Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 35

1.

Spinocerebellar ataxia type 2-neuronopathy or neuropathy?

Pelosi L, Iodice R, Antenora A, Kilfoyle D, Mulroy E, Rodrigues M, Roxburgh R, Iovino A, Filla A, Manganelli F, Santoro L.

Muscle Nerve. 2019 Sep;60(3):271-278. doi: 10.1002/mus.26613. Epub 2019 Jul 5.

PMID:
31228263
2.

Prediction of Survival With Long-Term Disease Progression in Most Common Spinocerebellar Ataxia.

Diallo A, Jacobi H, Cook A, Giunti P, Parkinson MH, Labrum R, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Panzeri M, Castaldo A, Rakowicz M, Rola R, Sulek A, Schmitz-Hübsch T, Schöls L, Hengel H, Baliko L, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Boesch S, Nachbauer W, Pandolfo M, Schulz JB, Bauer P, Jun-Suk K, Klockgether T, Tezenas du Montcel S.

Mov Disord. 2019 Aug;34(8):1220-1227. doi: 10.1002/mds.27739. Epub 2019 Jun 18.

PMID:
31211461
3.

Longitudinal study of a cohort of MSA-C patients in South Italy: survival and clinical features.

Lieto M, Roca A, Bruzzese D, Antenora A, Alfieri G, Saccà F, Bellofatto M, Bilo L, Barbato S, De Michele G, Filla A.

Neurol Sci. 2019 Oct;40(10):2105-2109. doi: 10.1007/s10072-019-03948-7. Epub 2019 May 31.

PMID:
31152261
4.

Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks.

Rucco R, Liparoti M, Jacini F, Baselice F, Antenora A, De Michele G, Criscuolo C, Vettoliere A, Mandolesi L, Sorrentino G, Sorrentino P.

Neurol Sci. 2019 May;40(5):979-984. doi: 10.1007/s10072-019-3725-y. Epub 2019 Feb 8.

5.

Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study.

D'Amore A, Tessa A, Casali C, Dotti MT, Filla A, Silvestri G, Antenora A, Astrea G, Barghigiani M, Battini R, Battisti C, Bruno I, Cereda C, Dato C, Di Iorio G, Donadio V, Felicori M, Fini N, Fiorillo C, Gallone S, Gemignani F, Gigli GL, Graziano C, Guerrini R, Gurrieri F, Kariminejad A, Lieto M, Marques LourenḈo C, Malandrini A, Mandich P, Marcotulli C, Mari F, Massacesi L, Melone MAB, Mignarri A, Milone R, Musumeci O, Pegoraro E, Perna A, Petrucci A, Pini A, Pochiero F, Pons MR, Ricca I, Rossi S, Seri M, Stanzial F, Tinelli F, Toscano A, Valente M, Federico A, Rubegni A, Santorelli FM.

Front Neurol. 2018 Dec 4;9:981. doi: 10.3389/fneur.2018.00981. eCollection 2018.

6.

Reversible Valproate-Induced Subacute Encephalopathy Associated With a MT-ATP8 Variant in the Mitochondrial Genome.

De Michele G, Sorrentino P, Nesti C, Rubegni A, Ruggiero L, Peluso S, Antenora A, Quarantelli M, Filla A, De Michele G, Santorelli FM.

Front Neurol. 2018 Aug 30;9:728. doi: 10.3389/fneur.2018.00728. eCollection 2018.

7.

Prevalence and phenotype of the c.1529C>T SPG7 variant in adult-onset cerebellar ataxia in Italy.

Mancini C, Giorgio E, Rubegni A, Pradotto L, Bagnoli S, Rubino E, Prontera P, Cavalieri S, Di Gregorio E, Ferrero M, Pozzi E, Riberi E, Ferrero P, Nigro P, Mauro A, Zibetti M, Tessa A, Barghigiani M, Antenora A, Sirchia F, Piacentini S, Silvestri G, De Michele G, Filla A, Orsi L, Santorelli FM, Brusco A.

Eur J Neurol. 2019 Jan;26(1):80-86. doi: 10.1111/ene.13768. Epub 2018 Sep 3.

8.

Predictors of survival in spinocerebellar ataxia type 2 population from Southern Italy.

Antenora A, Bruzzese D, Lieto M, Roca A, Florio MT, Peluso S, Saccà F, De Michele G, Santorelli FM, Filla A.

