Andrea Secco
Overview
Explore the profile of Andrea Secco including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
152
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Recent Articles
1.
Pezzotta F, Sarale N, Spacco G, Tantari G, Bertelli E, Bracciolini G, et al.
Children (Basel)
. 2024 Oct;
11(10).
PMID: 39457190
The case report shows the safety and efficacy of insulin treatment with Advanced Hybrid Closed Loop (AHCL) system in a young patient affected by permanent neonatal diabetes mellitus (PNDM) due...
2.
Baroncelli G, Comberiati P, Aversa T, Baronio F, Cassio A, Chiarito M, et al.
Front Endocrinol (Lausanne)
. 2024 May;
15:1383681.
PMID: 38706696
Rickets results from impaired mineralization of growing bone due to alterations in calcium and phosphate homeostasis. Clinical signs of rickets are related to the age of the patient, the duration...
3.
Bruzzi P, Vannelli S, Scarano E, Di Iorgi N, Parpagnoli M, Salerno M, et al.
Endocr Connect
. 2023 Apr;
12(7).
PMID: 37014306
Objective: This Italian survey aims to evaluate real-life long-term efficacy and safety of recombinant human growth hormone (rhGH) therapy in children with short stature homeobox-containing gene deficiency disorders (SHOX-D) and...
4.
Mellone S, Bertelli E, Roviglione B, Vurchio D, Ronzani S, Secco A, et al.
Genes (Basel)
. 2022 Dec;
13(12).
PMID: 36553457
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders caused by enzyme deficiencies required for cortisol biosynthesis in the adrenal cortex. The majority of CAH are due to...
5.
Cairello F, Gagliardi M, Magrassi S, Secco A, Strozzi M, Felici E
Cardiol Young
. 2022 Feb;
:1-2.
PMID: 35193728
DiGeorge syndrome has heterogeneous clinical presentation, and for this reason, its diagnosis can be challenging and may be missed. Since CHDs are very common in this patients, they can be...
6.
Elli F, Mattinzoli D, Lucca C, Piu M, Maffini M, Costanza J, et al.
J Bone Miner Res
. 2021 Dec;
37(3):465-474.
PMID: 34897794
Skeletal disorders, including both isolated and syndromic brachydactyly type E, derive from genetic defects affecting the fine tuning of the network of pathways involved in skeletogenesis and growth-plate development. Alterations...
7.
Fanelli A, Vannelli S, Babu D, Mellone S, Cucci A, Monzani A, et al.
Mol Genet Genomic Med
. 2021 Nov;
10(1):e1793.
PMID: 34811950
Background: SHOX enhancer CNVs, affecting one or more of the seven recognized evolutionary conserved non-coding elements (CNEs) represent one of the most frequent cause of SHOX-haploinsufficiency. During the diagnostic workflow...
8.
Lundie D, Secco A
Rev Sci Instrum
. 2020 Aug;
91(7):079501.
PMID: 32752789
The Hiden pQA portable gas analyzer is a versatile mass spectrometer suitable for broad application ranges where analysis of dissolved species in liquid samples is required. The system's gas analysis...
9.
Catarinucci L, Colella R, Mainetti L, Patrono L, Pieretti S, Secco A, et al.
Lab Anim (NY)
. 2014 Aug;
43(9):321-7.
PMID: 25141063
Evaluating the behavior of mice and rats has substantially contributed to the progress of research in many scientific fields. Researchers commonly observe recorded video of animal behavior and manually record...
10.
Secco A, Allegri A, Di Iorgi N, Napoli F, Calcagno A, Bertelli E, et al.
Eur J Endocrinol
. 2011 Jul;
165(3):411-20.
PMID: 21750044
Objective: Controversies exist about posterior pituitary (PP) function in subjects with ectopic PP (EPP) and with cerebral midline defects and/or their co-occurrence. We investigate water and electrolyte disturbances in patients...