Federico A - 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: federico a. 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

Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Rufa A, De Stefano N, Dotti MT, Bianchi S, Sicurelli F, Stromillo ML, D'Aniello B, Federico A. Rufa A, et al. Among authors: federico a. Arch Neurol. 2004 Apr;61(4):577-80. doi: 10.1001/archneur.61.4.577. Arch Neurol. 2004. PMID: 15096408

3

A novel NOTCH3 frameshift deletion and mitochondrial abnormalities in a patient with CADASIL.

Dotti MT, De Stefano N, Bianchi S, Malandrini A, Battisti C, Cardaioli E, Federico A. Dotti MT, et al. Among authors: federico a. Arch Neurol. 2004 Jun;61(6):942-5. doi: 10.1001/archneur.61.6.942. Arch Neurol. 2004. PMID: 15210536

4

Peripheral neuropathy in CADASIL.

Sicurelli F, Dotti MT, De Stefano N, Malandrini A, Mondelli M, Bianchi S, Federico A. Sicurelli F, et al. Among authors: federico a. J Neurol. 2005 Oct;252(10):1206-9. doi: 10.1007/s00415-005-0837-5. Epub 2005 Apr 15. J Neurol. 2005. PMID: 15827866

5

Physiology and pathology of notch signalling system.

Bianchi S, Dotti MT, Federico A. Bianchi S, et al. Among authors: federico a. J Cell Physiol. 2006 May;207(2):300-8. doi: 10.1002/jcp.20542. J Cell Physiol. 2006. PMID: 16270334 Review.

6

A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in an octogenarian paucisymptomatic patient.

Pescini F, Bianchi S, Salvadori E, Poggesi A, Dotti MT, Federico A, Inzitari D, Pantoni L. Pescini F, et al. Among authors: federico a. J Neurol Sci. 2008 Apr 15;267(1-2):170-3. doi: 10.1016/j.jns.2007.10.017. Epub 2007 Nov 19. J Neurol Sci. 2008. PMID: 18022198

7

Impaired vasoreactivity in mildly disabled CADASIL patients.

Campolo J, De Maria R, Frontali M, Taroni F, Inzitari D, Federico A, Romano S, Puca E, Mariotti C, Tomasello C, Pantoni L, Pescini F, Dotti MT, Stromillo ML, De Stefano N, Tavani A, Parodi O. Campolo J, et al. Among authors: federico a. J Neurol Neurosurg Psychiatry. 2012 Mar;83(3):268-74. doi: 10.1136/jnnp-2011-300080. Epub 2011 Nov 9. J Neurol Neurosurg Psychiatry. 2012. PMID: 22072702

8

Hereditary cerebral small vessel diseases: a review.

Federico A, Di Donato I, Bianchi S, Di Palma C, Taglia I, Dotti MT. Federico A, et al. J Neurol Sci. 2012 Nov 15;322(1-2):25-30. doi: 10.1016/j.jns.2012.07.041. Epub 2012 Aug 4. J Neurol Sci. 2012. PMID: 22868088 Review.

9

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: federico a. Stroke. 2012 Nov;43(11):2871-6. doi: 10.1161/STROKEAHA.112.665927. Epub 2012 Sep 20. Stroke. 2012. PMID: 22996955

10

First deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASIL.

Bianchi S, Dotti MT, Gallus GN, D'Eramo C, Di Donato I, Bernardi L, Maletta R, Puccio G, Bruni AC, Federico A. Bianchi S, et al. Among authors: federico a. Neurobiol Aging. 2013 Sep;34(9):2234.e9-12. doi: 10.1016/j.neurobiolaging.2013.03.005. Epub 2013 Apr 12. Neurobiol Aging. 2013. PMID: 23587639

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