Neurol Sci. 2018 Nov;39(11):1857-1860. doi: 10.1007/s10072-018-3504-1. Epub 2018 Jul 21.

PMID:
30030635
9.

Long-term evolution of patient-reported outcome measures in spinocerebellar ataxias.

Jacobi H, du Montcel ST, Bauer P, Giunti P, Cook A, Labrum R, Parkinson MH, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Sarro L, Rakowicz M, Sulek A, Sobanska A, Schmitz-Hübsch T, Schöls L, Hengel H, Baliko L, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Szymanski S, Boesch S, Nachbauer W, Kang JS, Pandolfo M, Schulz JB, Melac AT, Diallo A, Klockgether T.

J Neurol. 2018 Sep;265(9):2040-2051. doi: 10.1007/s00415-018-8954-0. Epub 2018 Jun 29.

PMID:
29959555
10.

Animal-Assisted Therapy in Elderly Patients: Evidence and Controversies in Dementia and Psychiatric Disorders and Future Perspectives in Other Neurological Diseases.

Peluso S, De Rosa A, De Lucia N, Antenora A, Illario M, Esposito M, De Michele G.

J Geriatr Psychiatry Neurol. 2018 May;31(3):149-157. doi: 10.1177/0891988718774634. Epub 2018 May 15. Review.

PMID:
29764282
11.

Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study.

Diallo A, Jacobi H, Cook A, Labrum R, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Panzeri M, Rakowicz M, Sobanska A, Sulek A, Schmitz-Hübsch T, Schöls L, Hengel H, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Boesch S, Pandolfo M, Schulz JB, Bauer P, Giunti P, Kang JS, Klockgether T, Tezenas du Montcel S.

Lancet Neurol. 2018 Apr;17(4):327-334. doi: 10.1016/S1474-4422(18)30042-5. Epub 2018 Mar 13.

PMID:
29553382
12.

Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial.

Schöls L, Rattay TW, Martus P, Meisner C, Baets J, Fischer I, Jägle C, Fraidakis MJ, Martinuzzi A, Saute JA, Scarlato M, Antenora A, Stendel C, Höflinger P, Lourenco CM, Abreu L, Smets K, Paucar M, Deconinck T, Bis DM, Wiethoff S, Bauer P, Arnoldi A, Marques W, Jardim LB, Hauser S, Criscuolo C, Filla A, Züchner S, Bassi MT, Klopstock T, De Jonghe P, Björkhem I, Schüle R.

Brain. 2017 Dec 1;140(12):3112-3127. doi: 10.1093/brain/awx273.

13.

The Multiple Faces of Spinocerebellar Ataxia type 2.

Antenora A, Rinaldi C, Roca A, Pane C, Lieto M, Saccà F, Peluso S, De Michele G, Filla A.

Ann Clin Transl Neurol. 2017 Aug 10;4(9):687-695. doi: 10.1002/acn3.437. eCollection 2017 Sep. Review.

14.

Body Mass Index Decline Is Related to Spinocerebellar Ataxia Disease Progression.

Diallo A, Jacobi H, Schmitz-Hübsch T, Cook A, Labrum R, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Panzeri M, Rakowicz M, Sobanska A, Sulek A, Schöls L, Hengel H, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Boesch S, Pandolfo M, Schulz JB, Bauer P, Giunti P, Baliko L, Parkinson MH, Kang JS, Klockgether T, Tezenas du Montcel S.

Mov Disord Clin Pract. 2017 Aug 11;4(5):689-697. doi: 10.1002/mdc3.12522. eCollection 2017 Sep-Oct.

15.

Chorea-acanthocytosis without chorea: Expanding the clinical phenotype.

Peluso S, Bilo L, Esposito M, Antenora A, De Rosa A, Pappatà S, De Michele G.

Parkinsonism Relat Disord. 2017 Aug;41:124-126. doi: 10.1016/j.parkreldis.2017.05.013. Epub 2017 May 17. No abstract available.

PMID:
28551324
16.

The magnetic apraxia of Denny-Brown.

Peluso S, De Michele G, Antenora A, De Rosa A, Bilo L.

Neurology. 2016 Aug 9;87(6):644. doi: 10.1212/WNL.0000000000002954. No abstract available. Erratum in: Neurology. 2017 Apr 11;88(15):1483.

