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Items: 50

1.

Management of dysphagia in Huntington's disease: a descriptive review.

Pizzorni N, Pirola F, Ciammola A, Schindler A.

Neurol Sci. 2020 Jan 27. doi: 10.1007/s10072-020-04265-0. [Epub ahead of print] Review.

PMID:
31989345
2.

A Novel Mutation of GFAP Causing Adult-Onset Alexander Disease.

Ciammola A, Sangalli D, Sassone J, Poletti B, Carelli L, Banfi P, Pappacoda G, Ceccherini I, Grossi A, Maderna L, Pingue M, Girotti F, Silani V.

Front Neurol. 2019 Nov 6;10:1124. doi: 10.3389/fneur.2019.01124. eCollection 2019.

3.

A Novel Approach for Investigating Parkinson's Disease Personality and Its Association With Clinical and Psychological Aspects.

Carelli L, Solca F, Torre S, Pasquini J, Morelli C, Pezzati R, Mancini F, Ciammola A, Silani V, Poletti B.

Front Psychol. 2019 Oct 11;10:2265. doi: 10.3389/fpsyg.2019.02265. eCollection 2019.

4.

Early Dyskinesias in Parkinson's Disease Patients With Parkin Mutation: A Primary Corticostriatal Synaptopathy?

Sassone J, Valtorta F, Ciammola A.

Front Neurosci. 2019 Mar 26;13:273. doi: 10.3389/fnins.2019.00273. eCollection 2019. Review.

5.

Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis.

Fusilli C, Migliore S, Mazza T, Consoli F, De Luca A, Barbagallo G, Ciammola A, Gatto EM, Cesarini M, Etcheverry JL, Parisi V, Al-Oraimi M, Al-Harrasi S, Al-Salmi Q, Marano M, Vonsattel JG, Sabatini U, Landwehrmeyer GB, Squitieri F.

Lancet Neurol. 2018 Nov;17(11):986-993. doi: 10.1016/S1474-4422(18)30294-1. Epub 2018 Sep 19.

PMID:
30243861
6.

The Arrows and Colors Cognitive Test (ACCT): A new verbal-motor free cognitive measure for executive functions in ALS.

Poletti B, Carelli L, Faini A, Solca F, Meriggi P, Lafronza A, Ciringione L, Pedroli E, Ticozzi N, Ciammola A, Cipresso P, Riva G, Silani V.

PLoS One. 2018 Aug 9;13(8):e0200953. doi: 10.1371/journal.pone.0200953. eCollection 2018.

7.

Cognitive-behavioral longitudinal assessment in ALS: the Italian Edinburgh Cognitive and Behavioral ALS screen (ECAS).

Poletti B, Solca F, Carelli L, Faini A, Madotto F, Lafronza A, Monti A, Zago S, Ciammola A, Ratti A, Ticozzi N, Abrahams S, Silani V.

Amyotroph Lateral Scler Frontotemporal Degener. 2018 Aug;19(5-6):387-395. doi: 10.1080/21678421.2018.1473443. Epub 2018 May 26.

PMID:
29804470
8.

The Complex Interplay Between Depression/Anxiety and Executive Functioning: Insights From the ECAS in a Large ALS Population.

Carelli L, Solca F, Faini A, Madotto F, Lafronza A, Monti A, Zago S, Doretti A, Ciammola A, Ticozzi N, Silani V, Poletti B.

Front Psychol. 2018 Apr 5;9:450. doi: 10.3389/fpsyg.2018.00450. eCollection 2018.

9.

Cortical thickness, stance control, and arithmetic skill: An exploratory study in premanifest Huntington disease.

Nanetti L, Contarino VE, Castaldo A, Sarro L, Bachoud-Levi AC, Giavazzi M, Frittoli S, Ciammola A, Rizzo E, Gellera C, Bruzzone MG, Taroni F, Grisoli M, Mariotti C.

Parkinsonism Relat Disord. 2018 Jun;51:17-23. doi: 10.1016/j.parkreldis.2018.02.033. Epub 2018 Feb 23.

PMID:
29496355
10.

Parkin absence accelerates microtubule aging in dopaminergic neurons.

Cartelli D, Amadeo A, Calogero AM, Casagrande FVM, De Gregorio C, Gioria M, Kuzumaki N, Costa I, Sassone J, Ciammola A, Hattori N, Okano H, Goldwurm S, Roybon L, Pezzoli G, Cappelletti G.

Neurobiol Aging. 2018 Jan;61:66-74. doi: 10.1016/j.neurobiolaging.2017.09.010. Epub 2017 Sep 20.

PMID:
29040870
11.

