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Page 1
Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.
Livide G, Epistolato MC, Amenduni M, Disciglio V, Marozza A, Mencarelli MA, Toti P, Lazzi S, Hadjistilianou T, De Francesco S, D'Ambrosio A, Renieri A, Ariani F. Livide G, et al. Among authors: marozza a. Pathol Oncol Res. 2012 Jul;18(3):703-12. doi: 10.1007/s12253-012-9498-8. Epub 2012 Jan 26. Pathol Oncol Res. 2012. PMID: 22278416 Free article.
p53 Arg72Pro and MDM2 309 SNPs in hereditary retinoblastoma.
Epistolato MC, Disciglio V, Livide G, Berchialla P, Mencarelli MA, Marozza A, Amenduni M, Hadjistilianou T, De Francesco S, Acquaviva A, Toti P, Cetta F, Ariani F, De Marchi M, Renieri A, Giachino D. Epistolato MC, et al. Among authors: marozza a. J Hum Genet. 2011 Sep;56(9):685-6. doi: 10.1038/jhg.2011.82. Epub 2011 Aug 4. J Hum Genet. 2011. PMID: 21814224 Free article.
Array comparative genomic hybridization in retinoma and retinoblastoma tissues.
Sampieri K, Amenduni M, Papa FT, Katzaki E, Mencarelli MA, Marozza A, Epistolato MC, Toti P, Lazzi S, Bruttini M, De Filippis R, De Francesco S, Longo I, Meloni I, Mari F, Acquaviva A, Hadjistilianou T, Renieri A, Ariani F. Sampieri K, et al. Among authors: marozza a. Cancer Sci. 2009 Mar;100(3):465-71. doi: 10.1111/j.1349-7006.2008.01070.x. Epub 2009 Jan 29. Cancer Sci. 2009. PMID: 19183342 Free PMC article.
Next generation sequencing in sporadic retinoblastoma patients reveals somatic mosaicism.
Amitrano S, Marozza A, Somma S, Imperatore V, Hadjistilianou T, De Francesco S, Toti P, Galimberti D, Meloni I, Cetta F, Piu P, Di Marco C, Dosa L, Lo Rizzo C, Carignani G, Mencarelli MA, Mari F, Renieri A, Ariani F. Amitrano S, et al. Among authors: marozza a. Eur J Hum Genet. 2015 Nov;23(11):1523-30. doi: 10.1038/ejhg.2015.6. Epub 2015 Feb 25. Eur J Hum Genet. 2015. PMID: 25712084 Free PMC article.
Interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndrome.
Disciglio V, Lo Rizzo C, Mencarelli MA, Mucciolo M, Marozza A, Di Marco C, Massarelli A, Canocchi V, Baldassarri M, Ndoni E, Frullanti E, Amabile S, Anderlid BM, Metcalfe K, Le Caignec C, David A, Fryer A, Boute O, Joris A, Greco D, Pecile V, Battini R, Novelli A, Fichera M, Romano C, Mari F, Renieri A. Disciglio V, et al. Among authors: marozza a. Am J Med Genet A. 2014 Jul;164A(7):1666-76. doi: 10.1002/ajmg.a.36513. Epub 2014 Apr 3. Am J Med Genet A. 2014. PMID: 24700646
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria.
Artuso R, Mencarelli MA, Polli R, Sartori S, Ariani F, Pollazzon M, Marozza A, Cilio MR, Specchio N, Vigevano F, Vecchi M, Boniver C, Dalla Bernardina B, Parmeggiani A, Buoni S, Hayek G, Mari F, Renieri A, Murgia A. Artuso R, et al. Among authors: marozza a. Brain Dev. 2010 Jan;32(1):17-24. doi: 10.1016/j.braindev.2009.02.004. Epub 2009 Apr 10. Brain Dev. 2010. PMID: 19362436
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability.
Mari F, Marozza A, Mencarelli MA, Lo Rizzo C, Fallerini C, Dosa L, Di Marco C, Carignani G, Baldassarri M, Cianci P, Vivarelli R, Vascotto M, Grosso S, Rubegni P, Caffarelli C, Pretegiani E, Fimiani M, Garavelli L, Cristofoli F, Vermeesch JR, Nuti R, Dotti MT, Balestri P, Hayek J, Selicorni A, Renieri A. Mari F, et al. Among authors: marozza a. Brain Dev. 2015 May;37(5):527-36. doi: 10.1016/j.braindev.2014.08.009. Epub 2014 Sep 22. Brain Dev. 2015. PMID: 25249037
19 results