These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
206 related articles for article (PubMed ID: 31072341)
1. Early screening the small bowel is key to protect Peutz-Jeghers syndrome patients from surgery: a novel mutation c.243delG in STK11 gene. Jiang YL; Zhao ZY; Li BR; Li J; Jin XW; Yu ED; Xu XD; Ning SB BMC Gastroenterol; 2019 May; 19(1):70. PubMed ID: 31072341 [TBL] [Abstract][Full Text] [Related]
2. Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl. Zhao ZY; Jiang YL; Li BR; Li J; Jin XW; Yu ED; Ning SB BMC Surg; 2018 Apr; 18(1):24. PubMed ID: 29685139 [TBL] [Abstract][Full Text] [Related]
3. A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report. Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Sun SH; Ning SB Medicine (Baltimore); 2017 Dec; 96(49):e8591. PubMed ID: 29245219 [TBL] [Abstract][Full Text] [Related]
4. Extremely young case of small bowel intussusception due to Peutz-Jeghers syndrome with nonsense mutation of STK11. Sado T; Nakayama Y; Kato S; Homma H; Kusakari M; Hidaka N; Gomi S; Takamizawa S; Kosho T; Saito S; Sugano K Clin J Gastroenterol; 2019 Oct; 12(5):429-433. PubMed ID: 30888642 [TBL] [Abstract][Full Text] [Related]
5. Follow-up and surgical management of Peutz-Jeghers syndrome in children. Vidal I; Podevin G; Piloquet H; Le Rhun M; Frémond B; Aubert D; Leclair MD; Héloury Y J Pediatr Gastroenterol Nutr; 2009 Apr; 48(4):419-25. PubMed ID: 19330929 [TBL] [Abstract][Full Text] [Related]
6. Mutation analysis of related genes in hamartoma polyp tissue of Peutz-Jeghers syndrome. Zhang Z; Duan FX; Gu GL; Yu PF World J Gastroenterol; 2020 Apr; 26(16):1926-1937. PubMed ID: 32390703 [TBL] [Abstract][Full Text] [Related]
7. Endoscopic therapy of small-bowel polyps by double-balloon enteroscopy in patients with Peutz-Jeghers syndrome. Gao H; van Lier MG; Poley JW; Kuipers EJ; van Leerdam ME; Mensink PB Gastrointest Endosc; 2010 Apr; 71(4):768-73. PubMed ID: 20188368 [TBL] [Abstract][Full Text] [Related]
8. Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation. Zhao HM; Yang YJ; Duan JQ; Ouyang HJ; Liu L; Yi LC; Xiao ZH; Zheng Y; Peng L; Attard TM; Li DY; You JY J Pediatr Gastroenterol Nutr; 2019 Feb; 68(2):199-206. PubMed ID: 30334930 [TBL] [Abstract][Full Text] [Related]
9. STK11 status and intussusception risk in Peutz-Jeghers syndrome. Hearle N; Schumacher V; Menko FH; Olschwang S; Boardman LA; Gille JJ; Keller JJ; Westerman AM; Scott RJ; Lim W; Trimbath JD; Giardiello FM; Gruber SB; Offerhaus GJ; Rooij FW; Wilson JH; Hansmann A; Möslein G; Royer-Pokora B; Vogel T; Phillips RK; Spigelman AD; Houlston RS J Med Genet; 2006 Aug; 43(8):e41. PubMed ID: 16882735 [TBL] [Abstract][Full Text] [Related]
10. Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient. Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Ning SB; Sun SH BMC Med Genet; 2017 Nov; 18(1):130. PubMed ID: 29141581 [TBL] [Abstract][Full Text] [Related]
11. Clinical features, endoscopic polypectomy and STK11 gene mutation in a nine-month-old Peutz-Jeghers syndrome Chinese infant. Huang ZH; Song Z; Zhang P; Wu J; Huang Y World J Gastroenterol; 2016 Mar; 22(11):3261-7. PubMed ID: 27004004 [TBL] [Abstract][Full Text] [Related]
13. A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome. Yoo JH; Yoo JH; Choi YJ; Kang JG; Sun YK; Ki CS; Lee KA; Choi JR BMC Med Genet; 2008 May; 9():44. PubMed ID: 18495044 [TBL] [Abstract][Full Text] [Related]
14. A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report. Chen JH; Zheng JJ; Guo Q; Liu C; Luo B; Tang SB; Cheng JD; Huang EW BMC Med Genet; 2017 Feb; 18(1):19. PubMed ID: 28231849 [TBL] [Abstract][Full Text] [Related]
15. Identification of a novel de novo STK11 mutation in a Chinese child with Peutz-Jeghers syndrome. Liu WL; Li F; He ZX; Jiang HY; Ai R; Zhu XP; Chen XX; Ma HW J Int Med Res; 2011; 39(5):2033-8. PubMed ID: 22118009 [TBL] [Abstract][Full Text] [Related]
16. Peutz-Jeghers syndrome: early clinical expression of a new STK11 gene variant. Brito S; Póvoas M; Dupont J; Lopes AI BMJ Case Rep; 2015 Oct; 2015():. PubMed ID: 26430231 [TBL] [Abstract][Full Text] [Related]
17. A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients. Thakur N; Reddy DN; Rao GV; Mohankrishna P; Singh L; Chandak GR BMC Med Genet; 2006 Sep; 7():73. PubMed ID: 17010210 [TBL] [Abstract][Full Text] [Related]
18. Low-level parental mosaicism in an apparent de novo case of Peutz-Jeghers syndrome. Butel-Simoes GI; Spigelman AD; Scott RJ; Vilain RE Fam Cancer; 2019 Jan; 18(1):109-112. PubMed ID: 29948449 [TBL] [Abstract][Full Text] [Related]
19. Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome. Tan H; Mei L; Huang Y; Yang P; Li H; Peng Y; Chen C; Wei X; Pan Q; Liang D; Wu L BMC Med Genet; 2016 Nov; 17(1):77. PubMed ID: 27821076 [TBL] [Abstract][Full Text] [Related]