Brain-Computer Interface for Clinical Purposes: Cognitive Assessment and Rehabilitation.

Carelli L, Solca F, Faini A, Meriggi P, Sangalli D, Cipresso P, Riva G, Ticozzi N, Ciammola A, Silani V, Poletti B.

Biomed Res Int. 2017;2017:1695290. doi: 10.1155/2017/1695290. Epub 2017 Aug 23. Review.

12.

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.

Parkinsonism Relat Disord. 2017 Nov;44:142-146. doi: 10.1016/j.parkreldis.2017.08.021. Epub 2017 Aug 26.

PMID:
28851564
13.

Neuropsychiatric Burden in Huntington's Disease.

Paoli RA, Botturi A, Ciammola A, Silani V, Prunas C, Lucchiari C, Zugno E, Caletti E.

Brain Sci. 2017 Jun 16;7(6). pii: E67. doi: 10.3390/brainsci7060067. Review.

14.

An eye-tracker controlled cognitive battery: overcoming verbal-motor limitations in ALS.

Poletti B, Carelli L, Solca F, Lafronza A, Pedroli E, Faini A, Ticozzi N, Ciammola A, Meriggi P, Cipresso P, Lulé D, Ludolph AC, Riva G, Silani V.

J Neurol. 2017 Jun;264(6):1136-1145. doi: 10.1007/s00415-017-8506-z. Epub 2017 May 13.

PMID:
28503706
15.

Cognitive-constructivist Approach in Medical Settings: The Use of Personal Meaning Questionnaire for Neurological Patients' Personality Investigation.

Poletti B, Carelli L, Lafronza A, Solca F, Faini A, Ciammola A, Grobberio M, Raimondi V, Pezzati R, Ardito RB, Silani V.

Front Psychol. 2017 Apr 11;8:582. doi: 10.3389/fpsyg.2017.00582. eCollection 2017.

16.

The synaptic function of parkin.

Sassone J, Serratto G, Valtorta F, Silani V, Passafaro M, Ciammola A.

Brain. 2017 Sep 1;140(9):2265-2272. doi: 10.1093/brain/awx006. Review.

PMID:
28335015
17.

An eye-tracking controlled neuropsychological battery for cognitive assessment in neurological diseases.

Poletti B, Carelli L, Solca F, Lafronza A, Pedroli E, Faini A, Zago S, Ticozzi N, Ciammola A, Morelli C, Meriggi P, Cipresso P, Lulé D, Ludolph AC, Riva G, Silani V.

Neurol Sci. 2017 Apr;38(4):595-603. doi: 10.1007/s10072-016-2807-3. Epub 2017 Jan 11.

PMID:
28078566
18.

Cerebral microbleeds: A new presenting feature of chromosome 22q11.2 deletion syndrome.

Bonati MT, Vanelli C, Sangalli D, Sina C, Giardino D, Sassone J, Girotti F, Silani V, Ciammola A.

J Neurol Sci. 2016 Sep 15;368:300-3. doi: 10.1016/j.jns.2016.07.044. Epub 2016 Jul 19. No abstract available.

PMID:
27538653
19.

Bcl-2/adenovirus E1B 19-kDa interacting protein (BNip3) has a key role in the mitochondrial dysfunction induced by mutant huntingtin.

Sassone F, Margulets V, Maraschi A, Rodighiero S, Passafaro M, Silani V, Ciammola A, Kirshenbaum LA, Sassone J.

Hum Mol Genet. 2015 Nov 15;24(22):6530-9. doi: 10.1093/hmg/ddv362. Epub 2015 Sep 10.

PMID:
26358776
20.

Counterfactual Thinking Deficit in Huntington's Disease.

Solca F, Poletti B, Zago S, Crespi C, Sassone F, Lafronza A, Maraschi AM, Sassone J, Silani V, Ciammola A.

PLoS One. 2015 Jun 12;10(6):e0126773. doi: 10.1371/journal.pone.0126773. eCollection 2015.

21.

Parkin regulates kainate receptors by interacting with the GluK2 subunit.

Maraschi A, Ciammola A, Folci A, Sassone F, Ronzitti G, Cappelletti G, Silani V, Sato S, Hattori N, Mazzanti M, Chieregatti E, Mulle C, Passafaro M, Sassone J.

Nat Commun. 2014 Oct 15;5:5182. doi: 10.1038/ncomms6182.

22.

Defining the role of the Bcl-2 family proteins in Huntington's disease.

Sassone J, Maraschi A, Sassone F, Silani V, Ciammola A.

Cell Death Dis. 2013 Aug 15;4:e772. doi: 10.1038/cddis.2013.300. Review.

