Li J - Search Results

1

Regional cerebral activity abnormality in pregnant women with antenatal depression.

Cheng B, Wang X, Zhou Y, Li J, Zhao Y, Xia S, Zuo Y, Meng Y, Deng W, Guo Y, Wang S. Cheng B, et al. Among authors: li j. J Affect Disord. 2020 Sep 1;274:381-388. doi: 10.1016/j.jad.2020.05.107. Epub 2020 May 23. J Affect Disord. 2020. PMID: 32663967

2

Cerebral Regional Homogeneity Alternation of Pregnant Women With Antenatal Depression During the Pandemic.

Cheng B, Meng Y, Zhou Y, Li J, Zeng J, Tan X, Zhang K, Luo Y, Zhang Y. Cheng B, et al. Among authors: li j. Front Psychiatry. 2021 Apr 20;12:627871. doi: 10.3389/fpsyt.2021.627871. eCollection 2021. Front Psychiatry. 2021. PMID: 33959047 Free PMC article.

3

Novel mutation in the ASXL3 gene in a Chinese boy with microcephaly and speech impairment: A case report.

Li JR, Huang Z, Lu Y, Ji QY, Jiang MY, Yang F. Li JR, et al. World J Clin Cases. 2020 Dec 26;8(24):6465-6472. doi: 10.12998/wjcc.v8.i24.6465. World J Clin Cases. 2020. PMID: 33392332 Free PMC article.

4

Could early life DHA supplementation benefit neurodevelopment? A systematic review and meta-analysis.

Hu R, Xu J, Hua Y, Li Y, Li J. Hu R, et al. Among authors: li y, li j. Front Neurol. 2024 Apr 5;15:1295788. doi: 10.3389/fneur.2024.1295788. eCollection 2024. Front Neurol. 2024. PMID: 38645744 Free PMC article.

5

Menkes disease diagnosed by a novel ATP7A frameshift mutation in a patient with infantile spasms-a case report.

Li J, Hu R, Wang J, Yu R, Xiong F, Jiang M. Li J, et al. Transl Pediatr. 2021 Jul;10(7):1965-1971. doi: 10.21037/tp-21-275. Transl Pediatr. 2021. PMID: 34430447 Free PMC article.

6

A de novo heterozygous variant in KAT6A is associated with a newly named neurodevelopmental disorder Arboleda-Tham syndrome-a case report.

Jiang M, Yang L, Wu J, Xiong F, Li J. Jiang M, et al. Among authors: li j. Transl Pediatr. 2021 Jun;10(6):1748-1754. doi: 10.21037/tp-21-206. Transl Pediatr. 2021. PMID: 34295791 Free PMC article.

7

A novel frameshift mutation of DVL1-induced Robinow syndrome: A case report and literature review.

Hu R, Qiu Y, Li Y, Li J. Hu R, et al. Among authors: li y, li j. Mol Genet Genomic Med. 2022 Mar;10(3):e1886. doi: 10.1002/mgg3.1886. Epub 2022 Feb 9. Mol Genet Genomic Med. 2022. PMID: 35137569 Free PMC article. Review.

8

Myhre Syndrome Misdiagnosed as Marfan Syndrome: an Educational Presentation.

Li J, Zhu T, Yang S, Yang F, Wu J, Xiong F. Li J, et al. Braz J Cardiovasc Surg. 2021 Oct 17;36(5):700-702. doi: 10.21470/1678-9741-2020-0592. Braz J Cardiovasc Surg. 2021. PMID: 34236823 Free PMC article.

9

The effect of iron supplementation in preterm infants at different gestational ages.

Ruan S, Li J, Xiong F, Qie D, Lu Y, Yang S, Tang Z, Yang F. Ruan S, et al. Among authors: li j. BMC Pediatr. 2024 Aug 20;24(1):530. doi: 10.1186/s12887-024-04996-5. BMC Pediatr. 2024. PMID: 39164675 Free PMC article.

10

Hypoxic exposure activates the B cell-specific Moloney murine leukaemia virus integration site 1/PI3K/Akt axis and promotes EMT in leukaemia stem cells.

Jiang M, He G, Li J, Li J, Guo X, Gao J. Jiang M, et al. Among authors: li j. Oncol Lett. 2021 Feb;21(2):98. doi: 10.3892/ol.2020.12359. Epub 2020 Dec 8. Oncol Lett. 2021. PMID: 33376531 Free PMC article.

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