IRIS
SANTORO, LUCIO
 Distribuzione geografica
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Continente #
NA - Nord America 11.700
AS - Asia 11.135
EU - Europa 8.394
SA - Sud America 1.525
Continente sconosciuto - Info sul continente non disponibili 541
AF - Africa 285
OC - Oceania 21
Totale 33.601
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Nazione #
US - Stati Uniti d'America 11.186
SG - Singapore 5.050
RU - Federazione Russa 3.797
VN - Vietnam 2.039
CN - Cina 2.006
IT - Italia 1.622
BR - Brasile 1.240
HK - Hong Kong 932
DE - Germania 531
NL - Olanda 442
FI - Finlandia 397
FR - Francia 373
CA - Canada 312
UA - Ucraina 299
GB - Regno Unito 242
IE - Irlanda 212
BD - Bangladesh 182
SE - Svezia 180
IN - India 170
JP - Giappone 168
AR - Argentina 108
MX - Messico 92
ZA - Sudafrica 73
CI - Costa d'Avorio 64
PL - Polonia 64
KR - Corea 60
PH - Filippine 55
IQ - Iraq 53
TH - Thailandia 53
PK - Pakistan 51
ES - Italia 49
TR - Turchia 47
ID - Indonesia 45
EC - Ecuador 37
VE - Venezuela 35
TW - Taiwan 30
CO - Colombia 29
AT - Austria 28
MA - Marocco 26
CZ - Repubblica Ceca 24
BE - Belgio 23
LT - Lituania 23
TN - Tunisia 23
CL - Cile 21
JM - Giamaica 21
JO - Giordania 19
IR - Iran 18
MY - Malesia 17
UY - Uruguay 17
DZ - Algeria 16
PE - Perù 16
AE - Emirati Arabi Uniti 15
AU - Australia 15
UZ - Uzbekistan 15
CR - Costa Rica 14
KE - Kenya 14
PY - Paraguay 13
EG - Egitto 12
CH - Svizzera 11
KZ - Kazakistan 11
LB - Libano 11
DK - Danimarca 10
TT - Trinidad e Tobago 10
AZ - Azerbaigian 9
IL - Israele 9
BB - Barbados 8
DO - Repubblica Dominicana 8
GT - Guatemala 8
HN - Honduras 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
SV - El Salvador 6
BO - Bolivia 5
ET - Etiopia 5
GR - Grecia 5
PT - Portogallo 5
QA - Qatar 5
RO - Romania 5
RS - Serbia 5
SN - Senegal 5
BG - Bulgaria 4
CY - Cipro 4
GA - Gabon 4
MU - Mauritius 4
NG - Nigeria 4
NO - Norvegia 4
BA - Bosnia-Erzegovina 3
BH - Bahrain 3
BS - Bahamas 3
CG - Congo 3
CV - Capo Verde 3
CW - ???statistics.table.value.countryCode.CW??? 3
DM - Dominica 3
KW - Kuwait 3
Totale 32.968
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Città #
Singapore 2.344
San Jose 1.794
Chandler 936
Moscow 901
Ashburn 896
Hong Kong 875
Beijing 660
Ho Chi Minh City 574
Hanoi 475
Santa Clara 423
Amsterdam 360
Naples 328
Council Bluffs 311
Los Angeles 301
Millbury 295
Jacksonville 293
The Dalles 280
Lauterbourg 267
Princeton 260
Boston 228
Dallas 218
Hefei 189
Nanjing 173
Munich 161
New York 160
Napoli 157
Buffalo 144
Tokyo 144
Ottawa 133
Wilmington 126
São Paulo 119
Seattle 116
Des Moines 110
Phoenix 108
Redondo Beach 95
Haiphong 94
Chicago 82
Orem 76
Da Nang 75
Houston 71
Brooklyn 65
Frankfurt am Main 64
Rome 63
Montreal 58
Warsaw 57
Nanchang 56
Helsinki 55
Turku 54
Shenyang 51
Lawrence 46
Milan 46
Mexico City 44
Tianjin 44
Toronto 44
Chennai 43
Stockholm 42
Denver 40
London 40
Atlanta 39
Hebei 38
Nuremberg 38
Rio de Janeiro 38
Biên Hòa 37
Lappeenranta 37
Poplar 36
Johannesburg 33
Woodbridge 33
Dong Ket 32
Norwalk 31
Hải Dương 30
Jiaxing 30
San Francisco 30
Baronissi 28
Brasília 28
Columbus 28
Kronberg 28
Augusta 27
Washington 27
Boardman 25
Can Tho 25
Mumbai 25
Belo Horizonte 24
Dublin 24
Dearborn 23
Nocera Inferiore 23
Dhaka 22
Redwood City 22
Seoul 22
Falkenstein 21
Shanghai 21
Changsha 20
Lahore 20
Manchester 20
Curitiba 19
Falls Church 19
Ankara 18
Baghdad 18
Pune 18
Amman 17
Guangzhou 17
Totale 17.375
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Nome #
SISTEMA NERVOSO. Neurologia - Neurochirurgia - Neuroradiologia 241
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry 231
A wavelet application for interpreting the EEG readings 209
microRNAs as biomarkers in Pompe disease 195
Anodal transcranial direct current stimulation of motor cortex does not ameliorate spasticity in multiple sclerosis 194
Early predictive factors of disability in CIDP 189
Electrophysiological comparison between males and females in HNPP. 186
Chronic inflammatory demyelinating polyneuropathy mimicking an acute painful diabetic neuropathy. 185
