1 陈静, GarraldaM, 程文红. ICD-11精神与行为障碍(草案)关于神经发育障碍诊断标准的进展[J]. 中华精神科杂志, 2017, 50(6): 411-413. DOI: 10.3760/cma.j.issn.1006-7884.2017.06.003.
2 Thapar A, Cooper M, Rutter M. Neurodevelopmental disorders[J]. Lancet Psychiatry, 2017, 4(4): 339-346. PMID: 27979720. DOI: 10.1016/S2215-0366(16)30376-5.
3 Thomas R, Sanders S, Doust J, et al. Prevalence of attention-deficit/hyperactivity disorder: a systematic review and meta-analysis[J]. Pediatrics, 2015, 135(4): e994-e1001. PMID: 25733754. DOI: 10.1542/peds.2014-3482.
4 Maenner MJ, Shaw KA, Bakian AV, et al. Prevalence and characteristics of autism spectrum disorder among children aged 8 years—autism and developmental disabilities monitoring network, 11 sites, United States, 2018[J]. MMWR Surveill Summ, 2021, 70(11): 1-16. PMID: 34855725. PMCID: PMC8639024. DOI: 10.15585/mmwr.ss7011a1.
5 辛莹莹, 孙丹, 刘智胜. 儿童抽动障碍及其共患病治疗进展[J]. 中华儿科杂志, 2022, 60(3): 263-266. PMID: 35240753. DOI: 10.3760/cma.j.cn112140-20210806-00653.
6 中华医学会儿科学分会神经学组, 中国医师协会神经内科分会儿童神经疾病专业委员会. 儿童智力障碍或全面发育迟缓病因诊断策略专家共识[J]. 中华儿科杂志, 2018, 56(11): 806-810. PMID: 30392203. DOI: 10.3760/cma.j.issn.0578-1310.2018.11.003.
7 Homberg JR, Kyzar EJ, Nguyen M, et al. Understanding autism and other neurodevelopmental disorders through experimental translational neurobehavioral models[J]. Neurosci Biobehav Rev, 2016, 65: 292-312. PMID: 27048961. DOI: 10.1016/j.neubiorev.2016.03.013.
8 张红梅, 薛曼, 王斌, 等. 孤独症谱系障碍早期遗传诊断和治疗研究进展[J]. 中华精神科杂志, 2022, 55(3): 232-237. DOI: 10.3760/cma.j.cn113661-20211123-00339.
9 Freeman RD, Fast DK, Burd L, et al. An international perspective on Tourette syndrome: selected findings from 3,500 individuals in 22 countries[J]. Dev Med Child Neurol, 2000, 42(7): 436-447. PMID: 10972415. DOI: 10.1017/s0012162200000839.
10 Piton A, Redin C, Mandel JL. XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing[J]. Am J Hum Genet, 2013, 93(2): 368-383. PMID: 23871722. PMCID: PMC3738825. DOI: 10.1016/j.ajhg.2013.06.013.
11 Topper S, Ober C, Das S. Exome sequencing and the genetics of intellectual disability[J]. Clin Genet, 2011, 80(2): 117-126. PMID: 21627642. PMCID: PMC4343531. DOI: 10.1111/j.1399-0004.2011.01720.x.
12 Miles JH. Autism spectrum disorders—a genetics review[J]. Genet Med, 2011, 13(4): 278-294. PMID: 21358411. DOI: 10.1097/GIM.0b013e3181ff67ba.
13 Ben-Shachar S, Lanpher B, German JR, et al. Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders[J]. J Med Genet, 2009, 46(6): 382-388. PMID: 19289393. PMCID: PMC2776649. DOI: 10.1136/jmg.2008.064378.
14 彭镜, 尹飞. 重视儿童神经发育障碍性疾病的病因及临床研究[J]. 中国医师杂志, 2018, 20(9): 1281-1283. DOI: 10.3760/cma.j.issn.1008-1372.2018.09.001.
