Redaelli S - Search Results

1

Partial duplication of the PARK2 gene in a child with developmental delay and her normal mother: a second report.

Mariani M, Crosti F, Redaelli S, Fossati C, Piras R, Biondi A, Dalprà L, Selicorni A. Mariani M, et al. Among authors: redaelli s. Am J Med Genet B Neuropsychiatr Genet. 2013 Jul;162B(5):485-6. doi: 10.1002/ajmg.b.32173. Epub 2013 Jun 6. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23740672 No abstract available.

2

AhRR and PPP1R3C: Potential Prognostic Biomarkers for Serous Ovarian Cancer.

Ardizzoia A, Jemma A, Redaelli S, Silva M, Bentivegna A, Lavitrano M, Conconi D. Ardizzoia A, et al. Among authors: redaelli s. Int J Mol Sci. 2023 Jul 14;24(14):11455. doi: 10.3390/ijms241411455. Int J Mol Sci. 2023. PMID: 37511212 Free PMC article.

3

Insights into the Peritumoural Brain Zone of Glioblastoma: CDK4 and EXT2 May Be Potential Drivers of Malignancy.

Giambra M, Di Cristofori A, Conconi D, Marzorati M, Redaelli S, Zambuto M, Rocca A, Roumy L, Carrabba G, Lavitrano M, Roversi G, Giussani C, Bentivegna A. Giambra M, et al. Among authors: redaelli s. Int J Mol Sci. 2023 Feb 2;24(3):2835. doi: 10.3390/ijms24032835. Int J Mol Sci. 2023. PMID: 36769158 Free PMC article.

4

Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature.

Redaelli S, Sala E, Roncaglia N, Colombo C, Crosti F, Villa N, Tagliabue P, Cappellini A, Dalprà L. Redaelli S, et al. Prenat Diagn. 2005 Feb;25(2):140-7. doi: 10.1002/pd.1093. Prenat Diagn. 2005. PMID: 15712378 Review.

5

Fetal trisomy 5 mosaicism: case report and literature review.

Villa N, Redaelli S, Borroni C, Colombo C, Roncaglia N, Sala E, Crosti F, Cappellini A, Dalprà L. Villa N, et al. Among authors: redaelli s. Am J Med Genet A. 2007 Oct 1;143A(19):2343-6. doi: 10.1002/ajmg.a.31909. Am J Med Genet A. 2007. PMID: 17702005 Review. No abstract available.

6

Ophthalmic features in a dysmorphic boy with chromosome 4q deletion and duplication.

Parentin F, Fabretto A, Benussi DG, Petix V, Marchetti F, Dalprà L, Redaelli S, Pensiero S, Pecile V. Parentin F, et al. Among authors: redaelli s. Ophthalmic Genet. 2009 Jun;30(2):103-5. doi: 10.1080/13816810802592559. Ophthalmic Genet. 2009. PMID: 19373683

7

A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome.

Martinoli E, Zuccotti GV, Pogliani L, Volontè M, Venturin M, Fortina P, Ertel A, Redaelli S, Riva P, Dalprà L. Martinoli E, et al. Among authors: redaelli s. Am J Med Genet A. 2010 Apr;152A(4):1043-5. doi: 10.1002/ajmg.a.33335. Am J Med Genet A. 2010. PMID: 20358625 No abstract available.

8

Familial subtelomeric rearrangement of chromosomes 19 and 20: a new contribution to partial distal 19q trisomy.

Lenzini E, Drigo P, Redaelli S, Mammi I, Rosa-Rizzotto M, Dalprà L. Lenzini E, et al. Among authors: redaelli s. Genet Test Mol Biomarkers. 2010 Oct;14(5):695-701. doi: 10.1089/gtmb.2010.0079. Epub 2010 Sep 20. Genet Test Mol Biomarkers. 2010. PMID: 20854099

9

Cytogenetics of premature ovarian failure: an investigation on 269 affected women.

Baronchelli S, Conconi D, Panzeri E, Bentivegna A, Redaelli S, Lissoni S, Saccheri F, Villa N, Crosti F, Sala E, Martinoli E, Volontè M, Marozzi A, Dalprà L. Baronchelli S, et al. Among authors: redaelli s. J Biomed Biotechnol. 2011;2011:370195. doi: 10.1155/2011/370195. Epub 2011 Jan 17. J Biomed Biotechnol. 2011. PMID: 21318170 Free PMC article.

10

A de novo supernumerary genomic discontinuous ring chromosome 21 in a child with mild intellectual disability.

Villa N, Bentivegna A, Ertel A, Redaelli S, Colombo C, Nacinovich R, Broggi F, Lissoni S, Bungaro S, Addya S, Fortina P, Dalprà L. Villa N, et al. Among authors: redaelli s. Am J Med Genet A. 2011 Jun;155A(6):1425-31. doi: 10.1002/ajmg.a.34010. Epub 2011 May 13. Am J Med Genet A. 2011. PMID: 21574245

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