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

Expression of MMP-2, MMP-9 and TIMP-2 in pituitary tumors and their relationship with cavernous sinus invasion.

垂体肿瘤中 MMP-2、MMP-9 和 TIMP-2 的表达及其与海绵窦侵犯的关系

Thé B Freire Ane Caroline, Jallad Raquel S, Batista Rafael L, Glezer Andrea, Machado Marcio C, Ochman Gilberto, Cescato Valter A, Cunha Neto Malebranche Berardo Carneiro, Frassetto Fernando P, de Medeiros Raphael S S, Trarbach Ericka B

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies

在患有垂体激素联合缺乏症的患者中发现的FGFR1和PROKR2罕见变异

Correa, Fernanda A; Trarbach, Ericka B; Tusset, Cintia; Latronico, Ana Claudia; Montenegro, Luciana R; Carvalho, Luciani R; Franca, Marcela M; Otto, Aline P; Costalonga, Everlayny F; Brito, Vinicius N; Abreu, Ana Paula; Nishi, Mirian Y; Jorge, Alexander A L; Arnhold, Ivo J P; Sidis, Yisrael; Pitteloud, Nelly; Mendonca, Berenice B

Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay

促性腺激素释放激素受体突变在青春期延迟患者中的作用

Beneduzzi, Daiane; Trarbach, Ericka B; Min, Le; Jorge, Alexander A L; Garmes, Heraldo M; Renk, Alessandra Covallero; Fichna, Marta; Fichna, Piotr; Arantes, Karina A; Costa, Elaine M F; Zhang, Anna; Adeola, Oluwaseun; Wen, Junping; Carroll, Rona S; Mendonça, Berenice B; Kaiser, Ursula B; Latronico, Ana Claudia; Silveira, Letícia F G

Copy number variation associated with Kallmann syndrome: new genetics insights from genome-wide studies

与卡尔曼综合征相关的拷贝数变异:来自全基因组研究的新遗传学见解

Trarbach, Ericka B

Nonsense mutations in FGF8 gene causing different degrees of human gonadotropin-releasing deficiency

FGF8基因的无义突变导致不同程度的人类促性腺激素释放激素缺乏症。

Trarbach, Ericka B; Abreu, Ana Paula; Silveira, Leticia Ferreira Gontijo; Garmes, Heraldo Mendes; Baptista, Maria Tereza M; Teles, Milena Gurgel; Costa, Elaine M F; Mohammadi, Moosa; Pitteloud, Nelly; Mendonca, Berenice B; Latronico, Ana Claudia