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Items: 1 to 50 of 352

1.

International Guidelines for the Treatment of Huntington's Disease.

Bachoud-Lévi AC, Ferreira J, Massart R, Youssov K, Rosser A, Busse M, Craufurd D, Reilmann R, De Michele G, Rae D, Squitieri F, Seppi K, Perrine C, Scherer-Gagou C, Audrey O, Verny C, Burgunder JM.

Front Neurol. 2019 Jul 3;10:710. doi: 10.3389/fneur.2019.00710. eCollection 2019.

2.

PERK-Mediated Unfolded Protein Response Activation and Oxidative Stress in PARK20 Fibroblasts.

Amodio G, Moltedo O, Fasano D, Zerillo L, Oliveti M, Di Pietro P, Faraonio R, Barone P, Pellecchia MT, De Rosa A, De Michele G, Polishchuk E, Polishchuk R, Bonifati V, Nitsch L, Pierantoni GM, Renna M, Criscuolo C, Paladino S, Remondelli P.

Front Neurosci. 2019 Jun 27;13:673. doi: 10.3389/fnins.2019.00673. eCollection 2019.

3.

Screening for Niemann-Pick type C disease in neurodegenerative diseases.

Boenzi S, Dardis A, Russo P, Bellofatto M, Imbriglio T, Fico T, De Michele G, De Rosa A.

J Clin Neurosci. 2019 Oct;68:266-267. doi: 10.1016/j.jocn.2019.06.025. Epub 2019 Jun 17.

PMID:
31221578
4.

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
5.

LRP10 variants in Parkinson's disease and dementia with Lewy bodies in the South-West of the Netherlands.

Vergouw LJM, Ruitenberg A, Wong TH, Melhem S, Breedveld GJ, Criscuolo C, De Michele G, de Jong FJ, Bonifati V, van Swieten JC, Quadri M.

Parkinsonism Relat Disord. 2019 May 25. pii: S1353-8020(19)30258-5. doi: 10.1016/j.parkreldis.2019.05.037. [Epub ahead of print]

PMID:
31147221
6.

Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian families.

De Michele G, Lieto M, Galatolo D, Salvatore E, Cocozza S, Barghigiani M, Tessa A, Baldacci J, Pappatà S, Filla A, De Michele G, Santorelli FM.

Parkinsonism Relat Disord. 2019 May 14. pii: S1353-8020(19)30222-6. doi: 10.1016/j.parkreldis.2019.05.001. [Epub ahead of print]

PMID:
31126790
7.

Degenerative and acquired sporadic adult onset ataxia.

Lieto M, Roca A, Santorelli FM, Fico T, De Michele G, Bellofatto M, Saccà F, De Michele G, Filla A.

Neurol Sci. 2019 Jul;40(7):1335-1342. doi: 10.1007/s10072-019-03856-w. Epub 2019 Mar 29. Review.

PMID:
30927137
8.

The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease.

De Rosa A, Nettore IC, Cantone E, Maione L, Desiderio S, Peluso S, Saccà F, Manganelli F, Bruzzese D, Colao A, De Michele G, Macchia PE.

Neurol Sci. 2019 Jul;40(7):1351-1356. doi: 10.1007/s10072-019-03842-2. Epub 2019 Mar 20.

PMID:
30895397
9.

Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family.

Ramos EM, Roca A, Chumchim N, Dokuru DR, Van Berlo V, De Michele G, Lieto M, Tedeschi E, De Michele G, Coppola G.

Neurogenetics. 2019 May;20(2):99-102. doi: 10.1007/s10048-019-00571-8. Epub 2019 Mar 21.

PMID:
30895394
10.

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.

11.

Management of Hereditary Spastic Paraplegia: A Systematic Review of the Literature.

Bellofatto M, De Michele G, Iovino A, Filla A, Santorelli FM.

Front Neurol. 2019 Jan 22;10:3. doi: 10.3389/fneur.2019.00003. eCollection 2019.

12.

DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease.

Castaldo I, De Rosa M, Romano A, Zuchegna C, Squitieri F, Mechelli R, Peluso S, Borrelli C, Del Mondo A, Salvatore E, Vescovi LA, Migliore S, De Michele G, Ristori G, Romano S, Avvedimento EV, Porcellini A.

