IRIS
SANTORO, LUCIO
 Distribuzione geografica
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Continente #
AS - Asia 11.054
NA - Nord America 10.566
EU - Europa 8.298
SA - Sud America 1.489
AF - Africa 283
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 4
Totale 31.715
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Nazione #
US - Stati Uniti d'America 10.134
SG - Singapore 5.045
RU - Federazione Russa 3.796
VN - Vietnam 2.038
CN - Cina 1.992
IT - Italia 1.548
BR - Brasile 1.222
HK - Hong Kong 930
DE - Germania 531
NL - Olanda 440
FI - Finlandia 397
FR - Francia 367
UA - Ucraina 297
CA - Canada 275
GB - Regno Unito 237
IE - Irlanda 211
SE - Svezia 180
IN - India 169
JP - Giappone 167
BD - Bangladesh 134
AR - Argentina 103
MX - Messico 89
ZA - Sudafrica 73
CI - Costa d'Avorio 64
PL - Polonia 63
KR - Corea 60
PH - Filippine 54
IQ - Iraq 53
TH - Thailandia 53
PK - Pakistan 51
ES - Italia 49
TR - Turchia 47
ID - Indonesia 41
EC - Ecuador 34
VE - Venezuela 31
TW - Taiwan 30
AT - Austria 28
MA - Marocco 26
CO - Colombia 25
LT - Lituania 23
TN - Tunisia 23
BE - Belgio 22
CZ - Repubblica Ceca 22
CL - Cile 21
JO - Giordania 19
IR - Iran 18
UY - Uruguay 17
DZ - Algeria 16
PE - Perù 16
AE - Emirati Arabi Uniti 15
AU - Australia 15
UZ - Uzbekistan 15
KE - Kenya 14
MY - Malesia 14
EG - Egitto 12
JM - Giamaica 12
CH - Svizzera 11
KZ - Kazakistan 11
LB - Libano 11
PY - Paraguay 11
DK - Danimarca 10
AZ - Azerbaigian 9
DO - Repubblica Dominicana 8
IL - Israele 8
OM - Oman 8
SA - Arabia Saudita 8
HR - Croazia 7
HU - Ungheria 7
NP - Nepal 7
PS - Palestinian Territory 7
AL - Albania 6
AM - Armenia 6
CR - Costa Rica 6
BB - Barbados 5
BO - Bolivia 5
ET - Etiopia 5
GR - Grecia 5
GT - Guatemala 5
HN - Honduras 5
QA - Qatar 5
RO - Romania 5
RS - Serbia 5
SN - Senegal 5
TT - Trinidad e Tobago 5
BG - Bulgaria 4
CY - Cipro 4
GA - Gabon 4
MU - Mauritius 4
NG - Nigeria 4
NO - Norvegia 4
PT - Portogallo 4
BA - Bosnia-Erzegovina 3
BH - Bahrain 3
CG - Congo 3
CV - Capo Verde 3
CW - ???statistics.table.value.countryCode.CW??? 3
DM - Dominica 3
KW - Kuwait 3
LV - Lettonia 3
SI - Slovenia 3
Totale 31.629
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Città #
Singapore 2.342
San Jose 1.490
Chandler 936
Moscow 901
Hong Kong 874
Ashburn 834
Beijing 657
Ho Chi Minh City 573
Hanoi 475
Santa Clara 409
Amsterdam 360
Naples 320
Millbury 295
Los Angeles 292
Jacksonville 290
The Dalles 280
Lauterbourg 267
Princeton 260
Boston 228
Dallas 215
Hefei 189
Nanjing 173
Munich 161
Napoli 157
New York 155
Tokyo 143
Buffalo 138
Ottawa 133
Wilmington 126
Seattle 115
São Paulo 112
Des Moines 109
Redondo Beach 95
Haiphong 94
Da Nang 75
Council Bluffs 74
Orem 74
Chicago 73
Houston 65
Frankfurt am Main 64
Rome 58
Brooklyn 57
Warsaw 57
Montreal 56
Nanchang 56
Helsinki 55
Turku 54
Shenyang 51
Lawrence 46
Mexico City 44
Tianjin 44
Chennai 43
Stockholm 42
London 40
Denver 39
Hebei 38
Milan 38
Nuremberg 38
Toronto 38
Biên Hòa 37
Lappeenranta 37
Poplar 36
Rio de Janeiro 36
Atlanta 35
Johannesburg 33
Woodbridge 33
Dong Ket 32
Norwalk 31
Hải Dương 30
Jiaxing 30
San Francisco 29
Baronissi 28
Columbus 28
Kronberg 28
Augusta 27
Brasília 27
Phoenix 27
Can Tho 25
Mumbai 25
Boardman 24
Washington 24
Belo Horizonte 23
Dearborn 23
Dublin 23
Nocera Inferiore 23
Dhaka 22
Redwood City 22
Seoul 22
Falkenstein 21
Shanghai 21
Lahore 20
Manchester 20
Changsha 19
Curitiba 19
Falls Church 19
Ankara 18
Baghdad 18
Pune 18
Amman 17
Guangzhou 17
Totale 16.564
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Nome #
SISTEMA NERVOSO. Neurologia - Neurochirurgia - Neuroradiologia 237
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry 224
A wavelet application for interpreting the EEG readings 203
Anodal transcranial direct current stimulation of motor cortex does not ameliorate spasticity in multiple sclerosis 187
microRNAs as biomarkers in Pompe disease 187
Early predictive factors of disability in CIDP 186
Electrophysiological comparison between males and females in HNPP. 182
A compound score to screen patients with hereditary transthyretin amyloidosis 180
Chronic inflammatory demyelinating polyneuropathy mimicking an acute painful diabetic neuropathy. 178
