Cinnante CM - Search Results

1

Intracerebral haemorrhage, a possible presentation in Churg-Strauss syndrome: case report and review of the literature.

Mencacci NE, Bersano A, Cinnante CM, Ciammola A, Corti S, Meroni PL, Silani V. Mencacci NE, et al. Among authors: cinnante cm. J Neurol Sci. 2011 Feb 15;301(1-2):107-11. doi: 10.1016/j.jns.2010.10.016. Epub 2010 Nov 20. J Neurol Sci. 2011. PMID: 21094960 Review.

2

Safety of carotid stenting for stroke prevention: need of an independent outcome assessor.

Lanfranconi S, Bersano A, D'Adda E, Ballabio E, Gattinoni M, Cinnante C, Nuzzi P, Isalberti M, Branca V, Candelise L. Lanfranconi S, et al. Neurol Sci. 2009 Apr;30(2):93-7. doi: 10.1007/s10072-009-0012-3. Epub 2009 Feb 3. Neurol Sci. 2009. PMID: 19189045

3

Transthyretin Asn90 variant: amyloidogenic or non-amyloidogenic role.

Bersano A, Del Bo R, Ballabio E, Cinnante C, Lanfranconi S, Comi GP, Baron P, Bresolin N, Candelise L. Bersano A, et al. J Neurol Sci. 2009 Sep 15;284(1-2):113-5. doi: 10.1016/j.jns.2009.04.015. Epub 2009 May 9. J Neurol Sci. 2009. PMID: 19428025

4

A cortically blind patient with preserved visual imagery.

Zago S, Corti S, Bersano A, Baron P, Conti G, Ballabio E, Lanfranconi S, Cinnante C, Costa A, Cappellari A, Bresolin N. Zago S, et al. Cogn Behav Neurol. 2010 Mar;23(1):44-8. doi: 10.1097/WNN.0b013e3181bf2e6e. Cogn Behav Neurol. 2010. PMID: 20299863

5

Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant.

Bersano A, Ranieri M, Ciammola A, Cinnante C, Lanfranconi S, Dotti MT, Candelise L, Baschirotto C, Ghione I, Ballabio E, Bresolin N, Bassi MT. Bersano A, et al. Funct Neurol. 2012 Oct-Dec;27(4):247-52. Funct Neurol. 2012. PMID: 23597439 Free PMC article.

6

X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene.

Ciammola A, Carrera P, Di Fonzo A, Sassone J, Villa R, Poletti B, Ferrari M, Girotti F, Monfrini E, Buongarzone G, Silani V, Cinnante CM, Mignogna ML, D'Adamo P, Bonati MT. Ciammola A, et al. Among authors: cinnante cm. Parkinsonism Relat Disord. 2017 Nov;44:142-146. doi: 10.1016/j.parkreldis.2017.08.021. Epub 2017 Aug 26. Parkinsonism Relat Disord. 2017. PMID: 28851564

7

A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature.

Brusa R, Magri F, Papadimitriou D, Govoni A, Del Bo R, Ciscato P, Savarese M, Cinnante C, Walter MC, Abicht A, Bulst S, Corti S, Moggio M, Bresolin N, Nigro V, Comi GP. Brusa R, et al. Neuromuscul Disord. 2018 Jun;28(6):532-537. doi: 10.1016/j.nmd.2018.04.006. Epub 2018 Apr 13. Neuromuscul Disord. 2018. PMID: 29759638 Review.

8

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the Literature.

Gagliardi D, Faravelli I, Villa L, Pero G, Cinnante C, Brusa R, Mauri E, Tresoldi L, Magri F, Govoni A, Bresolin N, Comi GP, Corti S. Gagliardi D, et al. Front Neurol. 2018 Aug 2;9:619. doi: 10.3389/fneur.2018.00619. eCollection 2018. Front Neurol. 2018. PMID: 30116219 Free PMC article.

9

Stormorken Syndrome Caused by a p.R304W STIM1 Mutation: The First Italian Patient and a Review of the Literature.

Borsani O, Piga D, Costa S, Govoni A, Magri F, Artoni A, Cinnante CM, Fagiolari G, Ciscato P, Moggio M, Bresolin N, Comi GP, Corti S. Borsani O, et al. Among authors: cinnante cm. Front Neurol. 2018 Oct 15;9:859. doi: 10.3389/fneur.2018.00859. eCollection 2018. Front Neurol. 2018. PMID: 30374325 Free PMC article.

10

Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis.

Brusa R, Faravelli I, Gagliardi D, Magri F, Cogiamanian F, Saccomanno D, Cinnante C, Mauri E, Abati E, Bresolin N, Corti S, Comi GP. Brusa R, et al. Front Neurol. 2019 Aug 13;10:823. doi: 10.3389/fneur.2019.00823. eCollection 2019. Front Neurol. 2019. PMID: 31456730 Free PMC article.

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