Ann Neurol. 2019 Feb;85(2):296-301. doi: 10.1002/ana.25393. Epub 2019 Jan 13.

PMID:
30549309
13.

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.

14.

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.

PMID:
30098094
15.

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
16.

The Italian version of the quick mild cognitive impairment (Qmci-I) screen: normative study on 307 healthy subjects.

Iavarone A, Carpinelli Mazzi M, Russo G, D'Anna F, Peluso S, Mazzeo P, De Luca V, De Michele G, Iaccarino G, Abete P, Milan G, Garofalo E, Musella C, O'Caoimh R, Molloy W, De Joanna G, Manzo V, Ambra FI, Postiglione A, Illario M; Working Group.

Aging Clin Exp Res. 2019 Mar;31(3):353-360. doi: 10.1007/s40520-018-0981-2. Epub 2018 Jun 8.

PMID:
29949025
17.

LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study.

Quadri M, Mandemakers W, Grochowska MM, Masius R, Geut H, Fabrizio E, Breedveld GJ, Kuipers D, Minneboo M, Vergouw LJM, Carreras Mascaro A, Yonova-Doing E, Simons E, Zhao T, Di Fonzo AB, Chang HC, Parchi P, Melis M, Correia Guedes L, Criscuolo C, Thomas A, Brouwer RWW, Heijsman D, Ingrassia AMT, Calandra Buonaura G, Rood JP, Capellari S, Rozemuller AJ, Sarchioto M, Fen Chien H, Vanacore N, Olgiati S, Wu-Chou YH, Yeh TH, Boon AJW, Hoogers SE, Ghazvini M, IJpma AS, van IJcken WFJ, Onofrj M, Barone P, Nicholl DJ, Puschmann A, De Mari M, Kievit AJ, Barbosa E, De Michele G, Majoor-Krakauer D, van Swieten JC, de Jong FJ, Ferreira JJ, Cossu G, Lu CS, Meco G, Cortelli P, van de Berg WDJ, Bonifati V; International Parkinsonism Genetics Network.

Lancet Neurol. 2018 Jul;17(7):597-608. doi: 10.1016/S1474-4422(18)30179-0. Epub 2018 Jun 7.

PMID:
29887161
18.

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
19.

Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations.

Severino M, Lualdi S, Fiorillo C, Striano P, De Toni T, Peluso S, De Michele G, Rossi A, Filocamo M, Bruno C.

J Neurol. 2018 Jun;265(6):1419-1425. doi: 10.1007/s00415-018-8826-7. Epub 2018 Apr 17.

PMID:
29666984
20.

Closing-in Phenomenon in Huntington's Disease: A Neuropsychological Marker of Frontal/Executive Dysfunction.

De Lucia N, Peluso S, Roca A, Russo CV, Massarelli M, De Michele G, Di Maio L, Salvatore E, De Michele G.

Arch Clin Neuropsychol. 2019 Feb 1;34(1):24-30. doi: 10.1093/arclin/acy020.

PMID:
29554249
21.

Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations.

Fasano D, Parisi S, Pierantoni GM, De Rosa A, Picillo M, Amodio G, Pellecchia MT, Barone P, Moltedo O, Bonifati V, De Michele G, Nitsch L, Remondelli P, Criscuolo C, Paladino S.

Cell Death Dis. 2018 Mar 7;9(3):385. doi: 10.1038/s41419-018-0410-7.

22.

Adult normative values for the PATA Rate Test.

Pane C, Costabile T, Salvati A, Aurisicchio DL, Abate F, Liguori A, Paciello F, Peluso S, Manganelli F, De Michele G, Filla A, Saccà F.

J Neurol. 2018 May;265(5):1102-1105. doi: 10.1007/s00415-018-8820-0. Epub 2018 Mar 6.

PMID:
29511862
23.

Spinocerebellar Ataxia Tethering PCR: A Rapid Genetic Test for the Diagnosis of Spinocerebellar Ataxia Types 1, 2, 3, 6, and 7 by PCR and Capillary Electrophoresis.

Cagnoli C, Brussino A, Mancini C, Ferrone M, Orsi L, Salmin P, Pappi P, Giorgio E, Pozzi E, Cavalieri S, Di Gregorio E, Ferrero M, Filla A, De Michele G, Gellera C, Mariotti C, Nethisinghe S, Giunti P, Stevanin G, Brusco A.

