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Cited by in CrossRef
For: Huang ZH, Song Z, Zhang P, Wu J, Huang Y. Clinical features, endoscopic polypectomy and STK11 gene mutation in a nine-month-old Peutz-Jeghers syndrome Chinese infant. World J Gastroenterol 2016; 22(11): 3261-3267 [PMID: 27004004 DOI: 10.3748/wjg.v22.i11.3261]
URL: https://www.wjgnet.com/1007-9327/full/v22/i11/3261.htm
Number Citing Articles
1
Yu-Liang Jiang, Xiao-Dong Xu, Bai-Rong Li, En-Da Yu, Zi-Ye Zhao, Hong Liu. Delayed diagnosis of Peutz–Jeghers syndrome due to pathological information loss or mistake in family/personal historyOrphanet Journal of Rare Diseases 2021; 16(1) doi: 10.1186/s13023-021-01900-7
2
Zofia Nevozinskaya, Iryna Korsunskaya, Luiza Sakaniya, Yury Perlamutrov, Vladimir Sobolev. Peutz–Jeghers syndrome in dermatologyActa Dermatovenerologica Alpina Pannonica et Adriatica 2019; 28(3) doi: 10.15570/actaapa.2019.33
3
Jonathan J Neville, Sarah Ellul, Costa Healy. Ileo-ileal intussusception secondary to a Peutz-Jeghers hamartomatous polyp in an infantBMJ Case Reports 2024; 17(7): e261464 doi: 10.1136/bcr-2024-261464
4
Zi-Ye Zhao, Yu-Liang Jiang, Bai-Rong Li, Fu Yang, Jing Li, Xiao-Wei Jin, Shu-Han Sun, Shou-Bin Ning. A novel germline mutation (c.A527G) in STK11 gene causes Peutz–Jeghers syndrome in a Chinese girlMedicine 2017; 96(49): e8591 doi: 10.1097/MD.0000000000008591
5
Priyanka Maity, Nandini Das, Uttara Chatterjee, Dhananjay Basak. Sex-Cord Tumor with Annular Tubules with Unusual Morphology in an Infant with Peutz-Jeghers SyndromeFetal and Pediatric Pathology 2022; 41(2): 306 doi: 10.1080/15513815.2020.1786200
6
Shuai Yang, Hong Xu, Ying Zhang, Changbo Tao, Peisheng Jin. A case of labial lentigines in Peutz-Jeghers syndrome treated using a Q-switched alexandrite laserChinese Journal of Plastic and Reconstructive Surgery 2021; 3(3): 147 doi: 10.1016/j.cjprs.2021.09.006
7
Hong‐Mei Zhao, Yong‐Jia Yang, Jia‐Qi Duan, Hong‐Juan Ouyang, Li Liu, Li‐Chun Yi, Zheng‐Hui Xiao, Yu Zheng, Lv Peng, Thomas M. Attard, Ding‐You Li, Jie‐Yu You. Clinical and Genetic Study of Children With Peutz‐Jeghers Syndrome Identifies a High Frequency of STK11 De Novo MutationJournal of Pediatric Gastroenterology and Nutrition 2019; 68(2): 199 doi: 10.1097/MPG.0000000000002166