De Gasperi R - Search Results

1

Lack of chronic neuroinflammation in the absence of focal hemorrhage in a rat model of low-energy blast-induced TBI.

Gama Sosa MA, De Gasperi R, Perez Garcia GS, Sosa H, Searcy C, Vargas D, Janssen PL, Perez GM, Tschiffely AE, Janssen WG, McCarron RM, Hof PR, Haghighi FG, Ahlers ST, Elder GA. Gama Sosa MA, et al. Among authors: de gasperi r. Acta Neuropathol Commun. 2017 Nov 10;5(1):80. doi: 10.1186/s40478-017-0483-z. Acta Neuropathol Commun. 2017. PMID: 29126430 Free PMC article.

2

Modifications of ganglioside patterns in human meningiomas.

Berra B, Riboni L, De Gasperi R, Gaini SM, Ragnotti G. Berra B, et al. Among authors: de gasperi r. J Neurochem. 1983 Mar;40(3):777-82. doi: 10.1111/j.1471-4159.1983.tb08046.x. J Neurochem. 1983. PMID: 6827275

3

Correction of the galactocerebrosidase deficiency in globoid cell leukodystrophy-cultured cells by SL3-3 retroviral-mediated gene transfer.

Gama Sosa MA, de Gasperi R, Undevia S, Yeretsian J, Rouse SC 2nd, Lyerla TA, Kolodny EH. Gama Sosa MA, et al. Among authors: de gasperi r. Biochem Biophys Res Commun. 1996 Jan 26;218(3):766-71. doi: 10.1006/bbrc.1996.0136. Biochem Biophys Res Commun. 1996. PMID: 8579588 Free article.

4

Substitution of alanine543 with a threonine residue at the carboxy terminal end of the beta-chain is associated with thermolabile hexosaminidase B in a Jewish family of Oriental ancestry.

De Gasperi R, Gama Sosa MA, Grebner EE, Mansfield D, Battistini S, Sartorato EL, Raghavan SS, Davis JG, Kolodny EH. De Gasperi R, et al. Biochem Mol Med. 1995 Oct;56(1):31-6. doi: 10.1006/bmme.1995.1053. Biochem Mol Med. 1995. PMID: 8593535 Free article.

5

Late-onset GM2 gangliosidosis: Ashkenazi Jewish family with an exon 5 mutation (Tyr180-->His) in the Hex A alpha-chain gene.

De Gasperi R, Gama Sosa MA, Battistini S, Yeretsian J, Raghavan S, Zelnik N, Leshinsky E, Kolodny EH. De Gasperi R, et al. Neurology. 1996 Aug;47(2):547-52. doi: 10.1212/wnl.47.2.547. Neurology. 1996. PMID: 8757036

6

Molecular heterogeneity of late-onset forms of globoid-cell leukodystrophy.

De Gasperi R, Gama Sosa MA, Sartorato EL, Battistini S, MacFarlane H, Gusella JF, Krivit W, Kolodny EH. De Gasperi R, et al. Am J Hum Genet. 1996 Dec;59(6):1233-42. Am J Hum Genet. 1996. PMID: 8940268 Free PMC article.

7

Adult-onset Krabbe's disease in siblings with novel mutations in the galactocerebrosidase gene.

Bernardini GL, Herrera DG, Carson D, DeGasperi R, Gama Sosa MA, Kolodny EH, Trifiletti R. Bernardini GL, et al. Ann Neurol. 1997 Jan;41(1):111-4. doi: 10.1002/ana.410410119. Ann Neurol. 1997. PMID: 9005874

8

Molecular basis of late-life globoid cell leukodystrophy.

De Gasperi R, Gama Sosa MA, Sartorato E, Battistini S, Raghavan S, Kolodny EH. De Gasperi R, et al. Hum Mutat. 1999;14(3):256-62. doi: 10.1002/(SICI)1098-1004(1999)14:3<256::AID-HUMU9>3.0.CO;2-6. Hum Mutat. 1999. PMID: 10477434

9

BAC and PAC DNA for the generation of transgenic animals.

Gama SM, De Gasperi R, Wen PH, Gonzalez EA, Kelley K, Lazzarini RA, Elder GA. Gama SM, et al. Among authors: de gasperi r. Biotechniques. 2002 Jul;33(1):51-3. doi: 10.2144/02331bm07. Biotechniques. 2002. PMID: 12139256 Free article. No abstract available.

10

Human midsized neurofilament subunit induces motor neuron disease in transgenic mice.

Gama Sosa MA, Friedrich VL Jr, DeGasperi R, Kelley K, Wen PH, Senturk E, Lazzarini RA, Elder GA. Gama Sosa MA, et al. Exp Neurol. 2003 Nov;184(1):408-19. doi: 10.1016/s0014-4886(03)00206-1. Exp Neurol. 2003. PMID: 14637110

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