Zicari E - Search Results

1

CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients.

Bianchi S, Zicari E, Carluccio A, Di Donato I, Pescini F, Nannucci S, Valenti R, Ragno M, Inzitari D, Pantoni L, Federico A, Dotti MT. Bianchi S, et al. Among authors: zicari e. J Neurol. 2015 Jan;262(1):134-41. doi: 10.1007/s00415-014-7533-2. Epub 2014 Oct 26. J Neurol. 2015. PMID: 25344745

2

High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiarities.

Bianchi S, Rufa A, Ragno M, D'Eramo C, Pescini F, Pantoni L, Cappelli A, Perretti A, Zicari E, Zolo P, Inzitari D, Dotti MT, Federico A. Bianchi S, et al. Among authors: zicari e. J Neurol. 2010 Jun;257(6):1039-42. doi: 10.1007/s00415-010-5481-z. Epub 2010 Feb 19. J Neurol. 2010. PMID: 20169447 No abstract available.

3

The Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale: a screening tool to select patients for NOTCH3 gene analysis.

Pescini F, Nannucci S, Bertaccini B, Salvadori E, Bianchi S, Ragno M, Sarti C, Valenti R, Zicari E, Moretti M, Chiti S, Stromillo ML, De Stefano N, Dotti MT, Federico A, Inzitari D, Pantoni L. Pescini F, et al. Among authors: zicari e. Stroke. 2012 Nov;43(11):2871-6. doi: 10.1161/STROKEAHA.112.665927. Epub 2012 Sep 20. Stroke. 2012. PMID: 22996955

4

Pulsating enophthalmos in an adult patient with type 1 neurofibromatosis.

Rufa A, Zicari E, Cerase A, Vallone IM, Dotti MT, Federico A. Rufa A, et al. Among authors: zicari e. Neurology. 2006 Dec 26;67(12):2169. doi: 10.1212/01.wnl.0000233833.03410.82. Neurology. 2006. PMID: 17190938 No abstract available.

5

Right-to-left shunt in CADASIL patients: prevalence and correlation with clinical and MRI findings.

Zicari E, Tassi R, Stromillo ML, Pellegrini M, Bianchi S, Cevenini G, Gistri M, De Stefano N, Federico A, Dotti MT. Zicari E, et al. Stroke. 2008 Jul;39(7):2155-7. doi: 10.1161/STROKEAHA.107.506311. Epub 2008 May 1. Stroke. 2008. PMID: 18451353

6

Plasma levels of asymmetric dimethylarginine in cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathy.

Rufa A, Blardi P, De Lalla A, Cevenini G, De Stefano N, Zicari E, Auteri A, Federico A, Dotti MT. Rufa A, et al. Among authors: zicari e. Cerebrovasc Dis. 2008;26(6):636-40. doi: 10.1159/000166840. Epub 2008 Nov 4. Cerebrovasc Dis. 2008. PMID: 18984949

7

Bone marrow-derived progenitor cells in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Pescini F, Cesari F, Giusti B, Sarti C, Zicari E, Bianchi S, Dotti MT, Federico A, Balestrino M, Enrico A, Gandolfo C, Gori AM, Abbate R, Pantoni L, Inzitari D. Pescini F, et al. Among authors: zicari e. Stroke. 2010 Feb;41(2):218-23. doi: 10.1161/STROKEAHA.109.563726. Epub 2009 Dec 24. Stroke. 2010. PMID: 20035077

8

Dysautonomic achalasia in two siblings with Sandhoff disease.

Pellegrini M, Zicari E, Dotti MT, Federico A. Pellegrini M, et al. Among authors: zicari e. J Neurol Sci. 2006 Feb 15;241(1-2):107-9. doi: 10.1016/j.jns.2005.11.001. Epub 2005 Dec 13. J Neurol Sci. 2006. PMID: 16352312

9

Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Piccirillo G, Magrì D, Mitra M, Rufa A, Zicari E, Stromillo ML, De Stefano N, Dotti MT. Piccirillo G, et al. Among authors: zicari e. Eur J Neurol. 2008 Nov;15(11):1216-21. doi: 10.1111/j.1468-1331.2008.02300.x. Epub 2008 Sep 18. Eur J Neurol. 2008. PMID: 18803652

10

A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss.

Cardaioli E, Da Pozzo P, Gallus GN, Malandrini A, Gambelli S, Gaudiano C, Malfatti E, Viscomi C, Zicari E, Berti G, Serni G, Dotti MT, Federico A. Cardaioli E, et al. Among authors: zicari e. Neuromuscul Disord. 2007 Oct;17(9-10):681-3. doi: 10.1016/j.nmd.2007.05.001. Epub 2007 Jul 5. Neuromuscul Disord. 2007. PMID: 17614276

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