Hu L - Search Results

1

Clinical and genetic spectrum of a large cohort of children with epilepsy in China.

Yang L, Kong Y, Dong X, Hu L, Lin Y, Chen X, Ni Q, Lu Y, Wu B, Wang H, Lu QR, Zhou W. Yang L, et al. Among authors: hu l. Genet Med. 2019 Mar;21(3):564-571. doi: 10.1038/s41436-018-0091-8. Epub 2018 Jun 21. Genet Med. 2019. PMID: 29930392 Free PMC article.

2

Flash visual evoked potentials are not specific enough to identify parieto-occipital lobe involvement in term neonates after significant hypoglycaemia.

Hu L, Gu Q, Zhu Z, Yang C, Chen C, Cao Y, Zhou W. Hu L, et al. Acta Paediatr. 2014 Aug;103(8):e329-33. doi: 10.1111/apa.12673. Epub 2014 May 19. Acta Paediatr. 2014. PMID: 24798709

3

Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients.

Fan ZC, Ni JW, Yang L, Hu LY, Ma SM, Mei M, Sun BJ, Wang HJ, Zhou WH. Fan ZC, et al. Among authors: hu ly. Mol Genet Genomic Med. 2015 Jun 29;3(6):526-36. doi: 10.1002/mgg3.162. eCollection 2015 Nov. Mol Genet Genomic Med. 2015. PMID: 26740944 Free PMC article.

4

Novel compound heterozygous mutations in the PEX1 gene in two Chinese newborns with Zellweger syndrome based on whole exome sequencing.

Ge MM, Hu L, Li Z, Cheng G, Yan K, Kong Y, Wang H, Yang L, Zhou W. Ge MM, et al. Among authors: hu l. Clin Chim Acta. 2017 Jul;470:24-28. doi: 10.1016/j.cca.2017.04.016. Epub 2017 Apr 19. Clin Chim Acta. 2017. PMID: 28432012

5

Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures.

Kong Y, Yan K, Hu L, Wang M, Dong X, Lu Y, Wu B, Wang H, Yang L, Zhou W. Kong Y, et al. Among authors: hu l. Clin Chim Acta. 2018 Aug;483:14-19. doi: 10.1016/j.cca.2018.03.027. Epub 2018 Apr 9. Clin Chim Acta. 2018. PMID: 29649454

6

A Novel MYCN Variant Associated with Intellectual Disability Regulates Neuronal Development.

Yu X, Hu L, Liu X, Zhan G, Mei M, Wang H, Zhang X, Qiu Z, Zhou W, Yang L. Yu X, et al. Among authors: hu l. Neurosci Bull. 2018 Oct;34(5):854-858. doi: 10.1007/s12264-018-0236-4. Epub 2018 May 21. Neurosci Bull. 2018. PMID: 29786759 Free PMC article. No abstract available.

7

Data on mutations and Clinical features in SCN1A or SCN2A gene.

Kong Y, Yan K, Hu L, Wang M, Dong X, Lu Y, Wu B, Wang H, Yang L, Zhou W. Kong Y, et al. Among authors: hu l. Data Brief. 2018 Aug 30;22:492-501. doi: 10.1016/j.dib.2018.08.122. eCollection 2019 Feb. Data Brief. 2018. PMID: 30619928 Free PMC article.

8

Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates.

Liu X, Mei M, Chen X, Lu Y, Dong X, Hu L, Hu X, Cheng G, Cao Y, Yang L, Zhou W. Liu X, et al. Among authors: hu x, hu l. Respir Res. 2019 Aug 5;20(1):174. doi: 10.1186/s12931-019-1148-1. Respir Res. 2019. PMID: 31382961 Free PMC article.

9

Genetic aetiology of early infant deaths in a neonatal intensive care unit.

Yang L, Liu X, Li Z, Zhang P, Wu B, Wang H, Hu L, Cheng G, Wang L, Zhou W. Yang L, et al. Among authors: hu l. J Med Genet. 2020 Mar;57(3):169-177. doi: 10.1136/jmedgenet-2019-106221. Epub 2019 Sep 9. J Med Genet. 2020. PMID: 31501239

10

Positive impact of COVID-19 on career choice in pediatric medical students: a longitudinal study.

Hu L, Wu H, Zhou W, Shen J, Qiu W, Zhang R, Wu J, Chai Y. Hu L, et al. Transl Pediatr. 2020 Jun;9(3):243-252. doi: 10.21037/tp-20-100. Transl Pediatr. 2020. PMID: 32775243 Free PMC article.

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