23.

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.

Funct Neurol. 2012 Oct-Dec;27(4):247-52.

24.

Charles Bonnet syndrome: two case reports and review of the literature.

Lerario A, Ciammola A, Poletti B, Girotti F, Silani V.

J Neurol. 2013 Apr;260(4):1180-6. doi: 10.1007/s00415-013-6857-7. Epub 2013 Feb 5. Review.

PMID:
23381616
25.

Ganglioside GM1 induces phosphorylation of mutant huntingtin and restores normal motor behavior in Huntington disease mice.

Di Pardo A, Maglione V, Alpaugh M, Horkey M, Atwal RS, Sassone J, Ciammola A, Steffan JS, Fouad K, Truant R, Sipione S.

Proc Natl Acad Sci U S A. 2012 Feb 28;109(9):3528-33. doi: 10.1073/pnas.1114502109. Epub 2012 Feb 13.

26.

Brain-derived neurotrophic factor in patients with Huntington's disease.

Zuccato C, Marullo M, Vitali B, Tarditi A, Mariotti C, Valenza M, Lahiri N, Wild EJ, Sassone J, Ciammola A, Bachoud-Lèvi AC, Tabrizi SJ, Di Donato S, Cattaneo E.

PLoS One. 2011;6(8):e22966. doi: 10.1371/journal.pone.0022966. Epub 2011 Aug 12.

27.

Atypical Parkinsonism Revealing a Late Onset, Rigid and Akinetic Form of Huntington's Disease.

Ciammola A, Sassone J, Poletti B, Mencacci N, Benti R, Silani V.

Case Rep Neurol Med. 2011;2011:696953. doi: 10.1155/2011/696953. Epub 2011 Sep 7.

28.

Late onset oculopharyngeal muscular dystrophy with prominent neurogenic features and short GCG trinucleotide expansion.

Piccolo G, Cortese A, Tavazzi E, Piccolo L, Sassone J, Ciammola A, Alfonsi E, Colombo I, Moggio M.

Muscle Nerve. 2011 Jan;43(1):141-2. doi: 10.1002/mus.21842. No abstract available.

PMID:
21171103
29.

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.

J Neurol Sci. 2011 Feb 15;301(1-2):107-11. doi: 10.1016/j.jns.2010.10.016. Epub 2010 Nov 20. Review.

PMID:
21094960
30.

Low anaerobic threshold and increased skeletal muscle lactate production in subjects with Huntington's disease.

Ciammola A, Sassone J, Sciacco M, Mencacci NE, Ripolone M, Bizzi C, Colciago C, Moggio M, Parati G, Silani V, Malfatto G.

Mov Disord. 2011 Jan;26(1):130-7. doi: 10.1002/mds.23258. Epub 2010 Oct 7.

31.

Mutant Huntingtin induces activation of the Bcl-2/adenovirus E1B 19-kDa interacting protein (BNip3).

Sassone J, Colciago C, Marchi P, Ascardi C, Alberti L, Di Pardo A, Zippel R, Sipione S, Silani V, Ciammola A.

Cell Death Dis. 2010;1:e7. doi: 10.1038/cddis.2009.6.

32.

Aripiprazole in the treatment of Huntington's disease: a case series.

Ciammola A, Sassone J, Colciago C, Mencacci NE, Poletti B, Ciarmiello A, Squitieri F, Silani V.

Neuropsychiatr Dis Treat. 2009;5:1-4. Epub 2009 Apr 8.

33.

Impaired PGC-1alpha function in muscle in Huntington's disease.

Chaturvedi RK, Adhihetty P, Shukla S, Hennessy T, Calingasan N, Yang L, Starkov A, Kiaei M, Cannella M, Sassone J, Ciammola A, Squitieri F, Beal MF.

Hum Mol Genet. 2009 Aug 15;18(16):3048-65. doi: 10.1093/hmg/ddp243. Epub 2009 May 21.

34.

Huntington's disease: the current state of research with peripheral tissues.

Sassone J, Colciago C, Cislaghi G, Silani V, Ciammola A.

Exp Neurol. 2009 Oct;219(2):385-97. doi: 10.1016/j.expneurol.2009.05.012. Epub 2009 May 19. Review.

PMID:
19460373
35.

Distinct brain volume changes correlating with clinical stage, disease progression rate, mutation size, and age at onset prediction as early biomarkers of brain atrophy in Huntington's disease.

Squitieri F, Cannella M, Simonelli M, Sassone J, Martino T, Venditti E, Ciammola A, Colonnese C, Frati L, Ciarmiello A.

