Similar articles for PMID: 31510723

Year	Number of Results
1994	1
2004	2
2006	2
2007	2
2008	4
2009	6
2010	9
2011	4
2012	3
2013	4
2014	4
2015	12
2016	14
2017	14
2018	12
2019	9
2020	13
2021	13
2022	12
2023	11
2024	0

1

[Clinical analysis of five cases of autism spectrum disorder complicated with epilepsy with chromosome copy number variation].

Li MY, Ye J, Huang ZY, Lin YC, Liu AH, Li LP, Chen J, Wang YP. Li MY, et al. Zhonghua Yi Xue Za Zhi. 2019 Sep 3;99(33):2615-2618. doi: 10.3760/cma.j.issn.0376-2491.2019.33.012. Zhonghua Yi Xue Za Zhi. 2019. PMID: 31510723 Chinese.

2

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.

Miller DT, Shen Y, Weiss LA, Korn J, Anselm I, Bridgemohan C, Cox GF, Dickinson H, Gentile J, Harris DJ, Hegde V, Hundley R, Khwaja O, Kothare S, Luedke C, Nasir R, Poduri A, Prasad K, Raffalli P, Reinhard A, Smith SE, Sobeih MM, Soul JS, Stoler J, Takeoka M, Tan WH, Thakuria J, Wolff R, Yusupov R, Gusella JF, Daly MJ, Wu BL. Miller DT, et al. J Med Genet. 2009 Apr;46(4):242-8. doi: 10.1136/jmg.2008.059907. Epub 2008 Sep 19. J Med Genet. 2009. PMID: 18805830 Free PMC article.

3

[Association between autism spectrum disorder and epilepsy in children].

Mei SL, Zhang Z, Liu X, Gao TT, Peng XX. Mei SL, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2017 May;19(5):549-554. doi: 10.7499/j.issn.1008-8830.2017.05.014. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 28506347 Free PMC article. Chinese.

4

[Analysis of clinical and genetic characteristics of epilepsy associated with chromosome 16p11.2 microdeletion].

Wang HS, Deng J, Wang XH, Chen CH, Wang X, Zhuo XW, Dai LF, Li H, Fang F. Wang HS, et al. Zhonghua Er Ke Za Zhi. 2022 Apr 2;60(4):339-344. doi: 10.3760/cma.j.cn112140-20211115-00953. Zhonghua Er Ke Za Zhi. 2022. PMID: 35385941 Chinese.

5

Clinical and Genetic Profile of Autism Spectrum Disorder-Epilepsy (ASD-E) Phenotype: Two Sides of the Same Coin!

Karunakaran S, Menon RN, Nair SS, Santhakumar S, Nair M, Sundaram S. Karunakaran S, et al. Clin EEG Neurosci. 2020 Nov;51(6):390-398. doi: 10.1177/1550059420909673. Epub 2020 Mar 2. Clin EEG Neurosci. 2020. PMID: 32114799

6

The effect of epilepsy on autistic symptom severity assessed by the social responsiveness scale in children with autism spectrum disorder.

Ko C, Kim N, Kim E, Song DH, Cheon KA. Ko C, et al. Behav Brain Funct. 2016 Jun 27;12(1):20. doi: 10.1186/s12993-016-0105-0. Behav Brain Funct. 2016. PMID: 27350381 Free PMC article.

7

15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.

Vanlerberghe C, Petit F, Malan V, Vincent-Delorme C, Bouquillon S, Boute O, Holder-Espinasse M, Delobel B, Duban B, Vallee L, Cuisset JM, Lemaitre MP, Vantyghem MC, Pigeyre M, Lanco-Dosen S, Plessis G, Gerard M, Decamp M, Mathieu M, Morin G, Jedraszak G, Bilan F, Gilbert-Dussardier B, Fauvert D, Roume J, Cormier-Daire V, Caumes R, Puechberty J, Genevieve D, Sarda P, Pinson L, Blanchet P, Lemeur N, Sheth F, Manouvrier-Hanu S, Andrieux J. Vanlerberghe C, et al. Eur J Med Genet. 2015 Mar;58(3):140-7. doi: 10.1016/j.ejmg.2015.01.002. Epub 2015 Jan 14. Eur J Med Genet. 2015. PMID: 25596525

8

[Analysis of gene mutation of early onset epileptic spasm with unknown reason].

Yang X, Pan G, Li WH, Zhang LM, Wu BB, Wang HJ, Zhang P, Zhou SZ. Yang X, et al. Zhonghua Er Ke Za Zhi. 2017 Nov 2;55(11):813-817. doi: 10.3760/cma.j.issn.0578-1310.2017.11.004. Zhonghua Er Ke Za Zhi. 2017. PMID: 29141310 Chinese.

9

Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.

Borlot F, Regan BM, Bassett AS, Stavropoulos DJ, Andrade DM. Borlot F, et al. JAMA Neurol. 2017 Nov 1;74(11):1301-1311. doi: 10.1001/jamaneurol.2017.1775. JAMA Neurol. 2017. PMID: 28846756 Free PMC article.

10

Behavioral characterization of dup15q syndrome: Toward meaningful endpoints for clinical trials.

DiStefano C, Wilson RB, Hyde C, Cook EH, Thibert RL, Reiter LT, Vogel-Farley V, Hipp J, Jeste S. DiStefano C, et al. Am J Med Genet A. 2020 Jan;182(1):71-84. doi: 10.1002/ajmg.a.61385. Epub 2019 Oct 26. Am J Med Genet A. 2020. PMID: 31654560 Free PMC article.

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