PMID:
27502963
17.

Be aware of Wolfram syndrome when examining ataxic patients.

Antenora A, Lieto M, Santorelli FM, Peluso S, Saccà F, De Michele G, Filla A.

J Neurol. 2016 Sep;263(9):1862-3. doi: 10.1007/s00415-016-8199-8. Epub 2016 Jun 17. No abstract available.

PMID:
27314960
18.

CCM3/PDCD10 gene mutation in cerebral cavernous malformations associated with hyperkeratotic cutaneous capillary venous malformations.

Bilo L, Antenora A, Peluso S, Procaccini EM, Quarantelli M, Mansueto G, Cigoli MS, Penco S, De Michele G.

J Dermatol. 2016 Aug;43(8):962-3. doi: 10.1111/1346-8138.13317. Epub 2016 Feb 20. No abstract available.

PMID:
26896283
19.

Long-term effect of epoetin alfa on clinical and biochemical markers in friedreich ataxia.

Saccà F, Puorro G, Marsili A, Antenora A, Pane C, Casali C, Marcotulli C, Defazio G, Liuzzi D, Tatillo C, Cambriglia DM, Schiano di Cola G, Giuliani L, Guardasole V, Salzano A, Ruvolo A, De Rosa A, Cittadini A, De Michele G, Filla A.

Mov Disord. 2016 May;31(5):734-41. doi: 10.1002/mds.26552. Epub 2016 Feb 16.

PMID:
26879839
20.

Parkinsonism in adult-onset Rasmussens's encephalitis: a clinical picture presenting as corticobasal syndrome.

Bilo L, Peluso S, Antenora A, De Rosa A, Esposito M, Barbato S, Pappatà S, De Michele G.

Int J Neurosci. 2016 Dec;126(12):1136-8. doi: 10.3109/00207454.2015.1135438. Epub 2016 Jan 25.

PMID:
26708103
21.

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.

Jacobi H, du Montcel ST, Bauer P, Giunti P, Cook A, Labrum R, Parkinson MH, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Panzeri M, Rakowicz M, Sulek A, Sobanska A, Schmitz-Hübsch T, Schöls L, Hengel H, Baliko L, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Szymanski S, Boesch S, Kang JS, Pandolfo M, Schulz JB, Molho S, Diallo A, Klockgether T.

Lancet Neurol. 2015 Nov;14(11):1101-8. doi: 10.1016/S1474-4422(15)00202-1. Epub 2015 Sep 13.

PMID:
26377379
22.

The Effect of Cerebellar Degeneration on Human Sensori-motor Plasticity.

Dubbioso R, Pellegrino G, Antenora A, De Michele G, Filla A, Santoro L, Manganelli F.

Brain Stimul. 2015 Nov-Dec;8(6):1144-50. doi: 10.1016/j.brs.2015.05.012. Epub 2015 Jun 16.

PMID:
26140957
23.

Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage.

Peluso S, De Rosa A, Antenora A, Lieto M, Criscuolo C, Barbieri F, Pappatà S, De Michele G.

Parkinsonism Relat Disord. 2015 Feb;21(2):156-8. doi: 10.1016/j.parkreldis.2014.10.029. Epub 2014 Nov 21. No abstract available.

PMID:
25483721
24.

PDCD10 gene mutations in multiple cerebral cavernous malformations.

Cigoli MS, Avemaria F, De Benedetti S, Gesu GP, Accorsi LG, Parmigiani S, Corona MF, Capra V, Mosca A, Giovannini S, Notturno F, Ciccocioppo F, Volpi L, Estienne M, De Michele G, Antenora A, Bilo L, Tavoni A, Zamponi N, Alfei E, Baranello G, Riva D, Penco S.

PLoS One. 2014 Oct 29;9(10):e110438. doi: 10.1371/journal.pone.0110438. eCollection 2014. Erratum in: PLoS One. 2015;10(4):e0123486.

25.

Metabolic Ataxias in Adults.

Antenora A, Filla A, Santorelli FM, Peluso S, Sacca F, De Michele G.

Curr Mol Med. 2014;14(8):959-970. doi: 10.2174/1566524014666141010131213.

PMID:
25323876
26.

