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

Incorporating health literacy in education for socially disadvantaged adults: an Australian feasibility study

将健康素养融入社会弱势成年人的教育:一项澳大利亚可行性研究

Muscat, Danielle M; Smith, Sian; Dhillon, Haryana M; Morony, Suzanne; Davis, Esther L; Luxford, Karen; Shepherd, Heather L; Hayen, Andrew; Comings, John; Nutbeam, Don; McCaffery, Kirsten

Evaluation of an Australian health literacy training program for socially disadvantaged adults attending basic education classes: study protocol for a cluster randomised controlled trial

一项针对参加基础教育课程的社会弱势成年人的澳大利亚健康素养培训项目的评估:一项整群随机对照试验的研究方案

McCaffery, Kirsten J; Morony, Suzanne; Muscat, Danielle M; Smith, Sian K; Shepherd, Heather L; Dhillon, Haryana M; Hayen, Andrew; Luxford, Karen; Meshreky, Wedyan; Comings, John; Nutbeam, Don

Maternal age as a potential explanation of the role of the L allele of the serotonin transporter gene in anxiety and depression in Asians

母亲年龄可能是血清素转运蛋白基因L等位基因在亚洲人焦虑和抑郁中发挥作用的潜在解释因素

Comings, David E; MacMurray, James P

Activation instead of blocking mesolimbic dopaminergic reward circuitry is a preferred modality in the long term treatment of reward deficiency syndrome (RDS): a commentary

激活而非阻断中脑边缘多巴胺奖赏回路是治疗奖赏缺乏综合征(RDS)的首选方法:评述

Blum, Kenneth; Chen, Amanda Lih Chuan; Chen, Thomas J H; Braverman, Eric R; Reinking, Jeffrey; Blum, Seth H; Cassel, Kimberly; Downs, Bernard W; Waite, Roger L; Williams, Lonna; Prihoda, Thomas J; Kerner, Mallory M; Palomo, Tomas; Comings, David E; Tung, Howard; Rhoades, Patrick; Oscar-Berman, Marlene

Towards a healthy baby: Congenital disorders and the new genetics in primary health care

迈向健康婴儿:先天性疾病与初级保健中的新遗传学

Lewis, Lara C; Chen, Lingyan; Hameed, L Shahul; Kitchen, Robert R; Maroteau, Cyrielle; Nagarajan, Shilpa R; Norlin, Jenny; Daly, Charlotte E; Szczerbinska, Iwona; Hjuler, Sara Toftegaard; Patel, Rahul; Livingstone, Eilidh J; Durrant, Tom N; Wondimu, Elisabeth; BasuRay, Soumik; Chandran, Anandhakumar; Lee, Wan-Hung; Hu, Sile; Gilboa, Barak; Grandi, Megan E; Toledo, Enrique M; Erikat, Abdullah H A; Hodson, Leanne; Haynes, William G; Pursell, Natalie W; Coppieters, Ken; Fleckner, Jan; Howson, Joanna M M; Andersen, Birgitte; Ruby, Maxwell A; Stevenson, Alan C; Herndon, C N; Comings, David E; Comings, David E; McPherson, Elizabeth

Evidence for an X-linked modifier gene affecting the expression of Tourette syndrome and its relevance to the increased frequency of speech, cognitive, and behavioral disorders in males

证据表明,X染色体连锁修饰基因会影响图雷特综合征的表达,并且与男性言语、认知和行为障碍发生率增加有关。

Comings, D E; Comings, B G

Medical genetics principles and practice

医学遗传学原理与实践

Verardo, Lucas Lima; Brito, Luiz F; Carolino, Nuno; Magalhães, Ana Fabrícia Braga; Brock, D J H; Comings, David E

Congenital and acquired cognitive disorders

先天性和后天性认知障碍

Jiratchariyakul, Weena; Beerhues, Ludger; Mahady, Gail B; Kummalue, Tanawan; Vongsakul, Molvibha; Tambuyzer, Tim; Ahmed, Tariq; Berckmans, Daniel; Balschun, Detlef; Aerts, Jean-Marie; Comings, David E

The biochemical genetics of man

人类的生物化学遗传学

Iversen, O H; Comings, David E

Determination of subfractions of amniotic fluid alpha-fetoprotein in diagnosing spina bifida and congenital nephrosis

羊水中甲胎蛋白亚组分的测定在脊柱裂和先天性肾病诊断中的应用

Ruoslahti, E; Pekkala, A; Comings, D E; Seppålå, M