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For: Jiang LX, Chen YR, Xu ZX, Zhang YH, Zhang Z, Yu PF, Dong ZW, Yang HR, Gu GL. Peutz-Jeghers syndrome without STK11 mutation may correlate with less severe clinical manifestations in Chinese patients. World J Gastroenterol 2023; 29(21): 3302-3317 [PMID: 37377590 DOI: 10.3748/wjg.v29.i21.3302]
URL: https://www.wjgnet.com/1009-3079/full/v29/i21/3302.htm
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Mustafa Yilmaz, Ogun Bebek, Yavuzhan Colak, Ayberk Türkyılmaz. Somatic STK11 mosaicism in a Turkish patient with Peutz-Jeghers syndromeFamilial Cancer 2024; 23(4): 641 doi: 10.1007/s10689-024-00405-z
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Tahir N. Khan, Chunyu Liu, Kai Lee Yap, Humayoon Shafique Satti, Ayaz Khan, Muhammad Safeer, Sheraz Khan, Naveed Altaf Malik, Feng Zhang, Muhammad Tariq, Erica E. Davis, Priya Gusain. Genetic Investigation and Transcriptome Profiling in a Nuclear Family With Peutz–Jeghers SyndromeHuman Mutation 2025; 2025(1) doi: 10.1155/humu/5530710
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Anqi Jiang, Yingfei Ye, Haowen Tan, Xiang Tao, Fenghua Ma, Hui Wang, Congjian Xu, Yu Kang. Gastric-type endocervical adenocarcinoma in situ as the presenting feature in a mosaic STK11 pathogenic variant carrier with a Peutz-Jeghers syndrome childFamilial Cancer 2025; 24(3) doi: 10.1007/s10689-025-00485-5
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Anne Marie Jelsig, John Gásdal Karstensen, Thomas V. Overeem Hansen. Progress report: Peutz–Jeghers syndromeFamilial Cancer 2024; 23(4): 409 doi: 10.1007/s10689-024-00362-7
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Myrto Skafida, Melani M Duvall, Kristin Zelley, Sarah E. Baldino, Garrett M Brodeur, Thomas Kolon, Sogol Mostoufi‐Moab, Suzanne P. MacFarland. Conservative management of gynecomastia in Peutz‐Jeghers syndrome: Case series and review of the literaturePediatric Blood & Cancer 2024; 71(10) doi: 10.1002/pbc.31180