (GI-AI) is indeed the...
5.
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...
6.
Tseretopoulou X, Ali S, Bryce J, Amin N, Atapattu N, Bachega T, et al.
J Endocr Soc
. 2024 Sep;
8(10):bvae145.
PMID: 39258010
Background: It is unclear whether targeted monitoring of acute adrenal insufficiency (AI) related adverse events (AE) such as sick day episodes (SDEs) and hospitalization rate in congenital adrenal hyperplasia (CAH)...
7.
Fava D, Guglielmi D, Pepino C, Angelelli A, Casalini E, Varotto C, et al.
J Clin Endocrinol Metab
. 2024 Jun;
110(1):78-90.
PMID: 38913686
Context: The 2019 American Association of Clinical Endocrinologists guidelines suggested peak GH-cutoffs to glucagon test (GST) of ≤3 and ≤1 µg/L in the diagnosis of permanent GH deficiency (GHD) during...
8.
Calcaterra V, Tornese G, Zuccotti G, Staiano A, Cherubini V, Gaudino R, et al.
Ital J Pediatr
. 2024 Apr;
50(1):73.
PMID: 38637868
Background: In response to the imperative need for standardized support for adolescent Gender Dysphoria (GD), the Italian Academy of Pediatrics, in collaboration with the Italian Society of Pediatrics, the Italian...
9.
Rossi A, Simeoli C, Pivonello R, Salerno M, Rosano C, Brunetti B, et al.
Rev Endocr Metab Disord
. 2024 Mar;
25(4):707-725.
PMID: 38556561
Hepatic glycogen storage diseases constitute a group of disorders due to defects in the enzymes and transporters involved in glycogen breakdown and synthesis in the liver. Although hypoglycemia and hepatomegaly...
10.
Chiarito M, Lattanzio C, DAscanio V, Capalbo D, Cavarzere P, Grandone A, et al.
Endocrine
. 2024 Mar;
84(2):727-734.
PMID: 38536547
Purpose: To investigate the incidence of nephrolithiasis in a cohort of children with congenital adrenal hyperplasia (CAH), and to study if there is an association with the metabolic control of...