Wang J - Search Results

1

Early‑onset epilepsy and microcephaly‑capillary malformation syndrome caused by a novel STAMBP mutation in a Chinese boy.

Wu F, Dai Y, Wang J, Cheng M, Wang Y, Li X, Yuan P, Liao S, Jiang L, Chen J, Yan L, Zhong M. Wu F, et al. Among authors: wang j, wang y. Mol Med Rep. 2019 Dec;20(6):5145-5151. doi: 10.3892/mmr.2019.10757. Epub 2019 Oct 17. Mol Med Rep. 2019. PMID: 31638258 Free PMC article. Review.

2

Hereditary folate malabsorption with a novel mutation on SLC46A1: A case report.

Tan J, Li X, Guo Y, Xie L, Wang J, Ma J, Jiang L. Tan J, et al. Among authors: wang j. Medicine (Baltimore). 2017 Dec;96(50):e8712. doi: 10.1097/MD.0000000000008712. Medicine (Baltimore). 2017. PMID: 29390264 Free PMC article.

3

De novo mutations of STXBP1 in Chinese children with early onset epileptic encephalopathy.

Li T, Cheng M, Wang J, Hong S, Li M, Liao S, Xie L, Jiang L. Li T, et al. Among authors: wang j. Genes Brain Behav. 2018 Nov;17(8):e12492. doi: 10.1111/gbb.12492. Epub 2018 Sep 12. Genes Brain Behav. 2018. PMID: 29896790 Free article.

4

Genetic and phenotypic characteristics of SCN1A-related epilepsy in Chinese children.

Fang ZX, Hong SQ, Li TS, Wang J, Xie LL, Han W, Jiang L. Fang ZX, et al. Among authors: wang j. Neuroreport. 2019 Jun 12;30(9):671-680. doi: 10.1097/WNR.0000000000001259. Neuroreport. 2019. PMID: 31009440

5

A girl with protein-losing enteropathy during a ketogenic diet: a case report.

Wang J, Jiang L, Cheng M. Wang J, et al. BMC Pediatr. 2020 Mar 3;20(1):102. doi: 10.1186/s12887-020-1991-8. BMC Pediatr. 2020. PMID: 32126979 Free PMC article.

6

Clinical Forms and GRIN2A Genotype of Severe End of Epileptic-Aphasia Spectrum Disorder.

Li X, Xie LL, Han W, Hong SQ, Ma JN, Wang J, Jiang L. Li X, et al. Among authors: wang j. Front Pediatr. 2020 Nov 6;8:574803. doi: 10.3389/fped.2020.574803. eCollection 2020. Front Pediatr. 2020. PMID: 33240831 Free PMC article.

7

Clinical characteristics of children with Guillain-Barré syndrome and factors associated with disease severity.

Luo HY, Li XJ, Cheng M, Wang J, Xie LL, Yao ZX, Jiang L. Luo HY, et al. Among authors: wang j. J Clin Neurosci. 2021 Oct;92:120-125. doi: 10.1016/j.jocn.2021.08.001. Epub 2021 Aug 9. J Clin Neurosci. 2021. PMID: 34509238

8

Hypoparathyroidism, neutropenia and nephrotic syndrome in a patient with mitochondrial trifunctional protein deficiency: A case report and review of the literature.

Li Y, He C, Li S, Wang J, Jiang L, Guo Y. Li Y, et al. Among authors: wang j. Eur J Med Genet. 2021 Dec;64(12):104344. doi: 10.1016/j.ejmg.2021.104344. Epub 2021 Sep 17. Eur J Med Genet. 2021. PMID: 34543737 Review.

9

Prospective control study of efficacy and influencing factors of a ketogenic diet on refractory epilepsy in children.

Feng L, Wang J, Li X, Hu Y, Hong S, Jiang L. Feng L, et al. Among authors: wang j. Transl Pediatr. 2022 Jan;11(1):138-148. doi: 10.21037/tp-21-595. Transl Pediatr. 2022. PMID: 35242660 Free PMC article.

10

External Assessment of the Anti-N-Methyl-D-Aspartate Receptor Encephalitis One-Year Functional Status Score in Chinese Pediatric Patients.

Luo H, Li Y, Zheng Y, Zhou L, Yang J, Fang Z, Jiang Y, Wang J, Yao Z, Chen M, Jiang L. Luo H, et al. Among authors: wang j. Front Immunol. 2022 Jun 23;13:889394. doi: 10.3389/fimmu.2022.889394. eCollection 2022. Front Immunol. 2022. PMID: 35812389 Free PMC article.

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