Zhao ZY - Search Results

1

Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.

Zhao ZY, Jiang YL, Li BR, Yang F, Li J, Jin XW, Ning SB, Sun SH. Zhao ZY, et al. BMC Med Genet. 2017 Nov 15;18(1):130. doi: 10.1186/s12881-017-0471-y. BMC Med Genet. 2017. PMID: 29141581 Free PMC article.

2

Detection and miss rates of autofluorescence imaging of adenomatous and polypoid lesions during colonoscopy: a systematic review and meta-analysis.

Zhao ZY, Guan YG, Li BR, Shan YQ, Yan FH, Gao YJ, Wang H, Lou Z, Fu CG, Yu ED. Zhao ZY, et al. Endosc Int Open. 2015 Jun;3(3):E226-35. doi: 10.1055/s-0034-1391708. Epub 2015 May 7. Endosc Int Open. 2015. PMID: 26171435 Free PMC article.

3

Drugs for Neuropathic Pain Are Promising in Treating Feed-induced Dystonia in Central Nervous System Disabled Children.

Zhao ZY, Jiang YL, Yu ED, Ning SB. Zhao ZY, et al. J Pediatr Gastroenterol Nutr. 2018 Jan;66(1):e25. doi: 10.1097/MPG.0000000000001738. J Pediatr Gastroenterol Nutr. 2018. PMID: 28902092 No abstract available.

4

A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.

Zhao ZY, Jiang YL, Li BR, Yang F, Li J, Jin XW, Ning SB, Sun SH. Zhao ZY, et al. Dig Dis Sci. 2017 Nov;62(11):3014-3020. doi: 10.1007/s10620-017-4741-5. Epub 2017 Oct 6. Dig Dis Sci. 2017. PMID: 28986664

5

A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report.

Zhao ZY, Jiang YL, Li BR, Yang F, Li J, Jin XW, Sun SH, Ning SB. Zhao ZY, et al. Medicine (Baltimore). 2017 Dec;96(49):e8591. doi: 10.1097/MD.0000000000008591. Medicine (Baltimore). 2017. PMID: 29245219 Free PMC article.

6

A novel mutation (c.855delG) in STK11 gene is associated with Peutz-Jeghers syndrome in a Chinese family.

Zhao ZY, Jiang YL, Li BR, Yu ED, Ning SB. Zhao ZY, et al. Dig Liver Dis. 2018 Mar;50(3):312-314. doi: 10.1016/j.dld.2017.12.007. Epub 2017 Dec 19. Dig Liver Dis. 2018. PMID: 29301733 No abstract available.

7

Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl.

Zhao ZY, Jiang YL, Li BR, Li J, Jin XW, Yu ED, Ning SB. Zhao ZY, et al. BMC Surg. 2018 Apr 23;18(1):24. doi: 10.1186/s12893-018-0357-8. BMC Surg. 2018. PMID: 29685139 Free PMC article.

8

A novel STK11 missense mutation (c.346G > T) causing Peutz-Jeghers syndrome in a Chinese male with a negative family history.

Zhao ZY, Jiang YL, Li BR, Yu ED, Ning SB. Zhao ZY, et al. Dig Liver Dis. 2018 Aug;50(8):864-866. doi: 10.1016/j.dld.2018.05.020. Epub 2018 Jun 4. Dig Liver Dis. 2018. PMID: 29921539 No abstract available.

9

The altered activity of P53 signaling pathway by STK11 gene mutations and its cancer phenotype in Peutz-Jeghers syndrome.

Jiang YL, Zhao ZY, Li BR, Yang F, Li J, Jin XW, Wang H, Yu ED, Sun SH, Ning SB. Jiang YL, et al. Among authors: zhao zy. BMC Med Genet. 2018 Aug 9;19(1):141. doi: 10.1186/s12881-018-0626-5. BMC Med Genet. 2018. PMID: 30092773 Free PMC article.

10

Adenoma miss rate determined by very shortly repeated colonoscopy: Retrospective analysis of data from a single tertiary medical center in China.

Wang CL, Huang ZP, Chen K, Yan FH, Zhu LL, Shan YQ, Gao YJ, Li BR, Wang H, Yu ED, Zhao ZY. Wang CL, et al. Among authors: zhao zy. Medicine (Baltimore). 2018 Sep;97(38):e12297. doi: 10.1097/MD.0000000000012297. Medicine (Baltimore). 2018. PMID: 30235675 Free PMC article.

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