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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1968 2
1969 4
1970 5
1971 2
1972 4
1973 4
1974 4
1975 2
1976 4
1977 1
1978 3
1979 2
1980 4
1981 1
1982 1
1983 2
1984 2
1985 3
1986 1
1987 3
1988 3
1989 3
1990 3
1991 3
1992 2
1993 2
1994 10
1995 9
1996 5
1997 3
1998 8
1999 12
2000 19
2001 18
2002 11
2003 19
2004 19
2005 17
2006 26
2007 19
2008 21
2009 23
2010 14
2011 26
2012 23
2013 21
2014 15
2015 17
2016 19
2017 21
2018 12
2019 15
2020 11
2021 17
2022 19
2023 11
2024 1

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528 results

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Page 1
Peutz-Jeghers syndrome: a systematic review and recommendations for management.
Beggs AD, Latchford AR, Vasen HF, Moslein G, Alonso A, Aretz S, Bertario L, Blanco I, Bülow S, Burn J, Capella G, Colas C, Friedl W, Møller P, Hes FJ, Järvinen H, Mecklin JP, Nagengast FM, Parc Y, Phillips RK, Hyer W, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJ, Wijnen JT, Clark SK, Hodgson SV. Beggs AD, et al. Gut. 2010 Jul;59(7):975-86. doi: 10.1136/gut.2009.198499. Gut. 2010. PMID: 20581245
Peutz-Jeghers syndrome (PJS, MIM175200) is an autosomal dominant condition defined by the development of characteristic polyps throughout the gastrointestinal tract and mucocutaneous pigmentation. ...The proposed guidelines contained in this article have been …
Peutz-Jeghers syndrome (PJS, MIM175200) is an autosomal dominant condition defined by the development of characteristic …
Peutz-Jeghers syndrome.
Tacheci I, Kopacova M, Bures J. Tacheci I, et al. Curr Opin Gastroenterol. 2021 May 1;37(3):245-254. doi: 10.1097/MOG.0000000000000718. Curr Opin Gastroenterol. 2021. PMID: 33591027 Review.
PURPOSE OF REVIEW: Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartomas and mucocutaneous pigmentations, caused by a germline mutation in the serine/ threonine kinase 11 or liver kin …
PURPOSE OF REVIEW: Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined b …
Pathology and genetics of hereditary colorectal cancer.
Ma H, Brosens LAA, Offerhaus GJA, Giardiello FM, de Leng WWJ, Montgomery EA. Ma H, et al. Pathology. 2018 Jan;50(1):49-59. doi: 10.1016/j.pathol.2017.09.004. Epub 2017 Nov 21. Pathology. 2018. PMID: 29169633 Review.
Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associated polyposis, Peutz-Jeghers syndrome, juvenile polyposis and Cowden/PTEN hamartoma syndrome. ...
Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associ …
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. Yamamoto H, et al. Digestion. 2023;104(5):335-347. doi: 10.1159/000529799. Epub 2023 Apr 13. Digestion. 2023. PMID: 37054692 Free article. Review.
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare disease characterized by the presence of hamartomatous polyposis throughout the gastrointestinal tract, except for the esophagus, along with characteristic mucocutaneous pigmentation. ...
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare disease characterized by the presence of hamartomatous polyposis thr …
Esophageal Cancer: An Updated Review.
DiSiena M, Perelman A, Birk J, Rezaizadeh H. DiSiena M, et al. South Med J. 2021 Mar;114(3):161-168. doi: 10.14423/SMJ.0000000000001226. South Med J. 2021. PMID: 33655310 Review.
This makes early detection of the utmost importance, and certain patients have been shown to have the benefit of screening/surveillance endoscopies, including those with Barrett's esophagus, lye-induced/caustic strictures, tylosis, and Peutz-Jeghers syndrome. …
This makes early detection of the utmost importance, and certain patients have been shown to have the benefit of screening/surveillance endo …
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Syngal S, Brand RE, Church JM, Giardiello FM, Hampel HL, Burt RW; American College of Gastroenterology. Syngal S, et al. Am J Gastroenterol. 2015 Feb;110(2):223-62; quiz 263. doi: 10.1038/ajg.2014.435. Epub 2015 Feb 3. Am J Gastroenterol. 2015. PMID: 25645574 Free PMC article. Review.
Genetic testing should be conducted in the context of pre- and post-test genetic counseling to ensure the patient's informed decision making. Patients who meet clinical criteria for a syndrome as well as those with identified pathogenic germline mutations should receive ap …
Genetic testing should be conducted in the context of pre- and post-test genetic counseling to ensure the patient's informed decision making …
Hereditary and familial colon cancer.
Jasperson KW, Tuohy TM, Neklason DW, Burt RW. Jasperson KW, et al. Gastroenterology. 2010 Jun;138(6):2044-58. doi: 10.1053/j.gastro.2010.01.054. Gastroenterology. 2010. PMID: 20420945 Free PMC article. Review.
Between 2% to 5% of all colon cancers arise in the setting of well-defined inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associated polyposis, and certain hamartomatous polyposis conditions. ...
Between 2% to 5% of all colon cancers arise in the setting of well-defined inherited syndromes, including Lynch syndrome, familial ad …
Genetic Predisposition to Colorectal Cancer: How Many and Which Genes to Test?
Rebuzzi F, Ulivi P, Tedaldi G. Rebuzzi F, et al. Int J Mol Sci. 2023 Jan 21;24(3):2137. doi: 10.3390/ijms24032137. Int J Mol Sci. 2023. PMID: 36768460 Free PMC article. Review.
Colorectal cancer is one of the most common tumors, and genetic predisposition is one of the key risk factors in the development of this malignancy. Lynch syndrome and familial adenomatous polyposis are the best-known genetic diseases associated with hereditary colorectal …
Colorectal cancer is one of the most common tumors, and genetic predisposition is one of the key risk factors in the development of this mal …
Ovarian sex cord-stromal tumours and their mimics.
Young RH. Young RH. Pathology. 2018 Jan;50(1):5-15. doi: 10.1016/j.pathol.2017.09.007. Epub 2017 Nov 11. Pathology. 2018. PMID: 29132723 Review.
The rare pure Sertoli cell tumour is briefly noted as is the sex cord tumour with annular tubules, well known because of its association in some cases with Peutz-Jeghers syndrome. Most do not have that association, however, but have their own interesting feat …
The rare pure Sertoli cell tumour is briefly noted as is the sex cord tumour with annular tubules, well known because of its association in …
Peutz-Jeghers syndrome.
McGarrity TJ, Kulin HE, Zaino RJ. McGarrity TJ, et al. Am J Gastroenterol. 2000 Mar;95(3):596-604. doi: 10.1111/j.1572-0241.2000.01831.x. Am J Gastroenterol. 2000. PMID: 10710046 Review.
Peutz-Jeghers syndrome (PJS) is an unusual polyposis syndrome that has enjoyed a rich and somewhat confusing history. Mucocutaneous pigmentation and diffuse gastrointestinal hamartomas are the hallmark features of this autosomal dominant inherited cond …
Peutz-Jeghers syndrome (PJS) is an unusual polyposis syndrome that has enjoyed a rich and somewhat confusing his …
528 results