Chiurazzi P - Search Results

1

Exfoliative Cytology and Genetic Analysis for a Non-Invasive Approach to the Diagnosis of White Sponge Nevus: Case Series.

Lajolo C, Cafiero C, Stigliano E, Grippaudo FR, Chiurazzi P, Grippaudo C. Lajolo C, et al. Among authors: chiurazzi p. Bioengineering (Basel). 2023 Jan 23;10(2):154. doi: 10.3390/bioengineering10020154. Bioengineering (Basel). 2023. PMID: 36829648 Free PMC article.

2

XLMR genes: update 1998.

Lubs H, Chiurazzi P, Arena J, Schwartz C, Tranebjaerg L, Neri G. Lubs H, et al. Among authors: chiurazzi p. Am J Med Genet. 1999 Apr 2;83(4):237-47. Am J Med Genet. 1999. PMID: 10208155 Review.

3

Genetics of mental retardation.

Chiurazzi P, Oostra BA. Chiurazzi P, et al. Curr Opin Pediatr. 2000 Dec;12(6):529-35. doi: 10.1097/00008480-200012000-00003. Curr Opin Pediatr. 2000. PMID: 11106270 Review.

4

XLMR genes: update 1992.

Neri G, Chiurazzi P, Arena F, Lubs HA, Glass IA. Neri G, et al. Among authors: chiurazzi p. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):373-82. doi: 10.1002/ajmg.1320430158. Am J Med Genet. 1992. PMID: 1605215 Review.

5

Bioinformatic analysis indicates that SARS-CoV-2 is unrelated to known artificial coronaviruses.

Dallavilla T, Bertelli M, Morresi A, Bushati V, Stuppia L, Beccari T, Chiurazzi P, Marceddu G. Dallavilla T, et al. Among authors: chiurazzi p. Eur Rev Med Pharmacol Sci. 2020 Apr;24(8):4558-4564. doi: 10.26355/eurrev_202004_21041. Eur Rev Med Pharmacol Sci. 2020. PMID: 32373995 Free article.

6

No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome.

Chiurazzi P, de Graaff E, Ng J, Verkerk AJ, Wolfson S, Fisch GS, Kozak L, Neri G, Oostra BA. Chiurazzi P, et al. Am J Med Genet. 1994 Jul 15;51(4):309-14. doi: 10.1002/ajmg.1320510405. Am J Med Genet. 1994. PMID: 7942992

7

Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications.

De Bonis ML, Cerase A, Matarazzo MR, Ferraro M, Strazzullo M, Hansen RS, Chiurazzi P, Neri G, D'Esposito M. De Bonis ML, et al. Among authors: chiurazzi p. Hum Mol Genet. 2006 Apr 1;15(7):1123-32. doi: 10.1093/hmg/ddl027. Epub 2006 Feb 24. Hum Mol Genet. 2006. PMID: 16500999

8

DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature.

Chiurazzi P, Pomponi MG, Sharrock A, Macpherson J, Lormeau S, Morel ML, Rousseau F. Chiurazzi P, et al. Am J Med Genet. 1999 Apr 2;83(4):347-9. Am J Med Genet. 1999. PMID: 10208178 No abstract available.

9

Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine.

Pietrobono R, Pomponi MG, Tabolacci E, Oostra B, Chiurazzi P, Neri G. Pietrobono R, et al. Among authors: chiurazzi p. Nucleic Acids Res. 2002 Jul 15;30(14):3278-85. doi: 10.1093/nar/gkf434. Nucleic Acids Res. 2002. PMID: 12136110 Free PMC article.

10

Double-blind, placebo-controlled study of L-acetylcarnitine for the treatment of hyperactive behavior in fragile X syndrome.

Torrioli MG, Vernacotola S, Mariotti P, Bianchi E, Calvani M, De Gaetano A, Chiurazzi P, Neri G. Torrioli MG, et al. Among authors: chiurazzi p. Am J Med Genet. 1999 Dec 3;87(4):366-8. Am J Med Genet. 1999. PMID: 10588848 Clinical Trial. No abstract available.

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