Pescini F - Search Results

1

First report of a pathogenic mutation on exon 24 of the NOTCH3 gene in a CADASIL family.

Valenti R, Bianchi S, Pescini F, D'Eramo C, Inzitari D, Dotti MT, Pantoni L. Valenti R, et al. Among authors: pescini f. J Neurol. 2011 Sep;258(9):1632-6. doi: 10.1007/s00415-011-5983-3. Epub 2011 Mar 16. J Neurol. 2011. PMID: 21409506

2

The serum metabolomic profiles of atrial fibrillation patients treated with direct oral anticoagulants or vitamin K antagonists.

Vignoli A, Gori AM, Berteotti M, Cesari F, Giusti B, Bertelli A, Kura A, Sticchi E, Salvadori E, Barbato C, Formelli B, Pescini F, Marcucci R, Tenori L, Poggesi A. Vignoli A, et al. Among authors: pescini f. Life Sci. 2024 Aug 15;351:122796. doi: 10.1016/j.lfs.2024.122796. Epub 2024 Jun 7. Life Sci. 2024. PMID: 38852797 Free article.

3

Thrombophilic risk factors and unusual clinical features in three Italian CADASIL patients.

Pantoni L, Sarti C, Pescini F, Bianchi S, Bartolini L, Nencini P, Basile AM, Lamassa M, Kalaria RN, Dotti MT, Federico A, Inzitari D. Pantoni L, et al. Among authors: pescini f. Eur J Neurol. 2004 Nov;11(11):782-7. doi: 10.1111/j.1468-1331.2004.00915.x. Eur J Neurol. 2004. PMID: 15525301

4

Postpartum psychiatric disturbances as an unrecognized onset of CADASIL.

Pantoni L, Pescini F, Inzitari D, Dotti MT. Pantoni L, et al. Among authors: pescini f. Acta Psychiatr Scand. 2005 Sep;112(3):241; author reply 242. doi: 10.1111/j.1600-0447.2005.00595.x. Acta Psychiatr Scand. 2005. PMID: 16095483 No abstract available.

5

Cerebellar arteriovenous malformation and vertebral artery aneurysm in a CADASIL patient.

Pescini F, Sarti C, Pantoni L, Mangiafico S, Bianchi S, Dotti MT, Federico A, Inzitari D. Pescini F, et al. Acta Neurol Scand. 2006 Jan;113(1):62-3. doi: 10.1111/j.1600-0404.2005.00539.x. Acta Neurol Scand. 2006. PMID: 16367901

6

First report of a Romanian CADASIL patient following immigration to Italy.

Pescini F, Bianchi S, Dotti MT, Federico A, Inzitari D, Pantoni L. Pescini F, et al. Eur J Neurol. 2007 Aug;14(8):e7-8. doi: 10.1111/j.1468-1331.2007.01743.x. Eur J Neurol. 2007. PMID: 17661999 No abstract available.

7

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. 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

8

Psychiatric disturbances in CADASIL: a brief review.

Valenti R, Poggesi A, Pescini F, Inzitari D, Pantoni L. Valenti R, et al. Among authors: pescini f. Acta Neurol Scand. 2008 Nov;118(5):291-5. doi: 10.1111/j.1600-0404.2008.01015.x. Epub 2008 Mar 26. Acta Neurol Scand. 2008. PMID: 18384453 Review.

9

The contribution of cerebrospinal fluid oligoclonal bands to the early diagnosis of multiple sclerosis.

Zipoli V, Hakiki B, Portaccio E, Lolli F, Siracusa G, Giannini M, Pantoni L, Pescini F, Sorbi S, Amato MP. Zipoli V, et al. Among authors: pescini f. Mult Scler. 2009 Apr;15(4):472-8. doi: 10.1177/1352458508100502. Epub 2009 Jan 19. Mult Scler. 2009. PMID: 19153171

10

Familial cerebral cavernous malformation: report of a further Italian family.

Nannucci S, Pescini F, Poggesi A, Ciolli L, Patrosso MC, Marocchi A, Inzitari D, Penco S, Pantoni L. Nannucci S, et al. Among authors: pescini f. Neurol Sci. 2009 Apr;30(2):143-7. doi: 10.1007/s10072-009-0020-3. Epub 2009 Jan 30. Neurol Sci. 2009. PMID: 19184323

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