VITA, Giuseppe
 Distribuzione geografica
Continente #
NA - Nord America 13.993
EU - Europa 13.066
AS - Asia 2.629
SA - Sud America 24
Continente sconosciuto - Info sul continente non disponibili 22
OC - Oceania 13
AF - Africa 5
Totale 29.752
Nazione #
US - Stati Uniti d'America 13.945
IE - Irlanda 4.493
SE - Svezia 2.851
CN - Cina 2.323
IT - Italia 1.213
UA - Ucraina 1.171
DE - Germania 1.033
PL - Polonia 726
FI - Finlandia 628
GB - Regno Unito 342
BE - Belgio 225
FR - Francia 210
IN - India 153
VN - Vietnam 50
CA - Canada 46
RU - Federazione Russa 46
AT - Austria 39
NL - Olanda 32
IR - Iran 29
HK - Hong Kong 24
EU - Europa 20
SG - Singapore 18
CZ - Repubblica Ceca 16
CL - Cile 12
ES - Italia 9
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
DK - Danimarca 3
SA - Arabia Saudita 3
TR - Turchia 3
CO - Colombia 2
GR - Grecia 2
IL - Israele 2
JP - Giappone 2
LV - Lettonia 2
PT - Portogallo 2
RS - Serbia 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
TW - Taiwan 1
ZA - Sudafrica 1
Totale 29.752
Città #
Dublin 4.490
Chandler 2.711
Jacksonville 2.557
Nyköping 1.765
Beijing 1.026
Princeton 740
Warsaw 722
Medford 642
Ashburn 629
Cambridge 622
Des Moines 502
Dearborn 487
Ann Arbor 482
Messina 303
Boardman 271
Brussels 211
Wilmington 202
San Mateo 173
Shenyang 170
Jinan 166
New York 166
Woodbridge 147
Bremen 127
Nanjing 117
Lancaster 115
Pune 98
Hebei 94
Ningbo 86
Tianjin 81
Zhengzhou 76
Houston 73
Taizhou 69
Haikou 65
Hangzhou 62
Seattle 59
Rome 57
Dong Ket 49
Norwalk 45
Leawood 37
Nanchang 37
Falls Church 35
Guangzhou 35
Vienna 35
Fuzhou 32
Augusta 31
Taiyuan 28
Changsha 26
Helsinki 26
Milan 25
Jiaxing 24
Ottawa 23
Washington 23
Auburn Hills 22
Ardabil 21
Monmouth Junction 19
Redwood City 18
Lanzhou 17
Nürnberg 17
London 15
Palo Del Colle 15
Mumbai 14
Brno 13
Catania 13
Duncan 12
Waanrode 12
Central 11
Civitavecchia 11
Saint Petersburg 11
Clearwater 9
Napoli 9
Toronto 9
Chicago 8
Los Angeles 8
Hong Kong 7
Livorno 7
Riposto 7
Bologna 6
Cagliari 6
Kemerovo 6
Mountain View 6
Padova 6
Palermo 6
Paris 6
Seelze 6
Tappahannock 6
Verona 6
Collegeville 5
Fairfield 5
Hanover 5
Kunming 5
North Brunswick 5
Novokuznetsk 5
Piazza Armerina 5
Salerno 5
Torino 5
Aci Sant'antonio 4
Bari 4
Fort Worth 4
Greifswald 4
Las Vegas 4
Totale 21.304
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) 137
HATTR italian registry: preliminary data from the collaborative network of telethon GUP 15010 study 120
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 108
Parenteral nutrition improves nutritional status, autonomic symptoms and quality of life in transthyretin amyloid polyneuropathy 102
Agenesis of the Internal Carotid Artery Associated with Generalized Epilepsy 95
Health-related quality of life and functional changes in DMD: A 12-month longitudinal cohort study 92
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy 90
Characterization and functional analysis of the human microRNA 363 in glioblastoma transfected cell lines 85
Fahr's syndrome: local inflammatory factors in the pathogenesis of calcification 85
Hippo signaling pathway is altered in Duchenne muscular dystrophy 84
Miotonia congenita, epilessia, schizofrenia: un'insolita associazione 83
Mioclono segmentale in un caso di siringomielia 83
Patisiran, an RNAi therapeutic, for hereditary transthyretin amyloidosis 83
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) 83
Functional changes in Duchenne muscular dystrophy: A 12-month longitudinal cohort study. 81
Juvenile limb-girdle myasthenia gravis 78
Onset of hypothyroidism with polymyositis-like clinical features in elderly patients 78
A CMT1A PATIENT WITH PAINFUL AND DISABLING SYMPTOMS: FAST RECOVERY AFTER IVIG TREATMENT. 78
Awareness and behavioural and psychological symptoms of dementia (BPSD) impact in Alzheimer's disease 78