Jaw-Opening Oromandibular Dystonia Associated With Spinocerebellar Ataxia Type 2.

Antenora A, Peluso S, Saccà F, De Michele G, Filla A.

Mov Disord Clin Pract. 2014 May 26;1(2):121-122. doi: 10.1002/mdc3.12032. eCollection 2014 Jun. No abstract available.

27.

A novel PSEN1 mutation in a patient with sporadic early-onset Alzheimer's disease and prominent cerebellar ataxia.

Testi S, Peluso S, Fabrizi GM, Antenora A, Russo CV, Pappatà S, Padovani A, Ferrarini M, Filla A.

J Alzheimers Dis. 2014;41(3):709-14. doi: 10.3233/JAD-140081.

PMID:
24718101
28.

Parkinsonism may be part of the symptom complex of DOOR syndrome.

Bilo L, Peluso S, Antenora A, De Rosa A, Auletta G, Pappatà S, De Michele G.

Parkinsonism Relat Disord. 2014 Apr;20(4):463-5. doi: 10.1016/j.parkreldis.2014.01.014. Epub 2014 Jan 23. No abstract available.

PMID:
24486243
29.

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.

Jacobi H, Reetz K, du Montcel ST, Bauer P, Mariotti C, Nanetti L, Rakowicz M, Sulek A, Durr A, Charles P, Filla A, Antenora A, Schöls L, Schicks J, Infante J, Kang JS, Timmann D, Di Fabio R, Masciullo M, Baliko L, Melegh B, Boesch S, Bürk K, Peltz A, Schulz JB, Dufaure-Garé I, Klockgether T.

Lancet Neurol. 2013 Jul;12(7):650-8. doi: 10.1016/S1474-4422(13)70104-2. Epub 2013 May 22. Erratum in: Lancet Neurol. 2013 Jul;12(7):630.

PMID:
23707147
30.

Somatosensory temporal discrimination threshold is increased in patients with cerebellar atrophy.

Manganelli F, Dubbioso R, Pisciotta C, Antenora A, Nolano M, De Michele G, Filla A, Berardelli A, Santoro L.

Cerebellum. 2013 Aug;12(4):456-9. doi: 10.1007/s12311-012-0435-x.

PMID:
23288507
31.

Clinical use of frataxin measurement in a patient with a novel deletion in the FXN gene.

Saccà F, Marsili A, Puorro G, Antenora A, Pane C, Tessa A, Scoppettuolo P, Nesti C, Brescia Morra V, De Michele G, Santorelli FM, Filla A.

J Neurol. 2013 Apr;260(4):1116-21. doi: 10.1007/s00415-012-6770-5. Epub 2012 Nov 30.

PMID:
23196337
32.

Antiphospholipid-related chorea.

Peluso S, Antenora A, De Rosa A, Roca A, Maddaluno G, Brescia Morra V, De Michele G.

Front Neurol. 2012 Oct 22;3:150. doi: 10.3389/fneur.2012.00150. eCollection 2012.

33.

Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit.

Saccà F, Piro R, De Michele G, Acquaviva F, Antenora A, Carlomagno G, Cocozza S, Denaro A, Guacci A, Marsili A, Perrotta G, Puorro G, Cittadini A, Filla A.

Mov Disord. 2011 Mar;26(4):739-42. doi: 10.1002/mds.23435. Epub 2010 Nov 10.

PMID:
21506154
34.

A combined nucleic acid and protein analysis in Friedreich ataxia: implications for diagnosis, pathogenesis and clinical trial design.

Saccà F, Puorro G, Antenora A, Marsili A, Denaro A, Piro R, Sorrentino P, Pane C, Tessa A, Brescia Morra V, Cocozza S, De Michele G, Santorelli FM, Filla A.

PLoS One. 2011 Mar 11;6(3):e17627. doi: 10.1371/journal.pone.0017627.

35.

Complex phenotype in an Italian family with a novel mutation in SPG3A.

de Leva MF, Filla A, Criscuolo C, Tessa A, Pappatà S, Quarantelli M, Bilo L, Peluso S, Antenora A, Longo D, Santorelli FM, De Michele G.

J Neurol. 2010 Mar;257(3):328-31. doi: 10.1007/s00415-009-5311-3. Epub 2009 Sep 19.

PMID:
19768483

Supplemental Content

Loading ...
Support Center