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Cited by in CrossRef
For: Engin G, Eraslan S, Kayserili H, Kapran Y, Akman H, Akyuz A, Aykan NF. Imatinib response of gastrointestinal stromal tumor patients with germline mutation on KIT exon 13: A family report. World J Radiol 2017; 9(9): 365-370 [PMID: 29098070 DOI: 10.4329/wjr.v9.i9.365]
URL: https://www.wjgnet.com/1949-8470/full/v9/i9/365.htm
Number Citing Articles
1
Jing Qi, He-Li Liu, Feng Ren, Sheng Liu, Wei Shi, Wei-Hang Liu, Gao-Qiang Cai, Guo-Qing Liao. Preoperative adjuvant therapy for locally advanced and recurrent/metastatic gastrointestinal stromal tumors: a retrospective studyWorld Journal of Surgical Oncology 2020; 18(1) doi: 10.1186/s12957-020-01840-9
2
K. M. Ingley, M. Zatzman, A. M. Fontebasso, W. Lo, V. Subasri, A. Goldenberg, Y. Li, S. Davidson, N. Kanwar, L. Waldman, L. Brunga, Y. Babichev, E. G. Demicco, A. Gupta, M. Szybowska, S. Thipphavong, D. Malkin, A. Villani, A. Shlien, R. A. Gladdy, R. H. Kim. Genomic and clinical characterization of a familial GIST kindred intolerant to imatinibnpj Genomic Medicine 2024; 9(1) doi: 10.1038/s41525-024-00405-z
3
Newton A.C.S. Wong, Christel Garcia-Petit, Adam Dangoor, Nicola Andrew. A literature review and database of how the primary KIT/PDGFRA variant of a gastrointestinal stromal tumour predicts for sensitivity to imatinibCancer Genetics 2022; : 46 doi: 10.1016/j.cancergen.2022.09.002
4
Rola H. Ali, Ahmad R. Alsaber, Asit K. Mohanty, Abdulsalam Alnajjar, Eiman M. A. Mohammed, Mona Alateeqi, Hiba Jama, Ammar Almarzooq, Noelle Benobaid, Zainab Alqallaf, Amir A. Ahmed, Shakir Bahzad, Mohammad Alkandari. Molecular Profiling of KIT/PDGFRA-Mutant and Wild-Type Gastrointestinal Stromal Tumors (GISTs) with Clinicopathological Correlation: An 18-Year Experience at a Tertiary Center in KuwaitCancers 2024; 16(16): 2907 doi: 10.3390/cancers16162907
5
Mara Fornasarig, Daniela Gasparotto, Luisa Foltran, Michele Campigotto, Sara Lombardi, Elisa Del Savio, Angela Buonadonna, Fabio Puglisi, Sandro Sulfaro, Vincenzo Canzonieri, Renato Cannizzaro, Roberta Maestro. A Novel Kindred with Familial Gastrointestinal Stromal Tumors Caused by a Rare KIT Germline Mutation (N655K): Clinico-Pathological Presentation and TKI SensitivityJournal of Personalized Medicine 2020; 10(4): 234 doi: 10.3390/jpm10040234