VITA, Giuseppe
 Distribuzione geografica
Continente #
NA - Nord America 14.074
EU - Europa 12.468
AS - Asia 3.109
SA - Sud America 24
Continente sconosciuto - Info sul continente non disponibili 22
OC - Oceania 13
AF - Africa 6
Totale 29.716
Nazione #
US - Stati Uniti d'America 14.024
IE - Irlanda 3.919
SE - Svezia 2.860
CN - Cina 2.334
IT - Italia 1.271
UA - Ucraina 1.171
DE - Germania 1.041
PL - Polonia 726
FI - Finlandia 631
SG - Singapore 358
GB - Regno Unito 347
IN - India 275
FR - Francia 213
BE - Belgio 110
VN - Vietnam 50
CA - Canada 48
RU - Federazione Russa 46
NL - Olanda 32
IR - Iran 30
AT - Austria 27
HK - Hong Kong 26
CZ - Repubblica Ceca 23
EU - Europa 20
ES - Italia 16
CL - Cile 12
AU - Australia 8
RO - Romania 8
KR - Corea 7
CH - Svizzera 6
BR - Brasile 5
NZ - Nuova Zelanda 5
PH - Filippine 5
EC - Ecuador 4
NO - Norvegia 4
PT - Portogallo 4
DK - Danimarca 3
RS - Serbia 3
SA - Arabia Saudita 3
TR - Turchia 3
TW - Taiwan 3
CO - Colombia 2
GR - Grecia 2
IL - Israele 2
JP - Giappone 2
LV - Lettonia 2
MY - Malesia 2
TH - Thailandia 2
UG - Uganda 2
A1 - Anonimo 1
A2 - ???statistics.table.value.countryCode.A2??? 1
AR - Argentina 1
AZ - Azerbaigian 1
DM - Dominica 1
EG - Egitto 1
HU - Ungheria 1
ID - Indonesia 1
IQ - Iraq 1
KH - Cambogia 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LT - Lituania 1
LU - Lussemburgo 1
MA - Marocco 1
MX - Messico 1
PK - Pakistan 1
TG - Togo 1
ZA - Sudafrica 1
Totale 29.716
Città #
Dublin 3.915
Chandler 2.716
Jacksonville 2.557
Nyköping 1.768
Beijing 1.026
Princeton 741
Warsaw 722
Medford 643
Ashburn 631
Cambridge 622
Des Moines 502
Dearborn 487
Ann Arbor 482
Messina 308
Boardman 289
Wilmington 202
Singapore 196
San Mateo 173
Shenyang 170
New York 168
Jinan 166
Woodbridge 147
Bremen 128
Hyderabad 124
Nanjing 117
Lancaster 115
Pune 98
Brussels 96
Hebei 94
Ningbo 86
Tianjin 81
Zhengzhou 76
Houston 73
Taizhou 69
Haikou 65
Rome 63
Hangzhou 62
Seattle 59
Dong Ket 49
Los Angeles 48
Norwalk 45
Leawood 37
Nanchang 37
Falls Church 35
Guangzhou 35
Fuzhou 32
Augusta 31
Taiyuan 28
Milan 27
Vienna 27
Changsha 26
Helsinki 26
Jiaxing 24
Ottawa 24
Washington 23
Auburn Hills 22
Ardabil 21
Brno 19
Monmouth Junction 19
Redwood City 18
Catania 17
Lanzhou 17
London 17
Nürnberg 17
Palo Del Colle 15
Mumbai 14
Duncan 12
Waanrode 12
Central 11
Civitavecchia 11
Saint Petersburg 11
Bologna 9
Clearwater 9
Hong Kong 9
Napoli 9
Toronto 9
Chicago 8
Reggio Calabria 8
Livorno 7
Munich 7
Riposto 7
Villamayor 7
Cagliari 6
Kemerovo 6
Lappeenranta 6
Mountain View 6
Padova 6
Palermo 6
Paris 6
Shanghai 6
Tappahannock 6
Verona 6
Collegeville 5
Fairfield 5
Hanover 5
Kunming 5
Naples 5
North Brunswick 5
Novokuznetsk 5
Piazza Armerina 5
Totale 21.033
Nome #
Severe rhabdomyolysis in a patient with “Heat Stroke” 192
6MWT performance correlates with peripheral neuropathy but not with cardiac involvement in patients with hereditary transthyretin amyloidosis (hATTR) 131
HATTR italian registry: preliminary data from the collaborative network of telethon GUP 15010 study 122
Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic Area 113
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 113
Deficit multiplo di Acyl-CoA deidrogenasi responsivo alla riboflavina (MADD-RR): studio clinico, biochimico, genetico e spettroscopico 109
Parenteral nutrition improves nutritional status, autonomic symptoms and quality of life in transthyretin amyloid polyneuropathy 101
Awareness and behavioural and psychological symptoms of dementia (BPSD) impact in Alzheimer's disease 93
Health-related quality of life and functional changes in DMD: A 12-month longitudinal cohort study 91
Agenesis of the Internal Carotid Artery Associated with Generalized Epilepsy 91
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy 89
Patisiran, an RNAi therapeutic, for hereditary transthyretin amyloidosis 87
Hippo signaling pathway is altered in Duchenne muscular dystrophy 85
Mioclono segmentale in un caso di siringomielia 83
Fahr's syndrome: local inflammatory factors in the pathogenesis of calcification 83
Miotonia congenita, epilessia, schizofrenia: un'insolita associazione 82
Characterization and functional analysis of the human microRNA 363 in glioblastoma transfected cell lines 82
Vacuolated PAS-positive lymphocytes on blood smear: An easy screening tool and a possible biomarker for monitoring therapeutic responses in Late Onset Pompe Disease (LOPD) 81
Onset of hypothyroidism with polymyositis-like clinical features in elderly patients 80
