Peluso S - Search Results

1

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. De Rosa A, et al. Among authors: peluso s. J Parkinsons Dis. 2014;4(1):123-8. doi: 10.3233/JPD-130312. J Parkinsons Dis. 2014. PMID: 24496098

2

The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern Italy.

Criscuolo C, De Rosa A, Guacci A, Simons EJ, Breedveld GJ, Peluso S, Volpe G, Filla A, Oostra BA, Bonifati V, De Michele G. Criscuolo C, et al. Among authors: peluso s. Mov Disord. 2011 Aug 1;26(9):1733-6. doi: 10.1002/mds.23735. Epub 2011 Apr 29. Mov Disord. 2011. PMID: 21538529

3

A case of restless leg syndrome in a family with LRRK2 gene mutation.

De Rosa A, Guacci A, Peluso S, Del Gaudio L, Massarelli M, Barbato S, Criscuolo C, De Michele G. De Rosa A, et al. Among authors: peluso s. Int J Neurosci. 2013 Apr;123(4):283-5. doi: 10.3109/00207454.2012.756485. Epub 2013 Feb 4. Int J Neurosci. 2013. PMID: 23227859

4

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. De Rosa A, et al. Among authors: peluso s. J Neurol. 2014 Nov;261(11):2204-8. doi: 10.1007/s00415-014-7477-6. Epub 2014 Sep 3. J Neurol. 2014. PMID: 25182701

5

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. De Rosa A, et al. Among authors: peluso s. J Nucl Cardiol. 2017 Feb;24(1):103-107. doi: 10.1007/s12350-015-0332-z. Epub 2015 Dec 1. J Nucl Cardiol. 2017. PMID: 26626785

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. De Rosa A, et al. Among authors: peluso s. Geriatr Nurs. 2016 Nov-Dec;37(6):434-439. doi: 10.1016/j.gerinurse.2016.06.012. Epub 2016 Jul 18. Geriatr Nurs. 2016. PMID: 27444659

7

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. Dubbioso R, et al. Among authors: peluso s. Mov Disord. 2017 Jun;32(6):947-948. doi: 10.1002/mds.27012. Epub 2017 Apr 17. Mov Disord. 2017. PMID: 28419556 No abstract available.

8

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. De Rosa A, et al. Among authors: peluso s. Parkinsonism Relat Disord. 2018 Feb;47:80-83. doi: 10.1016/j.parkreldis.2017.12.008. Epub 2017 Dec 9. Parkinsonism Relat Disord. 2018. PMID: 29249679

9

GBA-Related Parkinson's Disease: Dissection of Genotype-Phenotype Correlates in a Large Italian Cohort.

Petrucci S, Ginevrino M, Trezzi I, Monfrini E, Ricciardi L, Albanese A, Avenali M, Barone P, Bentivoglio AR, Bonifati V, Bove F, Bonanni L, Brusa L, Cereda C, Cossu G, Criscuolo C, Dati G, De Rosa A, Eleopra R, Fabbrini G, Fadda L, Garbellini M, Minafra B, Onofrj M, Pacchetti C, Palmieri I, Pellecchia MT, Petracca M, Picillo M, Pisani A, Vallelunga A, Zangaglia R, Di Fonzo A, Morgante F, Valente EM; ITA-GENE-PD Study Group. Petrucci S, et al. Mov Disord. 2020 Nov;35(11):2106-2111. doi: 10.1002/mds.28195. Epub 2020 Jul 13. Mov Disord. 2020. PMID: 32658388

10

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. Criscuolo C, et al. Among authors: peluso s. Acta Neurol Scand. 2016 Jun;133(6):410-4. doi: 10.1111/ane.12476. Epub 2015 Sep 15. Acta Neurol Scand. 2016. PMID: 26370385

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