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A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype.
Berardinelli F, di Masi A, Salvatore M, Banerjee S, Myung K, De Villartay JP, Revy P, Plebani A, Soresina A, Taruscio D, Tanzarella C, Antoccia A. Berardinelli F, et al. Among authors: salvatore m. Eur J Med Genet. 2007 May-Jun;50(3):176-87. doi: 10.1016/j.ejmg.2007.01.006. Epub 2007 Feb 21. Eur J Med Genet. 2007. PMID: 17395558
The Italian external quality assessment scheme in classical cytogenetics: four years of activity.
Floridia G, Falbo V, Censi F, Tosto F, Salvatore M, Baroncini A, Battaglia P, Conti A, Donti E, La Starza R, Nitsch L, Pierluigi M, Piombo G, Susca F, Mancini M, Mecucci C, Calzolari E, Dagna Bricarelli F, Guanti G, Taruscio D. Floridia G, et al. Among authors: salvatore m. Community Genet. 2008;11(5):295-303. doi: 10.1159/000121401. Epub 2008 May 20. Community Genet. 2008. PMID: 18493128
Altered microRNA Expression Patterns in Hepatoblastoma Patients.
Magrelli A, Azzalin G, Salvatore M, Viganotti M, Tosto F, Colombo T, Devito R, Di Masi A, Antoccia A, Lorenzetti S, Maranghi F, Mantovani A, Tanzarella C, Macino G, Taruscio D. Magrelli A, et al. Among authors: salvatore m. Transl Oncol. 2009 Aug 18;2(3):157-63. doi: 10.1593/tlo.09124. Transl Oncol. 2009. PMID: 19701500 Free PMC article.
Complex multipathways alterations and oxidative stress are associated with Hailey-Hailey disease.
Cialfi S, Oliviero C, Ceccarelli S, Marchese C, Barbieri L, Biolcati G, Uccelletti D, Palleschi C, Barboni L, De Bernardo C, Grammatico P, Magrelli A, Salvatore M, Taruscio D, Frati L, Gulino A, Screpanti I, Talora C. Cialfi S, et al. Among authors: salvatore m. Br J Dermatol. 2010 Mar;162(3):518-26. doi: 10.1111/j.1365-2133.2009.09500.x. Epub 2009 Nov 9. Br J Dermatol. 2010. PMID: 19903178
1,326 results