A CMT1A PATIENT WITH PAINFUL AND DISABLING SYMPTOMS: FAST RECOVERY AFTER IVIG TREATMENT. 79
Myasthenia Gravis: Unusual Presentations and Diagnostic Pitfalls 78
Nusinersen in type 1 spinal muscular atrophy: Twelve-month real-world data 77
Functional changes in Duchenne muscular dystrophy: A 12-month longitudinal cohort study. 76
Nerve conduction velocity in CMT1A: what else can we tell? 76
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 76
Juvenile limb-girdle myasthenia gravis 75
Modulation of neuronal nitric oxide synthase and apoptosis by the isoflavone genistein in Mdx mice 74
Increase in synchronization of autonomic rhythms between individuals when listening to music 74
BILATERAL PARAMEDIAN THALAMIC INFARCT AFTER OCCLUSION OF THE ARTERY OF PERCHERON. 73
A comparative analysis of somatic and autonomic neuropathy in chronic alcoholics. 72
A NOVEL SERUM MICRORNA SIGNATURE TO SCREEN TRANSTHYRETIN-RELATED FAMILIAL AMYLOID POLYNEUROPATHY 72
The soy isoflavone genistein blunts nuclear factor kappa-B, MAPKs and TNF-α activation and ameliorates muscle function and morphology in mdx mice. 72
An observational study of functional abilities in infants, children, and adults with type 1 SMA 71
NLRP3 inflammasome CSF expression and neuropsychological changes in idiopathic normal pressure hydrocephalus 71
Serial scanning with 99mTc-3, 3-diphosphono-1, 2-propanodicarboxylic acid (99mTc-DPD) for early detection of cardiac amyloid deposition and prediction of clinical worsening in subjects carrying a transthyretin gene mutation 71
Progressiva comparsa di miopatia, neuropatia e miastenia in un paziente con ipotiroidismo primario autoimmune. 70
Diagnosi precoce di amiloidosi cardiaca familiare tramite risonanza magnetica cardiaca. 70
Histological effects of givinostat in boys with Duchenne muscular dystrophy 70
Expanded access program with Nusinersen in SMA type I in Italy: Strengths and pitfalls of a successful experience 70
La deformazione longitudinale e radiale del ventricolo sinistro è ridotta nell’amiloidosi cardiaca familiare: studio con ecocardiogramma bi-dimensionale e risonanza magnetica cardiaca. 69
Sport activity in Charcot-Marie-Tooth disease: A case study of a Paralympic swimmer 69
Circulating microRNAs Profile in Patients With Transthyretin Variant Amyloidosis 69
A Phase 1/2 Study of Flavocoxid, an Oral NF-κB Inhibitor, in Duchenne Muscular Dystrophy 69
Is rigid spine syndrome a distinct clinical entity? 68
Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathies 68
Clinical and genetic characterization in two families with muscle phosphofructokinase deficiency 68
Extra-muscle involvement in Xp21-linked muscular dystrophy: an evoked potentials and electroretinography study 67
A CLSM study of dystrophin associated proteins and some extra-cellular matrix components in human skeletal muscle 67
Espressione della Transglutaminasi 2 e della sua isoforma short nei tumori astrogliali umani 67
Clinical and genotypic of narcoleptic from North eastern Sicily: our sleep centre experience 67
Phenotypic variability of TTR Val122Ile mutation: a Caucasian patient with axonal neuropathy and normal heart 67
Integrated care of muscular dystrophies in Italy. Part 1. Pharmacological treatment and rehabilitative interventions 67
Inotersen treatment for patients with Hereditary transthyretin amyloidosis 67
NF-kB blockade reduces skeletal muscle degeneration and enhances muscle function in mdx mice. 66
Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci 66
Potenziali evocati nelle distrofie muscolari Xp21-linked 66
ANT1 expression and RAGE-NF-kB pathway activation in sporadic inclusion-body myositis 66
Novel outcome measures for Charcot-Marie-Tooth disease: Validation and reliability of the 6-min walk test and StepWatch™ Activity Monitor and identification of the walking features related to higher quality of life 66
Behaviour of vinculin and talin in perineurial cells in healthy subjects and in subjects affected by diabteic neuropathy 65
TRANSTHYRETIN AMYLOIDOSIS IN SOUTHERN ITALY POPULATION: DESCRIPTION OF A COHORT OF PATIENTS WITH PHE64LEU MUTATION AND LATE ONSET 65
alpha7/beta1 integrin distribution in correlation with talin-vinculin system 65
Analisi dello stato di metilazione del promoter di O6-methylguanine DNA methyltransferase (MGMT) e TMS1/ASC: possibili implicazioni cliniche e prognostiche nei gliomi cerebrali diffusi di basso grado 65
