Magrinelli F - Search Results

1

Detection and Characterization of a De Novo Alu Retrotransposition Event Causing NKX2-1-Related Disorder.

Magrinelli F, Rocca C, Simone R, Zenezini Chiozzi R, Jaunmuktane Z, Mencacci NE, Tinazzi M, Jayawant S, Nemeth AH, Demidov G, Houlden H, Bhatia KP. Magrinelli F, et al. Mov Disord. 2023 Feb;38(2):347-353. doi: 10.1002/mds.29280. Epub 2022 Nov 23. Mov Disord. 2023. PMID: 36420574

2

Twelve-year Follow-up of A Large Italian Family with Atypical Phenotypes of DYT1-dystonia.

Magrinelli F, Bacchin R, Tinazzi M, Gambarin M. Magrinelli F, et al. Mov Disord Clin Pract. 2018 Dec 30;6(2):166-170. doi: 10.1002/mdc3.12712. eCollection 2019 Feb. Mov Disord Clin Pract. 2018. PMID: 30838317 Free PMC article.

3

Ciliary Dysfunction: The Hairy Explanation of Normal Pressure Hydrocephalus?

Mulroy E, Latorre A, Magrinelli F, Bhatia KP. Mulroy E, et al. Among authors: magrinelli f. Mov Disord Clin Pract. 2019 Dec 20;7(1):30-31. doi: 10.1002/mdc3.12880. eCollection 2020 Jan. Mov Disord Clin Pract. 2019. PMID: 31970208 Free PMC article. No abstract available.

4

Upper camptocormia in Parkinson's disease: Neurophysiological and imaging findings of both central and peripheral pathophysiological mechanisms.

Magrinelli F, Geroin C, Squintani G, Gandolfi M, Rizzo G, Barillari M, Vattemi G, Morgante F, Tinazzi M. Magrinelli F, et al. Parkinsonism Relat Disord. 2020 Feb;71:28-34. doi: 10.1016/j.parkreldis.2020.01.004. Epub 2020 Jan 11. Parkinsonism Relat Disord. 2020. PMID: 31981996

5

Huntington disease like 2 (HDL-2) with parkinsonism and abnormal DAT-SPECT - A novel observation.

Mulroy E, Latorre A, Menozzi E, Teh PC, Magrinelli F, Bhatia KP. Mulroy E, et al. Among authors: magrinelli f. Parkinsonism Relat Disord. 2020 Feb;71:46-48. doi: 10.1016/j.parkreldis.2020.01.008. Epub 2020 Jan 16. Parkinsonism Relat Disord. 2020. PMID: 32028232 No abstract available.

6

Unravelling the enigma of cortical tremor and other forms of cortical myoclonus.

Latorre A, Rocchi L, Magrinelli F, Mulroy E, Berardelli A, Rothwell JC, Bhatia KP. Latorre A, et al. Among authors: magrinelli f. Brain. 2020 Sep 1;143(9):2653-2663. doi: 10.1093/brain/awaa129. Brain. 2020. PMID: 32417917 Review.

7

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. Neurology. 2020 Sep 15;95(11):500-501. doi: 10.1212/WNL.0000000000010502. Epub 2020 Aug 4. Neurology. 2020. PMID: 32753446 No abstract available.

8

Isolated and combined genetic tremor syndromes: a critical appraisal based on the 2018 MDS criteria.

Magrinelli F, Latorre A, Balint B, Mackenzie M, Mulroy E, Stamelou M, Tinazzi M, Bhatia KP. Magrinelli F, et al. Parkinsonism Relat Disord. 2020 Aug;77:121-140. doi: 10.1016/j.parkreldis.2020.04.010. Epub 2020 Jun 15. Parkinsonism Relat Disord. 2020. PMID: 32818815 Review.

9

A new family with GLRB-related hyperekplexia showing chorea in homo- and heterozygous variant carriers.

Estevez-Fraga C, Magrinelli F, Latorre A, Cordivari C, Houlden H, Tinazzi M, Hemingway C, Tabrizi SJ, Bhatia KP. Estevez-Fraga C, et al. Among authors: magrinelli f. Parkinsonism Relat Disord. 2020 Oct;79:97-99. doi: 10.1016/j.parkreldis.2020.08.016. Epub 2020 Aug 18. Parkinsonism Relat Disord. 2020. PMID: 32911248 No abstract available.

10

Reply: Pentameric repeat expansions: cortical myoclonus or cortical tremor? and Cortical tremor: a tantalizing conundrum between cortex and cerebellum.

Latorre A, Rocchi L, Magrinelli F, Mulroy E, Berardelli A, Rothwell JC, Bhatia KP. Latorre A, et al. Among authors: magrinelli f. Brain. 2020 Oct 1;143(10):e88. doi: 10.1093/brain/awaa261. Brain. 2020. PMID: 33011762 No abstract available.

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