Grandis M - Search Results

1

Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies.

Mandich P, Fossa P, Capponi S, Geroldi A, Acquaviva M, Gulli R, Ciotti P, Manganelli F, Grandis M, Bellone E. Mandich P, et al. Among authors: grandis m. Eur J Hum Genet. 2009 Sep;17(9):1129-34. doi: 10.1038/ejhg.2009.37. Epub 2009 Mar 18. Eur J Hum Genet. 2009. PMID: 19293842 Free PMC article.

2

Comparing the Impact of COVID-19 on Vaccinated and Unvaccinated Patients Affected by Myasthenia Gravis.

Scarsi E, Massucco S, Ferraro PM, Cella A, Grisanti SG, Assini A, Beronio A, Della Cava F, Gemelli C, Bandini F, Serrati C, Del Sette M, Schenone A, Benedetti L, Prada V, Grandis M. Scarsi E, et al. Among authors: grandis m. Life (Basel). 2023 Apr 21;13(4):1064. doi: 10.3390/life13041064. Life (Basel). 2023. PMID: 37109594 Free PMC article.

3

The D355V mutation decreases EGR2 binding to an element within the Cx32 promoter.

Musso M, Balestra P, Bellone E, Cassandrini D, Di Maria E, Doria LL, Grandis M, Mancardi GL, Schenone A, Levi G, Ajmar F, Mandich P. Musso M, et al. Among authors: grandis m. Neurobiol Dis. 2001 Aug;8(4):700-6. doi: 10.1006/nbdi.2001.0397. Neurobiol Dis. 2001. PMID: 11493034

4

Phenotypic clustering in MPZ mutations.

Shy ME, Jáni A, Krajewski K, Grandis M, Lewis RA, Li J, Shy RR, Balsamo J, Lilien J, Garbern JY, Kamholz J. Shy ME, et al. Among authors: grandis m. Brain. 2004 Feb;127(Pt 2):371-84. doi: 10.1093/brain/awh048. Epub 2004 Jan 7. Brain. 2004. PMID: 14711881 Review.

5

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

6

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

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

Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease.

Mandich P, Grandis M, Geroldi A, Acquaviva M, Varese A, Gulli R, Ciotti P, Bellone E. Mandich P, et al. Among authors: grandis m. J Hum Genet. 2008;53(6):529-533. doi: 10.1007/s10038-008-0280-4. Epub 2008 Apr 1. J Hum Genet. 2008. PMID: 18379723

9

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

10

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

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