Xu Y - Search Results

1

A term neonate with early myoclonic encephalopathy caused by RARS2 gene variants: a case report.

Xu Y, Wu BB, Wang HJ, Zhou SZ, Cheng GQ, Zhou YF. Xu Y, et al. Transl Pediatr. 2020 Oct;9(5):707-712. doi: 10.21037/tp-20-110. Transl Pediatr. 2020. PMID: 33209735 Free PMC article.

2

Development and validation of Auto-Neo-electroencephalography (EEG) to estimate brain age and predict report conclusion for electroencephalography monitoring data in neonatal intensive care units.

Dong X, Kong Y, Xu Y, Zhou Y, Wang X, Xiao T, Chen B, Lu Y, Cheng G, Zhou W. Dong X, et al. Among authors: xu y. Ann Transl Med. 2021 Aug;9(16):1290. doi: 10.21037/atm-21-1564. Ann Transl Med. 2021. PMID: 34532427 Free PMC article.

3

Early initial video-electro-encephalography combined with variant location predict prognosis of KCNQ2-related disorder.

Xu Y, Dou YL, Chen X, Dong XR, Wang XH, Wu BB, Cheng GQ, Zhou YF. Xu Y, et al. BMC Pediatr. 2021 Oct 28;21(1):477. doi: 10.1186/s12887-021-02946-z. BMC Pediatr. 2021. PMID: 34711204 Free PMC article.

4

Generation of an induced pluripotent stem cell line (FDCHI007-A) derived from a patient with developmental and epileptic encephalopathy Type 31 carrying heterozygous c.545C > A mutation in DNM1 gene.

Xu Y, Wang X, Qiu T, Wang J, Wang Y, Wu B, Zhou Y. Xu Y, et al. Stem Cell Res. 2022 Apr;60:102709. doi: 10.1016/j.scr.2022.102709. Epub 2022 Feb 12. Stem Cell Res. 2022. PMID: 35184021 Free article.

5

Clinical Study of 30 Novel KCNQ2 Variants/Deletions in KCNQ2-Related Disorders.

Xiao T, Chen X, Xu Y, Chen H, Dong X, Yang L, Wu B, Chen L, Li L, Zhuang D, Chen D, Zhou Y, Wang H, Zhou W. Xiao T, et al. Among authors: xu y. Front Mol Neurosci. 2022 Apr 26;15:809810. doi: 10.3389/fnmol.2022.809810. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35557555 Free PMC article.

6

Identification of genetic characteristics in pediatric epilepsy with focal cortical dysplasia type 2 using deep whole-exome sequencing.

Xu Y, Zhao R, Wang M, Wang XH, Wang Y, Li H, Ma YY, Wu BB, Zhou YF. Xu Y, et al. Mol Genet Genomic Med. 2022 Dec;10(12):e2086. doi: 10.1002/mgg3.2086. Epub 2022 Nov 7. Mol Genet Genomic Med. 2022. PMID: 36342087 Free PMC article.

7

Brain development in newborns and infants after ECMO.

Yan K, Tang LK, Xiao FF, Zhang P, Cheng GQ, Wang LS, Lu CM, Ge MM, Hu LY, Zhou YF, Xiao TT, Xu Y, Yin ZQ, Yan GF, Lu GP, Li Q, Zhou WH. Yan K, et al. Among authors: xu y. World J Pediatr. 2024 Jan 19. doi: 10.1007/s12519-023-00768-w. Online ahead of print. World J Pediatr. 2024. PMID: 38238638 Review.

8

Physicians' perception toward non-invasive prenatal testing through the eye of the Rogers' diffusion of innovation theory in China.

Wei Y, Shi L, Ming J, He L, Xu Y, Chen Y. Wei Y, et al. Among authors: xu y. Int J Technol Assess Health Care. 2020 Jun;36(3):239-244. doi: 10.1017/S0266462320000136. Epub 2020 Apr 28. Int J Technol Assess Health Care. 2020. PMID: 32340647

9

Investigation on the frailty status of the elderly inpatients in Shanghai using the FRAIL (fatigue, resistance, ambulation, illness, and loss) questionnaire.

Wei Y, Cao Y, Yang X, Xu Y. Wei Y, et al. Among authors: xu y. Medicine (Baltimore). 2018 May;97(18):e0581. doi: 10.1097/MD.0000000000010581. Medicine (Baltimore). 2018. PMID: 29718855 Free PMC article.

10

Molecular characterization of fluoroquinolone-resistant Mycobacterium tuberculosis clinical isolates from Shanghai, China.

Zhu C, Zhang Y, Shen Y, Siu GK, Wu W, Qian X, Deng G, Xu Y, Lau R, Fan X, Zhang W, Lu H, Yam WC. Zhu C, et al. Among authors: xu y. Diagn Microbiol Infect Dis. 2012 Jul;73(3):260-3. doi: 10.1016/j.diagmicrobio.2012.03.025. Epub 2012 May 4. Diagn Microbiol Infect Dis. 2012. PMID: 22560167 Free article.

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