PubRank

Fabrizio Salvi

Author PubWeight™ 74.44‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron 2010 7.87
2 A prospective open-label study of endovascular treatment of chronic cerebrospinal venous insufficiency. J Vasc Surg 2009 7.58
3 Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. Brain 2006 3.16
4 The value of cerebral Doppler venous haemodynamics in the assessment of multiple sclerosis. J Neurol Sci 2009 2.10
5 Usefulness and limitations of 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy in the aetiological diagnosis of amyloidotic cardiomyopathy. Eur J Nucl Med Mol Imaging 2010 1.98
6 Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types. Circulation 2009 1.93
7 A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Hum Mol Genet 2009 1.93
8 Transthyretin-related amyloidoses and the heart: a clinical overview. Nat Rev Cardiol 2010 1.81
9 Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective. Eur Heart J 2012 1.77
10 Guideline of transthyretin-related hereditary amyloidosis for clinicians. Orphanet J Rare Dis 2013 1.68
11 Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. Brain 2012 1.67
12 Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation. Neurobiol Aging 2009 1.62
13 Noninvasive etiologic diagnosis of cardiac amyloidosis using 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy. J Am Coll Cardiol 2005 1.55
14 Amyotrophic lateral sclerosis with mutation of the Cu/Zn superoxide dismutase gene (SOD1) in a patient with Down syndrome. Neuromuscul Disord 2007 1.44
15 Changes of cine cerebrospinal fluid dynamics in patients with multiple sclerosis treated with percutaneous transluminal angioplasty: a case-control study. J Vasc Interv Radiol 2013 1.43
16 FUS mutations in sporadic amyotrophic lateral sclerosis. Neurobiol Aging 2010 1.42
17 A novel T137A SOD1 mutation in an Italian family with two subjects affected by amyotrophic lateral sclerosis. Amyotroph Lateral Scler 2011 1.42
18 Intracranial venous haemodynamics in multiple sclerosis. Curr Neurovasc Res 2007 1.38
19 Multicenter case-control study on restless legs syndrome in multiple sclerosis: the REMS study. Sleep 2008 1.22
20 Role of (99m)Tc-DPD scintigraphy in diagnosis and prognosis of hereditary transthyretin-related cardiac amyloidosis. JACC Cardiovasc Imaging 2011 1.19
21 C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population. Neurobiol Aging 2012 1.13
22 Hypoperfusion of brain parenchyma is associated with the severity of chronic cerebrospinal venous insufficiency in patients with multiple sclerosis: a cross-sectional preliminary report. BMC Med 2011 1.04
23 MRI predictors of long-term evolution in amyotrophic lateral sclerosis. Eur J Neurosci 2010 1.03
24 Usefulness of 99mTc-DPD scintigraphy in cardiac amyloidosis. J Am Coll Cardiol 2008 1.03
25 Brain white matter damage in SCA1 and SCA2. An in vivo study using voxel-based morphometry, histogram analysis of mean diffusivity and tract-based spatial statistics. Neuroimage 2008 1.00
26 Primary diffuse meningeal melanomatosis: radiologic-pathologic correlation. AJNR Am J Neuroradiol 2003 0.96
27 Altered collagen expression in jugular veins in multiple sclerosis. Cardiovasc Pathol 2012 0.94
28 Brain white matter tracts degeneration in Friedreich ataxia. An in vivo MRI study using tract-based spatial statistics and voxel-based morphometry. Neuroimage 2007 0.93
29 Assessment of brain white matter fiber bundle atrophy in patients with Friedreich ataxia. Radiology 2010 0.93
30 Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis. BMC Med Genet 2010 0.92
31 Endothelial nitric oxide synthase gene polymorphisms in Behçet's disease. J Rheumatol 2002 0.91
32 Phenotypic and genotypic heterogeneity in transthyretin-related cardiac amyloidosis: towards tailoring of therapeutic strategies? Amyloid 2006 0.91
33 Adult Alexander's disease without leukoencephalopathy. Ann Neurol 2005 0.90
34 Factor V Leiden and prothrombin gene G20210A mutations in Italian patients with Behçet's disease and deep vein thrombosis. Arthritis Rheum 2004 0.89
35 Combined heart and liver transplantation for familial amyloidotic neuropathy: considerations from the hepatic point of view. Liver Transpl 2003 0.89
36 Oncocytic modifications in rectal adenocarcinomas after radio and chemotherapy. Virchows Arch 2005 0.87
37 Genetic microheterogeneity of human transthyretin detected by IEF. Electrophoresis 2007 0.86
38 Vascular endothelial growth factor gene polymorphisms in Behçet's disease. J Rheumatol 2004 0.86
39 Gender-related risk of myocardial involvement in systemic amyloidosis. Amyloid 2008 0.84
40 Cardiac amyloidosis: the great pretender. Heart Fail Rev 2015 0.84
41 Amyloidoma of the brachial plexus. Surg Neurol 2003 0.83
42 ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias. Neuroimage 2004 0.82
43 Magnetization transfer and diffusion tensor MR imaging of acute disseminated encephalomyelitis. AJNR Am J Neuroradiol 2002 0.82
44 Epidemiology of amyotrophic lateral sclerosis in Emilia Romagna Region (Italy): A population based study. Amyotroph Lateral Scler Frontotemporal Degener 2014 0.81
45 Brain structural damage in spinocerebellar ataxia type 1 : a VBM study. J Neurol 2008 0.81
46 Neurodegeneration in friedreich's ataxia is associated with a mixed activation pattern of the brain. A fMRI study. Hum Brain Mapp 2011 0.81
47 Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis. BMC Med Genet 2012 0.80
48 Radiotherapy in Italy for non-small cell lung cancer: patterns of care survey. Tumori 2012 0.80
49 Muscle oxygen consumption by NIRS and mobility in multiple sclerosis patients. BMC Neurol 2013 0.80
50 Identification of TTR-related subclinical amyloidosis with 99mTc-DPD scintigraphy. JACC Cardiovasc Imaging 2014 0.79
51 Proton MR spectroscopy of the cerebellum and pons in patients with degenerative ataxia. Radiology 2002 0.78
52 CC chemokine receptor 5 polymorphism in Italian patients with Behcet's disease. Rheumatology (Oxford) 2012 0.78
53 Prognostic Evaluation of Disease Outcome in Solid Tumors Investigated With 64Cu-ATSM PET/CT. Clin Nucl Med 2016 0.77
54 Female sex as a possible protective factor from myocardial involvement in transthyretin-related amyloidoses. Arch Intern Med 2005 0.77
55 Efficacy and safety of venous angioplasty of the extracranial veins for multiple sclerosis. Brave dreams study (brain venous drainage exploited against multiple sclerosis): study protocol for a randomized controlled trial. Trials 2012 0.76
56 Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point. Liver Int 2006 0.75
57 High MUC2 immunohistochemical expression is a predictor of poor response to preoperative radiochemotherapy (RCT) in rectal adenocarcinoma. Appl Immunohistochem Mol Morphol 2008 0.75
58 PLA1/A2 polymorphism of the platelet glycoprotein receptors IIIA in Behçet's disease. Clin Exp Rheumatol 2011 0.75
59 Parkinsonism in polycythaemia vera probably due to manganism. Mov Disord 2008 0.75
60 Severe peripheral motor neuropathy in a patient with Hodgkin lymphoma treated with brentuximab vedotin. Leuk Lymphoma 2013 0.75