164 related articles for article (PubMed ID: 37167130)
1. [The course and clinical manifestations of Peutz-Jeghers syndrome in the Russian population].
Savelyeva ТA; Ponomarenko АA; Shelygin YA; Kuzminov АM; Vyshegorodtsev DV; Loginova АN; Pikunov DY; Goncharova ЕP; Likutov АA; Mainovskaya ОA; Tsukanov АS
Ter Arkh; 2023 Mar; 95(2):145-151. PubMed ID: 37167130
[TBL] [Abstract][Full Text] [Related]
2. Novel germline STK11 variants and breast cancer phenotype identified in an Indian cohort of Peutz-Jeghers syndrome.
Lipsa A; Kowtal P; Sarin R
Hum Mol Genet; 2019 Jun; 28(11):1885-1893. PubMed ID: 30689838
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Peutz-Jeghers Syndrome with Adenomatous Change in a Fifteen-month-old Boy].
Lee KS; Lee SH; Myong NH
Korean J Gastroenterol; 2015 Aug; 66(2):106-10. PubMed ID: 26289244
[TBL] [Abstract][Full Text] [Related]
5. An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.
Daniell J; Plazzer JP; Perera A; Macrae F
Fam Cancer; 2018 Jul; 17(3):421-427. PubMed ID: 28900777
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome.
Huang Z; Miao S; Wang L; Zhang P; Wu B; Wu J; Huang Y
BMC Gastroenterol; 2015 Nov; 15():166. PubMed ID: 26607058
[TBL] [Abstract][Full Text] [Related]
8. Clinical Guidelines for Diagnosis and Management of Peutz-Jeghers Syndrome in Children and Adults.
Yamamoto H; Sakamoto H; Kumagai H; Abe T; Ishiguro S; Uchida K; Kawasaki Y; Saida Y; Sano Y; Takeuchi Y; Tajika M; Nakajima T; Banno K; Funasaka Y; Hori S; Yamaguchi T; Yoshida T; Ishikawa H; Iwama T; Okazaki Y; Saito Y; Matsuura N; Mutoh M; Tomita N; Akiyama T; Yamamoto T; Ishida H; Nakayama Y
Digestion; 2023; 104(5):335-347. PubMed ID: 37054692
[TBL] [Abstract][Full Text] [Related]
9. Disease pattern in Danish patients with Peutz-Jeghers syndrome.
Jelsig AM; Qvist N; Sunde L; Brusgaard K; Hansen T; Wikman FP; Nielsen CB; Nielsen IK; Gerdes AM; Bojesen A; Ousager LB
Int J Colorectal Dis; 2016 May; 31(5):997-1004. PubMed ID: 26979979
[TBL] [Abstract][Full Text] [Related]
10. Clinical features, diagnosis, and treatment of Peutz-Jeghers syndrome: Experience with 566 Chinese cases.
Xu ZX; Jiang LX; Chen YR; Zhang YH; Zhang Z; Yu PF; Dong ZW; Yang HR; Gu GL
World J Gastroenterol; 2023 Mar; 29(10):1627-1637. PubMed ID: 36970589
[TBL] [Abstract][Full Text] [Related]
11. Nasal polyposis in Peutz-Jeghers syndrome: a distinct histopathological and molecular genetic entity.
de Leng WW; Westerman AM; Weterman MA; Jansen M; van Dekken H; Giardiello FM; de Rooij FW; Paul Wilson JH; Offerhaus GJ; Keller JJ
J Clin Pathol; 2007 Apr; 60(4):392-6. PubMed ID: 16775120
[TBL] [Abstract][Full Text] [Related]
12. Peutz-Jeghers syndrome without
Jiang LX; Chen YR; Xu ZX; Zhang YH; Zhang Z; Yu PF; Dong ZW; Yang HR; Gu GL
World J Gastroenterol; 2023 Jun; 29(21):3302-3317. PubMed ID: 37377590
[TBL] [Abstract][Full Text] [Related]
13. Two cases of somatic STK11 mosaicism in Danish patients with Peutz-Jeghers syndrome.
Jelsig AM; Bertelsen B; Forss I; Karstensen JG
Fam Cancer; 2021 Jan; 20(1):55-59. PubMed ID: 32504210
[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. 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]
16. [Hereditary predisposition to cancers of the digestive tract, breast, gynecological and gonadal: focus on the Peutz-Jeghers].
Turpin A; Cattan S; Leclerc J; Wacrenier A; Manouvrier-Hanu S; Buisine MP; Lejeune-Dumoulin S
Bull Cancer; 2014 Sep; 101(9):813-22. PubMed ID: 25036236
[TBL] [Abstract][Full Text] [Related]
17. Peutz-Jeghers syndrome: risks of a hereditary condition.
Westerman AM; Wilson JH
Scand J Gastroenterol Suppl; 1999; 230():64-70. PubMed ID: 10499464
[TBL] [Abstract][Full Text] [Related]
18. STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.
Wang Z; Wu B; Mosig RA; Chen Y; Ye F; Zhang Y; Gong W; Gong L; Huang F; Wang X; Nie B; Zheng H; Cui M; Wang Y; Wang J; Chen C; Polydorides AD; Zhang DY; Martignetti JA; Jiang B
Hum Mutat; 2014 Jul; 35(7):851-8. PubMed ID: 24652667
[TBL] [Abstract][Full Text] [Related]
19. 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]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
