Similar articles for PMID: 28434922

Year	Number of Results
1997	1
1998	1
2000	1
2001	2
2004	2
2005	4
2006	4
2007	3
2008	1
2010	6
2011	5
2012	13
2013	11
2014	10
2015	11
2016	5
2017	2
2019	10
2020	6
2021	2
2022	9
2023	2
2024	0

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. Guaraldi F, et al. Eur J Med Genet. 2017 Jul;60(7):380-384. doi: 10.1016/j.ejmg.2017.04.010. Epub 2017 Apr 18. Eur J Med Genet. 2017. PMID: 28434922 Review.

2

Aggressive juvenile polyposis in children with chromosome 10q23 deletion.

Septer S, Zhang L, Lawson CE, Cocjin J, Attard T, Ardinger HH. Septer S, et al. World J Gastroenterol. 2013;19(14):2286-92. doi: 10.3748/wjg.v19.i14.2286. World J Gastroenterol. 2013. PMID: 23599658 Free PMC article.

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. Hiljadnikova Bajro M, et al. J Appl Genet. 2013 Feb;54(1):43-7. doi: 10.1007/s13353-012-0115-z. Epub 2012 Sep 21. J Appl Genet. 2013. PMID: 22993021

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. Oliveira PH, et al. J Pediatr Surg. 2013 Jan;48(1):e33-7. doi: 10.1016/j.jpedsurg.2012.09.067. J Pediatr Surg. 2013. PMID: 23331837 Free article.

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. Alimi A, et al. Am J Med Genet A. 2015 Jun;167(6):1305-8. doi: 10.1002/ajmg.a.36876. Epub 2015 Apr 5. Am J Med Genet A. 2015. PMID: 25846706 Free PMC article.

6

Juvenile polyposis and other intestinal polyposis syndromes with microdeletions of chromosome 10q22-23.

Dahdaleh FS, Carr JC, Calva D, Howe JR. Dahdaleh FS, et al. Clin Genet. 2012 Feb;81(2):110-6. doi: 10.1111/j.1399-0004.2011.01763.x. Epub 2011 Sep 6. Clin Genet. 2012. PMID: 21834858 Free PMC article. Review.

7

Chromosome 10q23 Deletion Syndrome: An Overlap of Bannayan-Riley-Ruvalcaba Syndrome and Juvenile Polyposis Syndrome.

Waisbourd-Zinman O, Mamula P, Piccoli DA. Waisbourd-Zinman O, et al. J Paediatr Child Health. 2016 Aug;52(8):852. doi: 10.1111/jpc.13289. J Paediatr Child Health. 2016. PMID: 27535890 No abstract available.

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. Boland CR, et al. Gastroenterology. 2022 Jun;162(7):2063-2085. doi: 10.1053/j.gastro.2022.02.021. Epub 2022 Apr 26. Gastroenterology. 2022. PMID: 35487791

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. Boland CR, et al. Am J Gastroenterol. 2022 Jun 1;117(6):846-864. doi: 10.14309/ajg.0000000000001755. Epub 2022 Apr 26. Am J Gastroenterol. 2022. PMID: 35471415

10

Interstitial deletion of 10q23.1 and confirmation of three 10qdel syndromes.

Singh S, Aftimos S, George A, Love DR. Singh S, et al. Singapore Med J. 2011 Jul;52(7):e143-6. Singapore Med J. 2011. PMID: 21808946 Free article.

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