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

Growth Hormone Withdrawal in Mid-Puberty: No Impact on Near Adult Height in Adolescents With Transient Idiopathic GHD

青春期中期生长激素撤退:对患有短暂性特发性生长激素缺乏症的青少年接近成年时的身高无影响

Vliegenthart, Joeri; Wit, Jan M; Bakker, Boudewijn; Boot, Annemieke M; de Bruin, Christiaan; Finken, Martijn J J; van der Heyden, Josine C; Hokken-Koelega, Anita C S; van der Kamp, Hetty J; van Mil, Edgar G; Sas, Theo C J; Schott, Dina A; van Setten, Petra; Straetemans, Saartje; van Tellingen, Vera; Touwslager, Robbert N H; van Trotsenburg, A S Paul; Voorhoeve, Paul G; Rings, Edmond H H M; van den Akker, Erica L T; van der Kaay, Danielle C M

Iodine deficiency in the first pregnancy trimester and intelligence in adolescence

妊娠早期碘缺乏与青春期智力

Keestra, Sarai M; Königs, Marsh; van Welie, Nienke; Dreyer, Kim; Oosterlaan, Jaap; Mijatovic, Velja; Roseboom, Tessa J; Finken, Martijn J J

Clustered cardiometabolic risk in pregnancy and dysmenorrhea in offspring: Results from a prospective birth cohort study

妊娠期聚集性心血管代谢风险与后代痛经:一项前瞻性出生队列研究的结果

Zhou, Siyu; Shkarpa, Nikol; Brouwer, Cathy; van den Boogaard, Emmy; Finken, Martijn J J; Twickler, Marcel Th B; Vrijkotte, Tanja G M

HRQoL in Adolescents with Idiopathic Isolated GHD: rhGH (Dis)continuation in Mid-Puberty

特发性孤立性生长激素缺乏症青少年患者的健康相关生活质量:青春期中期rhGH(停)用

Vliegenthart, Joeri; Busschbach, Jan; Rings, Edmond H H M; van den Akker, Erica L T; van der Kaay, Danielle C M; Bakker, Boudewijn; Boot, Annemieke M; de Bruin, Christiaan; Finken, Martijn J J; van der Heyden, Josine C; Hokken-Koelega, Anita C S; van der Kamp, Hetty J; van Mil, Edgar G; Sas, Theo C J; Schott, D A; van Setten, Petra A; Straetemans, Saartje; van Tellingen, Vera; Touwslager, Robbert N H; Paul van Trotsenburg, A S; Voorhoeve, Paul G; Wit, Jan M

Maternal thyroid function in the first half of pregnancy and neurodevelopmental outcomes in early adolescence in the Amsterdam Born Children and their Development (ABCD) cohort

阿姆斯特丹出生儿童及其发展(ABCD)队列研究中,孕早期母亲甲状腺功能与青春期早期神经发育结果的关系

Keestra, Sarai M; de Rooij, Susanne R; Roseboom, Tessa J; Königs, Marsh; Vrijkotte, Tanja Gm; Finken, Martijn J J

Long-term child outcomes after prenatal aspirin exposure: A 4-year follow-up of a randomized controlled trial (the APRIL study)

产前服用阿司匹林对儿童长期影响:一项随机对照试验的 4 年随访(APRIL 研究)

van Limburg Stirum, Emilie V J; van 't Hooft, Janneke; Landman, Anadeijda J E M C; Finken, Martijn J J; Ravelli, Anita C J; Leemhuis, Aleid G; Pajkrt, Eva; Oudijk, Martijn A; de Boer, Marjon A

Development of 24-Hour Rhythms in Cortisol Secretion Across Infancy: A Systematic Review and Meta-Analysis of Individual Participant Data

婴儿期皮质醇分泌24小时节律的发育:基于个体参与者数据的系统评价和荟萃分析

Kervezee, Laura; Romijn, Michelle; van de Weijer, Kirsten N G; Chen, Britney S J; Burchell, George L; Tollenaar, Marieke S; Tamayo-Ortiz, Marcela; Philbrook, Lauren E; de Weerth, Carolina; Cao, Yang; Rotteveel, Joost; Eiden, Rina D; Azar, Rima; Bush, Nicole R; Chis, Adina; Kmita, Grazyna; Clearfield, Melissa W; Beijers, Roseriet; Gröschl, Michael; Wudy, Stefan A; Kalsbeek, Andries; Mörelius, Evalotte; Finken, Martijn J J

Identification of a Novel CYP11B2 Variant in a Family with Varying Degrees of Aldosterone Synthase Deficiency

在一个患有不同程度醛固酮合酶缺乏症的家族中发现一种新的 CYP11B2 变异

Mark R. Garrelfs, Tuula Rinne, Jacquelien J. Hillebrand, Peter Lauffer, Merijn W. Bijlsma, Hedi L Claahsen-van der Grinten, Nicole de Leeuw, Martijn J. J. Finken, Joost Rotteveel, Nitash Zwaveling-Soonawala, Max Nieuwdorp, A. S. Paul van Trotsenburg, Christiaan F. Mooij

Neurodevelopmental outcomes of school-age children conceived after hysterosalpingography with oil-based or water-based iodinated contrast: long-term follow-up of a nationwide randomized controlled trial

使用油基或水基碘造影剂进行子宫输卵管造影后受孕的学龄儿童的神经发育结局:一项全国性随机对照试验的长期随访

Keestra, Sarai M; Van Welie, Nienke; Dreyer, Kim; Van Eekelen, Rik; Roseboom, Tessa J; Oosterlaan, Jaap; Mol, Ben W; Finken, Martijn J J; Mijatovic, Velja; Königs, Marsh

Biallelic variants in the SLC13A1 sulfate transporter gene cause hyposulfatemia with a mild spondylo-epi-metaphyseal dysplasia

SLC13A1硫酸盐转运蛋白基因的双等位基因变异会导致低硫酸血症,并伴有轻度脊椎骨骺干骺端发育不良。

van de Kamp, Jiddeke M; Bökenkamp, Arend; Smith, Desiree E C; Wamelink, Mirjam M C; Jansen, Erwin E W; Struys, Eduard A; Waisfisz, Quinten; Verkleij, Marieke; Hartmann, Michaela F; Wang, Rong; Wudy, Stefan A; Paganini, Chiara; Rossi, Antonio; Finken, Martijn J J