Electrophysiological characterization of adult-onset Niemann?Pick type C disease 173
Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI 173
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 171
Six-minute walk test is reliable and sensitive in detecting response to therapy in CIDP 169
Small nerve fiber involvement in CMT1A 168
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability. 164
Brain damage in glycogen storage disease type I 163
Muscle fiber type disproportion (FTD) in a family with mutations in theLMNAgene 162
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 161
Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonism 161
Motor performance deterioration accelerates after 50 years of age in Charcot-Marie-Tooth type 1a patients 160
Evaluation of the motor cortex by magnetic stimulation in patients with Alzheimer disease 158
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease 157
Skin innervation across amyotrophic lateral sclerosis clinical stages: new prognostic biomarkers 156
Spasmodic dysphonia follow-up with videolaryngoscopy and voice spectrography during treatment with botulinum toxin 156
Postural instability in Charcot-Marie-Tooth 1A disease 156
Evaluation of sudomotor function in diabetes using the dynamic sweat test. 155
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 154
The Heterogeneity of Early Parkinson?s Disease: A Cluster Analysis on Newly Diagnosed Untreated Patients 154
Gender differences in non-motor symptoms in early, drug naïve Parkinson's disease 154
Serum epidermal growth factor predicts cognitive functions in early, drug-naive Parkinson's disease patients. 153
Long-term therapy with miglustat and cognitive decline in the adult form of Niemann-Pick disease type C: a case report 153
Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathy 151
Isolated intracranial Mycobacterium avium complex granulomas in an immune-competent man 151
Electrophysiological characterisation in hereditary spastic paraplegia type 5. 151
Ataxia with oculomotor apraxia type 1 in southern italy: late onset and variable phenotype. 150
Subclinical neurological involvement does not develop if Wilson's disease is treated early 150
Case of acute motor conduction block neuropathy (AMCBN) 147
Central cholinergic dysfunction in the adult form of Niemann Pick disease type C: a further link with Alzheimer's disease? 147
Modifications of brain tissue volumes in facioscapulohumeral dystrophy. 146
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs 146
A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder 145
Cervical dystonia patients display subclinical gait changes 145
Multimodal evoked potentials follow up in multiple sclerosis patients under fingolimod therapy 142
Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype 141
A rare mutation in MYH7 gene occurs with overlapping phenotype. 139
Interpreting Genetic Variants in Titin in Patients With Muscle Disorders 139
Cutaneous sensory and autonomic denervation in Progressive Supranuclear Palsy 139
Quantification of myelinated endings and mechanoreceptors in human digital skin 138
Executive functions are impaired in heterozygote patients with oculopharyngeal muscular dystrophy 138
A Novel mutat of melin protein zero associated with an axonal form of Charcot-Marie.Tooth disease 137
Congenital myopathies: Clinical phenotypes and new diagnostic tools 137
Different cortical excitability profiles in hereditary brain iron and copper accumulation 137
Neurophysiologic evaluation of central-peripheral sensory and motor pudendal pathways in primary premature ejaculation. 135
Absent innervation of skin and sweat glands in congenital insensitivity to pain with anhidrosis 134
Validation of the Italian version of the Neuropathic Pain Symptom Inventory in peripheral nervous system diseases 134
Study of multimodal evoked potentials in patients with type 1 Gaucher's disease. 133
Analysis of macrodeletions in the dystrophin gene in patients from southern Italy and correlation between genotype and phenotype. The presence/absence of the III hinge region of the dystrophin protein affects the phenotype. 132
The analysis of epidermal nerve fibre spatial distribution improves the diagnostic yield of skin biopsy 132