15 黄开拓, 张烨, 赵睿, 等. 孤独症谱系障碍的遗传学研究进展[J]. 中华医学遗传学杂志, 2022, 39(1): 103-107. PMID: 34964979. DOI: 10.3760/cma.j.cn511374-20201012-00710.
16 Vissers LE, Gilissen C, Veltman JA. Genetic studies in intellectual disability and related disorders[J]. Nat Rev Genet, 2016, 17(1): 9-18. PMID: 26503795. DOI: 10.1038/nrg3999.
17 Rojas-Charry L, Nardi L, Methner A, et al. Abnormalities of synaptic mitochondria in autism spectrum disorder and related neurodevelopmental disorders[J]. J Mol Med (Berl), 2021, 99(2): 161-178. PMID: 33340060. PMCID: PMC7819932. DOI: 10.1007/s00109-020-02018-2.
18 Wang C, Geng H, Liu W, et al. Prenatal, perinatal, and postnatal factors associated with autism: a meta-analysis[J]. Medicine (Baltimore), 2017, 96(18): e6696. PMID: 28471964. PMCID: PMC5419910. DOI: 10.1097/MD.0000000000006696.
19 Saxena R, Babadi M, Namvarhaghighi H, et al. Role of environmental factors and epigenetics in autism spectrum disorders[J]. Prog Mol Biol Transl Sci, 2020, 173: 35-60. PMID: 32711816. DOI: 10.1016/bs.pmbts.2020.05.002.
20 Thapar A, Cooper M. Attention deficit hyperactivity disorder[J]. Lancet, 2016, 387(10024): 1240-1250. PMID: 26386541. DOI: 10.1016/S0140-6736(15)00238-X.
21 刘雨睿, 刘静, 罗娟, 等. 157例语言发育迟缓儿童的发育特征及影响因素分析[J]. 内蒙古医学杂志, 2019, 51(2): 135-137. DOI: 10.16096/J.cnki.nmgyxzz.2019.51.02.003.
22 Han VX, Patel S, Jones HF, et al. Maternal immune activation and neuroinflammation in human neurodevelopmental disorders[J]. Nat Rev Neurol, 2021, 17(9): 564-579. PMID: 34341569. DOI: 10.1038/s41582-021-00530-8.
23 Filipello F, Morini R, Corradini I, et al. The microglial innate immune receptor TREM2 is required for synapse elimination and normal brain connectivity[J]. Immunity, 2018, 48(5): 979-991.e8. PMID: 29752066. DOI: 10.1016/j.immuni.2018.04.016.
24 Shen L, Zhang K, Feng C, et al. iTRAQ-based proteomic analysis reveals protein profile in plasma from children with autism[J]. Proteomics Clin Appl, 2018, 12(3): e1700085. PMID: 29274201. DOI: 10.1002/prca.201700085.
25 Parker-Athill EC, Ehrhart J, Tan J, et al. Cytokine correlations in youth with tic disorders[J]. J Child Adolesc Psychopharmacol, 2015, 25(1): 86-92. PMID: 25658821. PMCID: PMC4340338. DOI: 10.1089/cap.2014.0103.
26 Sharma SR, Gonda X, Tarazi FI. Autism spectrum disorder: classification, diagnosis and therapy[J]. Pharmacol Ther, 2018, 190: 91-104. PMID: 29763648. DOI: 10.1016/j.pharmthera.2018.05.007.
27 Dan Z, Mao X, Liu Q, et al. Altered gut microbial profile is associated with abnormal metabolism activity of autism spectrum disorder[J]. Gut Microbes, 2020, 11(5): 1246-1267. PMID: 32312186. PMCID: PMC7524265. DOI: 10.1080/19490976.2020.1747329.
28 Strati F, Cavalieri D, Albanese D, et al. New evidences on the altered gut microbiota in autism spectrum disorders[J]. Microbiome, 2017, 5(1): 24. PMID: 28222761. PMCID: PMC5320696. DOI: 10.1186/s40168-017-0242-1.
