Grandis M - Search Results

1

Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement.

Geroldi A, Ponti C, Mammi A, Patrone S, Gotta F, Trevisan L, Sanguineri F, Origone P, Gaudio A, La Barbera A, Cataldi M, Gemelli C, Massucco S, Schenone A, Lanteri P, Fiorillo C, Grandis M, Mandich P, Bellone E. Geroldi A, et al. Among authors: grandis m. Pediatr Neurol. 2024 May;154:4-8. doi: 10.1016/j.pediatrneurol.2024.02.002. Epub 2024 Feb 10. Pediatr Neurol. 2024. PMID: 38428336

2

Placebo effect in chronic inflammatory demyelinating polyneuropathy: The PATH study and a systematic review.

Lewis RA, Cornblath DR, Hartung HP, Sobue G, Lawo JP, Mielke O, Durn BL, Bril V, Merkies ISJ, Bassett P, Cleasby A, van Schaik IN; PATH study group. Lewis RA, et al. J Peripher Nerv Syst. 2020 Sep;25(3):230-237. doi: 10.1111/jns.12402. Epub 2020 Aug 5. J Peripher Nerv Syst. 2020. PMID: 32627277 Free PMC article.

3

Glycans of myelin proteins.

Sedzik J, Jastrzebski JP, Grandis M. Sedzik J, et al. Among authors: grandis m. J Neurosci Res. 2015 Jan;93(1):1-18. doi: 10.1002/jnr.23462. Epub 2014 Sep 12. J Neurosci Res. 2015. PMID: 25213400 Review.

4

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

5

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

6

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

7

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

8

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

9

Relapses after treatment with rituximab in a patient with multiple sclerosis and anti myelin-associated glycoprotein polyneuropathy.

Benedetti L, Franciotta D, Vigo T, Grandis M, Fiorina E, Ghiglione E, Roccatagliata L, Mancardi GL, Uccelli A, Schenone A. Benedetti L, et al. Among authors: grandis m. Arch Neurol. 2007 Oct;64(10):1531-3. doi: 10.1001/archneur.64.10.1531. Arch Neurol. 2007. PMID: 17923639

10

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

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