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Mar 21, 2016 (publication date) through Apr 25, 2024
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Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| 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] |
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| 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 history. Orphanet Journal of Rare Diseases 2021; 16(1) doi: 10.1186/s13023-021-01900-7
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| 2 |
Zofia Nevozinskaya, Iryna Korsunskaya, Luiza Sakaniya, Yury Perlamutrov, Vladimir Sobolev. Peutz–Jeghers syndrome in dermatology. Acta Dermatovenerologica Alpina Pannonica et Adriatica 2019; 28(3) doi: 10.15570/actaapa.2019.33
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| 3 |
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 girl. Medicine 2017; 96(49): e8591 doi: 10.1097/MD.0000000000008591
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| 4 |
Priyanka Maity, Nandini Das, Uttara Chatterjee, Dhananjay Basak. Sex-Cord Tumor with Annular Tubules with Unusual Morphology in an Infant with Peutz-Jeghers Syndrome. Fetal and Pediatric Pathology 2022; 41(2): 306 doi: 10.1080/15513815.2020.1786200
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| 5 |
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 laser. Chinese Journal of Plastic and Reconstructive Surgery 2021; 3(3): 147 doi: 10.1016/j.cjprs.2021.09.006
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| 6 |
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 Mutation. Journal of Pediatric Gastroenterology and Nutrition 2019; 68(2): 199 doi: 10.1097/MPG.0000000000002166
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