Giannini F - Search Results

1

A new mutation in DNM2 gene in a large Italian family.

Lopergolo D, Bocci S, Pinto AM, Valentino F, Doddato G, Ginanneschi F, Volpi N, Renieri A, Giannini F. Lopergolo D, et al. Among authors: giannini f. Neurol Sci. 2021 Jun;42(6):2509-2513. doi: 10.1007/s10072-020-04972-8. Epub 2021 Jan 18. Neurol Sci. 2021. PMID: 33459893

2

Rhabdomyolysis in an elderly multitreated patient: multiple drug interactions after statin withdrawal.

Ginanneschi F, Volpi N, Giannini F, Rocchi R, Donati D, Aglianò M, Lorenzoni P, Rossi A. Ginanneschi F, et al. Among authors: giannini f. J Neurol Sci. 2014 Jan 15;336(1-2):284-7. doi: 10.1016/j.jns.2013.10.040. Epub 2013 Nov 6. J Neurol Sci. 2014. PMID: 24252882

3

Sporadic hereditary motor and sensory neuropathies: Advances in the diagnosis using next generation sequencing technology.

Fallerini C, Carignani G, Capoccitti G, Federico A, Rufa A, Pinto AM, Rizzo CL, Rossi A, Mari F, Mencarelli MA, Giannini F, Renieri A. Fallerini C, et al. Among authors: giannini f. J Neurol Sci. 2015 Dec 15;359(1-2):409-17. doi: 10.1016/j.jns.2015.09.377. Epub 2015 Oct 9. J Neurol Sci. 2015. PMID: 26481167

4

Major motor-functional determinants associated with poor self-reported health-related quality of life in myasthenia gravis patients.

Cioncoloni D, Casali S, Ginanneschi F, Carone M, Veronica B, Rossi A, Giannini F. Cioncoloni D, et al. Among authors: giannini f. Neurol Sci. 2016 May;37(5):717-23. doi: 10.1007/s10072-016-2556-3. Epub 2016 Apr 1. Neurol Sci. 2016. PMID: 27038315

5

Multifocal motor neuropathy occurring after acute motor axonal neuropathy: two stages of the same disease?

Bocci S, Giannini F, Volpi N, Rossi A, Ginanneschi F. Bocci S, et al. Among authors: giannini f. Neurol Sci. 2022 Feb;43(2):1463-1465. doi: 10.1007/s10072-021-05725-x. Epub 2021 Nov 20. Neurol Sci. 2022. PMID: 34800200 No abstract available.

6

A Novel Variant in Superoxide Dismutase 1 Gene (p.V119M) in Als Patients with Pure Lower Motor Neuron Presentation.

Ricci C, Giannini F, Riolo G, Bocci S, Casali S, Battistini S. Ricci C, et al. Among authors: giannini f. Genes (Basel). 2021 Sep 29;12(10):1544. doi: 10.3390/genes12101544. Genes (Basel). 2021. PMID: 34680939 Free PMC article.

7

D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings.

Giannini F, Battistini S, Mancuso M, Greco G, Ricci C, Volpi N, Del Corona A, Piazza S, Siciliano G. Giannini F, et al. Amyotroph Lateral Scler. 2010;11(1-2):216-9. doi: 10.3109/17482960902721642. Amyotroph Lateral Scler. 2010. PMID: 20184519

8

Incidence of ulnar neuropathy at the elbow in the province of Siena (Italy).

Mondelli M, Giannini F, Ballerini M, Ginanneschi F, Martorelli E. Mondelli M, et al. Among authors: giannini f. J Neurol Sci. 2005 Jul 15;234(1-2):5-10. doi: 10.1016/j.jns.2005.02.010. Epub 2005 Apr 20. J Neurol Sci. 2005. PMID: 15993135

9

Clinical Features and Outcome of the Guillain-Barre Syndrome: A Single-Center 11-Year Experience.

Ginanneschi F, Giannini F, Sicurelli F, Battisti C, Capoccitti G, Bartalini S, Mignarri A, Volpi N, Cioncoloni D, Franci L, De Stefano N, Rossi A. Ginanneschi F, et al. Among authors: giannini f. Front Neurol. 2022 Jun 29;13:856091. doi: 10.3389/fneur.2022.856091. eCollection 2022. Front Neurol. 2022. PMID: 35860488 Free PMC article.

10

Novel POLG mutations and variable clinical phenotypes in 13 Italian patients.

Da Pozzo P, Cardaioli E, Rubegni A, Gallus GN, Malandrini A, Rufa A, Battisti C, Carluccio MA, Rocchi R, Giannini F, Bianchi A, Mancuso M, Siciliano G, Dotti MT, Federico A. Da Pozzo P, et al. Among authors: giannini f. Neurol Sci. 2017 Apr;38(4):563-570. doi: 10.1007/s10072-016-2734-3. Epub 2017 Jan 27. Neurol Sci. 2017. PMID: 28130605

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