Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (6355)
All Articles published online
|
Publishing Process of This Article
|
Mar 16, 2013 (publication date) through Nov 26, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Gastrointestinal Endoscopy
ISSN
1948-5190
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Yajima H, Isomoto H, Nishioka H, Yamaguchi N, Ohnita K, Ichikawa T, Takeshima F, Shikuwa S, Ito M, Nakao K, Tsukamoto K, Kohno S. Novel serine/threonine kinase 11 gene mutations in Peutz-Jeghers syndrome patients and endoscopic management. World J Gastrointest Endosc 2013; 5(3): 102-110 [PMID: 23515270 DOI: 10.4253/wjge.v5.i3.102] |
|---|---|
| URL: | https://www.wjgnet.com/1007-9327/full/v5/i3/102.htm |
| Number | Citing Articles |
| 1 |
Zhiheng Huang, Shijian Miao, Lin Wang, Ping Zhang, Bingbing Wu, Jie Wu, Ying Huang. Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome. BMC Gastroenterology 2015; 15(1) doi: 10.1186/s12876-015-0397-9
|
| 2 |
Jenifer Loureiro, Gian Luigi Menegazzo, Lucas Vergamini, Roberto Carmagnani Pestana, Fernanda Bellotti Formiga, Marcella Guilherme Carolino de Sousa, Thais Yuka Takahashi, Felipe Silveira, Paulo de Azeredo Passos Candelária, Dino Martini Filho, Fang Chia Bin. Diagnostic difficulty in Peutz–Jeghers syndrome. Journal of Coloproctology 2015; 35(01): 067 doi: 10.1016/j.jcol.2014.08.012
|
| 3 |
Shun-ichi Misawa, Misuzu Takeda, Hiroto Sakamoto, Yasushi Kirii, Hiroyoshi Ota, Hiroyuki Takagi. Spontaneous rupture of a giant gastrointestinal stromal tumor of the jejunum: a case report and literature review. World Journal of Surgical Oncology 2014; 12(1): 153 doi: 10.1186/1477-7819-12-153
|
| 4 |
Hu Tan, Xianda Wei, Pu Yang, Yanru Huang, Haoxian Li, Desheng Liang, Lingqian Wu. A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report. Familial Cancer 2017; 16(3): 417 doi: 10.1007/s10689-016-9963-8
|
| 5 |
Ola A. Hussein, Hany A. Labib, Rasha Haggag, Maha Mahmoud Hamed Sakr. Phe354Leu polymorphism of the liver kinase B1 gene as a prognostic factor in adult egyptian patients with acute myeloid leukemia. Heliyon 2023; 9(5): e15415 doi: 10.1016/j.heliyon.2023.e15415
|
| 6 |
Matteo Fassan, Michele Simbolo, Emilio Bria, Andrea Mafficini, Sara Pilotto, Paola Capelli, Maria Bencivenga, Sara Pecori, Claudio Luchini, Diogo Neves, Giona Turri, Caterina Vicentini, Licia Montagna, Anna Tomezzoli, Giampaolo Tortora, Marco Chilosi, Giovanni De Manzoni, Aldo Scarpa. High-throughput mutation profiling identifies novel molecular dysregulation in high-grade intraepithelial neoplasia and early gastric cancers. Gastric Cancer 2014; 17(3): 442 doi: 10.1007/s10120-013-0315-1
|
| 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 Mutation. Journal of Pediatric Gastroenterology and Nutrition 2019; 68(2): 199 doi: 10.1097/MPG.0000000000002166
|