Abbruzzese M - Search Results

1

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: abbruzzese m. Mol Cell Neurosci. 2005 Apr;28(4):703-14. doi: 10.1016/j.mcn.2004.11.016. Mol Cell Neurosci. 2005. PMID: 15797717

2

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: abbruzzese m. Neurobiol Dis. 2004 Jun;16(1):263-73. doi: 10.1016/j.nbd.2004.02.007. Neurobiol Dis. 2004. PMID: 15207283

3

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

4

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. Among authors: abbruzzese m. Eur J Neurosci. 2006 Mar;23(6):1445-52. doi: 10.1111/j.1460-9568.2006.04666.x. Eur J Neurosci. 2006. PMID: 16553608

5

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

6

Sonography of the median nerve in Charcot-Marie-Tooth disease.

Martinoli C, Schenone A, Bianchi S, Mandich P, Caponetto C, Abbruzzese M, Derchi LE. Martinoli C, et al. Among authors: abbruzzese m. AJR Am J Roentgenol. 2002 Jun;178(6):1553-6. doi: 10.2214/ajr.178.6.1781553. AJR Am J Roentgenol. 2002. PMID: 12034637

7

17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1.

Mancardi GL, Uccelli A, Bellone E, Sghirlanzoni A, Mandich P, Pareyson D, Schenone A, Abbruzzese M, Ajmar F. Mancardi GL, et al. Among authors: abbruzzese m. Eur Neurol. 1994;34(3):135-9. doi: 10.1159/000117026. Eur Neurol. 1994. PMID: 8033938

8

Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies.

Schenone A, Nobbio L, Caponnetto C, Abbruzzese M, Mandich P, Bellone E, Ajmar F, Gherardi G, Windebank AJ, Mancardi G. Schenone A, et al. Among authors: abbruzzese m. Ann Neurol. 1997 Dec;42(6):866-72. doi: 10.1002/ana.410420607. Ann Neurol. 1997. PMID: 9403478

9

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: abbruzzese m. Ann Neurol. 2001 Jul;50(1):47-55. doi: 10.1002/ana.1034. Ann Neurol. 2001. PMID: 11456309

10

Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families.

Bellone E, Mandich P, Mancardi GL, Schenone A, Uccelli A, Abbruzzese M, Sghirlanzoni A, Pareyson D, Ajmar F. Bellone E, et al. Among authors: abbruzzese m. J Med Genet. 1992 Jul;29(7):492-3. J Med Genet. 1992. PMID: 1640430 Free PMC article. No abstract available.

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