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

Age dependency of body mass index distribution in childhood and adolescent inpatients with anorexia nervosa with a focus on DSM-5 and ICD-11 weight criteria and severity specifiers

儿童和青少年神经性厌食症住院患者的体重指数分布与年龄的关系,重点关注DSM-5和ICD-11体重标准和严重程度指标

Engelhardt, Christian; Föcker, Manuel; Bühren, Katharina; Dahmen, Brigitte; Becker, Katja; Weber, Linda; Correll, Christoph U; Egberts, Karin Maria; Ehrlich, Stefan; Roessner, Veit; Fleischhaker, Christian; von Gontard, Alexander; Hahn, Freia; Jenetzky, Ekkehart; Kaess, Michael; Legenbauer, Tanja; Renner, Tobias J; Schulze, Ulrike M E; Sinzig, Judith; Wessing, Ida; Antony, Gisela; Herpertz-Dahlmann, Beate; Peters, Triinu; Hebebrand, Johannes

Reasons for admission and variance of body weight at referral in female inpatients with anorexia nervosa in Germany

德国女性神经性厌食症住院患者的入院原因及转诊时体重变化

Peters, Triinu; Kolar, David; Föcker, Manuel; Bühren, Katharina; Dahmen, Brigitte; Becker, Katja; Weber, Linda; Correll, Christoph U; Jaite, Charlotte; Egberts, Karin M; Romanos, Marcel; Ehrlich, Stefan; Seidel, Maria; Roessner, Veit; Fleischhaker, Christian; von Gontard, Alexander; Hahn, Freia; Huss, Michael; Kaess, Michael; Legenbauer, Tanja; Renner, Tobias J; Schulze, Ulrike M E; Sinzig, Judith; Wessing, Ida; Antony, Gisela; Herpertz-Dahlmann, Beate; Gradl-Dietsch, Gertraud; Hebebrand, Johannes

Seasonal variation of BMI at admission in German adolescents with anorexia nervosa

德国青少年神经性厌食症患者入院时BMI的季节性变化

Kolar, David R; Bühren, Katharina; Herpertz-Dahlmann, Beate; Becker, Katja; Egberts, Karin; Ehrlich, Stefan; Fleischhaker, Christian; von Gontard, Alexander; Hahn, Freia; Huss, Michael; Jaite, Charlotte; Kaess, Michael; Legenbauer, Tanja; Renner, Tobias J; Roessner, Veit; Schulze, Ulrike; Sinzig, Judith; Wessing, Ida; Hebebrand, Johannes; Föcker, Manuel; Jenetzky, Ekkehart

Diagnostic and Clinical Management of Skull Fractures in Children

儿童颅骨骨折的诊断和临床处理

Arneitz, Christoph; Sinzig, Maria; Fasching, Günter

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

全基因组罕见拷贝数变异分析揭示PARK2是注意力缺陷/多动障碍的候选基因

Jarick, I; Volckmar, A-L; Pütter, C; Pechlivanis, S; Nguyen, T T; Dauvermann, M R; Beck, S; Albayrak, Ö; Scherag, S; Gilsbach, S; Cichon, S; Hoffmann, P; Degenhardt, F; Nöthen, M M; Schreiber, S; Wichmann, H-E; Jöckel, K-H; Heinrich, J; Tiesler, C M T; Faraone, S V; Walitza, S; Sinzig, J; Freitag, C; Meyer, J; Herpertz-Dahlmann, B; Lehmkuhl, G; Renner, T J; Warnke, A; Romanos, M; Lesch, K-P; Reif, A; Schimmelmann, B G; Hebebrand, J; Scherag, A; Hinney, A

Rare mutations of CACNB2 found in autism spectrum disease-affected families alter calcium channel function

在自闭症谱系障碍患者家族中发现的CACNB2罕见突变会改变钙通道功能。

Breitenkamp, Alexandra F S; Matthes, Jan; Nass, Robert Daniel; Sinzig, Judith; Lehmkuhl, Gerd; Nürnberg, Peter; Herzig, Stefan

IL-1β-driven neutrophilia preserves antibacterial defense in the absence of the kinase IKKβ

IL-1β 驱动的中性粒细胞增多症在缺乏激酶 IKKβ 的情况下保留了抗菌防御能力

Li-Chung Hsu, Thomas Enzler, Jun Seita, Anjuli M Timmer, Chih-Yuan Lee, Ting-Yu Lai, Guann-Yi Yu, Liang-Chuan Lai, Vladislav Temkin, Ursula Sinzig, Thiha Aung, Victor Nizet, Irving L Weissman, Michael Karin

Aortic development and anomalies

主动脉发育和异常

Kau, Thomas; Sinzig, Marietta; Gasser, Johann; Lesnik, Gerald; Rabitsch, Egon; Celedin, Stefan; Eicher, Wolfgang; Illiasch, Herbert; Hausegger, Klaus Armin