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease 184
A compound score to screen patients with hereditary transthyretin amyloidosis 184
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 179
Autonomic dysfunction is associated with disease progression and survival in amyotrophic lateral sclerosis: a prospective longitudinal cohort study 178
Electrophysiological characterization of adult-onset Niemann?Pick type C disease 178
Small nerve fiber involvement in CMT1A 175
Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI 175
Six-minute walk test is reliable and sensitive in detecting response to therapy in CIDP 175
Brain damage in glycogen storage disease type I 169
Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonism 167
Muscle fiber type disproportion (FTD) in a family with mutations in theLMNAgene 166
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability. 166
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 165
Motor performance deterioration accelerates after 50 years of age in Charcot-Marie-Tooth type 1a patients 165
Skin innervation across amyotrophic lateral sclerosis clinical stages: new prognostic biomarkers 163
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 161
Evaluation of the motor cortex by magnetic stimulation in patients with Alzheimer disease 160
Evaluation of sudomotor function in diabetes using the dynamic sweat test. 160
Spasmodic dysphonia follow-up with videolaryngoscopy and voice spectrography during treatment with botulinum toxin 160
The Heterogeneity of Early Parkinson?s Disease: A Cluster Analysis on Newly Diagnosed Untreated Patients 158
Postural instability in Charcot-Marie-Tooth 1A disease 158
Serum epidermal growth factor predicts cognitive functions in early, drug-naive Parkinson's disease patients. 157
Long-term therapy with miglustat and cognitive decline in the adult form of Niemann-Pick disease type C: a case report 157
Gender differences in non-motor symptoms in early, drug naïve Parkinson's disease 157
Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathy 155
Subclinical neurological involvement does not develop if Wilson's disease is treated early 155
Isolated intracranial Mycobacterium avium complex granulomas in an immune-competent man 154
Ataxia with oculomotor apraxia type 1 in southern italy: late onset and variable phenotype. 154
Electrophysiological characterisation in hereditary spastic paraplegia type 5. 154
Case of acute motor conduction block neuropathy (AMCBN) 150
Central cholinergic dysfunction in the adult form of Niemann Pick disease type C: a further link with Alzheimer's disease? 150
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs 149
Modifications of brain tissue volumes in facioscapulohumeral dystrophy. 148
A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder 147
Cervical dystonia patients display subclinical gait changes 147
Cutaneous sensory and autonomic denervation in Progressive Supranuclear Palsy 147
Multimodal evoked potentials follow up in multiple sclerosis patients under fingolimod therapy 145
A rare mutation in MYH7 gene occurs with overlapping phenotype. 144
Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype 143
Interpreting Genetic Variants in Titin in Patients With Muscle Disorders 143
Executive functions are impaired in heterozygote patients with oculopharyngeal muscular dystrophy 142
Congenital myopathies: Clinical phenotypes and new diagnostic tools 142
Quantification of myelinated endings and mechanoreceptors in human digital skin 141
Different cortical excitability profiles in hereditary brain iron and copper accumulation 140
A Novel mutat of melin protein zero associated with an axonal form of Charcot-Marie.Tooth disease 139
Study of multimodal evoked potentials in patients with type 1 Gaucher's disease. 138
Validation of the Italian version of the Neuropathic Pain Symptom Inventory in peripheral nervous system diseases 138
Neurophysiologic evaluation of central-peripheral sensory and motor pudendal pathways in primary premature ejaculation. 137
