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Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism.
Magrinelli F, Mehta S, Di Lazzaro G, Latorre A, Edwards MJ, Balint B, Basu P, Kobylecki C, Groppa S, Hegde A, Mulroy E, Estevez-Fraga C, Arora A, Kumar H, Schneider SA, Lewis PA, Jaunmuktane Z, Revesz T, Gandhi S, Wood NW, Hardy JA, Tinazzi M, Lal V, Houlden H, Bhatia KP. Magrinelli F, et al. Among authors: di lazzaro g. Mov Disord. 2022 Jan;37(1):148-161. doi: 10.1002/mds.28807. Epub 2021 Oct 8. Mov Disord. 2022. PMID: 34622992
X-Linked Parkinsonism: Phenotypic and Genetic Heterogeneity.
Di Lazzaro G, Magrinelli F, Estevez-Fraga C, Valente EM, Pisani A, Bhatia KP. Di Lazzaro G, et al. Mov Disord. 2021 Jul;36(7):1511-1525. doi: 10.1002/mds.28565. Epub 2021 May 7. Mov Disord. 2021. PMID: 33960519 Review.
Ethnic Differences in Dystonia Prevalence and Phenotype.
Mulroy E, Macerollo A, Scotton S, Cociasu I, Di Lazzaro G, Bashir S, Doherty J, Hamid S, Mooney N, Batla A, Morgante F, Bhatia KP. Mulroy E, et al. Among authors: di lazzaro g. Mov Disord. 2022 Jun;37(6):1323-1325. doi: 10.1002/mds.29034. Epub 2022 May 2. Mov Disord. 2022. PMID: 35500158 No abstract available.
The Need to Tic.
Di Lazzaro G, Magrinelli F, Ganos C, Bhatia KP. Di Lazzaro G, et al. Mov Disord Clin Pract. 2020 Aug 14;7(7):863-864. doi: 10.1002/mdc3.13023. eCollection 2020 Oct. Mov Disord Clin Pract. 2020. PMID: 33043087 Free PMC article. No abstract available.
Late-Onset Chorea in JAK2-Associated Essential Thrombocythemia.
Koya Kutty S, Di Lazzaro G, Magrinelli F, Mulroy E, Latorre A, Bhatia KP. Koya Kutty S, et al. Among authors: di lazzaro g. Mov Disord Clin Pract. 2020 Nov 24;8(1):145-148. doi: 10.1002/mdc3.13105. eCollection 2021 Jan. Mov Disord Clin Pract. 2020. PMID: 33426172 Free PMC article. No abstract available.
Huntington disease-like phenotype in a patient with ANO3 mutation.
Koya Kutty S, Mulroy E, Magrinelli F, Di Lazzaro G, Latorre A, Bhatia KP. Koya Kutty S, et al. Among authors: di lazzaro g. Parkinsonism Relat Disord. 2021 Sep;90:120-122. doi: 10.1016/j.parkreldis.2021.02.022. Epub 2021 Feb 20. Parkinsonism Relat Disord. 2021. PMID: 33640251 No abstract available.
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
Criss-cross gait: A clue to glucose transporter type 1 deficiency syndrome.
Magrinelli F, Mulroy E, Schneider SA, Latorre A, Di Lazzaro G, Hennig A, Grünewald S, De Vivo DC, Bhatia KP. Magrinelli F, et al. Among authors: di lazzaro g. Neurology. 2020 Sep 15;95(11):500-501. doi: 10.1212/WNL.0000000000010502. Epub 2020 Aug 4. Neurology. 2020. PMID: 32753446 No abstract available.
Idiopathic Non-task-Specific Upper Limb Dystonia, a Neglected Form of Dystonia.
Defazio G, Ercoli T, Erro R, Pellicciari R, Mascia MM, Fabbrini G, Albanese A, Lalli S, Eleopra R, Barone P, Marchese R, Ceravolo R, Scaglione C, Liguori R, Esposito M, Bentivoglio AR, Bertolasi L, Altavista MC, Bono F, Pisani A, Girlanda P, Berardelli A; Italian Dystonia Registry Participants. Defazio G, et al. Mov Disord. 2020 Nov;35(11):2038-2045. doi: 10.1002/mds.28199. Epub 2020 Jul 14. Mov Disord. 2020. PMID: 32662572
59 results