Salvatore M - Search Results

1

Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob disease.

Salvatore M, Pocchiari M, Cardone F, Petraroli R, D'Alessandro M, Galveź S, Brown P, Macćhi G, Fieschi C, Colosimo C. Salvatore M, et al. J Neurol Neurosurg Psychiatry. 1996 Jul;61(1):111-2. doi: 10.1136/jnnp.61.1.111. J Neurol Neurosurg Psychiatry. 1996. PMID: 8676137 Free PMC article. No abstract available.

2

Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation).

Barbanti P, Fabbrini G, Salvatore M, Petraroli R, Cardone F, Maras B, Equestre M, Macchi G, Lenzi GL, Pocchiari M. Barbanti P, et al. Among authors: salvatore m. Neurology. 1996 Sep;47(3):734-41. doi: 10.1212/wnl.47.3.734. Neurology. 1996. PMID: 8797472

3

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.

Pocchiari M, Salvatore M, Cutruzzolá F, Genuardi M, Allocatelli CT, Masullo C, Macchi G, Alemá G, Galgani S, Xi YG, et al. Pocchiari M, et al. Among authors: salvatore m. Ann Neurol. 1993 Dec;34(6):802-7. doi: 10.1002/ana.410340608. Ann Neurol. 1993. PMID: 7902693

4

Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.

Salvatore M, Genuardi M, Petraroli R, Masullo C, D'Alessandro M, Pocchiari M. Salvatore M, et al. Hum Genet. 1994 Oct;94(4):375-9. doi: 10.1007/BF00201596. Hum Genet. 1994. PMID: 7927332

5

Apolipoprotein E in sporadic and familial Creutzfeldt-Jakob disease.

Salvatore M, Seeber AC, Nacmias B, Petraroli R, D'Alessandro M, Sorbi S, Pocchiari M. Salvatore M, et al. Neurosci Lett. 1995 Oct 20;199(2):95-8. doi: 10.1016/0304-3940(95)12030-8. Neurosci Lett. 1995. PMID: 8584252 Clinical Trial.

6

Alpha1 antichymotrypsin signal peptide polymorphism in sporadic Creutzfeldt-Jakob disease.

Salvatore M, Seeber AC, Nacmias B, Petraroli R, Sorbi S, Pocchiari M. Salvatore M, et al. Neurosci Lett. 1997 May 16;227(2):140-2. doi: 10.1016/s0304-3940(97)00308-x. Neurosci Lett. 1997. PMID: 9180223

7

Creutzfeldt-Jakob disease after non-commercial dura mater graft.

Pocchiari M, Masullo C, Salvatore M, Genuardi M, Galgani S. Pocchiari M, et al. Among authors: salvatore m. Lancet. 1992 Sep 5;340(8819):614-5. doi: 10.1016/0140-6736(92)92153-7. Lancet. 1992. PMID: 1355193 No abstract available.

8

Progressive dementia in a young patient with a homozygous deletion of the PrP gene.

Masullo C, Salvatore M, Macchi G, Genuardi M, Pocchiari M. Masullo C, et al. Among authors: salvatore m. Ann N Y Acad Sci. 1994 Jun 6;724:358-60. doi: 10.1111/j.1749-6632.1994.tb38931.x. Ann N Y Acad Sci. 1994. PMID: 8030960 No abstract available.

9

Experimental drug treatment of scrapie: a pathogenetic basis for rationale therapeutics.

Pocchiari M, Salvatore M, Ladogana A, Ingrosso L, Xi YG, Cibati M, Masullo C. Pocchiari M, et al. Among authors: salvatore m. Eur J Epidemiol. 1991 Sep;7(5):556-61. doi: 10.1007/BF00143139. Eur J Epidemiol. 1991. PMID: 1761115 Review.

10

Sulphate polyanions prolong the incubation period of scrapie-infected hamsters.

Ladogana A, Casaccia P, Ingrosso L, Cibati M, Salvatore M, Xi YG, Masullo C, Pocchiari M. Ladogana A, et al. Among authors: salvatore m. J Gen Virol. 1992 Mar;73 ( Pt 3):661-5. doi: 10.1099/0022-1317-73-3-661. J Gen Virol. 1992. PMID: 1372039

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