日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Late-onset dyshormonogenic goitrous hypothyroidism due to a homozygous mutation of the SLC26A7 gene: a case report

由SLC26A7基因纯合突变引起的迟发性甲状腺激素分泌异常性甲状腺肿:病例报告

Sciarroni, Elisabetta; Montanelli, Lucia; Di Cosmo, Caterina; Bagattini, Brunella; Comi, Simone; Pignata, Luisa; Brancatella, Alessandro; De Marco, Giuseppina; Ferrarini, Eleonora; Nencetti, Chiara; Sessa, Maria Rita; Latrofa, Francesco; Santini, Ferruccio; Tonacchera, Massimo; Agretti, Patrizia

Characterization of a novel mutation V136L in bone morphogenetic protein 15 identified in a woman affected by POI.

对一名患有 POI 的女性体内发现的骨形态发生蛋白 15 中的新突变 V136L 进行表征

Ferrarini Eleonora, De Marco Giuseppina, Orsolini Francesca, Gianetti Elena, Benelli Elena, Fruzzetti Franca, Simoncini Tommaso, Agretti Patrizia, Tonacchera Massimo

Clinical features, risk of mass enlargement, and development of endocrine hyperfunction in patients with adrenal incidentalomas: a long-term follow-up study

肾上腺偶发瘤患者的临床特征、肿块增大风险及内分泌功能亢进的发生:一项长期随访研究

Falcetta, Pierpaolo; Orsolini, Francesca; Benelli, Elena; Agretti, Patrizia; Vitti, Paolo; Di Cosmo, Caterina; Tonacchera, Massimo

Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism

在同一家族的四名成员中鉴定出一种新的pax8基因序列变异:从先天性甲状腺功能减退伴甲状腺发育不全到轻度亚临床甲状腺功能减退。

Vincenzi, Monica; Camilot, Marta; Ferrarini, Eleonora; Teofoli, Francesca; Venturi, Giacomo; Gaudino, Rossella; Cavarzere, Paolo; De Marco, Giuseppina; Agretti, Patrizia; Dimida, Antonio; Tonacchera, Massimo; Boner, Attilio; Antoniazzi, Franco

Metabolic engineering of the iodine content in Arabidopsis

拟南芥碘含量的代谢工程

Landini, Martina; Gonzali, Silvia; Kiferle, Claudia; Tonacchera, Massimo; Agretti, Patrizia; Dimida, Antonio; Vitti, Paolo; Alpi, Amedeo; Pinchera, Aldo; Perata, Pierdomenico