Sagnelli A - Search Results

1

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

2

X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutation.

Sagnelli A, Piscosquito G, Chiapparini L, Ciano C, Salsano E, Saveri P, Milani M, Taroni F, Pareyson D. Sagnelli A, et al. J Peripher Nerv Syst. 2014 Jun;19(2):183-6. doi: 10.1111/jns5.12070. J Peripher Nerv Syst. 2014. PMID: 24863494

3

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.

4

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.

5

Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patient.

Sagnelli A, Scaioli V, Piscosquito G, Salsano E, Dalla Bella E, Gellera C, Pareyson D. Sagnelli A, et al. Neuromuscul Disord. 2015 Oct;25(10):800-1. doi: 10.1016/j.nmd.2015.07.015. Epub 2015 Jul 29. Neuromuscul Disord. 2015. PMID: 26298608

6

Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation.

Di Bella D, Pareyson D, Savoiardo M, Farina L, Ciano C, Caldarazzo S, Sagnelli A, Bonato S, Nava S, Bresolin N, Tedeschi G, Taroni F, Salsano E. Di Bella D, et al. Among authors: sagnelli a. Neurology. 2014 Sep 23;83(13):1217-8. doi: 10.1212/WNL.0000000000000812. Epub 2014 Aug 15. Neurology. 2014. PMID: 25128180 Free article. No abstract available.

7

Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings.

Sagnelli A, Magri S, Farina L, Chiapparini L, Marotta G, Tonduti D, Consonni M, Scigliuolo GM, Benti R, Pareyson D, Taroni F, Salsano E, Di Bella D. Sagnelli A, et al. J Neurol. 2016 Mar;263(3):591-3. doi: 10.1007/s00415-016-8020-8. Epub 2016 Jan 25. J Neurol. 2016. PMID: 26810722 No abstract available.

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

Lack of benefit of acetyl-dl-leucine in patients with multiple system atrophy of the cerebellar type.

Scigliuolo GM, Sagnelli A, Brenna G, Pareyson D, Salsano E. Scigliuolo GM, et al. Among authors: sagnelli a. J Neurol Sci. 2017 Aug 15;379:12-13. doi: 10.1016/j.jns.2017.05.020. Epub 2017 May 11. J Neurol Sci. 2017. PMID: 28716222 Clinical Trial. No abstract available.

10

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

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