Thermosensitive hereditary neuropathy with liability to pressure palsy. 131
Two families with novel PMP22 point mutations: genotype-phenotype correlation. 130
Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular study. 130
The genetic basis of undiagnosed muscular dystrophies and myopathies 130
Loss of cutaneous large and small fibers in naive and l-dopa-treated PD patients 130
Reply (Acute motor conduction block neuropathy or acute multifocal motor neuropathy: an attempt at a nosological systematization) 129
Somatosensory Temporal Discrimination Threshold Is Increased in Patients with Cerebellar Atrophy. 129
Atypical clinical and radiological presentation of cryptococcal choroid plexitis in an immunocompetent woman 129
Anti-GAD antibody ocular flutter: expanding the spectrum of autoimmune ocular motor disorders 129
Copy number variants account for a tiny fraction of undiagnosed myopathic patients 128
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 128
A 5-year clinical follow-up study from the Italian National Registry for FSHD 128
Postganglionic Sudomotor Assessment in Early Stage of Multiple System Atrophy and Parkinson Disease: A Morpho-functional Study 128
Axonal degeneration in systemic sclerosis can be reverted by factors improving tissue oxygenation 127
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. 127
Correlation between phenotype and CTG repeats in myotonic dystrophy patients from southern Italy. 127
Spinocerebellar ataxia type 2-neuronopathy or neuropathy? 127
In vivo evidence of cortical amyloid deposition in the adult form of Niemann Pick type C 127
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17 126
Congenital fiber type disproportion myopathy. Report of a case with late onset and myalgia. 126
The combined treatment with orbital and pretarsal botulinum toxin injections in the management of poorly responsive blepharospasm 126
The Effect of Cerebellar Degeneration on Human Sensori-motor Plasticity 126
Short-latency afferent inhibition in patients with Parkinson's disease and freezing of gait 126
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial 126
Diabetes mellitus in Kearns-Sayre syndrome: a case with a 10-year follow-up. 125
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 125
Autonomic nervous system involvement in a new CMT2B family. 124
Amiodarone-induced experimental acute neuropathy in rats. 123
Small-fiber involvement in spinobulbar muscular atrophy (Kennedy's disease). 122
Charcot-Marie-Tooth disease: New insights from skin biopsy 122
A novel family with axonal Charcot-Marie-Tooth disease caused by a mutation in the EGR2 gene 122
Autonomic dysfunction is associated with disease progression and survival in amyotrophic lateral sclerosis: a prospective longitudinal cohort study 121
A Novel CAPN1 Mutation Causes a Pure Hereditary Spastic Paraplegia in an Italian Family 121
Nerve conduction velocity in CMT1A: what else can we tell? 120
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 119
GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features. 119
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise" 119
Postexercise facilitation of motor evoked potentials following transcranial magnetic stimulation. A study in normal subjects 118
Lower limb involvement in adult-onset primary dystonia: frequency and clinical features. 118
GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course 118
Alterations of autophagy in the peripheral neuropathy Charcot-Marie-Tooth type 2B 118
A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family. 117
Totale 14.352
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Categoria #
all - tutte 103.001
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 103.001
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202139 0 0 0 0 0 0 0 0 0 0 0 39
2021/20221.531 35 1 6 9 24 22 9 67 225 152 269 712
2022/20232.242 324 221 59 159 247 220 8 193 319 330 122 40
2023/20241.632 56 216 343 81 83 185 28 188 14 31 295 112
2024/20258.324 426 423 48 91 261 305 879 544 689 854 3.073 731
2025/202615.101 1.674 997 1.608 1.508 2.671 605 1.871 879 1.818 1.010 358 102
Totale 32.252