230 related articles for article (PubMed ID: 26850131)
21. Hamartomatous polyposis syndromes: molecular genetics, neoplastic risk, and surveillance recommendations.
Wirtzfeld DA; Petrelli NJ; Rodriguez-Bigas MA
Ann Surg Oncol; 2001 May; 8(4):319-27. PubMed ID: 11352305
[TBL] [Abstract][Full Text] [Related]
22. Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations.
Ponti G; Ponz de Leon M; Maffei S; Pedroni M; Losi L; Di Gregorio C; Gismondi V; Scarselli A; Benatti P; Roncari B; Seidenari S; Pellacani G; Varotti C; Prete E; Varesco L; Roncucci L
Clin Genet; 2005 Nov; 68(5):442-7. PubMed ID: 16207212
[TBL] [Abstract][Full Text] [Related]
23. Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography.
Marsh DJ; Theodosopoulos G; Howell V; Richardson AL; Benn DE; Proos AL; Eng C; Robinson BG
Neoplasia; 2001; 3(3):236-44. PubMed ID: 11494117
[TBL] [Abstract][Full Text] [Related]
24. Pancreatic cancer screening in high-risk individuals with germline genetic mutations.
DaVee T; Coronel E; Papafragkakis C; Thaiudom S; Lanke G; Chakinala RC; Nogueras González GM; Bhutani MS; Ross WA; Weston BR; Lee JH
Gastrointest Endosc; 2018 Jun; 87(6):1443-1450. PubMed ID: 29309780
[TBL] [Abstract][Full Text] [Related]
25. Polyposis syndromes in children and adolescents: a case series data analysis.
Cohen S; Gorodnichenco A; Weiss B; Lerner A; Ben-Tov A; Yaron A; Reif S
Eur J Gastroenterol Hepatol; 2014 Sep; 26(9):972-7. PubMed ID: 24999926
[TBL] [Abstract][Full Text] [Related]
26. Genetic testing by cancer site: colon (polyposis syndromes).
Jasperson KW
Cancer J; 2012; 18(4):328-33. PubMed ID: 22846733
[TBL] [Abstract][Full Text] [Related]
27. Rapid detection of germline mutations for hereditary gastrointestinal polyposis/cancers using HaloPlex target enrichment and high-throughput sequencing technologies.
Kohda M; Kumamoto K; Eguchi H; Hirata T; Tada Y; Tanakaya K; Akagi K; Takenoshita S; Iwama T; Ishida H; Okazaki Y
Fam Cancer; 2016 Oct; 15(4):553-62. PubMed ID: 26837502
[TBL] [Abstract][Full Text] [Related]
28. Familial colorectal cancer.
Lung MS; Trainer AH; Campbell I; Lipton L
Intern Med J; 2015 May; 45(5):482-91. PubMed ID: 25955461
[TBL] [Abstract][Full Text] [Related]
29. Mutation cluster region, association between germline and somatic mutations and genotype-phenotype correlation in upper gastrointestinal familial adenomatous polyposis.
Groves C; Lamlum H; Crabtree M; Williamson J; Taylor C; Bass S; Cuthbert-Heavens D; Hodgson S; Phillips R; Tomlinson I
Am J Pathol; 2002 Jun; 160(6):2055-61. PubMed ID: 12057910
[TBL] [Abstract][Full Text] [Related]
30. Lessons from the skin--cutaneous features of familial cancer.
Winship IM; Dudding TE
Lancet Oncol; 2008 May; 9(5):462-72. PubMed ID: 18452857
[TBL] [Abstract][Full Text] [Related]
31. A novel APC mutation associated with Gardner syndrome in a Chinese family.
Zeng M; Yao X; Pan Y; Gu H; Xiong F; Yin X; Wu B; Chen T
Gene; 2024 Feb; 896():148051. PubMed ID: 38043837
[TBL] [Abstract][Full Text] [Related]
32. [Muir-Torre syndrome and familial colorectal cancer: 2 families with molecular genetic analysis].
Doré MX; Dieumegard B; Grandjouan S; Avril MF; Martinet C; Ducreux M; Lasser P; Bressac-de Paillerets B
Ann Dermatol Venereol; 1999; 126(8-9):582-6. PubMed ID: 10530344
[TBL] [Abstract][Full Text] [Related]
33. Biallelic MYH germline mutations as cause of Muir-Torre syndrome.
Guillén-Ponce C; Castillejo A; Barberá VM; Pascual-Ramírez JC; Andrada E; Castillejo MI; Guarinós C; Molina-Garrido MJ; Carrato A; Soto JL
Fam Cancer; 2010 Jun; 9(2):151-4. PubMed ID: 19998059
[TBL] [Abstract][Full Text] [Related]
34. The genetics of hereditary colon cancer.
Rustgi AK
Genes Dev; 2007 Oct; 21(20):2525-38. PubMed ID: 17938238
[TBL] [Abstract][Full Text] [Related]
35. Polyposis syndromes: pediatric implications.
Hyer W
Gastrointest Endosc Clin N Am; 2001 Oct; 11(4):659-82, vi-vii. PubMed ID: 11689361
[TBL] [Abstract][Full Text] [Related]
36. [Sporadic and hereditary colorectal cancer. Pathogenetically different with different therapeutic indications].
Weitz J; Knaebel HP; Büchler MW
Chirurg; 2003 Aug; 74(8):717-25. PubMed ID: 12928792
[TBL] [Abstract][Full Text] [Related]
37. Pigmented ocular fundus lesions in the inherited gastrointestinal polyposis syndromes and in hereditary nonpolyposis colorectal cancer.
Traboulsi EI; Maumenee IH; Krush AJ; Giardiello FM; Levin LS; Hamilton SR
Ophthalmology; 1988 Jul; 95(7):964-9. PubMed ID: 2845322
[TBL] [Abstract][Full Text] [Related]
38. Differentiated thyroid carcinoma and intestinal polyposis syndromes.
Triggiani V; Angelo Giagulli V; Tafaro A; Resta F; Sabba C; Licchelli B; Guastamacchia E
Endocr Metab Immune Disord Drug Targets; 2012 Dec; 12(4):377-81. PubMed ID: 22463724
[TBL] [Abstract][Full Text] [Related]
39. [Overflow incontinence--a rare manifestation of Peutz-Jeghers syndrome].
Loff S; Wessel L; Wirth H; Waag KL
Chirurg; 1994 May; 65(5):491-3. PubMed ID: 8050305
[TBL] [Abstract][Full Text] [Related]
40. [Differential diagnosis of preneoplastic changes: intestinal polyps and polyposis syndromes (hereditary polyp syndromes].
Mróz A
Pol J Pathol; 2014 Dec; 65(4 Suppl 1):S12-25. PubMed ID: 26165029
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
