Anna Grandone
Overview
Explore the profile of Anna Grandone including associated specialties, affiliations and a list of published articles.
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Articles
92
Citations
828
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Recent Articles
1.
Guarino S, Calcaterra V, Di Sessa A, Labati L, Marrapodi M, Grandone A, et al.
BMC Med
. 2025 Feb;
23(1):123.
PMID: 40011875
Background: Thyroid hormone (TH) sensitivity at type 1 diabetes mellitus (T1DM) onset and its connection with acute kidney injury (AKI) has not been investigated. We aimed to evaluate changes in...
2.
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...
3.
Baroncelli G, Grandone A, Aversa A, Sessa M, Pelosini C, Michelucci A, et al.
Eur J Med Genet
. 2024 Jul;
70:104958.
PMID: 38950880
Background And Objective: X-linked hypophosphatemic rickets (XLH) is due to loss-of-function mutations in the phosphate-regulating endopeptidase homologue on the X chromosome (PHEX) that lead to increased fibroblast growth factor 23...
4.
Palumbo S, Palumbo D, Cirillo G, Giurato G, Aiello F, Del Giudice E, et al.
Clin Epigenetics
. 2024 Jun;
16(1):82.
PMID: 38909248
Background: Genetic and environmental factors are implicated in many developmental processes. Recent evidence, however, has suggested that epigenetic changes may also influence the onset of puberty or the susceptibility to...
5.
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...
6.
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...
7.
Seefried L, Alzahrani A, Arango Sancho P, Bacchetta J, Crowley R, Emma F, et al.
Orphanet J Rare Dis
. 2023 Oct;
18(Suppl 2):333.
PMID: 37885021
No abstract available.
8.
Spinelli C, Ghionzoli M, Sahli L, Guglielmo C, Frascella S, Romano S, et al.
Cancers (Basel)
. 2023 Jul;
15(14).
PMID: 37509342
DICER1 syndrome is a rare genetic disorder that predisposes patients to the development of malignant and non-malignant diseases. Presently, DICER1 syndrome diagnosis still occurs late, usually following surgical operations, affecting...
9.
Howard S, Fanis P, Nicolaides N, Grandone A
Front Endocrinol (Lausanne)
. 2023 Apr;
14:1178888.
PMID: 37008930
No abstract available.
10.
Bizzarri C, Capalbo D, Wasniewska M, Baronio F, Grandone A, Cappa M
Front Endocrinol (Lausanne)
. 2023 Mar;
14:1133376.
PMID: 36860362
Background: Despite the optimization of replacement therapy, adrenal crises still represent life-threatening emergencies in many children with adrenal insufficiency. Objective: We summarized current standards of clinical practice for adrenal crisis...