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Cited by in CrossRef
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 syndromeBMC 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 syndromeJournal 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 reviewWorld 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 reportFamilial 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 leukemiaHeliyon 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 cancersGastric 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 MutationJournal of Pediatric Gastroenterology and Nutrition 2019; 68(2): 199 doi: 10.1097/MPG.0000000000002166