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

Year Number of Results
1952 1
1956 1
1957 1
1971 1
1977 1
1986 2
1987 1
1988 1
1990 1
1992 1
1993 1
1994 1
1995 1
1996 1
1998 1
1999 1
2000 1
2001 3
2002 2
2003 1
2004 7
2005 7
2006 6
2007 3
2008 3
2009 2
2010 3
2011 5
2012 5
2013 9
2014 4
2015 3
2016 4
2017 7
2018 10
2019 12
2020 10
2021 12
2022 6
2023 3
2024 0

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129 results

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Page 1
Morphea after Silicone Implants.
Wollina U, Schönlebe J. Wollina U, et al. Acta Dermatovenerol Croat. 2023 Aug;31(1):45-47. Acta Dermatovenerol Croat. 2023. PMID: 37843092
A number of case reports suggested a possible link to adjuvant autoimmune syndrome (2), morphea of the breast (3-5), and systemic scleroderma (6-8), among others. ...We report the case of a 32-year-old female patient who developed morphea of the breasts after silicone impl …
A number of case reports suggested a possible link to adjuvant autoimmune syndrome (2), morphea of the breast (3-5), and systemic scl …
Familial intestinal polyposis and device assisted enteroscopy: where do we stand?
Losurdo G, Di Leo M, Rizzi S, Lacavalla I, Celiberto F, Iannone A, Rendina M, Ierardi E, Iabichino G, De Luca L, Di Leo A. Losurdo G, et al. Expert Rev Gastroenterol Hepatol. 2023 Jul-Dec;17(8):811-816. doi: 10.1080/17474124.2023.2242240. Epub 2023 Jul 29. Expert Rev Gastroenterol Hepatol. 2023. PMID: 37515779 Review.
The best known ones are familial adenomatous polyposis (FAP), Peutz-Jeghers (PJS), juvenile polyposis and Cowden syndromes, as well as conditions predisposing to cancer, such as Lynch syndrome. ...
The best known ones are familial adenomatous polyposis (FAP), Peutz-Jeghers (PJS), juvenile polyposis and Cowden syndromes, as well a …
Peutz-Jeghers syndrome without STK11 mutation may correlate with less severe clinical manifestations in Chinese patients.
Jiang LX, Chen YR, Xu ZX, Zhang YH, Zhang Z, Yu PF, Dong ZW, Yang HR, Gu GL. Jiang LX, et al. World J Gastroenterol. 2023 Jun 7;29(21):3302-3317. doi: 10.3748/wjg.v29.i21.3302. World J Gastroenterol. 2023. PMID: 37377590 Free PMC article. Clinical Trial.
BACKGROUND: Peutz-Jeghers syndrome (PJS) is an autosomal dominant genetic disease with skin mucosal pigment spots and gastrointestinal (GI) multiple hamartoma polyps as clinical characteristics. ...AIM: To investigates whether PJS patients with known S …
BACKGROUND: Peutz-Jeghers syndrome (PJS) is an autosomal dominant genetic disease with skin mucosal pigment spots and gastrointestina …
Sirolimus treatment of a PTEN hamartoma tumor syndrome presenting with melena.
Şahin GE, Hoşnut FÖ, Yeşil Ş, Lafcı NG, Gül AE, Şahin G. Şahin GE, et al. Turk J Pediatr. 2022;64(4):766-774. doi: 10.24953/turkjped.2021.5330. Turk J Pediatr. 2022. PMID: 36082652 Free article.
BACKGROUND: PTEN hamartoma tumor syndrome (PHTS) is an umbrella term including Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome (BRRS), PTEN-related Proteus syndrome (PS), and PTEN-related Proteus-like syndrome. ...CONCLUSIO …
BACKGROUND: PTEN hamartoma tumor syndrome (PHTS) is an umbrella term including Cowden syndrome (CS), Bannayan-Ri …
Long-term treatment of cancer-prone germline PTEN mutant mice with low-dose rapamycin extends lifespan and delays tumour development.