Usefulness of Combining Electrocardiographic and Echocardiographic Findings and Brain Natriuretic Peptide in Early Detection of Cardiac Amyloidosis in Subjects With Transthyretin Gene Mutation 65
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family 65
Analisi dello stato di metilazione del promoter di O6-methylguanine DNA methyltransferase (MGMT) e TMS1/ASC nei gliomi cerebrali diffusi di basso grado: possibili implicazioni cliniche e prognostiche. 65
Studio dell'espressione genica del muscolo scheletrico in pazienti affetti da glicogenosi II 64
Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism. 64
A checklist for clinical trials in rare disease: Obstacles and anticipatory actions-lessons learned from the FOR-DMD trial 64
A Nouvel serum MicroRNA signature to screen ATTR 64
Effect of exercise on telomere length and telomere proteins expression in mdx mice 64
Cardiac longitudinal and radial strain is impaired in TTR-FAP: a magnetic resonance and 2-dimensional strain echocardiography study 63
Adult-onset centronuclear myopathy: evidence against a neurogenic pathology. 63
Muscle Fat-Fraction and Mapping in Duchenne Muscular Dystrophy: Evaluation of Disease Distribution and Correlation with Clinical Assessments: A preliminary experience. 63
Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative study 63
Pilot study of flavocoxid in ambulant DMD patients. 63
Integrated care of muscular dystrophies in Italy. Part 2. Psychological treatments, social and welfare support, and financial costs 63
A decreased muscle content of HPRG correlates with the reduction of AMP deaminase activity observed in patients affected by myoadenylate deficiencies 62
Retinal and central nervous system involvement in Xp21-linked muscular dystrophy: an electroretinography and evoked potentials study 62
Telomere shortening and telomere-associated proteins in Duchenne muscular dystrophy. 62
Modulazione della lunghezza telomerica nei diversi gradi di tumore astrogliale nell'uomo. 62
ANT1 expression and RAGE-NF-kB pathway in sporadic inclusion body myositis. 62
A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): the study protocol 62
A 5-center experience with intrathecal administration of nusinersen in SMA1 in Italy letter to the editor of european journal of pediatric neurology regarding the manuscript “single-center experience with intrathecal administration of nusinersen in children with spinal muscular atrophy type 1” written by pechmann and colleagues” 62
Autoimmune juvenile limb-girdle myasthenia 62
A randomized placebo-controlled phase 3 trial of an antisense oligonucleotide, drisapersen, in duchenne muscular dystrophy 62
Expression of the tumor necrosis factor receptor-associated factors I and 2 and regulation of the nuclear factor-kappa B antiapoptotic activity in human gliomas 62
Telomere shortening is associated to TRF1 and PARP1 overexpression in Duchenne muscular dystrophy 62
Autonomic dysfunction in uremia 61
Cardiovascular autonomic control in Becker muscular dystrophy 61
Morphometric analysis of sciatic nerve and its main branches in the rabbit. 61
Intrathecal administration of Nusinersen in type 1 SMA: successful psychological program in a single Italian center 61
Espressione differenziale di un panel di miRNA in tumori cerebrali astrogliali con diverso grado di malignità. 61
Amyloid myopathy presenting with rhabdomyolysis: evidence of complement activation. 60
Dyscondrosteosis in a child with Becker muscular dystrophy: an unreported association between Xp21 gene (DMD/BMD) deletion and a novel homozygous SHOX gene mutation 60
Meccanismi antiapoptotici nf-kb-mediati in gliomi umani in vivo. 60
Le alterazioni neurologiche dell'uremico 60
Pilot study of flavocoxid in ambulant DMD patients. 60
Effects of teriparatide on bone mineral density and quality of life in Duchenne muscular dystrophy related osteoporosis: a case report 60
Advances in Treatment of ATTRv Amyloidosis: State of the Art and Future Prospects 60
Nusinersen versus sham control in later-onset spinal muscular atrophy 60
Totale 7.274
Categoria #
all - tutte 124.173
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 124.173


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20205.184 685 303 19 335 49 517 650 529 122 891 884 200
2020/20214.254 459 118 912 177 607 430 168 353 82 455 332 161
2021/20224.238 66 582 55 201 275 35 325 200 94 326 521 1.558
2022/202310.900 933 923 492 763 893 1.021 122 610 4.733 40 282 88
2023/20242.604 215 397 195 200 226 548 74 161 29 196 49 314
2024/2025146 146 0 0 0 0 0 0 0 0 0 0 0
Totale 30.624