CNS Neurosci Ther. 2009 Winter;15(1):1-11. doi: 10.1111/j.1755-5949.2008.00068.x.

36.

De novo seven extra repeat expanded mutation in the PRNP gene in an Italian patient with early onset dementia.

Cannella M, Martino T, Simonelli M, Ciammola A, Gradini R, Ciarmiello A, Gianfrancesco F, Squitieri F.

BMJ Case Rep. 2009;2009. pii: bcr08.2008.0711. doi: 10.1136/bcr.08.2008.0711. Epub 2009 Feb 2.

37.

The pseudopolyneuritic form of amyotrophic lateral sclerosis (Patrikios' disease).

Cappellari A, Ciammola A, Silani V.

Electromyogr Clin Neurophysiol. 2008 Mar;48(2):75-81.

PMID:
18435211
38.

Neuroprotective effects of riluzole in Huntington's disease.

Squitieri F, Ciammola A, Colonnese C, Ciarmiello A.

Eur J Nucl Med Mol Imaging. 2008 Jan;35(1):221-2. Epub 2007 Nov 6. No abstract available.

PMID:
17987289
39.

De novo seven extra repeat expanded mutation in the PRNP gene in an Italian patient with early onset dementia.

Cannella M, Martino T, Simonelli M, Ciammola A, Gradini R, Ciarmiello A, Gianfrancesco F, Squitieri F.

J Neurol Neurosurg Psychiatry. 2007 Dec;78(12):1411-3. Epub 2007 Aug 6. No abstract available.

40.

Low brain-derived neurotrophic factor (BDNF) levels in serum of Huntington's disease patients.

Ciammola A, Sassone J, Cannella M, Calza S, Poletti B, Frati L, Squitieri F, Silani V.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):574-7.

PMID:
17427191
41.

Central nervous system involvement in HCV-related mixed cryoglobulinemia.

Cappellari A, Origgi L, Spina MF, Yiannopoulou KG, Meola G, Vanoli M, Ciammola A, Gregorini F, Scorza R, Bresolin N.

Electromyogr Clin Neurophysiol. 2006 May-Jun;46(3):149-58.

PMID:
16918199
42.

Apoptosis induced by proteasome inhibition in human myoblast cultures.

Sassone J, Ciammola A, Tiloca C, Glionna M, Meola G, Mancinelli E, Silani V.

Eur J Histochem. 2006 Apr-Jun;50(2):109-18.

PMID:
16864121
43.

Increased apoptosis, Huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects.

Ciammola A, Sassone J, Alberti L, Meola G, Mancinelli E, Russo MA, Squitieri F, Silani V.

Cell Death Differ. 2006 Dec;13(12):2068-78. Epub 2006 May 26.

44.

Early peripheral nerve abnormalities in impaired glucose tolerance.

Cappellari A, Airaghi L, Capra R, Ciammola A, Branchi A, Levi Minzi G, Bresolin N.

Electromyogr Clin Neurophysiol. 2005 Jun;45(4):241-4.

PMID:
16083148
45.

Stem-cell therapy for amyotrophic lateral sclerosis.

Silani V, Cova L, Corbo M, Ciammola A, Polli E.

Lancet. 2004 Jul 10-16;364(9429):200-2. Review.

PMID:
15246734
46.

Stem cells in the treatment of amyotrophic lateral sclerosis (ALS).

Silani V, Fogh I, Ratti A, Sassone J, Ciammola A, Cova L.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2002 Dec;3(4):173-81. Review.

PMID:
12710505
47.

Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease.

Zuccato C, Ciammola A, Rigamonti D, Leavitt BR, Goffredo D, Conti L, MacDonald ME, Friedlander RM, Silani V, Hayden MR, Timmusk T, Sipione S, Cattaneo E.

Science. 2001 Jul 20;293(5529):493-8. Epub 2001 Jun 14.

48.

Motor neurones in culture as a model to study ALS.

Silani V, Braga M, Ciammola A, Cardin V, Scarlato G.

J Neurol. 2000 Mar;247 Suppl 1:I28-36. Review.

PMID:
10795884
49.

Motor neurone metabolism.

Silani V, Ciammola A, Pizzuti A, Cardin V, Scarlato G.

J Neurol Sci. 1999 Oct 31;169(1-2):161-9. Review.

PMID:
10540026
50.

Immunomagnetic isolation of human developing motor neurons.

Silani V, Brioschi A, Braga M, Ciammola A, Zhou FC, Bonifati C, Ratti A, Pizzuti A, Buscaglia M, Scarlato G.

Neuroreport. 1998 Apr 20;9(6):1143-7.

PMID:
9601683

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