Tibarewal P, Rathbone V, Constantinou G, Pearce W, Adil M, Varyova Z, Folkes L, Hampson A, Classen GAE, Alves A, Carvalho S, Scudamore CL, Vanhaesebroeck B. Tibarewal P, et al. J Pathol. 2022 Dec;258(4):382-394. doi: 10.1002/path.6009. Epub 2022 Oct 31. J Pathol. 2022. PMID: 36073856 Free PMC article.
Germline heterozygous PTEN gene alterations also underlie PTEN hamartoma tumour syndrome (PHTS), a rare human cancer-predisposition condition. ...However, this has not been explored in cancer prevention in a model of germline cancer predisposition, such as PHTS. …
Germline heterozygous PTEN gene alterations also underlie PTEN hamartoma tumour syndrome (PHTS), a rare human cancer-predispos …
A phase II study of TAS-117 in patients with advanced solid tumors harboring germline PTEN-inactivating mutations.
Rodón J, Funchain P, Laetsch TW, Arkenau HT, Hervieu A, Singer CF, Murciano-Goroff YR, Chawla SP, Anthony K, Yamamiya I, Liu M, Halim AB, Benhadji KA, Takahashi O, Delaloge S. Rodón J, et al. Future Oncol. 2022 Sep;18(30):3377-3387. doi: 10.2217/fon-2022-0305. Epub 2022 Aug 30. Future Oncol. 2022. PMID: 36039910 Free PMC article.
Germline mutations in the PTEN gene are a hallmark of PTEN hamartoma tumor syndrome, which includes Cowden syndrome, where they appear to elevate lifetime risk of cancer. ...Clinical Trial Registration: NCT04770246 (ClinicalTrials.gov)... …
Germline mutations in the PTEN gene are a hallmark of PTEN hamartoma tumor syndrome, which includes Cowden syndrome
Phenotypic Features of Cystic Lung Disease in Proteus Syndrome: A Clinical Trial.
Keppler-Noreuil KM, Burton-Akright J, Kleiner DE, Sapp JC, Lindhurst MJ, Han CG, Biesecker LG, Gochuico BR. Keppler-Noreuil KM, et al. Ann Am Thorac Soc. 2022 Nov;19(11):1871-1880. doi: 10.1513/AnnalsATS.202111-1214OC. Ann Am Thorac Soc. 2022. PMID: 35839129 Free PMC article.
Objectives: To define the phenotype of cystic lung disease in Proteus syndrome. Methods: Medical records, pulmonary function tests, and chest computed tomography of 39 individuals with Proteus syndrome evaluated at a single center were retrospectively reviewed. ... …
Objectives: To define the phenotype of cystic lung disease in Proteus syndrome. Methods: Medical records, pulmonary function tests, a …
Lip Papillomas in Cowden Disease: Carbon Dioxide Laser Vaporization.
Del Pozo Losada J, Barja López JM. Del Pozo Losada J, et al. Actas Dermosifiliogr. 2022 Jun;113(6):640-641. doi: 10.1016/j.ad.2020.08.018. Epub 2021 Jul 26. Actas Dermosifiliogr. 2022. PMID: 35730160 Free article. English, Spanish. No abstract available.
A randomized controlled trial of everolimus for neurocognitive symptoms in PTEN hamartoma tumor syndrome.
Srivastava S, Jo B, Zhang B, Frazier T, Gallagher AS, Peck F, Levin AR, Mondal S, Li Z, Filip-Dhima R, Geisel G, Dies KA, Diplock A, Eng C, Hanna R, Sahin M, Hardan A; Developmental Synaptopathies Consortium. Srivastava S, et al. Hum Mol Genet. 2022 Oct 10;31(20):3393-3404. doi: 10.1093/hmg/ddac111. Hum Mol Genet. 2022. PMID: 35594551 Free PMC article. Clinical Trial.
PTEN hamartoma tumor syndrome (PHTS) is a complex neurodevelopmental disorder characterized by mechanistic target of rapamycin (mTOR) overactivity. ...No placebo-controlled studies have examined mTOR inhibition on cognition and behavior in humans with PHTS with/with …
PTEN hamartoma tumor syndrome (PHTS) is a complex neurodevelopmental disorder characterized by mechanistic target of rapamycin …
129 results