Nusinersen in type 1 spinal muscular atrophy: Twelve-month real-world data 78
Myasthenia Gravis: Unusual Presentations and Diagnostic Pitfalls 77
Nerve conduction velocity in CMT1A: what else can we tell? 77
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 77
Increase in synchronization of autonomic rhythms between individuals when listening to music 76
A comparative analysis of somatic and autonomic neuropathy in chronic alcoholics. 75
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 75
alpha7/beta1 integrin distribution in correlation with talin-vinculin system 74
Modulation of neuronal nitric oxide synthase and apoptosis by the isoflavone genistein in Mdx mice 74
A NOVEL SERUM MICRORNA SIGNATURE TO SCREEN TRANSTHYRETIN-RELATED FAMILIAL AMYLOID POLYNEUROPATHY 74
The soy isoflavone genistein blunts nuclear factor kappa-B, MAPKs and TNF-α activation and ameliorates muscle function and morphology in mdx mice. 73
BILATERAL PARAMEDIAN THALAMIC INFARCT AFTER OCCLUSION OF THE ARTERY OF PERCHERON. 72
Clinical and genetic characterization in two families with muscle phosphofructokinase deficiency 71
Diagnosi precoce di amiloidosi cardiaca familiare tramite risonanza magnetica cardiaca. 70
Espressione della Transglutaminasi 2 e della sua isoforma short nei tumori astrogliali umani 70
Expanded access program with Nusinersen in SMA type I in Italy: Strengths and pitfalls of a successful experience 70
An observational study of functional abilities in infants, children, and adults with type 1 SMA 70
Is rigid spine syndrome a distinct clinical entity? 69
Clinical and genotypic of narcoleptic from North eastern Sicily: our sleep centre experience 69
Histological effects of givinostat in boys with Duchenne muscular dystrophy 69
Circulating microRNAs Profile in Patients With Transthyretin Variant Amyloidosis 69
Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathies 68
Sport activity in Charcot-Marie-Tooth disease: A case study of a Paralympic swimmer 68
Phenotypic variability of TTR Val122Ile mutation: a Caucasian patient with axonal neuropathy and normal heart 68
Inotersen treatment for patients with Hereditary transthyretin amyloidosis 68
A Nouvel serum MicroRNA signature to screen ATTR 68
NLRP3 inflammasome CSF expression and neuropsychological changes in idiopathic normal pressure hydrocephalus 68
NF-kB blockade reduces skeletal muscle degeneration and enhances muscle function in mdx mice. 67
Extra-muscle involvement in Xp21-linked muscular dystrophy: an evoked potentials and electroretinography study 67
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 67
Potenziali evocati nelle distrofie muscolari Xp21-linked 66
Studio dell'espressione genica del muscolo scheletrico in pazienti affetti da glicogenosi II 66
Usefulness of Combining Electrocardiographic and Echocardiographic Findings and Brain Natriuretic Peptide in Early Detection of Cardiac Amyloidosis in Subjects With Transthyretin Gene Mutation 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
A checklist for clinical trials in rare disease: Obstacles and anticipatory actions-lessons learned from the FOR-DMD trial 66
Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci 65
ANT1 expression and RAGE-NF-kB pathway activation in sporadic inclusion-body myositis 65
Progressiva comparsa di miopatia, neuropatia e miastenia in un paziente con ipotiroidismo primario autoimmune. 65
TRANSTHYRETIN AMYLOIDOSIS IN SOUTHERN ITALY POPULATION: DESCRIPTION OF A COHORT OF PATIENTS WITH PHE64LEU MUTATION AND LATE ONSET 65
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family 65
Pilot study of flavocoxid in ambulant DMD patients. 65
Integrated care of muscular dystrophies in Italy. Part 1. Pharmacological treatment and rehabilitative interventions 65
A CLSM study of dystrophin associated proteins and some extra-cellular matrix components in human skeletal muscle 64
