F
Fabrizio Salvi
Researcher at University of Bologna
Publications - 221
Citations - 14278
Fabrizio Salvi is an academic researcher from University of Bologna. The author has contributed to research in topics: Transthyretin & Chronic cerebrospinal venous insufficiency. The author has an hindex of 56, co-authored 213 publications receiving 12721 citations. Previous affiliations of Fabrizio Salvi include Academy for Urban School Leadership & University of Ferrara.
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Journal ArticleDOI
Tongue involvement in amyloidoses.
TL;DR: Two patients with amyloidotic peripheral neuropathy and remarkably different abnormal appearance of the tongue are reported, both of which have been diagnosed with TTR-amyloidosis.
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Metabolite Changes in Normal Appearing Cervical Spinal Cord in Two Patients with Multiple Sclerosis. A Proton MR Spectroscopic Analysis.
TL;DR: 2 cases of multiple sclerosis analyzed with Proton MR Spectroscopy (1H-MRS) with the voxel placed along the main axis of the normal appearing cervical spinal cord over three main space planes, orthogonally set will disclose biochemical changes in MS, even in normal appearing spinal cord.
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Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases
Anna Bartoletti-Stella,Silvia de Pasqua,Simone Baiardi,Ilaria Bartolomei,Giacomo Mengozzi,Giuseppe Orio,Francesca Pastorelli,Silvia Piras,Roberto Poda,Alberto Raggi,Michelangelo Stanzani Maserati,Martina Tarozzi,Rocco Liguori,Fabrizio Salvi,Piero Parchi,Sabina Capellari +15 more
TL;DR: 12 different pathogenic/likely pathogenic variants in 21 patients identified in a cohort of Italian patients affected by various neurodegenerative disorders are found, including 4 previously unreported.
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Diffuse Brain Hypoperfusion in Advanced Leukoencephalopathy with Calcifications and Cysts
Emanuele Bartolini,Andrea Bianchi,Ilaria Bartolomei,Alessandra Vella,Lapo Sali,Antonio Ciccarone,Fabrizio Salvi,Mario Mascalchi +7 more
TL;DR: It is speculated that cortical hypoperfusion may be related to cerebral atrophy or may reflect deafferentation secondary to severe leukoencephalopathy, and may possibly contribute to severe motor and cognitive impairment.
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Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point.
Paola Rimessi,Pietro Spitali,Yukio Ando,Vincenzo Mazzaferro,Francesca Pastorelli,Carlo Alberto Tassinari,Elisa Calzolari,Fabrizio Salvi,Alessandra Ferlini +8 more
TL;DR: Mutations in the transthyretin (TTR) gene cause familial amyloidotic polyneuropathy, an autosomal dominant peripheral neuropathy often associated with cardiomyopathy, and Liver transplant currently represents a powerful therapeutic approach for FAP patients.