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Items: 1 to 20 of 327

1.

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. 2017 May 6. doi: 10.1111/jnp.12125. [Epub ahead of print]

PMID:
28477351
2.

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 Apr 17. doi: 10.1002/mds.27012. [Epub ahead of print] No abstract available.

PMID:
28419556
3.

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.

4.

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
5.

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. 2016 Oct 12. [Epub ahead of print]

PMID:
27734308
6.

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.

7.

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
8.

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
9.

Clinical manifestations of intermediate allele carriers in Huntington disease.

Cubo E, Ramos-Arroyo MA, Martinez-Horta S, Martínez-Descalls A, Calvo S, Gil-Polo C; European HD Network..

Neurology. 2016 Aug 9;87(6):571-8. doi: 10.1212/WNL.0000000000002944. Epub 2016 Jul 8.

PMID:
27402890
10.

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
11.

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
12.

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
13.

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
14.

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
15.

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
16.

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
17.

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
18.

SPG5 and multiple sclerosis: clinical and genetic overlap?

Criscuolo C, Carbone R, Lieto M, Peluso S, Guacci A, Filla A, Quarantelli M, Lanzillo R, Morra VB, De Michele G.

Acta Neurol Scand. 2016 Jun;133(6):410-4. doi: 10.1111/ane.12476. Epub 2015 Sep 15.

PMID:
26370385
19.

ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.

Panza E, Escamilla-Honrubia JM, Marco-Marín C, Gougeard N, De Michele G, Morra VB, Liguori R, Salviati L, Donati MA, Cusano R, Pippucci T, Ravazzolo R, Németh AH, Smithson S, Davies S, Hurst JA, Bordo D, Rubio V, Seri M.

Brain. 2016 Jan;139(Pt 1):e3. doi: 10.1093/brain/awv247. Epub 2015 Aug 21. No abstract available.

PMID:
26297558
20.

A new model to study neurodegeneration in ataxia oculomotor apraxia type 2.

Becherel OJ, Sun J, Yeo AJ, Nayler S, Fogel BL, Gao F, Coppola G, Criscuolo C, De Michele G, Wolvetang E, Lavin MF.

Hum Mol Genet. 2015 Oct 15;24(20):5759-74. doi: 10.1093/hmg/ddv296. Epub 2015 Jul 30.

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