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

SUN-441 Crinecerfont Shows Favorable Trends in Improving Clinical Outcomes in Children and Adolescents With Classic Congenital Adrenal Hyperplasia: 1-Year Results From the CAHtalyst™ Pediatric Study

SUN-441 Crinecerfont 在改善经典型先天性肾上腺皮质增生症患儿和青少年的临床结局方面显示出良好的趋势:CAHtalyst™ 儿科研究的 1 年结果

Yang, Xue; Yao, Xiao; Qiu, Yinyuan; Sarafoglou, Kyriakie; Lekarev, Oksana; Loechner, Karen; Yang, Ming; Mick, Gail J; Dattani, Mehul T; Bettendorf, Markus; Clemente, Maria; Salerno, Mariacarolina; Farber, Robert H; Chan, Jean L; Rosales, Gelliza B G; Jeha, George S

Access to care among patients with osteogenesis imperfecta during the COVID-19 pandemic

COVID-19 大流行期间成骨不全患者的就医情况

Malina, Sara N; Flanagan, Jill C; Loechner, Karen J; Wu, Malinda

Biased Maintenance of Attention on Sad Faces in Clinically Depressed Youth: An Eye-Tracking Study

临床抑郁症青少年对悲伤面孔的注意力维持存在偏向性:一项眼动追踪研究

Buhl, Christina; Sfärlea, Anca; Loechner, Johanna; Starman-Wöhrle, Kornelija; Salemink, Elske; Schulte-Körne, Gerd; Platt, Belinda

Insulinoma in an adolescent female with weight loss: a case report and literature review on pediatric insulinomas

青少年女性体重减轻并发胰岛素瘤:病例报告及儿科胰岛素瘤文献综述

Gupta, Pranav; Loechner, Karen; Patterson, Briana C; Felner, Eric

Emotion Regulation as a Mediator in the Relationship Between Cognitive Biases and Depressive Symptoms in Depressed, At-risk and Healthy Children and Adolescents

情绪调节在认知偏差与抑郁症、高危抑郁症和健康儿童及青少年抑郁症状关系中的中介作用

Sfärlea, A; Takano, K; Buhl, C; Loechner, J; Greimel, E; Salemink, E; Schulte-Körne, G; Platt, B

Risk of Depression in the Offspring of Parents with Depression: The Role of Emotion Regulation, Cognitive Style, Parenting and Life Events

父母患有抑郁症的子女患抑郁症的风险:情绪调节、认知风格、养育方式和生活事件的作用

Loechner, Johanna; Sfärlea, Anca; Starman, Kornelija; Oort, Frans; Thomsen, Laura Asperud; Schulte-Körne, Gerd; Platt, Belinda

Qualitative evaluation of a preventive intervention for the offspring of parents with a history of depression

对有抑郁症病史的父母的子女进行预防性干预的定性评估

Claus, Nathalie; Marzano, Lisa; Loechner, Johanna; Starman, Kornelija; Voggt, Alessandra; Loy, Fabian; Wermuth, Inga; Haemmerle, Stephanie; Engelmann, Lina; Bley, Mirjam; Schulte-Koerne, Gerd; Platt, Belinda

How to assess communication skills? Development of the rating scale ComOn Check

如何评估沟通技巧?ComOn Check 评分量表的开发

Radziej, K; Loechner, J; Engerer, C; Niglio de Figueiredo, M; Freund, J; Sattel, H; Bachmann, C; Berberat, P O; Dinkel, A; Wuensch, A

Generalized arterial calcification of infancy and pseudoxanthoma elasticum can be caused by mutations in either ENPP1 or ABCC6

婴儿期全身性动脉钙化和假性黄色瘤可由ENPP1或ABCC6基因突变引起。

Nitschke, Yvonne; Baujat, Geneviève; Botschen, Ulrike; Wittkampf, Tanja; du Moulin, Marcel; Stella, Jacqueline; Le Merrer, Martine; Guest, Geneviève; Lambot, Karen; Tazarourte-Pinturier, Marie-Frederique; Chassaing, Nicolas; Roche, Olivier; Feenstra, Ilse; Loechner, Karen; Deshpande, Charu; Garber, Samuel J; Chikarmane, Rashmi; Steinmann, Beat; Shahinyan, Tatevik; Martorell, Loreto; Davies, Justin; Smith, Wendy E; Kahler, Stephen G; McCulloch, Mignon; Wraige, Elizabeth; Loidi, Lourdes; Höhne, Wolfgang; Martin, Ludovic; Hadj-Rabia, Smaïl; Terkeltaub, Robert; Rutsch, Frank

Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management

Kir6.2 (KCNJ11) V290M 突变纯合子和杂合子携带者先天性高胰岛素血症和葡萄糖敏感性增高:K(ATP) 通道失活机制及临床治疗

Loechner, Karen J; Akrouh, Alejandro; Kurata, Harley T; Dionisi-Vici, Carlo; Maiorana, Arianna; Pizzoferro, Milena; Rufini, Vittoria; de Ville de Goyet, Jean; Colombo, Carlo; Barbetti, Fabrizio; Koster, Joseph C; Nichols, Colin G