A Cassio
Overview
Explore the profile of A Cassio including associated specialties, affiliations and a list of published articles.
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Articles
57
Citations
303
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0
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Recent Articles
1.
Palumbo S, Cirillo G, Sanchez G, Aiello F, Fachin A, Baldo F, et al.
J Endocrinol Invest
. 2022 Dec;
46(6):1233-1240.
PMID: 36577869
Purpose: We aimed to investigate a cohort of female and male patients with idiopathic central precocious puberty (CPP), negative for Makorin Ring Finger Protein 3 (MKRN3) defect, by molecular screening...
2.
Barberi C, Di Natale V, Assirelli V, Bernardini L, Candela E, Cassio A
Front Endocrinol (Lausanne)
. 2022 Dec;
13:1032914.
PMID: 36531478
Sexual development is a complex mechanism activated by the hypothalamic-pituitary-gonadal axis. Over the last one hundred years there has been a decline in the age at puberty onset in industrialised...
3.
Baccelli F, Ortolano R, Conti F, Soncini E, Baronio F, Masetti R, et al.
Clin Immunol
. 2022 Oct;
245:109142.
PMID: 36182049
Autoimmune thyroid disease has been described as a complication of HSCT for different indications and as a manifestation of inborn errors of immunity, like SCID. A 1-month female was diagnosed...
4.
Gentilini D, Muzza M, de Filippis T, Vigone M, Weber G, Calzari L, et al.
J Endocrinol Invest
. 2022 Sep;
46(2):393-404.
PMID: 36071330
Purpose: The elevated frequency of discordance for congenital hypothyroidism (CH) phenotype between monozygotic twins suggests the involvement of non-mendelian mechanisms. The aim of the study was to investigate the role...
5.
Emma F, Cappa M, Antoniazzi F, Bianchi M, Chiodini I, Eller Vainicher C, et al.
Ital J Pediatr
. 2019 Jun;
45(1):67.
PMID: 31151476
Background: X-linked hypophosphatemic rickets (XLH) is the first cause of inherited hypophosphatemia and is caused by mutation in the PHEX gene, resulting in excessive expression of the phosphaturic factor FGF23....
6.
Tonti G, Maltoni G, Cassio A, Zucchini S
Acta Diabetol
. 2019 Apr;
56(9):1083-1086.
PMID: 30968194
No abstract available.
7.
Balsamo C, Zucchini S, Maltoni G, Rollo A, Martini A, Mazzanti L, et al.
J Endocrinol Invest
. 2015 Feb;
38(6):701-7.
PMID: 25722223
Background: Type 1 diabetes (T1DM) is an autoimmune disease often associated with thyroid abnormalities. Purpose: We investigated the correlation between thyroid function and metabolic derangement at onset and the influence...
8.
Cassio A, Corbetta C, Antonozzi I, Calaciura F, Caruso U, Cesaretti G, et al.
J Endocrinol Invest
. 2013 Feb;
36(3):195-203.
PMID: 23404215
The Italian screening program for primary congenital hypothyroidism (CH) is an integrated system including neonatal screening, diagnosis, treatment, follow-up, and nationwide surveillance of the disease. The aim of the Italian...
9.
Betterle C, Ghizzoni L, Cassio A, Baronio F, Cervato S, Garelli S, et al.
J Endocrinol Invest
. 2011 Nov;
35(10):877-81.
PMID: 22104652
Unlabelled: Autoimmune polyendocrinopathy-candidiasis-ectodermal- dystrophy (APECED), also known as autoimmune polyendocrine syndrome type 1 (APS-1), is a very rare disease. Diagnosis requires the presence of at least two of three major...
10.
Cassio A, Corrias A, Gualandi S, Tato L, Cesaretti G, Volta C, et al.
Clin Endocrinol (Oxf)
. 2006 Jan;
64(1):53-7.
PMID: 16402928
Objective: To evaluate the influence of sex as well as pubertal stage at diagnosis on the growth outcome of childhood thyrotoxicosis. Design: Retrospective, collaborative study. Patients And Methods: Longitudinal auxological...