Cacchiò G - Search Results

1

"CADASIL coma" in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutation.

Ragno M, Pianese L, Morroni M, Cacchiò G, Manca A, Di Marzio F, Silvestri S, Miceli C, Scarcella M, Onofrj M, Trojano L. Ragno M, et al. Among authors: cacchio g. Neurol Sci. 2013 Nov;34(11):1947-53. doi: 10.1007/s10072-013-1418-5. Epub 2013 Apr 10. Neurol Sci. 2013. PMID: 23572112

2

High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Cappelli A, Ragno M, Cacchiò G, Scarcella M, Staffolani P, Pianese L. Cappelli A, et al. Among authors: cacchio g. Neurosci Lett. 2009 Sep 22;462(2):176-8. doi: 10.1016/j.neulet.2009.06.087. Epub 2009 Jul 2. Neurosci Lett. 2009. PMID: 19576955

3

Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL).

Ragno M, Pianese L, Pinelli M, Silvestri S, Cacchiò G, Di Marzio F, Scarcella M, Coretti F, Altamura F, Monticelli A, Castaldo I. Ragno M, et al. Among authors: cacchio g. Neurogenetics. 2011 Nov;12(4):337-43. doi: 10.1007/s10048-011-0298-1. Epub 2011 Sep 1. Neurogenetics. 2011. PMID: 21881852

4

Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation.

Ragno M, Pianese L, Cacchiò G, Manca A, Scarcella M, Silvestri S, Di Marzio F, Caiazzo AR, Silvaggio F, Tasca G, Mirabella M, Trojano L. Ragno M, et al. Among authors: cacchio g. Neurosci Lett. 2012 Jan 6;506(1):116-20. doi: 10.1016/j.neulet.2011.10.062. Epub 2011 Nov 2. Neurosci Lett. 2012. PMID: 22079340

5

Parkinsonism is a late, not rare, feature of CADASIL: a study on Italian patients carrying the R1006C mutation.

Ragno M, Berbellini A, Cacchiò G, Manca A, Di Marzio F, Pianese L, De Rosa A, Silvestri S, Scarcella M, De Michele G. Ragno M, et al. Among authors: cacchio g. Stroke. 2013 Apr;44(4):1147-9. doi: 10.1161/STROKEAHA.111.000458. Epub 2013 Feb 14. Stroke. 2013. PMID: 23412372

6

First report of a homozygous mutation on exon 24 of the NOTCH3 gene in a paucisymptomatic CADASIL elderly patient.

Ragno M, Pianese L, Tiberi S, Cacchiò G, Paci C, Trojano L. Ragno M, et al. Among authors: cacchio g. Neurol Sci. 2022 Feb;43(2):1457-1458. doi: 10.1007/s10072-021-05706-0. Epub 2021 Nov 5. Neurol Sci. 2022. PMID: 34739617 No abstract available.

7

Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene.

Ragno M, Fabrizi GM, Cacchiò G, Scarcella M, Sirocchi G, Selvaggio F, Taioli F, Ferrarini M, Trojano L. Ragno M, et al. Among authors: cacchio g. Neurol Sci. 2006 Sep;27(4):252-6. doi: 10.1007/s10072-006-0679-7. Neurol Sci. 2006. PMID: 16998728

8

Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation.

Ragno M, Cacchiò G, Fabrizi GM, Scarcella M, Silvaggio F, Cavallaro T, Taioli F, Trojano L. Ragno M, et al. Among authors: cacchio g. Neurol Sci. 2007 Aug;28(4):181-4. doi: 10.1007/s10072-007-0817-x. Epub 2007 Aug 10. Neurol Sci. 2007. PMID: 17690848

9

Motor cortex cholinergic dysfunction in CADASIL: a transcranial magnetic demonstration.

Manganelli F, Ragno M, Cacchiò G, Iodice V, Trojano L, Silvaggio F, Scarcella M, Grazioli M, Santoro L, Perretti A. Manganelli F, et al. Among authors: cacchio g. Clin Neurophysiol. 2008 Feb;119(2):351-5. doi: 10.1016/j.clinph.2007.10.011. Epub 2007 Dec 11. Clin Neurophysiol. 2008. PMID: 18065265

10

Striatal [123I] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease.

Ragno M, Scarcella MG, Cacchiò G, Capellari S, Di Marzio F, Parchi P, Trojano L. Ragno M, et al. Among authors: cacchio g. Acta Neurol Scand. 2009 Feb;119(2):131-4. doi: 10.1111/j.1600-0404.2008.01075.x. Epub 2008 Jul 13. Acta Neurol Scand. 2009. PMID: 18638039

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