Salvi F - Search Results

1

Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective.

Rapezzi C, Quarta CC, Obici L, Perfetto F, Longhi S, Salvi F, Biagini E, Lorenzini M, Grigioni F, Leone O, Cappelli F, Palladini G, Rimessi P, Ferlini A, Arpesella G, Pinna AD, Merlini G, Perlini S. Rapezzi C, et al. Among authors: salvi f. Eur Heart J. 2013 Feb;34(7):520-8. doi: 10.1093/eurheartj/ehs123. Epub 2012 Jun 28. Eur Heart J. 2013. PMID: 22745357

2

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

3

Discrimination of peripheral polyneuropathies caused by TTR variant or diabetes in the same pedigree through protein studies.

Ferlini A, Romeo G, Tassinari CA, Saraiva MJ, Costa PP, Salvi F. Ferlini A, et al. Among authors: salvi f. Adv Neurol. 1988;48:201-8. Adv Neurol. 1988. PMID: 3334782 No abstract available.

4

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

5

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

6

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

7

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

8

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

9

Combined heart and liver transplantation for familial amyloidotic neuropathy: considerations from the hepatic point of view.

Grazi GL, Cescon M, Salvi F, Ercolani G, Ravaioli M, Arpesella G, Magelli C, Grigioni F, Cavallari A. Grazi GL, et al. Among authors: salvi f. Liver Transpl. 2003 Sep;9(9):986-92. doi: 10.1053/jlts.2003.50173. Liver Transpl. 2003. PMID: 12942463 Free article. Review.

10

Atypical familial motor neuropathy in patients with mutant TTR Ile68Leu.

Salvi F, Scaglione C, Michelucci R, Linke RP, Obici L, Ravani A, Rimessi P, Ferlini A, Meletti S, Cavallaro T, Tassinari CA, Martinelli P. Salvi F, et al. Amyloid. 2003 Sep;10(3):185-9. doi: 10.3109/13506120308998999. Amyloid. 2003. PMID: 14640031

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