Gemelli C - Search Results

1

Genetic Workup for Charcot-Marie-Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 Years.

Gemelli C, Geroldi A, Massucco S, Trevisan L, Callegari I, Marinelli L, Ursino G, Hamedani M, Mennella G, Stara S, Maggi G, Mori L, Schenone C, Gotta F, Patrone S, Mammi A, Origone P, Prada V, Nobbio L, Mandich P, Schenone A, Bellone E, Grandis M. Gemelli C, et al. Life (Basel). 2022 Mar 10;12(3):402. doi: 10.3390/life12030402. Life (Basel). 2022. PMID: 35330153 Free PMC article.

2

Influence of comorbidities on the phenotype of patients affected by Charcot-Marie-Tooth neuropathy type 1A.

Ursino G, Alberti MA, Grandis M, Reni L, Pareyson D, Bellone E, Gemelli C, Sabatelli M, Pisciotta C, Luigetti M, Santoro L, Massollo L, Schenone A. Ursino G, et al. Among authors: gemelli c. Neuromuscul Disord. 2013 Nov;23(11):902-6. doi: 10.1016/j.nmd.2013.07.002. Epub 2013 Jul 23. Neuromuscul Disord. 2013. PMID: 23891256

3

Tinetti and Berg balance scales correlate with disability in hereditary peripheral neuropathies: a preliminary study.

Monti Bragadin M, Francini L, Bellone E, Grandis M, Reni L, Canneva S, Gemelli C, Ursino G, Maggi G, Mori L, Schenone A. Monti Bragadin M, et al. Among authors: gemelli c. Eur J Phys Rehabil Med. 2015 Aug;51(4):423-7. Epub 2014 Dec 10. Eur J Phys Rehabil Med. 2015. PMID: 25491315 Free article.

4

Subcutaneous Immunoglobulins are a Valuable Treatment Option in Myasthenia Gravis.

Garnero M, Fabbri S, Gemelli C, Benedetti L, Mancardi GL, Schenone A, Grandis M. Garnero M, et al. Among authors: gemelli c. J Clin Neurol. 2018 Jan;14(1):98-99. doi: 10.3988/jcn.2018.14.1.98. Epub 2017 Sep 27. J Clin Neurol. 2018. PMID: 29141277 Free PMC article. No abstract available.

5

Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise".

Grandis M, Geroldi A, Gulli R, Manganelli F, Gotta F, Lamp M, Origone P, Trevisan L, Gemelli C, Fabbri S, Schenone A, Tozza S, Santoro L, Bellone E, Mandich P. Grandis M, et al. Among authors: gemelli c. Orphanet J Rare Dis. 2018 Oct 4;13(1):177. doi: 10.1186/s13023-018-0917-0. Orphanet J Rare Dis. 2018. PMID: 30286783 Free PMC article.

6

Hand Rehabilitation Treatment for Charcot-Marie-Tooth Disease: An Open Label Pilot Study.

Prada V, Schizzi S, Poggi I, Mori L, Gemelli C, Hamedani M, Accogli S, Maggi G, Grandis M, Mancardi GL, Schenone A. Prada V, et al. Among authors: gemelli c. J Neurol Neurophysiol. 2018 Jul 30;9(4):465. doi: 10.4172/2155-9562.1000465. J Neurol Neurophysiol. 2018. PMID: 30305981 Free PMC article.

7

Amyloid Cardiomyopathy in the Rare Transthyretin Tyr78Phe Mutation.

Tini G, Vianello PF, Gemelli C, Grandis M, Canepa M. Tini G, et al. Among authors: gemelli c. J Cardiovasc Transl Res. 2019 Dec;12(6):514-516. doi: 10.1007/s12265-018-9859-0. Epub 2019 Jan 2. J Cardiovasc Transl Res. 2019. PMID: 30604309 Review.

8

A novel mutation in the N-terminal acting-binding domain of Filamin C protein causing a distal myofibrillar myopathy.

Gemelli C, Prada V, Fiorillo C, Fabbri S, Maggi L, Geroldi A, Gibertini S, Mandich P, Trevisan L, Fossa P, Tagliafico AS, Schenone A, Grandis M. Gemelli C, et al. J Neurol Sci. 2019 Mar 15;398:75-78. doi: 10.1016/j.jns.2019.01.019. Epub 2019 Jan 17. J Neurol Sci. 2019. PMID: 30685713

9

A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs).

Pareyson D, Stojkovic T, Reilly MM, Leonard-Louis S, Laurà M, Blake J, Parman Y, Battaloglu E, Tazir M, Bellatache M, Bonello-Palot N, Lévy N, Sacconi S, Guimarães-Costa R, Attarian S, Latour P, Solé G, Megarbane A, Horvath R, Ricci G, Choi BO, Schenone A, Gemelli C, Geroldi A, Sabatelli M, Luigetti M, Santoro L, Manganelli F, Quattrone A, Valentino P, Murakami T, Scherer SS, Dankwa L, Shy ME, Bacon CJ, Herrmann DN, Zambon A, Tramacere I, Pisciotta C, Magri S, Previtali SC, Bolino A. Pareyson D, et al. Among authors: gemelli c. Ann Neurol. 2019 Jul;86(1):55-67. doi: 10.1002/ana.25500. Epub 2019 May 27. Ann Neurol. 2019. PMID: 31070812 Free PMC article.

10

Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotype.

Callegari I, Gemelli C, Geroldi A, Veneri F, Mandich P, D'Antonio M, Pareyson D, Shy ME, Schenone A, Prada V, Grandis M. Callegari I, et al. Among authors: gemelli c. J Neurol. 2019 Nov;266(11):2629-2645. doi: 10.1007/s00415-019-09453-3. Epub 2019 Jul 5. J Neurol. 2019. PMID: 31278453

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