Grandis M - Search Results

1

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: grandis m. Hum Mol Genet. 2022 Dec 16;31(24):4255-4274. doi: 10.1093/hmg/ddac170. Hum Mol Genet. 2022. PMID: 35908287 Free PMC article.

2

PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A.

Nobbio L, Mancardi G, Grandis M, Levi G, Suter U, Nave KA, Windebank AJ, Abbruzzese M, Schenone A. Nobbio L, et al. Among authors: grandis m. Ann Neurol. 2001 Jul;50(1):47-55. doi: 10.1002/ana.1034. Ann Neurol. 2001. PMID: 11456309

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. Among authors: grandis m. 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. Exp Neurol. 2004 Nov;190(1):213-23. doi: 10.1016/j.expneurol.2004.07.008. Exp Neurol. 2004. PMID: 15473994

5

Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside.

Li J, Bai Y, Ghandour K, Qin P, Grandis M, Trostinskaia A, Ianakova E, Wu X, Schenone A, Vallat JM, Kupsky WJ, Hatfield J, Shy ME. Li J, et al. Among authors: grandis m. Brain. 2005 May;128(Pt 5):1168-77. doi: 10.1093/brain/awh483. Epub 2005 Mar 17. Brain. 2005. PMID: 15774502

6

Predictors of response to rituximab in patients with neuropathy and anti-myelin associated glycoprotein immunoglobulin M.

Benedetti L, Briani C, Grandis M, Vigo T, Gobbi M, Ghiglione E, Carpo M, Cocito D, Caporale CM, Sormani MP, Mancardi GL, Nobile-Orazio E, Schenone A. Benedetti L, et al. Among authors: grandis m. J Peripher Nerv Syst. 2007 Jun;12(2):102-7. doi: 10.1111/j.1529-8027.2007.00129.x. J Peripher Nerv Syst. 2007. PMID: 17565535 Clinical Trial.

7

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. 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

8

Severe neuropathy after diphtheria-tetanus-pertussis vaccination in a child carrying a novel frame-shift mutation in the small heat-shock protein 27 gene.

Mandich P, Grandis M, Varese A, Geroldi A, Acquaviva M, Ciotti P, Gulli R, Doria-Lamba L, Fabrizi GM, Giribaldi G, Pizzuti A, Schenone A, Bellone E. Mandich P, et al. Among authors: grandis m. J Child Neurol. 2010 Jan;25(1):107-9. doi: 10.1177/0883073809334387. Epub 2009 May 11. J Child Neurol. 2010. PMID: 19435728

9

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. Among authors: grandis m. J Neuropathol Exp Neurol. 2009 May;68(5):441-55. doi: 10.1097/NEN.0b013e31819fa6ba. J Neuropathol Exp Neurol. 2009. PMID: 19525893

10

The spectrum of GNE mutations: allelic heterogeneity for a common phenotype.

Grandis M, Gulli R, Cassandrini D, Gazzerro E, Benedetti L, Narciso E, Nobbio L, Bruno C, Minetti C, Bellone E, Reni L, Mancardi GL, Mandich P, Schenone A. Grandis M, et al. Neurol Sci. 2010 Jun;31(3):377-80. doi: 10.1007/s10072-010-0248-y. Epub 2010 Mar 19. Neurol Sci. 2010. PMID: 20300792

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