29 Wright CF, FitzPatrick DR, Firth HV. Paediatric genomics: diagnosing rare disease in children[J]. Nat Rev Genet, 2018, 19(5): 253-268. PMID: 29398702. DOI: 10.1038/nrg.2017.116.
30 Bednarz HM, Kana RK. Advances, challenges, and promises in pediatric neuroimaging of neurodevelopmental disorders[J]. Neurosci Biobehav Rev, 2018, 90: 50-69. PMID: 29608989. DOI: 10.1016/j.neubiorev.2018.03.025.
31 张漫雪, 黄颐. 孤独症与多动症神经影像学比较研究进展[J]. 临床精神医学杂志, 2019, 29(3): 208-209. DOI: 10.3969/j.issn.1005-3220.2019.03.022.
32 胡爽, 李红, 张雅清, 等. 儿童孤独症的神经影像学研究进展[J]. 磁共振成像, 2021, 12(11): 105-108. DOI: 10.12015/issn.1674-8034.2021.11.026.
33 Jeste SS, Frohlich J, Loo SK. Electrophysiological biomarkers of diagnosis and outcome in neurodevelopmental disorders[J]. Curr Opin Neurol, 2015, 28(2): 110-116. PMID: 25710286. PMCID: PMC7334029. DOI: 10.1097/WCO.0000000000000181.
34 Khan MU, Aslani P. A review of factors influencing the three phases of medication adherence in people with attention-deficit/hyperactivity disorder[J]. J Child Adolesc Psychopharmacol, 2019, 29(6): 398-418. PMID: 31120328. DOI: 10.1089/cap.2018.0153.
35 Zyga O, Russ SW, Meeker H, et al. A preliminary investigation of a school-based musical theater intervention program for children with intellectual disabilities[J]. J Intellect Disabil, 2018, 22(3): 262-278. PMID: 28355942. DOI: 10.1177/1744629517699334.
36 刘乐, 钱昀, 江文庆, 等. 团体音乐治疗对注意缺陷多动障碍患儿治疗效果的研究[J]. 中国儿童保健杂志, 2020, 28(4): 399-402, 406. DOI: 10.11852/zgetbjzz2019-1489.
37 Habib M, Lardy C, Desiles T, et al. Music and dyslexia: a new musical training method to improve reading and related disorders[J]. Front Psychol, 2016, 7: 26. PMID: 26834689. PMCID: PMC4722115. DOI: 10.3389/fpsyg.2016.00026.
38 孟甜甜, 王朝晖. 经颅磁刺激在神经发育障碍性疾病中的应用进展[J]. 中国儿童保健杂志, 2020, 28(3): 292-294. DOI: 10.11852/zgetbjzz2019-0175.
39 Jensen NJ, Wodschow HZ, Nilsson M, et al. Effects of ketone bodies on brain metabolism and function in neurodegenerative diseases[J]. Int J Mol Sci, 2020, 21(22): 8767. PMID: 33233502. PMCID: PMC7699472. DOI: 10.3390/ijms21228767.
40 Kang DW, Adams JB, Vargason T, et al. Distinct fecal and plasma metabolites in children with autism spectrum disorders and their modulation after microbiota transfer therapy[J]. mSphere, 2020, 5(5): e00314-20. PMID: 33087514. PMCID: PMC7580952. DOI: 10.1128/mSphere.00314-20.
41 Zhao H, Shi Y, Luo X, et al. The effect of fecal microbiota transplantation on a child with Tourette syndrome[J]. Case Rep Med, 2017, 2017: 6165239. PMID: 29666652. PMCID: PMC5865276. DOI: 10.1155/2017/6165239.
42 Daily JL, Nash K, Jinwal U, et al. Adeno-associated virus-mediated rescue of the cognitive defects in a mouse model for Angelman syndrome[J]. PLoS One, 2011, 6(12): e27221. PMID: 22174738. PMCID: PMC3235088. DOI: 10.1371/journal.pone.0027221.