IRIS
SANTORO, LUCIO
 Distribuzione geografica
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Continente #
AS - Asia 8.320
NA - Nord America 7.748
EU - Europa 7.740
SA - Sud America 1.397
AF - Africa 231
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 4
Totale 25.455
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Nazione #
US - Stati Uniti d'America 7.394
SG - Singapore 4.753
RU - Federazione Russa 3.786
CN - Cina 1.756
IT - Italia 1.448
BR - Brasile 1.173
HK - Hong Kong 742
VN - Vietnam 531
DE - Germania 493
NL - Olanda 416
FI - Finlandia 384
UA - Ucraina 288
CA - Canada 232
IE - Irlanda 206
GB - Regno Unito 196
SE - Svezia 179
IN - India 118
AR - Argentina 90
FR - Francia 83
BD - Bangladesh 75
MX - Messico 73
CI - Costa d'Avorio 64
PL - Polonia 61
ZA - Sudafrica 61
ES - Italia 42
JP - Giappone 41
TR - Turchia 37
ID - Indonesia 31
KR - Corea 31
EC - Ecuador 29
AT - Austria 27
IQ - Iraq 27
PK - Pakistan 27
VE - Venezuela 25
CO - Colombia 23
BE - Belgio 22
LT - Lituania 21
CZ - Repubblica Ceca 20
IR - Iran 18
MA - Marocco 17
CL - Cile 16
TN - Tunisia 16
AE - Emirati Arabi Uniti 14
PE - Perù 14
KE - Kenya 12
UZ - Uzbekistan 12
UY - Uruguay 11
KZ - Kazakistan 10
AU - Australia 9
JO - Giordania 9
LB - Libano 9
PY - Paraguay 9
CH - Svizzera 8
AZ - Azerbaigian 7
DK - Danimarca 7
DO - Repubblica Dominicana 7
EG - Egitto 7
HU - Ungheria 7
IL - Israele 7
JM - Giamaica 7
MY - Malesia 6
NP - Nepal 6
SA - Arabia Saudita 6
AM - Armenia 5
DZ - Algeria 5
ET - Etiopia 5
GT - Guatemala 5
HR - Croazia 5
RO - Romania 5
TH - Thailandia 5
TT - Trinidad e Tobago 5
AL - Albania 4
BG - Bulgaria 4
BO - Bolivia 4
GA - Gabon 4
PS - Palestinian Territory 4
QA - Qatar 4
RS - Serbia 4
SN - Senegal 4
TW - Taiwan 4
BA - Bosnia-Erzegovina 3
BB - Barbados 3
CR - Costa Rica 3
CV - Capo Verde 3
CW - ???statistics.table.value.countryCode.CW??? 3
CY - Cipro 3
DM - Dominica 3
GR - Grecia 3
HN - Honduras 3
LV - Lettonia 3
MU - Mauritius 3
NG - Nigeria 3
NO - Norvegia 3
PH - Filippine 3
PT - Portogallo 3
TJ - Tagikistan 3
UG - Uganda 3
BF - Burkina Faso 2
BN - Brunei Darussalam 2
BY - Bielorussia 2
Totale 25.389
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Città #
Singapore 2.180
Chandler 936
Moscow 899
Hong Kong 738
Beijing 633
Ashburn 620
Santa Clara 386
Amsterdam 345
Naples 312
Millbury 293
Jacksonville 287
Princeton 259
Boston 225
Los Angeles 220
Dallas 197
Hefei 189
Ho Chi Minh City 182
Nanjing 173
Munich 160
Napoli 157
Ottawa 132
Buffalo 126
Wilmington 125
New York 117
Seattle 114
São Paulo 106
Des Moines 101
Hanoi 98
Redondo Beach 95
The Dalles 88
Houston 56
Warsaw 55
Nanchang 54
Turku 54
Chicago 52
Helsinki 52
Shenyang 51
Brooklyn 50
Rome 47
Lawrence 46
Tianjin 43
Stockholm 42
Mexico City 41
Montreal 41
Tokyo 39
Hebei 38
Nuremberg 36
Chennai 35
Orem 35
Rio de Janeiro 35
Denver 34
Frankfurt am Main 34
Lappeenranta 34
London 33
Woodbridge 33
Dong Ket 32
Milan 31
Norwalk 31
Haiphong 30
Jiaxing 29
Baronissi 28
Johannesburg 28
Kronberg 28
Poplar 28
Toronto 28
Atlanta 27
Augusta 27
Brasília 27
Boardman 24
Columbus 24
Dearborn 23
Mumbai 23
Nocera Inferiore 23
Belo Horizonte 22
Biên Hòa 22
Redwood City 22
Seoul 22
Washington 22
San Francisco 21
Falkenstein 20
Phoenix 20
Curitiba 19
Changsha 18
Dublin 18
Falls Church 18
Pune 17
Campinas 16
Dhaka 16
Kunming 16
Manchester 16
Porto Alegre 16
Ankara 15
San Mateo 15
Secaucus 15
Da Nang 14
Orange 14
Shanghai 14
Ann Arbor 13
Guayaquil 13
Lima 13
Totale 12.521
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Nome #
SISTEMA NERVOSO. Neurologia - Neurochirurgia - Neuroradiologia 205
A wavelet application for interpreting the EEG readings 175
Chronic inflammatory demyelinating polyneuropathy mimicking an acute painful diabetic neuropathy. 159
microRNAs as biomarkers in Pompe disease 157
Anodal transcranial direct current stimulation of motor cortex does not ameliorate spasticity in multiple sclerosis 156
Electrophysiological characterization of adult-onset Niemann?Pick type C disease 154
Electrophysiological comparison between males and females in HNPP. 151
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry 150
Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI 150
Early predictive factors of disability in CIDP 149
A compound score to screen patients with hereditary transthyretin amyloidosis 147
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability. 137
Six-minute walk test is reliable and sensitive in detecting response to therapy in CIDP 137
Small nerve fiber involvement in CMT1A 135
Ataxia with oculomotor apraxia type 1 in southern italy: late onset and variable phenotype. 135
Motor performance deterioration accelerates after 50 years of age in Charcot-Marie-Tooth type 1a patients 134
Brain damage in glycogen storage disease type I 133
Muscle fiber type disproportion (FTD) in a family with mutations in theLMNAgene 132
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 132
Isolated intracranial Mycobacterium avium complex granulomas in an immune-competent man 130
Electrophysiological characterisation in hereditary spastic paraplegia type 5. 130
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 130
Skin innervation across amyotrophic lateral sclerosis clinical stages: new prognostic biomarkers 128
Evaluation of the motor cortex by magnetic stimulation in patients with Alzheimer disease 127
Long-term therapy with miglustat and cognitive decline in the adult form of Niemann-Pick disease type C: a case report 126
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 125
Subclinical neurological involvement does not develop if Wilson's disease is treated early 125
Postural instability in Charcot-Marie-Tooth 1A disease 124
Cervical dystonia patients display subclinical gait changes 122
Evaluation of sudomotor function in diabetes using the dynamic sweat test. 120
A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder 120
Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonism 120
Study of multimodal evoked potentials in patients with type 1 Gaucher's disease. 119
The Heterogeneity of Early Parkinson?s Disease: A Cluster Analysis on Newly Diagnosed Untreated Patients 119
Different cortical excitability profiles in hereditary brain iron and copper accumulation 119
A rare mutation in MYH7 gene occurs with overlapping phenotype. 118
Diabetes mellitus in Kearns-Sayre syndrome: a case with a 10-year follow-up. 118
Modifications of brain tissue volumes in facioscapulohumeral dystrophy. 117
Serum epidermal growth factor predicts cognitive functions in early, drug-naive Parkinson's disease patients. 117
Gender differences in non-motor symptoms in early, drug naïve Parkinson's disease 117
A Novel mutat of melin protein zero associated with an axonal form of Charcot-Marie.Tooth disease 116
Spasmodic dysphonia follow-up with videolaryngoscopy and voice spectrography during treatment with botulinum toxin 116
Case of acute motor conduction block neuropathy (AMCBN) 115
Central cholinergic dysfunction in the adult form of Niemann Pick disease type C: a further link with Alzheimer's disease? 115
Cutaneous sensory and autonomic denervation in Progressive Supranuclear Palsy 115
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs 114
Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype 113
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17 113
Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular study. 113
Multimodal evoked potentials follow up in multiple sclerosis patients under fingolimod therapy 113
Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathy 112
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease 112
Executive functions are impaired in heterozygote patients with oculopharyngeal muscular dystrophy 112
Atypical clinical and radiological presentation of cryptococcal choroid plexitis in an immunocompetent woman 112
Congenital fiber type disproportion myopathy. Report of a case with late onset and myalgia. 111
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. 111
The Effect of Cerebellar Degeneration on Human Sensori-motor Plasticity 111
A 5-year clinical follow-up study from the Italian National Registry for FSHD 110
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. 109
Thermosensitive hereditary neuropathy with liability to pressure palsy. 109
