Li J - Search Results

1

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.

2

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

3

Case report: A rare case of TBL1XR1-RARB positive acute promyelocytic leukemia in child and review of the literature.

Jiang M, Li J, Wu J, Zhu Y, Gao J. Jiang M, et al. Among authors: li j. Front Oncol. 2022 Nov 16;12:1028089. doi: 10.3389/fonc.2022.1028089. eCollection 2022. Front Oncol. 2022. PMID: 36465368 Free PMC article.

4

A rare early-onset neonatal case of Birk-Barel syndrome presenting severe obstructive sleep apnea: a case report.

Zhang Q, Qin Z, Hu R, Li Y, Yang F, Li J. Zhang Q, et al. Among authors: li y, li j. Front Med (Lausanne). 2023 Jun 8;10:1180337. doi: 10.3389/fmed.2023.1180337. eCollection 2023. Front Med (Lausanne). 2023. PMID: 37358997 Free PMC article.

5

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.

6

Novel Compound Heterozygous PKLR Mutation Induced Pyruvate Kinase Deficiency With Persistent Pulmonary Hypertension in a Neonate: A Case Report.

Lin S, Hua X, Li J, Li Y. Lin S, et al. Among authors: li y, li j. Front Cardiovasc Med. 2022 Apr 26;9:872172. doi: 10.3389/fcvm.2022.872172. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 35557523 Free PMC article.

7

A novel compound heterozygous variant of ECEL1 induced joint dysfunction and cartilage degradation: a case report and literature review.

Jing S, Peng M, He Y, Hua Y, Li J, Li Y. Jing S, et al. Among authors: li y, li j. Front Neurol. 2024 Jan 24;15:1343025. doi: 10.3389/fneur.2024.1343025. eCollection 2024. Front Neurol. 2024. PMID: 38327621 Free PMC article.

8

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.

9

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.

10

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.

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