Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

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

Year Number of Results
1945 1
1950 1
1953 1
1954 1
1955 4
1956 6
1957 15
1958 14
1959 22
1960 15
1961 12
1962 20
1963 14
1964 21
1965 22
1966 19
1967 34
1968 23
1969 28
1970 35
1971 39
1972 29
1973 35
1974 31
1975 25
1976 19
1977 25
1978 22
1979 32
1980 26
1981 15
1982 23
1983 23
1984 28
1985 25
1986 32
1987 19
1988 17
1989 25
1990 22
1991 23
1992 13
1993 16
1994 31
1995 22
1996 21
1997 24
1998 48
1999 57
2000 57
2001 49
2002 50
2003 68
2004 76
2005 63
2006 83
2007 78
2008 77
2009 84
2010 79
2011 97
2012 82
2013 90
2014 80
2015 86
2016 82
2017 77
2018 72
2019 76
2020 66
2021 81
2022 96
2023 74
2024 71

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

2,802 results

Results by year

Filters applied: . Clear all
Page 1
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 …
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 …
Peutz-Jeghers Syndrome.
Sato E, Goto T, Honda H. Sato E, et al. JAMA Dermatol. 2022 Nov 1;158(11):1316. doi: 10.1001/jamadermatol.2022.3979. JAMA Dermatol. 2022. PMID: 36197686
Gastrointestinal aspects of Peutz-Jeghers syndrome.
Latchford AR, Clark SK. Latchford AR, et al. Best Pract Res Clin Gastroenterol. 2022 Jun-Aug;58-59:101789. doi: 10.1016/j.bpg.2022.101789. Epub 2022 Apr 6. Best Pract Res Clin Gastroenterol. 2022. PMID: 35988959 Review.
There are two main problems in the clinical management of the gastrointestinal (GI) tract in patients with Peutz-Jeghers syndrome (PJS), namely long-term cancer risk and managing polyp related complications (of which the most important clinically is intussusc …
There are two main problems in the clinical management of the gastrointestinal (GI) tract in patients with Peutz-Jeghers sy …
Peutz-Jeghers syndrome in dermatology.
Nevozinskaya Z, Korsunskaya I, Sakaniya L, Perlamutrov Y, Sobolev V. Nevozinskaya Z, et al. Acta Dermatovenerol Alp Pannonica Adriat. 2019 Sep;28(3):135-137. Acta Dermatovenerol Alp Pannonica Adriat. 2019. PMID: 31545393 Free article.
Peutz-Jeghers syndrome is a rare autosomal dominant disorder. Approximately 1:25,000 to 1:280,000 cases are registered annually. ...Patients with Peutz-Jeghers syndrome often develop various malignant neoplasms, mainly localized in the pa …
Peutz-Jeghers syndrome is a rare autosomal dominant disorder. Approximately 1:25,000 to 1:280,000 cases are registered …
Peutz-Jeghers syndrome: a new understanding.
Choi HS, Park YJ, Park JG. Choi HS, et al. J Korean Med Sci. 1999 Feb;14(1):2-7. doi: 10.3346/jkms.1999.14.1.2. J Korean Med Sci. 1999. PMID: 10102516 Free PMC article. Review.
Recently, Peutz-Jeghers syndrome susceptibility gene, encoding the serine threonine kinase STK11 (also called LKB1), was identified in families with Peutz-Jeghers syndrome. The identifications of germline mutations in families with Peu …
Recently, Peutz-Jeghers syndrome susceptibility gene, encoding the serine threonine kinase STK11 (also called LKB1), wa …
Peutz-Jeghers syndrome: management for recurrent intussusceptions.
Verma A, Kanneganti P, Kumar B, Upadhyaya VD, Mandelia A, Naik PB, Kumar T, Agarwal N. Verma A, et al. Pediatr Surg Int. 2024 Jun 2;40(1):148. doi: 10.1007/s00383-024-05723-y. Pediatr Surg Int. 2024. PMID: 38825635
BACKGROUND: Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder characterized by hamartomatous gastrointestinal polyps along with the characteristic mucocutaneous freckling. Multiple surgeries for recurrent intussusception in these children may lea …
BACKGROUND: Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder characterized by hamartomatous gastrointesti …
Peutz-Jeghers syndrome.
Heymann WR. Heymann WR. J Am Acad Dermatol. 2007 Sep;57(3):513-4. doi: 10.1016/j.jaad.2007.03.022. J Am Acad Dermatol. 2007. PMID: 17707154
[100 years Peutz-Jeghers syndrome].
de Jong MA, van Leerdam ME, Offerhaus GJAJ, Keller JJ. de Jong MA, et al. Ned Tijdschr Geneeskd. 2022 May 4;166:D6507. Ned Tijdschr Geneeskd. 2022. PMID: 35736377 Dutch.
In 2021 it was 100 years since drPeutz published his case report titled: 'a very remarkable case of familial polyposis of mucous membranes of intestinal tract and nasopharynx accompanied by peculiar pigmentations of skin and mucous membrane'. This is the first description of the …
In 2021 it was 100 years since drPeutz published his case report titled: 'a very remarkable case of familial polyposis of mucous membranes o …
[Management of the Peutz-Jeghers Syndrome].
Möslein G. Möslein G. Zentralbl Chir. 2023 Dec;148(6):492-501. doi: 10.1055/a-2109-3140. Epub 2023 Sep 5. Zentralbl Chir. 2023. PMID: 37669766 German.
The current evidence to guide management of Peutz-Jeghers Syndrome (PJS) is sparse. Here we summarise the European guidelines that were published in 2021 by the EHTG (European Hereditary Tumour Group), extended with new evidence on some aspects of clinical ma …
The current evidence to guide management of Peutz-Jeghers Syndrome (PJS) is sparse. Here we summarise the European guid …
2,802 results