175 related articles for article (PubMed ID: 30444588)
1. [Pilot clinical and genetic study of Russian patients with Peutz-Jeghers syndrome].
Shelygin YA; Pospekhova NI; Shubin VP; Kashnikov VN; Frolov SA; Kuzminov AM; Mainovskaya OA; Sachkov IY; Tsukanov AS
Vopr Onkol; 2016; 62(1):112-16. PubMed ID: 30444588
[TBL] [Abstract][Full Text] [Related]
2. Genetic screening for Peutz-Jeghers syndrome.
Ballhausen WG; Günther K
Expert Rev Mol Diagn; 2003 Jul; 3(4):471-9. PubMed ID: 12877386
[TBL] [Abstract][Full Text] [Related]
3. Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.
Resta N; Pierannunzio D; Lenato GM; Stella A; Capocaccia R; Bagnulo R; Lastella P; Susca FC; Bozzao C; Loconte DC; Sabbà C; Urso E; Sala P; Fornasarig M; Grammatico P; Piepoli A; Host C; Turchetti D; Viel A; Memo L; Giunti L; Stigliano V; Varesco L; Bertario L; Genuardi M; Lucci Cordisco E; Tibiletti MG; Di Gregorio C; Andriulli A; Ponz de Leon M;
Dig Liver Dis; 2013 Jul; 45(7):606-11. PubMed ID: 23415580
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Rare hereditary syndromes associated with polyposis and the development of malignant tumors].
Kazubskaya TP; Kozlova VM; Filippova MG; Тrofimov EI; Belev NF; Sokolova IN; Tamrazov RI; Pavlovskaya AI; Kondratyeva TT
Arkh Patol; 2016; 78(2):10-18. PubMed ID: 27070770
[TBL] [Abstract][Full Text] [Related]
6. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
Hemminki A; Markie D; Tomlinson I; Avizienyte E; Roth S; Loukola A; Bignell G; Warren W; Aminoff M; Höglund P; Järvinen H; Kristo P; Pelin K; Ridanpää M; Salovaara R; Toro T; Bodmer W; Olschwang S; Olsen AS; Stratton MR; de la Chapelle A; Aaltonen LA
Nature; 1998 Jan; 391(6663):184-7. PubMed ID: 9428765
[TBL] [Abstract][Full Text] [Related]
7. Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online.
Kruse R; Uhlhaas S; Lamberti C; Keller KM; Jackisch C; Steinhard J; Knöpfle G; Loff S; Back W; Stolte M; Jungck M; Propping P; Friedl W; Jenne DE
Hum Mutat; 1999; 13(3):257-8. PubMed ID: 10090485
[TBL] [Abstract][Full Text] [Related]
8. A Peutz-Jeghers syndrome family associated with sinonasal adenocarcinoma: 28 years follow up report.
Chiang JM; Chen TC
Fam Cancer; 2017 Oct; 16(4):555-560. PubMed ID: 28391433
[TBL] [Abstract][Full Text] [Related]
9. Genetic and epigenetic profiling of a solitary Peutz-Jeghers colon polyp.
Linhart H; Bormann F; Hutter B; Brors B; Lyko F
Cold Spring Harb Mol Case Stud; 2017 May; 3(3):a001610. PubMed ID: 28487883
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients.
Wang ZJ; Churchman M; Avizienyte E; McKeown C; Davies S; Evans DG; Ferguson A; Ellis I; Xu WH; Yan ZY; Aaltonen LA; Tomlinson IP
J Med Genet; 1999 May; 36(5):365-8. PubMed ID: 10353780
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Molecular insights into Peutz-Jeghers syndrome: two probands with a germline mutation of LKB1.
Hosogi H; Nagayama S; Kawamura J; Koshiba Y; Nomura A; Itami A; Okabe H; Satoh S; Watanabe G; Sakai Y
J Gastroenterol; 2008; 43(6):492-7. PubMed ID: 18600394
[TBL] [Abstract][Full Text] [Related]
14. Clinical and genetic analysis of Peutz-Jeghers syndrome patients in Taiwan.
Weng MT; Ni YH; Su YN; Wong JM; Wei SC
J Formos Med Assoc; 2010 May; 109(5):354-61. PubMed ID: 20497868
[TBL] [Abstract][Full Text] [Related]
15. Peutz-Jeghers syndrome: a new understanding.
Choi HS; Park YJ; Park JG
J Korean Med Sci; 1999 Feb; 14(1):2-7. PubMed ID: 10102516
[TBL] [Abstract][Full Text] [Related]
16. Frequency and spectrum of cancers in the 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; de Rooij FW; Wilson JH; Hansmann A; Möslein G; Royer-Pokora B; Vogel T; Phillips RK; Spigelman AD; Houlston RS
Clin Cancer Res; 2006 May; 12(10):3209-15. PubMed ID: 16707622
[TBL] [Abstract][Full Text] [Related]
17. Hamartomatous polyps - a clinical and molecular genetic study.
Jelsig AM
Dan Med J; 2016 Aug; 63(8):. PubMed ID: 27477802
[TBL] [Abstract][Full Text] [Related]
18. [Peutz-Jeghers syndrome].
Miyaki M
Nihon Rinsho; 2000 Jul; 58(7):1400-4. PubMed ID: 10921312
[TBL] [Abstract][Full Text] [Related]
19. Peutz-Jeghers syndrome polyps are polyclonal with expanded progenitor cell compartment.
de Leng WW; Jansen M; Keller JJ; de Gijsel M; Milne AN; Morsink FH; Weterman MA; Iacobuzio-Donahue CA; Clevers HC; Giardiello FM; Offerhaus GJ
Gut; 2007 Oct; 56(10):1475-6. PubMed ID: 17872577
[No Abstract] [Full Text] [Related]
20. Peutz-Jeghers syndrome: molecular analysis of a three-generation kindred with a novel defect in the serine threonine kinase gene STK11.
Trojan J; Brieger A; Raedle J; Roth WK; Zeuzem S
Am J Gastroenterol; 1999 Jan; 94(1):257-61. PubMed ID: 9934767
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
