Ravazzolo R - Search Results

1

Rarely occurring mutation of ACVR1 gene in Moroccan patient with fibrodysplasia ossificans progressiva.

Ratbi I, Bocciardi R, Regragui A, Ravazzolo R, Sefiani A. Ratbi I, et al. Among authors: ravazzolo r. Clin Rheumatol. 2010 Jan;29(1):119-21. doi: 10.1007/s10067-009-1283-z. Epub 2009 Oct 1. Clin Rheumatol. 2010. PMID: 19795179

2

Correction to: Rarely occurring mutation of ACVR1 gene in Moroccan patient with fibrodysplasia ossificans progressiva.

Ratbi I, Bocciardi R, Regragui A, Ravazzolo R, Sefiani A. Ratbi I, et al. Among authors: ravazzolo r. Clin Rheumatol. 2018 Mar;37(3):857. doi: 10.1007/s10067-017-3909-x. Clin Rheumatol. 2018. PMID: 29134511

3

High-throughput screening for modulators of ACVR1 transcription: discovery of potential therapeutics for fibrodysplasia ossificans progressiva.

Cappato S, Tonachini L, Giacopelli F, Tirone M, Galietta LJ, Sormani M, Giovenzana A, Spinelli AE, Canciani B, Brunelli S, Ravazzolo R, Bocciardi R. Cappato S, et al. Among authors: ravazzolo r. Dis Model Mech. 2016 Jun 1;9(6):685-96. doi: 10.1242/dmm.023929. Epub 2016 Apr 28. Dis Model Mech. 2016. PMID: 27125279 Free PMC article.

4

Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva.

Severino M, Bertamino M, Tortora D, Morana G, Uccella S, Bocciardi R, Ravazzolo R, Rossi A, Di Rocco M. Severino M, et al. Among authors: ravazzolo r. J Med Genet. 2016 Dec;53(12):859-864. doi: 10.1136/jmedgenet-2016-104076. Epub 2016 Aug 26. J Med Genet. 2016. PMID: 27565519

5

Hints on transcriptional control of essential players in heterotopic ossification of Fibrodysplasia Ossificans Progressiva.

Ravazzolo R, Cappato S, Bocciardi R. Ravazzolo R, et al. Bone. 2018 Apr;109:187-191. doi: 10.1016/j.bone.2017.10.028. Epub 2017 Oct 31. Bone. 2018. PMID: 29100956 Review.

6

The Horizon of a Therapy for Rare Genetic Diseases: A "Druggable" Future for Fibrodysplasia Ossificans Progressiva.

Cappato S, Giacopelli F, Ravazzolo R, Bocciardi R. Cappato S, et al. Among authors: ravazzolo r. Int J Mol Sci. 2018 Mar 26;19(4):989. doi: 10.3390/ijms19040989. Int J Mol Sci. 2018. PMID: 29587443 Free PMC article. Review.

7

Genomic Context and Mechanisms of the ACVR1 Mutation in Fibrodysplasia Ossificans Progressiva.

Ravazzolo R, Bocciardi R. Ravazzolo R, et al. Biomedicines. 2021 Feb 5;9(2):154. doi: 10.3390/biomedicines9020154. Biomedicines. 2021. PMID: 33562470 Free PMC article. Review.

8

Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva: confirmations and advancements.

Bocciardi R, Bordo D, Di Duca M, Di Rocco M, Ravazzolo R. Bocciardi R, et al. Among authors: ravazzolo r. Eur J Hum Genet. 2009 Mar;17(3):311-8. doi: 10.1038/ejhg.2008.178. Epub 2008 Oct 1. Eur J Hum Genet. 2009. PMID: 18830232 Free PMC article.

9

Is there a biological basis for treatment of fibrodysplasia ossificans progressiva with rosiglitazone? Potential benefits and undesired effects.

Bocciardi R, Ravazzolo R. Bocciardi R, et al. Among authors: ravazzolo r. PPAR Res. 2010;2010:541927. doi: 10.1155/2010/541927. Epub 2010 Jun 16. PPAR Res. 2010. PMID: 20613955 Free PMC article.

10

The role of the 3'UTR region in the regulation of the ACVR1/Alk-2 gene expression.

Mura M, Cappato S, Giacopelli F, Ravazzolo R, Bocciardi R. Mura M, et al. Among authors: ravazzolo r. PLoS One. 2012;7(12):e50958. doi: 10.1371/journal.pone.0050958. Epub 2012 Dec 5. PLoS One. 2012. PMID: 23227223 Free PMC article.

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