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Anna Elsa Maria Allegri

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Articles 21
Citations 238
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Recent Articles
1.
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...
2.
Fava D, Pepino C, Tosto V, Gastaldi R, Pepe A, Paoloni D, et al.
J Endocr Soc . 2023 Oct; 7(9):bvad094. PMID: 37873499
Context: Since the COVID-19 outbreak, the number of girls with suspected precocious puberty has increased. Objective: To compare the incidence of idiopathic central precocious puberty (ICPP) during COVID-19 with that...
3.
Fava D, Morandi F, Prigione I, Angelelli A, Bocca P, Pistorio A, et al.
J Endocr Soc . 2023 Aug; 7(9):bvad103. PMID: 37564886
Context: Rapid-onset obesity with central hypoventilation, hypothalamic dysfunction, and autonomic dysregulation with neural crest tumors (ROHHAD-NET) syndrome pathophysiology remains elusive. Acquired neuroimmunological dysfunction has been proposed as a possible pathogenetic...
4.
Patti G, Malerba F, Calevo M, Schiavone M, Scaglione M, Casalini E, et al.
Front Endocrinol (Lausanne) . 2023 Apr; 14:1172736. PMID: 37008915
[This corrects the article DOI: 10.3389/fendo.2022.975511.].
5.
Patti G, Malerba F, Calevo M, Schiavone M, Scaglione M, Casalini E, et al.
Front Endocrinol (Lausanne) . 2022 Sep; 13:975511. PMID: 36093089
Context: Data on pubertal timing in Silver Russell syndrome (SRS) are limited. Design And Methods: Retrospective observational study including twenty-three SRS patients [11p15 loss of methylation, (11p15 LOM, n=10) and...
6.
Fava D, Calandrino A, Calevo M, Allegri A, Napoli F, Gastaldi R, et al.
J Clin Endocrinol Metab . 2022 Jul; 107(10):e4132-e4143. PMID: 35881919
Context: The etiology of central precocious puberty (CPP) includes a spectrum of conditions. Girls younger than age 6 years with CPP should undergo cranial magnetic resonance imaging (MRI), but it...
7.
Morabito L, Allegri A, Capra A, Capasso M, Capra V, Garaventa A, et al.
Genes (Basel) . 2022 Apr; 13(4). PMID: 35456387
Osteogenesis imperfecta/Ehlers−Danlos (OI/EDS) overlap syndrome is a recently described disorder of connective tissue, characterized by mutation of COL1A1 (17q21.33) or COL1A2 (7q21.3) genes, that are involved in α-1 and α-2...
8.
Tannorella P, Minervino D, Guzzetti S, Vimercati A, Calzari L, Patti G, et al.
Genes (Basel) . 2021 Apr; 12(4). PMID: 33920573
Silver Russell Syndrome (SRS, MIM #180860) is a rare growth retardation disorder in which clinical diagnosis is based on six features: pre- and postnatal growth failure, relative macrocephaly, prominent forehead,...
9.
Bianco D, Napoli F, Morana G, Pistorio A, Allegri A, Fava D, et al.
J Clin Endocrinol Metab . 2020 Aug; 105(11). PMID: 32797230
Context: The etiology of central diabetes insipidus (CDI) in children is often unknown. Clinical and radiological features at disease onset do not allow discrimination between idiopathic forms and other conditions...
10.
Patti G, Guzzeti C, Di Iorgi N, Allegri A, Napoli F, Loche S, et al.
Best Pract Res Clin Endocrinol Metab . 2018 Aug; 32(4):425-444. PMID: 30086867
Central adrenal insufficiency (CAI) is a life-threatening condition caused by either pituitary disease (secondary adrenal insufficiency) or impaired hypothalamic function with inadequate CRH production (tertiary adrenal insufficiency). ACTH deficiency may...