137 related articles for article (PubMed ID: 28434922)
1. Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation.
Guaraldi F; Di Nardo G; Tarani L; Bertelli L; Susca FC; Bagnulo R; Resta N
Eur J Med Genet; 2017 Jul; 60(7):380-384. PubMed ID: 28434922
[TBL] [Abstract][Full Text] [Related]
2. Aggressive juvenile polyposis in children with chromosome 10q23 deletion.
Septer S; Zhang L; Lawson CE; Cocjin J; Attard T; Ardinger HH
World J Gastroenterol; 2013; 19(14):2286-92. PubMed ID: 23599658
[TBL] [Abstract][Full Text] [Related]
3. A new case with 10q23 interstitial deletion encompassing both PTEN and BMPR1A narrows the genetic region deleted in juvenile polyposis syndrome.
Hiljadnikova Bajro M; Sukarova-Angelovska E; Adélaïde J; Chaffanet M; Dimovski AJ
J Appl Genet; 2013 Feb; 54(1):43-7. PubMed ID: 22993021
[TBL] [Abstract][Full Text] [Related]
4. Juvenile polyposis of infancy in a child with deletion of BMPR1A and PTEN genes: surgical approach.
Oliveira PH; Cunha C; Almeida S; Ferreira R; Maia S; Saraiva JM; Lopes MF
J Pediatr Surg; 2013 Jan; 48(1):e33-7. PubMed ID: 23331837
[TBL] [Abstract][Full Text] [Related]
5. Overlap of Juvenile polyposis syndrome and Cowden syndrome due to de novo chromosome 10 deletion involving BMPR1A and PTEN: implications for treatment and surveillance.
Alimi A; Weeth-Feinstein LA; Stettner A; Caldera F; Weiss JM
Am J Med Genet A; 2015 Jun; 167(6):1305-8. PubMed ID: 25846706
[TBL] [Abstract][Full Text] [Related]
6. Juvenile polyposis and other intestinal polyposis syndromes with microdeletions of chromosome 10q22-23.
Dahdaleh FS; Carr JC; Calva D; Howe JR
Clin Genet; 2012 Feb; 81(2):110-6. PubMed ID: 21834858
[TBL] [Abstract][Full Text] [Related]
7. Chromosome 10q23 Deletion Syndrome: An Overlap of Bannayan-Riley-Ruvalcaba Syndrome and Juvenile Polyposis Syndrome.
Waisbourd-Zinman O; Mamula P; Piccoli DA
J Paediatr Child Health; 2016 Aug; 52(8):852. PubMed ID: 27535890
[No Abstract] [Full Text] [Related]
8. Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer.
Boland CR; Idos GE; Durno C; Giardiello FM; Anderson JC; Burke CA; Dominitz JA; Gross S; Gupta S; Jacobson BC; Patel SG; Shaukat A; Syngal S; Robertson DJ
Gastroenterology; 2022 Jun; 162(7):2063-2085. PubMed ID: 35487791
[TBL] [Abstract][Full Text] [Related]
9. Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer.
Boland CR; Idos GE; Durno C; Giardiello FM; Anderson JC; Burke CA; Dominitz JA; Gross S; Gupta S; Jacobson BC; Patel SG; Shaukat A; Syngal S; Robertson DJ
Am J Gastroenterol; 2022 Jun; 117(6):846-864. PubMed ID: 35471415
[TBL] [Abstract][Full Text] [Related]
10. Interstitial deletion of 10q23.1 and confirmation of three 10qdel syndromes.
Singh S; Aftimos S; George A; Love DR
Singapore Med J; 2011 Jul; 52(7):e143-6. PubMed ID: 21808946
[TBL] [Abstract][Full Text] [Related]
11. Patients with 10q22.3q23.1 recurrent deletion syndrome are at risk for juvenile polyposis.
Lecoquierre F; Cassinari K; Chambon P; Nicolas G; Malsa S; Marlin R; Assouline Y; Fléjou JF; Frebourg T; Houdayer C; Bera O; Baert-Desurmont S
Eur J Med Genet; 2020 Apr; 63(4):103773. PubMed ID: 31561016
[TBL] [Abstract][Full Text] [Related]
12. Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes.
Menko FH; Kneepkens CM; de Leeuw N; Peeters EA; Van Maldergem L; Kamsteeg EJ; Davidson R; Rozendaal L; Lasham CA; Peeters-Scholte CM; Jansweijer MC; Hilhorst-Hofstee Y; Gille JJ; Heins YM; Nieuwint AW; Sistermans EA
Clin Genet; 2008 Aug; 74(2):145-54. PubMed ID: 18510548
[TBL] [Abstract][Full Text] [Related]
13. Familial juvenile polyposis syndrome with a de novo germline missense variant in BMPR1A gene: a case report.
Liu Q; Liu M; Liu T; Yu Y
BMC Med Genet; 2020 Oct; 21(1):196. PubMed ID: 33032550
[TBL] [Abstract][Full Text] [Related]
14. Successful Treatment of Juvenile Polyposis of Infancy With Sirolimus.
Busoni VB; Orsi M; Lobos PA; D'Agostino D; Wagener M; De la Iglesia P; Fox VL
Pediatrics; 2019 Aug; 144(2):. PubMed ID: 31366686
[TBL] [Abstract][Full Text] [Related]
15. Genotype-defined cancer risk in juvenile polyposis syndrome.
Aytac E; Sulu B; Heald B; O'Malley M; LaGuardia L; Remzi FH; Kalady MF; Burke CA; Church JM
Br J Surg; 2015 Jan; 102(1):114-8. PubMed ID: 25389115
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Deletion of PTEN and BMPR1A on chromosome 10q23 is not always associated with juvenile polyposis of infancy.
Salviati L; Patricelli M; Guariso G; Sturniolo GC; Alaggio R; Bernardi F; Zuffardi O; Tenconi R
Am J Hum Genet; 2006 Sep; 79(3):593-6; author reply 596-7. PubMed ID: 16909400
[No Abstract] [Full Text] [Related]
18. BMPR1A mutations in juvenile polyposis affect cellular localization.
Howe JR; Dahdaleh FS; Carr JC; Wang D; Sherman SK; Howe JR
J Surg Res; 2013 Oct; 184(2):739-45. PubMed ID: 23433720
[TBL] [Abstract][Full Text] [Related]
19. [Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer].
Jelsig AM; Tørring PM; Qvist N; Bernstein I; Ousager LB
Ugeskr Laeger; 2013 Nov; 175(47A):. PubMed ID: 25353092
[TBL] [Abstract][Full Text] [Related]
20. mTOR inhibitors reduce enteropathy, intestinal bleeding and colectomy rate in patients with juvenile polyposis of infancy with PTEN-BMPR1A deletion.
Taylor H; Yerlioglu D; Phen C; Ballauff A; Nedelkopoulou N; Spier I; Loverdos I; Busoni VB; Heise J; Dale P; de Meij T; Sweet K; Cohen MC; Fox VL; Mas E; Aretz S; Eng C; Buderus S; Thomson M; Rojas I; Uhlig HH
Hum Mol Genet; 2021 Jun; 30(14):1273-1282. PubMed ID: 33822054
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