J Mol Diagn. 2018 May;20(3):289-297. doi: 10.1016/j.jmoldx.2017.12.006. Epub 2018 Feb 17.

PMID:
29462666
24.

Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy.

Caporali L, Iommarini L, La Morgia C, Olivieri A, Achilli A, Maresca A, Valentino ML, Capristo M, Tagliavini F, Del Dotto V, Zanna C, Liguori R, Barboni P, Carbonelli M, Cocetta V, Montopoli M, Martinuzzi A, Cenacchi G, De Michele G, Testa F, Nesti A, Simonelli F, Porcelli AM, Torroni A, Carelli V.

PLoS Genet. 2018 Feb 14;14(2):e1007210. doi: 10.1371/journal.pgen.1007210. eCollection 2018 Feb.

25.

Emotion Recognition and Psychological Comorbidity in Friedreich's Ataxia.

Costabile T, Capretti V, Abate F, Liguori A, Paciello F, Pane C, De Rosa A, Peluso S, De Michele G, Filla A, Saccà F.

Cerebellum. 2018 Jun;17(3):336-345. doi: 10.1007/s12311-018-0918-5.

PMID:
29327279
26.

The contribution of gender differences in motor, behavioral and cognitive features to functional capacity, independence and quality of life in patients with Huntington's disease.

Zielonka D, Ren M, De Michele G, Roos RAC, Squitieri F, Bentivoglio AR, Marcinkowski JT, Landwehrmeyer GB.

Parkinsonism Relat Disord. 2018 Apr;49:42-47. doi: 10.1016/j.parkreldis.2018.01.006. Epub 2018 Jan 5.

PMID:
29326033
27.

Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease.

De Rosa A, Peluso S, De Lucia N, Russo P, Annarumma I, Esposito M, Manganelli F, Brunetti A, De Michele G, Pappatà S.

Parkinsonism Relat Disord. 2018 Feb;47:80-83. doi: 10.1016/j.parkreldis.2017.12.008. Epub 2017 Dec 9.

PMID:
29249679
28.

Correction to: Peripheral markers of autophagy in polyglutamine diseases.

Puorro G, Marsili A, Sapone F, Pane C, De Rosa A, Peluso S, De Michele G, Filla A, Saccà F.

Neurol Sci. 2018 Jan;39(1):153. doi: 10.1007/s10072-017-3193-1.

PMID:
29147801
29.

A Biological Child Does Not Repair the Injustice of Breast Cancer at a Young Age.

De Michele G.

Narrat Inq Bioeth. 2017;7(2):113-114. doi: 10.1353/nib.2017.0033. No abstract available.

PMID:
29056633
30.

Narrative Symposium: Cancer and Fertility.

Yi A, De Michele G, Woodlief M, Fauvre M, Abrams R, Charne R, Warren TD, Ettinger B, Curran R, Rogers M, Hoffner B, Brown JJ, Schmuke AD, Mackey P, Frye J.

Narrat Inq Bioeth. 2017;7(2):111-E5. doi: 10.1353/nib.2017.0052. No abstract available.

PMID:
29056631
31.

Peripheral markers of autophagy in polyglutamine diseases.

Puorro G, Marsili A, Sapone F, Pane C, De Rosa A, Peluso S, De Michele G, Filla A, Saccà F.

Neurol Sci. 2018 Jan;39(1):149-152. doi: 10.1007/s10072-017-3156-6. Epub 2017 Oct 18. Erratum in: Neurol Sci. 2017 Nov 17;:.

PMID:
29046994
32.

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.

33.

Disruption of GABA(A)-mediated intracortical inhibition in patients with chorea-acanthocytosis.

Dubbioso R, Esposito M, Peluso S, Iodice R, De Michele G, Santoro L, Manganelli F.

Neurosci Lett. 2017 Jul 27;654:107-110. doi: 10.1016/j.neulet.2017.06.032. Epub 2017 Jun 20.

PMID:
28645789
34.

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
35.

Normalization of timed neuropsychological tests with the PATA rate and nine-hole pegboard tests.

Saccà F, Costabile T, Abate F, Liguori A, Paciello F, Pane C, De Rosa A, Manganelli F, De Michele G, Filla A.

