Yan K - Search Results

1

Neonatal Early-Onset Infection With SARS-CoV-2 in 33 Neonates Born to Mothers With COVID-19 in Wuhan, China.

Zeng L, Xia S, Yuan W, Yan K, Xiao F, Shao J, Zhou W. Zeng L, et al. Among authors: yan k. JAMA Pediatr. 2020 Jul 1;174(7):722-725. doi: 10.1001/jamapediatrics.2020.0878. JAMA Pediatr. 2020. PMID: 32215598 Free PMC article.

2

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: yan k. 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

3

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: yan k. 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

4

Biometry reference range of the corpus callosum in neonates: An observational study.

Gao Y, Yan K, Yang L, Cheng G, Zhou W. Gao Y, et al. Among authors: yan k. Medicine (Baltimore). 2018 Jun;97(24):e11071. doi: 10.1097/MD.0000000000011071. Medicine (Baltimore). 2018. PMID: 29901615 Free PMC article.

5

Early onset developmental delay and epilepsy in pediatric patients with WDR45 variants.

Chen H, Qian Y, Yu S, Xiao D, Guo X, Wang Q, Hao L, Yan K, Lu Y, Dong X, Zhou W, Wu B, Zhou S, Wang H. Chen H, et al. Among authors: yan k. Eur J Med Genet. 2019 Feb;62(2):149-160. doi: 10.1016/j.ejmg.2018.07.002. Epub 2018 Jul 6. Eur J Med Genet. 2019. PMID: 29981852

6

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: yan k. 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.

7

Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.

Chen X, Yan K, Gao Y, Wang H, Chen G, Wu B, Qin Q, Yang L, Zhou W. Chen X, et al. Among authors: yan k. BMC Med Genet. 2019 May 30;20(1):93. doi: 10.1186/s12881-019-0813-z. BMC Med Genet. 2019. PMID: 31146700 Free PMC article.

8

Relationship between phenotype and genotype of 102 Chinese newborns with Prader-Willi syndrome.

Ge MM, Gao YY, Wu BB, Yan K, Qin Q, Wang H, Zhou W, Yang L. Ge MM, et al. Among authors: yan k. Mol Biol Rep. 2019 Oct;46(5):4717-4724. doi: 10.1007/s11033-019-04916-2. Epub 2019 Jul 3. Mol Biol Rep. 2019. PMID: 31270759

9

Methadone versus morphine treatment outcomes in neonatal abstinence syndrome: A meta-analysis.

Xiao F, Yan K, Zhou W. Xiao F, et al. Among authors: yan k. J Paediatr Child Health. 2019 Oct;55(10):1177-1182. doi: 10.1111/jpc.14609. Epub 2019 Sep 3. J Paediatr Child Health. 2019. PMID: 31479559 Review.

10

What can we learn from neonates with COVID-19?

Xiao TT, Yan K, Wang LS, Zhou WH. Xiao TT, et al. Among authors: yan k. World J Pediatr. 2020 Jun;16(3):280-283. doi: 10.1007/s12519-020-00376-y. Epub 2020 Jun 10. World J Pediatr. 2020. PMID: 32524373 Free PMC article. No abstract available.

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