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Items: 1 to 20 of 40

1.

The Italian Dystonia Registry: rationale, design and preliminary findings.

Defazio G, Esposito M, Abbruzzese G, Scaglione CL, Fabbrini G, Ferrazzano G, Peluso S, Pellicciari R, Gigante AF, Cossu G, Arca R, Avanzino L, Bono F, Mazza MR, Bertolasi L, Bacchin R, Eleopra R, Lettieri C, Morgante F, Altavista MC, Polidori L, Liguori R, Misceo S, Squintani G, Tinazzi M, Ceravolo R, Unti E, Magistrelli L, Coletti Moja M, Modugno N, Petracca M, Tambasco N, Cotelli MS, Aguggia M, Pisani A, Romano M, Zibetti M, Bentivoglio AR, Albanese A, Girlanda P, Berardelli A.

Neurol Sci. 2017 Feb 18. doi: 10.1007/s10072-017-2839-3. [Epub ahead of print]

PMID:
28215037
2.

The occurrence of lateral shift in cervical dystonia.

Esposito M, Peluso S, Dubbioso R, Allocca R, Iorillo F, Coppola A, Santoro L.

Neurol Sci. 2017 Jan 4. doi: 10.1007/s10072-016-2799-z. [Epub ahead of print]

PMID:
28054172
3.

Adult-onset pure tic disorder after post-traumatic hypoxic lesions of the globus pallidus.

Criscuolo C, D'Amico A, Peluso S, Popolizio T, Pellecchia MT.

Parkinsonism Relat Disord. 2017 Jan;34:75-76. doi: 10.1016/j.parkreldis.2016.11.007. No abstract available.

PMID:
27887894
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. No abstract available.

PMID:
27885486
5.

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.

PMID:
27502963
6.

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.

PMID:
27444659
7.

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. No abstract available.

PMID:
27314960
8.

TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features.

Balestrini S, Milh M, Castiglioni C, Lüthy K, Finelli MJ, Verstreken P, Cardon A, Stražišar BG, Holder JL Jr, Lesca G, Mancardi MM, Poulat AL, Repetto GM, Banka S, Bilo L, Birkeland LE, Bosch F, Brockmann K, Cross JH, Doummar D, Félix TM, Giuliano F, Hori M, Hüning I, Kayserili H, Kini U, Lees MM, Meenakshi G, Mewasingh L, Pagnamenta AT, Peluso S, Mey A, Rice GM, Rosenfeld JA, Taylor JC, Troester MM, Stanley CM, Ville D, Walkiewicz M, Falace A, Fassio A, Lemke JR, Biskup S, Tardif J, Ajeawung NF, Tolun A, Corbett M, Gecz J, Afawi Z, Howell KB, Oliver KL, Berkovic SF, Scheffer IE, de Falco FA, Oliver PL, Striano P, Zara F, Campeau PM, Sisodiya SM.

Neurology. 2016 Jul 5;87(1):77-85. doi: 10.1212/WNL.0000000000002807.

9.

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. No abstract available.

PMID:
26896283
10.

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.

PMID:
26850715
11.

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.

PMID:
26708103
12.

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.

PMID:
26626785
13.

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.

PMID:
26370385
14.

Gain of hTERC: a genetic marker of malignancy in oral potentially malignant lesions.

Dorji T, Monti V, Fellegara G, Gabba S, Grazioli V, Repetti E, Marcialis C, Peluso S, Di Ruzza D, Neri F, Foschini MP.

Hum Pathol. 2015 Sep;46(9):1275-81. doi: 10.1016/j.humpath.2015.05.013.

PMID:
26170010
15.

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. No abstract available.

PMID:
25483721
16.

Metabolic Ataxias in Adults.

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

Curr Mol Med. 2014 Oct 10. [Epub ahead of print]

PMID:
25323876
17.

Screening for dopa-responsive dystonia in patients with Scans Without Evidence of Dopaminergic Deficiency (SWEDD).

De Rosa A, Carducci C, Carducci C, Peluso S, Lieto M, Mazzella A, Saccà F, Brescia Morra V, Pappatà S, Leuzzi V, De Michele G.

J Neurol. 2014 Nov;261(11):2204-8. doi: 10.1007/s00415-014-7477-6.

PMID:
25182701
18.

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
19.

Genetic screening for the LRRK2 R1441C and G2019S mutations in Parkinsonian patients from Campania.

De Rosa A, De Michele G, Guacci A, Carbone R, Lieto M, Peluso S, Picillo M, Barone P, Salemi F, Laiso A, Saccà F, Tessitore A, Pellecchia MT, Bonifati V, Criscuolo C.

J Parkinsons Dis. 2014;4(1):123-8. doi: 10.3233/JPD-130312.

PMID:
24496098
20.

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. No abstract available.

PMID:
24486243
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