儿童多动症分子遗传学研究进展
被引量:1
Recent advances of study on the biogenetic of attention deficit hyperactivity disorder
摘要
儿童多动综合征 (ADHD)的病因至今未明 ,家系研究和流行病学资料表明 ,ADHD的病因至少部分与基因相关。随着分子遗传学技术的发展 ,近年来对ADHD的多个候选基因进行了探讨 。
出处
《国外医学(临床生物化学与检验学分册)》
2004年第6期545-546,550,共3页
Foreign Medical Sciences(section of Clinical Biochemistry and Laboratory Medicine
参考文献13
-
1Retz W,Thome J,Blocher D,et al.Association of attention deficit hyperactivity disorder-related psychopathology and personality traits with the serotonin transporter promoter region polymorphism.Neurosci Lett,2002,319(3):133-136.
-
2Swanson J,Osterlaan J,Murias M,et al.Attention deficit/hyperactivity disorder children with a 7-repeat allel of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychologecal tests of attention.Proc Nat1 Acad Sci
-
3Quist JF,Barr CL,Schachar R,et al.Evidence for the serotonin HTR2A receptor gene as a susceptibility factor in attention deficit hyperactivity disorder.Mol Psychiatry,2000,5(5):537-541.
-
4Jiang S,Xin R,Lin S,et al.Linkage studies between attention deficit hyperactivity disorder and the monoumine oxidase genes.Am J Med Genet,2001,105(8):783-788.
-
5Barr CL,Wigg K,Malone M,et al.Linkage study of catachol-o-methyltransferase and attention-deficit hyperactivity disorder.Am J Med Genet,1999,88(6):710-713.
-
6Warren RP,Odell JD,Warren WL,et al.Strong association of the third hypervariable region of HLA-DR beta 1 with autism.J Neuroimmunol,1996,67(2):97-102.
-
7Odell JD,Warren RP,Warren WL,et al.Association of genes within the major histocompatibility complex with attention deficit hyperactivity disorder.Neuropsychobiology,1997,35(4):181-186.
-
8Seeger G,Schloss P,Schmidt MH.Functional polymorphism within the promoter of the serotonin transporter gene is associated with severe hyperkinetic disorders.Mol Psychiatry,2001,6(2):235-238.
-
9Gill M,Daly G,Heron S,et al.Confirmation of association between attention deficit hyperactivity disorder and a dopamine transporter polymorphism.Mol Psychiatry,1997,2(4):211-213.
-
10Barr CL,Wigg KG,Wu J,et al.Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorder.Am J Med Genet,2000,96(1):114-117.
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-
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-
2黄秋玲,唐洪丽.多巴胺转运体与儿童注意缺陷障碍研究进展[J].国外医学(儿科学分册),2004,31(6):320-323. 被引量:1
-
3钱秋谨,王玉凤,周儒伦,杨莉,李君.多巴胺转运体蛋白基因G352A多态性与注意缺陷多动障碍的关联分析[J].北京大学学报(医学版),2004,36(6):626-629. 被引量:4
-
4张浩波,王玉凤,李君,汪冰,杨莉.多巴胺β羟化酶基因与伴破坏性行为障碍的注意缺陷多动障碍的关联分析[J].中华儿科杂志,2005,43(1):26-30. 被引量:13
-
5Bush G, Luu P, Posner MI. Cognitive and emotional influences in the anterior cingulated cortex. Trends Cogn Sci 2000;4(6):215-22.
-
6MacDonald AW 3rd, Cohen JD, Stenger VA, et al. Dissociating the rale of the dorslateral prefrontal and anterior cingulated cortex in cognitive contro.Science 2000;288 (5472): 1835-38.
-
7Wigg K, Zai G, Schachar R, et al. Attention deficit hyperactivity disorder and the gene for dopamine beta-hydroxyylase. A m J Psychiatry 2002;159(6):1046-48.
-
8Smith KM,Daly M,Fischer M,et al. Association of the dopamine betahydroxylase gene with attention deficit hyperactivity disorder:enetic analysis of the Mil waukee longitudinal study .Am JMed Genet 2003;119(1):77-85.
-
9Lubar JF.Neocortical dynamics:implications for understanding the role of neurofeedback and related techniques for the enhancement of attention.Appl Psychophysiol Biofeedback 1997;22(2):111-26.
-
10李雅妹,孙晓勉.注意缺陷障碍的脑电图研究进展[J].国外医学(儿科学分册),2003,30(4):200-202. 被引量:5
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-
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-
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-
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-
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-
5陈新.各型注意缺陷多动障碍患者脑电图的改变[J].临床神经病学杂志,2013,26(1):47-48. 被引量:3
-
6陈世英.多动症儿童认知注意损害与脑电变化病损机制[J].中国医药科学,2013,3(10):20-22. 被引量:2
-
7王玉英,王治国,王惠峰.儿童醒脑方联合经颅微电流刺激疗法治疗儿童注意力缺陷多动障碍症30例疗效观察[J].河北中医,2014,36(1):70-71.
-
8王真真,刘文龙,张娟,赵旭.常规脑电图在儿童注意缺陷多动障碍诊断中的应用[J].中国妇幼保健,2018,33(17):3947-3949. 被引量:4
-
9冯锴,王俊宏,任昕昕.从脑与“五神藏”的关系浅论儿童多动症病机关键[J].中医学报,2019,34(6):1137-1140. 被引量:10
-
10张洁,刘世燕,丁士炬.注意缺陷多动症患儿脑电图结果分析比较[J].大家健康(学术版),2014(24):61-61.
-
1王柠,陈万金,慕容慎行.我国神经遗传病学研究50年回顾[J].中华神经科杂志,2005,38(3):156-160. 被引量:2
-
2谢春格,谢秋幼,李洵桦.脊髓小脑性共济失调的分子遗传学研究进展[J].国际遗传学杂志,2008,31(5):373-376.
-
3张申,王俊岭(综述),唐北沙(审校).常染色体隐性遗传共济失调的临床及分子遗传学特征[J].卒中与神经疾病,2009,16(2):127-128.
-
4薛潮彪,洪晓虹.精神分裂症内表型与眼球运动测验研究[J].中华行为医学与脑科学杂志,2012,21(4):376-378. 被引量:2
-
5张玥.注意缺陷多动障碍的分子遗传学研究进展[J].医学文选,2006,25(2):314-316. 被引量:1
-
6邹海强,马敬红,赵保健.欧洲神经科学协会联盟关于神经遗传病的分子诊断指南:运动神经元病、周围神经病和肌肉病[J].中华临床医师杂志(电子版),2012,6(24):8295-8300. 被引量:1
-
7胡国芹,杨程青,张晨,易正辉.精神分裂症与5-羟色胺2A受体基因T102C多态性研究进展[J].中国神经精神疾病杂志,2014,40(6):383-384. 被引量:3
-
8李涛,刘协和,胡应.多巴胺转运体基因与双相情感障碍[J].中华医学遗传学杂志,1996,13(5):273-277. 被引量:3
-
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