These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
217 related articles for article (PubMed ID: 37307869)
1. Novel dermatological and skeletal features associated with PTEN variant in PTEN hamartoma tumor syndrome. Comeau D; Allain V; Maillet-Lebel N; Ben Amor M Eur J Med Genet; 2023 Aug; 66(8):104798. PubMed ID: 37307869 [TBL] [Abstract][Full Text] [Related]
2. PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol. Piccione M; Fragapane T; Antona V; Giachino D; Cupido F; Corsello G Am J Med Genet A; 2013 Nov; 161A(11):2902-8. PubMed ID: 24123798 [TBL] [Abstract][Full Text] [Related]
3. Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations. Yehia L; Ni Y; Sesock K; Niazi F; Fletcher B; Chen HJL; LaFramboise T; Eng C PLoS Genet; 2018 Apr; 14(4):e1007352. PubMed ID: 29684080 [TBL] [Abstract][Full Text] [Related]
5. Breast cancer risk and clinical implications for germline PTEN mutation carriers. Ngeow J; Sesock K; Eng C Breast Cancer Res Treat; 2017 Aug; 165(1):1-8. PubMed ID: 26700035 [TBL] [Abstract][Full Text] [Related]
6. Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes. Pezzolesi MG; Li Y; Zhou XP; Pilarski R; Shen L; Eng C Am J Hum Genet; 2006 Nov; 79(5):923-34. PubMed ID: 17033968 [TBL] [Abstract][Full Text] [Related]
7. Imaging of PTEN-related abnormalities in the central nervous system. Dhamija R; Hoxworth JM Clin Imaging; 2020 Apr; 60(2):180-185. PubMed ID: 31927175 [TBL] [Abstract][Full Text] [Related]
8. PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes. Kurek KC; Howard E; Tennant LB; Upton J; Alomari AI; Burrows PE; Chalache K; Harris DJ; Trenor CC; Eng C; Fishman SJ; Mulliken JB; Perez-Atayde AR; Kozakewich HP Am J Surg Pathol; 2012 May; 36(5):671-87. PubMed ID: 22446940 [TBL] [Abstract][Full Text] [Related]
9. PTEN germline mutations in patients initially tested for other hereditary cancer syndromes: would use of risk assessment tools reduce genetic testing? Mester JL; Moore RA; Eng C Oncologist; 2013; 18(10):1083-90. PubMed ID: 24037976 [TBL] [Abstract][Full Text] [Related]
10. Analysis of prevalence and degree of macrocephaly in patients with germline PTEN mutations and of brain weight in Pten knock-in murine model. Mester JL; Tilot AK; Rybicki LA; Frazier TW; Eng C Eur J Hum Genet; 2011 Jul; 19(7):763-8. PubMed ID: 21343951 [TBL] [Abstract][Full Text] [Related]
11. PTEN Hamartoma tumor syndrome in childhood: A review of the clinical literature. Macken WL; Tischkowitz M; Lachlan KL Am J Med Genet C Semin Med Genet; 2019 Dec; 181(4):591-610. PubMed ID: 31609537 [TBL] [Abstract][Full Text] [Related]
12. Thyroid pathology in PTEN-hamartoma tumor syndrome: characteristic findings of a distinct entity. Laury AR; Bongiovanni M; Tille JC; Kozakewich H; Nosé V Thyroid; 2011 Feb; 21(2):135-44. PubMed ID: 21190448 [TBL] [Abstract][Full Text] [Related]
13. Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome. Busa T; Milh M; Degardin N; Girard N; Sigaudy S; Longy M; Olshchwang S; Sobol H; Chabrol B; Philip N Eur J Paediatr Neurol; 2015 Mar; 19(2):188-92. PubMed ID: 25549896 [TBL] [Abstract][Full Text] [Related]
15. Looking for the hidden mutation: Bannayan-Riley-Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A. Golas MM; Auber B; Ripperger T; Pabst B; Schmidt G; Morlot M; Diebold U; Steinemann D; Schlegelberger B; Morlot S Am J Med Genet A; 2019 Jul; 179(7):1383-1389. PubMed ID: 31062505 [TBL] [Abstract][Full Text] [Related]
16. Genetic and phenotypic heterogeneity in the PTEN hamartoma tumour syndrome. Orloff MS; Eng C Oncogene; 2008 Sep; 27(41):5387-97. PubMed ID: 18794875 [TBL] [Abstract][Full Text] [Related]
17. Thyroid Pathology Findings in Cowden Syndrome: A Clue for the Diagnosis of the PTEN Hamartoma Tumor Syndrome. Cameselle-Teijeiro J; Fachal C; Cabezas-Agrícola JM; Alfonsín-Barreiro N; Abdulkader I; Vega-Gliemmo A; Hermo JA Am J Clin Pathol; 2015 Aug; 144(2):322-8. PubMed ID: 26185318 [TBL] [Abstract][Full Text] [Related]
18. Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations. Sherman SK; Maxwell JE; Qian Q; Bellizzi AM; Braun TA; Iannettoni MD; Darbro BW; Howe JR Cancer Genet; 2015; 208(1-2):41-6. PubMed ID: 25554686 [TBL] [Abstract][Full Text] [Related]
19. Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway. Zhou XP; Waite KA; Pilarski R; Hampel H; Fernandez MJ; Bos C; Dasouki M; Feldman GL; Greenberg LA; Ivanovich J; Matloff E; Patterson A; Pierpont ME; Russo D; Nassif NT; Eng C Am J Hum Genet; 2003 Aug; 73(2):404-11. PubMed ID: 12844284 [TBL] [Abstract][Full Text] [Related]