Nobbio L - Search Results

1

Different cellular and molecular mechanisms for early and late-onset myelin protein zero mutations.

Grandis M, Vigo T, Passalacqua M, Jain M, Scazzola S, La Padula V, Brucal M, Benvenuto F, Nobbio L, Cadoni A, Mancardi GL, Kamholz J, Shy ME, Schenone A. Grandis M, et al. Among authors: nobbio l. Hum Mol Genet. 2008 Jul 1;17(13):1877-89. doi: 10.1093/hmg/ddn083. Epub 2008 Mar 12. Hum Mol Genet. 2008. PMID: 18337304

2

Gain of glycosylation: a new pathomechanism of myelin protein zero mutations.

Prada V, Passalacqua M, Bono M, Luzzi P, Scazzola S, Nobbio LA, Capponi S, Bellone E, Mandich P, Mancardi G, Shy M, Schenone A, Grandis M. Prada V, et al. Ann Neurol. 2012 Mar;71(3):427-31. doi: 10.1002/ana.22695. Ann Neurol. 2012. PMID: 22451207 Free PMC article.

3

Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A disease.

Nobbio L, Vigo T, Abbruzzese M, Levi G, Brancolini C, Mantero S, Grandis M, Benedetti L, Mancardi G, Schenone A. Nobbio L, et al. Neurobiol Dis. 2004 Jun;16(1):263-73. doi: 10.1016/j.nbd.2004.02.007. Neurobiol Dis. 2004. PMID: 15207283

4

Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease.

Grandis M, Leandri M, Vigo T, Cilli M, Sereda MW, Gherardi G, Benedetti L, Mancardi G, Abbruzzese M, Nave KA, Nobbio L, Schenone A. Grandis M, et al. Among authors: nobbio l. Exp Neurol. 2004 Nov;190(1):213-23. doi: 10.1016/j.expneurol.2004.07.008. Exp Neurol. 2004. PMID: 15473994

5

Experimental Charcot-Marie-Tooth type 1A: a cDNA microarrays analysis.

Vigo T, Nobbio L, Hummelen PV, Abbruzzese M, Mancardi G, Verpoorten N, Verhoeven K, Sereda MW, Nave KA, Timmerman V, Schenone A. Vigo T, et al. Among authors: nobbio l. Mol Cell Neurosci. 2005 Apr;28(4):703-14. doi: 10.1016/j.mcn.2004.11.016. Mol Cell Neurosci. 2005. PMID: 15797717

6

Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease.

Nobbio L, Gherardi G, Vigo T, Passalacqua M, Melloni E, Abbruzzese M, Mancardi G, Nave KA, Schenone A. Nobbio L, et al. Eur J Neurosci. 2006 Mar;23(6):1445-52. doi: 10.1111/j.1460-9568.2006.04666.x. Eur J Neurosci. 2006. PMID: 16553608

7

Impaired expression of ciliary neurotrophic factor in Charcot-Marie-Tooth type 1A neuropathy.

Nobbio L, Fiorese F, Vigo T, Cilli M, Gherardi G, Grandis M, Melcangi RC, Mancardi G, Abbruzzese M, Schenone A. Nobbio L, et al. J Neuropathol Exp Neurol. 2009 May;68(5):441-55. doi: 10.1097/NEN.0b013e31819fa6ba. J Neuropathol Exp Neurol. 2009. PMID: 19525893

8

P2X7-mediated increased intracellular calcium causes functional derangement in Schwann cells from rats with CMT1A neuropathy.

Nobbio L, Sturla L, Fiorese F, Usai C, Basile G, Moreschi I, Benvenuto F, Zocchi E, De Flora A, Schenone A, Bruzzone S. Nobbio L, et al. J Biol Chem. 2009 Aug 21;284(34):23146-58. doi: 10.1074/jbc.M109.027128. Epub 2009 Jun 22. J Biol Chem. 2009. PMID: 19546221 Free PMC article.

9

A novel mouse model of CMT1B identifies hyperglycosylation as a new pathogenetic mechanism.

Veneri FA, Prada V, Mastrangelo R, Ferri C, Nobbio L, Passalacqua M, Milanesi M, Bianchi F, Del Carro U, Vallat JM, Duong P, Svaren J, Schenone A, Grandis M, D'Antonio M. Veneri FA, et al. Among authors: nobbio l. Hum Mol Genet. 2022 Dec 16;31(24):4255-4274. doi: 10.1093/hmg/ddac170. Hum Mol Genet. 2022. PMID: 35908287 Free PMC article.

10

Inherited neuropathies.

Schenone A, Nobbio L, Monti Bragadin M, Ursino G, Grandis M. Schenone A, et al. Among authors: nobbio l. Curr Treat Options Neurol. 2011 Apr;13(2):160-79. doi: 10.1007/s11940-011-0115-z. Curr Treat Options Neurol. 2011. PMID: 21286948

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