J Neuropsychol. 2018 Sep;12(3):471-483. doi: 10.1111/jnp.12125. Epub 2017 May 6.

PMID:
28477351
36.

Does motor cortex plasticity depend on the type of mutation in the leucine-rich repeat kinase 2 gene?

Dubbioso R, de Rosa A, Esposito M, Peluso S, Iodice R, de Michele G, Santoro L, Manganelli F.

Mov Disord. 2017 Jun;32(6):947-948. doi: 10.1002/mds.27012. Epub 2017 Apr 17. No abstract available.

PMID:
28419556
37.

Stability of erythropoietin repackaging in polypropylene syringes for clinical use.

Marsili A, Puorro G, Pane C, de Rosa A, Defazio G, Casali C, Cittadini A, de Michele G, Florio BE, Filla A, Saccà F.

Saudi Pharm J. 2017 Feb;25(2):290-293. doi: 10.1016/j.jsps.2016.01.003. Epub 2016 Jan 14.

38.

Pathological laughter as onset symptom in atypical parkinsonisms.

De Rosa A, Pappatà S, Peluso S, Saccà F, Lieto M, Filla A, De Michele G.

J Neurol. 2017 Jan;264(1):182-184. doi: 10.1007/s00415-016-8351-5. Epub 2016 Nov 24. No abstract available.

PMID:
27885486
39.

Functional MRI signal fluctuations highlight altered resting brain activity in Huntington's disease.

Sarappa C, Salvatore E, Filla A, Cocozza S, Russo CV, Saccà F, Brunetti A, De Michele G, Quarantelli M.

Brain Imaging Behav. 2017 Oct;11(5):1459-1469. doi: 10.1007/s11682-016-9630-6.

PMID:
27734308
40.

Impulsive-compulsive behaviors in parkin-associated Parkinson disease.

Morgante F, Fasano A, Ginevrino M, Petrucci S, Ricciardi L, Bove F, Criscuolo C, Moccia M, De Rosa A, Sorbera C, Bentivoglio AR, Barone P, De Michele G, Pellecchia MT, Valente EM.

Neurology. 2016 Oct 4;87(14):1436-1441. Epub 2016 Sep 2.

41.

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
42.

Infusion treatments and deep brain stimulation in Parkinson's Disease: The role of nursing.

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

Geriatr Nurs. 2016 Nov - Dec;37(6):434-439. doi: 10.1016/j.gerinurse.2016.06.012. Epub 2016 Jul 18.

PMID:
27444659
43.

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
44.

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
45.

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
46.

Parkinsonism in a pair of monozygotic CADASIL twins sharing the R1006C mutation: a transcranial sonography study.

Ragno M, Sanguigni S, Manca A, Pianese L, Paci C, Berbellini A, Cozzolino V, Gobbato R, Peluso S, De Michele G.

Neurol Sci. 2016 Jun;37(6):875-81. doi: 10.1007/s10072-016-2497-x. Epub 2016 Feb 5.

PMID:
26850715
47.

Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonism.

De Rosa A, Pellegrino T, Pappatà S, Lieto M, Bonifati V, Palma V, Topa A, Santoro L, Bilo L, Cuocolo A, De Michele G.

Parkinsonism Relat Disord. 2016 Feb;23:102-5. doi: 10.1016/j.parkreldis.2015.12.006. Epub 2015 Dec 18.

PMID:
26725142
48.

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
49.

Myocardial 123I-metaiodobenzylguanidine scintigraphy in patients with homozygous and heterozygous parkin mutations.

De Rosa A, Pellegrino T, Pappatà S, Pellecchia MT, Peluso S, Saccà F, Barone P, Cuocolo A, De Michele G.

J Nucl Cardiol. 2017 Feb;24(1):103-107. doi: 10.1007/s12350-015-0332-z. Epub 2015 Dec 1.

PMID:
26626785
50.

Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Criscuolo C, Procaccini C, Meschini MC, Cianflone A, Carbone R, Doccini S, Devos D, Nesti C, Vuillaume I, Pellegrino M, Filla A, De Michele G, Matarese G, Santorelli FM.

J Neurol. 2015 Dec;262(12):2755-63. doi: 10.1007/s00415-015-7911-4. Epub 2015 Nov 3.

PMID:
26530509

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