Salvi F - Search Results

1

Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findings.

Ferlini A, Salvi F, Uncini A, el-Chami J, Winter P, Altland K, Repetto M, Littardi M, Campoleoni A, Vezzoni P, Patrosso MC. Ferlini A, et al. Among authors: salvi f. Clin Genet. 1996 Jan;49(1):10-4. doi: 10.1111/j.1399-0004.1996.tb04317.x. Clin Genet. 1996. PMID: 8721565

2

Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosis.

Patrosso MC, Salvi F, De Grandis D, Vezzoni P, Jacobson DR, Ferlini A. Patrosso MC, et al. Among authors: salvi f. Am J Med Genet. 1998 May 1;77(2):135-8. doi: 10.1002/(sici)1096-8628(19980501)77:2<135::aid-ajmg5>3.0.co;2-r. Am J Med Genet. 1998. PMID: 9605286

3

Molecular strategies in genetic diagnosis of transthyretin-related hereditary amyloidosis.

Ferlini A, Fini S, Salvi F, Patrosso MC, Vezzoni P, Forabosco A. Ferlini A, et al. Among authors: salvi f. FASEB J. 1992 Jul;6(10):2864-6. doi: 10.1096/fasebj.6.10.1353040. FASEB J. 1992. PMID: 1353040

4

Electromyographic findings in transthyretin (TTR)-related familial amyloid polyneuropathy (FAP).

Montagna P, Marchello L, Plasmati R, Ferlini A, Patrosso MC, Salvi F. Montagna P, et al. Among authors: salvi f. Electroencephalogr Clin Neurophysiol. 1996 Oct;101(5):423-30. Electroencephalogr Clin Neurophysiol. 1996. PMID: 8913196

5

Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel hot spot' in codon 47.

Ferlini A, Obici L, Manzati E, Biadi O, Tarantino E, Conigli P, Merlini G, D'Alessandro M, Mazzaferro V, Tassinari CA, Salvi F. Ferlini A, et al. Among authors: salvi f. Clin Genet. 2000 Apr;57(4):284-90. doi: 10.1034/j.1399-0004.2000.570407.x. Clin Genet. 2000. PMID: 10845569

6

Haplotype analysis of common transthyretin mutations.

Almeida MR, Aoyama-Oishi N, Sakaki Y, Holmgren G, Ulf D, Ferlini A, Salvi F, Munar-Oués M, Benson MD, Skinner M, et al. Almeida MR, et al. Among authors: salvi f. Hum Genet. 1995 Sep;96(3):350-4. doi: 10.1007/BF00210422. Hum Genet. 1995. PMID: 7649556

7

A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosis.

Ferlini A, Patrosso MC, Repetto M, Frattini A, Villa A, Fini S, Salvi F, Vezzoni P, Forabosco A. Ferlini A, et al. Among authors: salvi f. Hum Mutat. 1994;4(1):61-4. doi: 10.1002/humu.1380040110. Hum Mutat. 1994. PMID: 7951260 No abstract available.

8

Transthyretin-related TTR hereditary amyloidosis of the vitreous body. Clinical and molecular characterization in two Italian families.

Salvi F, Salvi G, Volpe R, Mencucci R, Plasmati R, Michelucci R, Gobbi P, Santangelo M, Ferlini A, Forabosco A, et al. Salvi F, et al. Among authors: salvi g. Ophthalmic Paediatr Genet. 1993 Mar;14(1):9-16. doi: 10.3109/13816819309087617. Ophthalmic Paediatr Genet. 1993. PMID: 8345958

9

Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis.

Almeida MR, Ferlini A, Forabosco A, Gawinowicz M, Costa PP, Salvi F, Plasmati R, Tassinari CA, Altland K, Saraiva MJ. Almeida MR, et al. Among authors: salvi f. Hum Mutat. 1992;1(3):211-5. doi: 10.1002/humu.1380010306. Hum Mutat. 1992. PMID: 1301926

10

Transthyretin amyloidosis and superficial siderosis of the CNS.

Mascalchi M, Salvi F, Pirini MG, D'Errico A, Ferlini A, Lolli F, Plasmati R, Tessa C, Villari N, Tassinari CA. Mascalchi M, et al. Among authors: salvi f. Neurology. 1999 Oct 22;53(7):1498-503. doi: 10.1212/wnl.53.7.1498. Neurology. 1999. PMID: 10534258

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