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 64
La deformazione longitudinale e radiale del ventricolo sinistro è ridotta nell’amiloidosi cardiaca familiare: studio con ecocardiogramma bi-dimensionale e risonanza magnetica cardiaca. 64
Muscle Fat-Fraction and Mapping in Duchenne Muscular Dystrophy: Evaluation of Disease Distribution and Correlation with Clinical Assessments: A preliminary experience. 64
Morphometric analysis of sciatic nerve and its main branches in the rabbit. 64
Effect of exercise on telomere length and telomere proteins expression in mdx mice 64
Behaviour of vinculin and talin in perineurial cells in healthy subjects and in subjects affected by diabteic neuropathy 63
A decreased muscle content of HPRG correlates with the reduction of AMP deaminase activity observed in patients affected by myoadenylate deficiencies 63
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
Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative study 63
Integrated care of muscular dystrophies in Italy. Part 2. Psychological treatments, social and welfare support, and financial costs 63
Autoimmune juvenile limb-girdle myasthenia 63
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. 63
Retinal and central nervous system involvement in Xp21-linked muscular dystrophy: an electroretinography and evoked potentials study 62
Inverse correlation between TRF-1 (telomeric-repeat binding factor 1) and histological grade of malignant brain tumors 62
VEGF overexpression via adeno-associated virus gene transfer promotes skeletal muscle regeneration and enhances muscle function in mdx mice 62
Cardiovascular autonomic control in Becker muscular dystrophy 62
Meccanismi antiapoptotici nf-kb-mediati in gliomi umani in vivo. 62
Effects of teriparatide on bone mineral density and quality of life in Duchenne muscular dystrophy related osteoporosis: a case report 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
A randomized placebo-controlled phase 3 trial of an antisense oligonucleotide, drisapersen, in duchenne muscular dystrophy 62
Amyloid myopathy presenting with rhabdomyolysis: evidence of complement activation. 61
Autonomic dysfunction in uremia 61
Atomic force microscopy investigation in Duchenne muscular dystrophy and polymyositis muscles 61
Modulazione della lunghezza telomerica nei diversi gradi di tumore astrogliale nell'uomo. 61
ANT1 expression and RAGE-NF-kB pathway in sporadic inclusion body myositis. 61
CARDIOVASCULAR AUTONOMIC DYSFUNCTION IN MULTIPLE-SCLEROSIS IS LIKELY RELATED TO BRAIN-STEM LESIONS 61
Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism. 61
Intrathecal administration of Nusinersen in type 1 SMA: successful psychological program in a single Italian center 61
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 61
“A CLSM study of dystrophin associated proteins and some extra-cellular matrix components in human skeletal muscle.” 61
Telomere shortening and telomere-associated proteins in Duchenne muscular dystrophy. 60
Outcome measures in Duchenne muscular dystrophy: validation of the Pediatric Quality of Life InventoryTM Neuromuscular Module in the Italian population and correlation with other functional assessments. 60
Pilot study of serial casting of ankles in muscular dystrophy patients. 60
Advances in Treatment of ATTRv Amyloidosis: State of the Art and Future Prospects 60
Totale 7.298
Categoria #
all - tutte 105.890
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 105.890


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019100 0 0 0 0 0 0 0 0 17 40 22 21
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
2021/20224.229 66 582 55 201 275 35 324 200 91 323 521 1.556
2022/202311.500 931 920 491 762 891 1.020 126 619 5.295 54 298 93
2023/20242.183 234 401 223 240 276 547 74 160 28 0 0 0
Totale 30.648