Chen S - Search Results

1

De novo variants of DEAF1 cause intellectual disability in six Chinese patients.

Chen S, Deng X, Xiong J, He F, Yang L, Chen B, Chen C, Zhang C, Yang L, Peng J, Yin F. Chen S, et al. Among authors: chen b, chen c. Clin Chim Acta. 2021 Jul;518:17-21. doi: 10.1016/j.cca.2021.02.026. Epub 2021 Mar 9. Clin Chim Acta. 2021. PMID: 33705764

2

The mutation of insulin receptor substrate-1 gene in Chinese patients with non-insulin-dependent diabetes mellitus.

Zeng W, Peng J, Wan X, Chen S, Song H. Zeng W, et al. Among authors: chen s. Chin Med J (Engl). 2000 Jan;113(1):80-3. doi: 10.3901/jme.2000.11.080. Chin Med J (Engl). 2000. PMID: 11775217

3

[Recurrent convulsion and pulmonary infection complicated by psychomotor retardation in an infant].

Xiong J, Peng J, Duan HL, Chen C, Wang XL, Chen SM, Yin F. Xiong J, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Feb;20(2):154-157. doi: 10.7499/j.issn.1008-8830.2018.02.014. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 29429466 Free PMC article. Chinese.

4

Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes.

Xiong J, Chen S, Pang N, Deng X, Yang L, He F, Wu L, Chen C, Yin F, Peng J. Xiong J, et al. Among authors: chen s, chen c. Front Neurosci. 2019 Apr 11;13:349. doi: 10.3389/fnins.2019.00349. eCollection 2019. Front Neurosci. 2019. PMID: 31031587 Free PMC article.

5

[Application of ventricular shunt for children with post-infective hydrocephalus].

Chen S, Peng J, Deng X, Wu L, Xiong J, Duan H, Peng P, Yin F. Chen S, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2019 Nov 28;44(11):1230-1237. doi: 10.11817/j.issn.1672-7347.2019.180345. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2019. PMID: 31919317 Free article. Chinese.

6

The Recommendations for the Management of Chinese Children With Epilepsy During the COVID-19 Outbreak.

Chen B, Kessi M, Chen S, Xiong J, Wu L, Deng X, Yang L, He F, Yin F, Peng J. Chen B, et al. Among authors: chen s. Front Pediatr. 2020 Aug 25;8:495. doi: 10.3389/fped.2020.00495. eCollection 2020. Front Pediatr. 2020. PMID: 32984209 Free PMC article.

7

Cardio-facio-cutaneous syndrome with BRAF gene mutation: A case report and literature review.

Chen B, Chen S, Xiong J, Yin F. Chen B, et al. Among authors: chen s. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2021 Apr 28;46(4):432-437. doi: 10.11817/j.issn.1672-7347.2021.190756. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2021. PMID: 33967092 Free PMC article. Review. Chinese, English.

8

Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patients.

Xiong J, Duan H, Chen S, Kessi M, He F, Deng X, Zhang C, Yang L, Peng J, Yin F. Xiong J, et al. Among authors: chen s. BMC Med Genomics. 2021 Jul 9;14(1):182. doi: 10.1186/s12920-021-01028-4. BMC Med Genomics. 2021. PMID: 34243774 Free PMC article.

9

Autism spectrum disorder and comorbid neurodevelopmental disorders (ASD-NDDs): Clinical and genetic profile of a pediatric cohort.

Chen S, Xiong J, Chen B, Zhang C, Deng X, He F, Yang L, Chen C, Peng J, Yin F. Chen S, et al. Among authors: chen b, chen c. Clin Chim Acta. 2022 Jan 1;524:179-186. doi: 10.1016/j.cca.2021.11.014. Epub 2021 Nov 17. Clin Chim Acta. 2022. PMID: 34800434

10

Urine Organic Acids as Metabolic Indicators for Global Developmental Delay/Intellectual Disability in Chinese Children.

Chen B, Zhan Y, Kessi M, Chen S, Xiong J, Deng X, Yang L, Peng J, Yin F, He F. Chen B, et al. Among authors: chen s. Front Mol Biosci. 2021 Dec 22;8:792319. doi: 10.3389/fmolb.2021.792319. eCollection 2021. Front Mol Biosci. 2021. PMID: 35036412 Free PMC article.

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