Sagnelli A[au] - Search Results

Year	Number of Results
2010	2
2011	1
2012	4
2013	2
2014	4
2015	4
2016	5
2017	3
2018	1
2020	1
2021	1
2024	0

1

Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis.

Elia AE, Lalli S, Monsurrò MR, Sagnelli A, Taiello AC, Reggiori B, La Bella V, Tedeschi G, Albanese A. Elia AE, et al. Among authors: sagnelli a. Eur J Neurol. 2016 Jan;23(1):45-52. doi: 10.1111/ene.12664. Epub 2015 Feb 9. Eur J Neurol. 2016. PMID: 25664595 Free PMC article. Clinical Trial.

2

Inherited neuropathies: an update.

Sagnelli A, Piscosquito G, Pareyson D. Sagnelli A, et al. J Neurol. 2013 Oct;260(10):2684-90. doi: 10.1007/s00415-013-7113-x. Epub 2013 Sep 24. J Neurol. 2013. PMID: 24061768 Review.

3

Mitochondrial dynamics and inherited peripheral nerve diseases.

Pareyson D, Saveri P, Sagnelli A, Piscosquito G. Pareyson D, et al. Among authors: sagnelli a. Neurosci Lett. 2015 Jun 2;596:66-77. doi: 10.1016/j.neulet.2015.04.001. Epub 2015 Apr 3. Neurosci Lett. 2015. PMID: 25847151 Review.

4

Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and Future.

Weydt P, Sagnelli A, Rosenbohm A, Fratta P, Pradat PF, Ludolph AC, Pareyson D. Weydt P, et al. Among authors: sagnelli a. J Mol Neurosci. 2016 Mar;58(3):379-87. doi: 10.1007/s12031-015-0682-7. Epub 2015 Nov 14. J Mol Neurosci. 2016. PMID: 26572537 Review.

5

Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.

Cortese A, Laurà M, Casali C, Nishino I, Hayashi YK, Magri S, Taroni F, Stuani C, Saveri P, Moggio M, Ripolone M, Prelle A, Pisciotta C, Sagnelli A, Pichiecchio A, Reilly MM, Buratti E, Pareyson D. Cortese A, et al. Among authors: sagnelli a. Eur J Neurol. 2018 Jan;25(1):154-163. doi: 10.1111/ene.13478. Epub 2017 Dec 2. Eur J Neurol. 2018. PMID: 29029362

6

Influenza Vaccine Hesitancy in Patients with Multiple Sclerosis: A Monocentric Observational Study.

Ziello A, Scavone C, Di Battista ME, Salvatore S, Di Giulio Cesare D, Moreggia O, Allegorico L, Sagnelli A, Barbato S, Manzo V, Capuano A, Maniscalco GT. Ziello A, et al. Among authors: sagnelli a. Brain Sci. 2021 Jul 5;11(7):890. doi: 10.3390/brainsci11070890. Brain Sci. 2021. PMID: 34356125 Free PMC article.

7

Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy.

Pareyson D, Fratta P, Pradat PF, Sorarù G, Finsterer J, Vissing J, Jokela ME, Udd B, Ludolph AC, Sagnelli A, Weydt P. Pareyson D, et al. Among authors: sagnelli a. J Mol Neurosci. 2016 Mar;58(3):394-400. doi: 10.1007/s12031-015-0704-5. Epub 2016 Jan 7. J Mol Neurosci. 2016. PMID: 26744358

8

Adult polyglucosan body disease in a patient originally diagnosed with Fabry's disease.

Sagnelli A, Savoiardo M, Marchesi C, Morandi L, Mora M, Morbin M, Farina L, Mazzeo A, Toscano A, Pagliarani S, Lucchiari S, Comi GP, Salsano E, Pareyson D. Sagnelli A, et al. Neuromuscul Disord. 2014 Mar;24(3):272-6. doi: 10.1016/j.nmd.2013.11.006. Epub 2013 Nov 19. Neuromuscul Disord. 2014. PMID: 24380807

9

Amyotrophic lateral sclerosis and multiple sclerosis overlap: a case report.

Trojsi F, Sagnelli A, Cirillo G, Piccirillo G, Femiano C, Izzo F, Monsurrò MR, Tedeschi G. Trojsi F, et al. Among authors: sagnelli a. Case Rep Med. 2012;2012:324685. doi: 10.1155/2012/324685. Epub 2012 Dec 24. Case Rep Med. 2012. PMID: 23326272 Free PMC article.

10

Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy.

Sagnelli A, Piscosquito G, Di Bella D, Fadda L, Melzi L, Morico A, Ciano C, Taroni F, Facchetti D, Salsano E, Pareyson D. Sagnelli A, et al. J Peripher Nerv Syst. 2017 Mar;22(1):59-63. doi: 10.1111/jns.12200. J Peripher Nerv Syst. 2017. PMID: 27982499

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