Congenital myopathies: Clinical phenotypes and new diagnostic tools 109
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 109
Short-latency afferent inhibition in patients with Parkinson's disease and freezing of gait 108
Blockade of glutamate mGlu5 receptors in a rat model of neuropathic pain prevents early over-expression of pro-apoptotic genes and morphological changes in dorsal horn lamina II 106
Anti-GAD antibody ocular flutter: expanding the spectrum of autoimmune ocular motor disorders 106
Quantification of myelinated endings and mechanoreceptors in human digital skin 105
GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features. 105
Correlation between phenotype and CTG repeats in myotonic dystrophy patients from southern Italy. 104
Somatosensory Temporal Discrimination Threshold Is Increased in Patients with Cerebellar Atrophy. 104
Charcot-Marie-Tooth disease: New insights from skin biopsy 104
Loss of cutaneous large and small fibers in naive and l-dopa-treated PD patients 104
Spinocerebellar ataxia type 2-neuronopathy or neuropathy? 104
Axonal degeneration in systemic sclerosis can be reverted by factors improving tissue oxygenation 103
A Novel CAPN1 Mutation Causes a Pure Hereditary Spastic Paraplegia in an Italian Family 103
The genetic basis of undiagnosed muscular dystrophies and myopathies 103
In vivo evidence of cortical amyloid deposition in the adult form of Niemann Pick type C 103
Postexercise facilitation of motor evoked potentials following transcranial magnetic stimulation. A study in normal subjects 102
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 102
Autonomic nervous system involvement in a new CMT2B family. 102
The role of skin biopsy in differentiating small fiber neuropathy from ganglionopathy 102
Interpreting Genetic Variants in Titin in Patients With Muscle Disorders 102
Absent innervation of skin and sweat glands in congenital insensitivity to pain with anhidrosis 101
Validation of the Italian version of the Neuropathic Pain Symptom Inventory in peripheral nervous system diseases 101
Reply (Acute motor conduction block neuropathy or acute multifocal motor neuropathy: an attempt at a nosological systematization) 101
Nerve conduction velocity in CMT1A: what else can we tell? 101
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial 101
Postganglionic Sudomotor Assessment in Early Stage of Multiple System Atrophy and Parkinson Disease: A Morpho-functional Study 101
Age at onset and symptom spread in primary adult-onset blepharospasm and cervical dystonia 100
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: Experience of the FSHD Italian National Registry 100
Copy number variants account for a tiny fraction of undiagnosed myopathic patients 100
Neurophysiologic evaluation of central-peripheral sensory and motor pudendal pathways in primary premature ejaculation. 99
Amiodarone-induced experimental acute neuropathy in rats. 99
A novel family with axonal Charcot-Marie-Tooth disease caused by a mutation in the EGR2 gene 99
Alterations of autophagy in the peripheral neuropathy Charcot-Marie-Tooth type 2B 99
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 98
GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course 98
Two families with novel PMP22 point mutations: genotype-phenotype correlation. 97
Sural nerve and epidermal vascular abnormalities in a case of POEMS syndrome. 97
A second family with hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibres, detected in the same geographic area as the first family. 97
A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family. 97
Totale 11.727
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Categoria #
all - tutte 87.504
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 87.504
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021564 0 0 0 0 0 129 74 46 84 37 155 39
2021/20221.526 35 1 6 9 24 21 9 67 225 151 269 709
2022/20232.241 323 221 59 159 247 220 8 193 319 330 122 40
2023/20241.631 56 216 343 81 83 185 28 188 14 31 294 112
2024/20258.308 425 419 48 91 260 304 877 543 689 852 3.069 731
2025/20268.863 1.668 996 1.605 1.504 2.664 426 0 0 0 0 0 0
Totale 25.986