The analysis of epidermal nerve fibre spatial distribution improves the diagnostic yield of skin biopsy 137
Postganglionic Sudomotor Assessment in Early Stage of Multiple System Atrophy and Parkinson Disease: A Morpho-functional Study 137
Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular study. 136
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. 136
Absent innervation of skin and sweat glands in congenital insensitivity to pain with anhidrosis 135
Thermosensitive hereditary neuropathy with liability to pressure palsy. 134
Anti-GAD antibody ocular flutter: expanding the spectrum of autoimmune ocular motor disorders 134
Two families with novel PMP22 point mutations: genotype-phenotype correlation. 133
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. 133
Short-latency afferent inhibition in patients with Parkinson's disease and freezing of gait 133
The genetic basis of undiagnosed muscular dystrophies and myopathies 133
Copy number variants account for a tiny fraction of undiagnosed myopathic patients 133
Spinocerebellar ataxia type 2-neuronopathy or neuropathy? 133
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 133
A 5-year clinical follow-up study from the Italian National Registry for FSHD 133
Reply (Acute motor conduction block neuropathy or acute multifocal motor neuropathy: an attempt at a nosological systematization) 132
Somatosensory Temporal Discrimination Threshold Is Increased in Patients with Cerebellar Atrophy. 132
Atypical clinical and radiological presentation of cryptococcal choroid plexitis in an immunocompetent woman 132
Small fiber pathology parallels disease progression in Parkinson disease: a longitudinal study 132
Correlation between phenotype and CTG repeats in myotonic dystrophy patients from southern Italy. 131
Loss of cutaneous large and small fibers in naive and l-dopa-treated PD patients 131
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 130
The Effect of Cerebellar Degeneration on Human Sensori-motor Plasticity 130
In vivo evidence of cortical amyloid deposition in the adult form of Niemann Pick type C 130
Axonal degeneration in systemic sclerosis can be reverted by factors improving tissue oxygenation 129
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17 129
The combined treatment with orbital and pretarsal botulinum toxin injections in the management of poorly responsive blepharospasm 129
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial 129
Diabetes mellitus in Kearns-Sayre syndrome: a case with a 10-year follow-up. 128
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 128
Congenital fiber type disproportion myopathy. Report of a case with late onset and myalgia. 128
A novel family with axonal Charcot-Marie-Tooth disease caused by a mutation in the EGR2 gene 126
Small-fiber involvement in spinobulbar muscular atrophy (Kennedy's disease). 125
Lower limb involvement in adult-onset primary dystonia: frequency and clinical features. 125
Amiodarone-induced experimental acute neuropathy in rats. 125
Autonomic nervous system involvement in a new CMT2B family. 125
Charcot-Marie-Tooth disease: New insights from skin biopsy 125
A Novel CAPN1 Mutation Causes a Pure Hereditary Spastic Paraplegia in an Italian Family 124
Nine-year case history of monofocal motor neuropathy. 123
Quantification of pilomotor nerves: a new tool to evaluate autonomic involvement in diabetes. 123
GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features. 123
Nerve conduction velocity in CMT1A: what else can we tell? 123
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise" 123
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: Experience of the FSHD Italian National Registry 122
Totale 14.854
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Categoria #
all - tutte 113.898
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 113.898
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.495 0 0 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
2025/202615.311 1.674 997 1.608 1.508 2.671 605 1.871 879 1.818 1.010 358 312
2026/20271.139 320 492 327 0 0 0 0 0 0 0 0 0
Totale 33.601