IRIS
SANTORO, LUCIO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 5.201
EU - Europa 2.908
AS - Asia 1.694
AF - Africa 60
SA - Sud America 8
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 9.874
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 5.053
IT - Italia 1.235
SG - Singapore 928
CN - Cina 659
NL - Olanda 368
FI - Finlandia 278
UA - Ucraina 254
DE - Germania 217
IE - Irlanda 203
CA - Canada 146
SE - Svezia 138
GB - Regno Unito 75
CI - Costa d'Avorio 58
RU - Federazione Russa 45
FR - Francia 34
VN - Vietnam 32
IN - India 30
BE - Belgio 15
CZ - Repubblica Ceca 13
IR - Iran 12
TR - Turchia 10
HK - Hong Kong 8
KR - Corea 8
BR - Brasile 5
ES - Italia 5
CH - Svizzera 4
DK - Danimarca 3
GR - Grecia 3
LT - Lituania 3
RO - Romania 3
TW - Taiwan 3
AU - Australia 2
CL - Cile 2
HR - Croazia 2
HU - Ungheria 2
PL - Polonia 2
PT - Portogallo 2
TH - Thailandia 2
AE - Emirati Arabi Uniti 1
AT - Austria 1
BG - Bulgaria 1
CO - Colombia 1
DO - Repubblica Dominicana 1
EE - Estonia 1
EU - Europa 1
GL - Groenlandia 1
JP - Giappone 1
MT - Malta 1
NG - Nigeria 1
ZA - Sudafrica 1
Totale 9.874
Salva come PNG Salva come JPEG
Città #
Chandler 936
Singapore 774
Santa Clara 349
Amsterdam 331
Millbury 295
Jacksonville 286
Naples 278
Ashburn 263
Princeton 260
Boston 206
Nanjing 173
Beijing 160
Napoli 157
Ottawa 129
Wilmington 122
Des Moines 101
Seattle 72
Nanchang 54
Shenyang 50
Lawrence 46
Hebei 38
Woodbridge 33
Dong Ket 32
Helsinki 31
Houston 31
Norwalk 31
Jiaxing 30
Baronissi 28
Kronberg 28
Rome 28
Tianjin 28
Augusta 24
Boardman 23
Dearborn 23
Nocera Inferiore 23
Redwood City 22
Milan 21
Washington 20
Falls Church 19
Changsha 17
Munich 17
Dublin 15
Kunming 15
Pune 15
Dallas 14
Orange 14
San Mateo 14
Ann Arbor 13
Brno 12
Toronto 12
Los Angeles 11
Shanghai 11
Leawood 10
Waanrode 10
Ardabil 9
Monmouth Junction 9
Salerno 9
Fairfield 8
Hangzhou 7
Wuhan 7
Zhengzhou 7
Falkenstein 6
London 6
Moscow 6
Palermo 6
Shenzhen 6
Brescia 5
Bristol 5
Fremont 5
Hong Kong 5
Lappeenranta 5
New York 5
Poggiomarino 5
Ankara 4
Campagna 4
Castellammare Di Stabia 4
Fort Worth 4
Guangzhou 4
Indiana 4
Lanzhou 4
Newark 4
Osimo 4
Paris 4
Pisa 4
Pozzuoli 4
San Genesio Ed Uniti 4
Senigallia 4
Seregno 4
Springfield 4
Verona 4
Aversa 3
Bari 3
Brewer 3
Brussels 3
Cerro Maggiore 3
Florence 3
Frankfurt am Main 3
Genoa 3
Leiden 3
Madrid 3
Totale 5.974
Salva come PNG Salva come JPEG
Nome #
SISTEMA NERVOSO. Neurologia - Neurochirurgia - Neuroradiologia 143
A wavelet application for interpreting the EEG readings 122
Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI 100
Chronic inflammatory demyelinating polyneuropathy mimicking an acute painful diabetic neuropathy. 79
Small nerve fiber involvement in CMT1A 74
Motor performance deterioration accelerates after 50 years of age in Charcot-Marie-Tooth type 1a patients 70
Anodal transcranial direct current stimulation of motor cortex does not ameliorate spasticity in multiple sclerosis 69
Ataxia with oculomotor apraxia type 1 in southern italy: late onset and variable phenotype. 67
Electrophysiological characterization of adult-onset Niemann?Pick type C disease 66
Isolated intracranial Mycobacterium avium complex granulomas in an immune-competent man 66
A novel mutation in SACS gene in a family from southern Italy 64
microRNAs as biomarkers in Pompe disease 64
Six-minute walk test is reliable and sensitive in detecting response to therapy in CIDP 62
A Novel mutat of melin protein zero associated with an axonal form of Charcot-Marie.Tooth disease 59
The Heterogeneity of Early Parkinson?s Disease: A Cluster Analysis on Newly Diagnosed Untreated Patients 58
Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonism 56
Early predictive factors of disability in CIDP 56
Evaluation of the motor cortex by magnetic stimulation in patients with Alzheimer disease 55
Cervical dystonia patients display subclinical gait changes 55
Muscle fiber type disproportion (FTD) in a family with mutations in theLMNAgene 54
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17 54
Brain damage in glycogen storage disease type I 53
Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype 52
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 52
The Effect of Cerebellar Degeneration on Human Sensori-motor Plasticity 52
Subclinical neurological involvement does not develop if Wilson's disease is treated early 52
Long-term therapy with miglustat and cognitive decline in the adult form of Niemann-Pick disease type C: a case report 52
RYR1 sequence variants in myopathies: expression and functional studies in two families 51
A rare mutation in MYH7 gene occurs with overlapping phenotype. 50
Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations. 50
Modifications of brain tissue volumes in facioscapulohumeral dystrophy. 50
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 50
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. 50
Study of multimodal evoked potentials in patients with type 1 Gaucher's disease. 49
Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular study. 49
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 49
Spasmodic dysphonia follow-up with videolaryngoscopy and voice spectrography during treatment with botulinum toxin 49
A 5-year clinical follow-up study from the Italian National Registry for FSHD 49
Autonomic dysfunction in children with Hirschsprung's disease 48
Electrophysiological characterisation in hereditary spastic paraplegia type 5. 48
A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder 48
Postural instability in Charcot-Marie-Tooth 1A disease 48
Different cortical excitability profiles in hereditary brain iron and copper accumulation 48
Prevalence and characteristics of peripheral neuropathy in hepatitis C virus population. 47
Analysis of dystrophin gene deletions indicates that the hinge III region of the protein correlates with disease severity 47
Centronuclear myopathies: genotype-phenotype correlation and frequency of defined genetic forms in an Italian cohort 47
Alterations of autophagy in the peripheral neuropathy Charcot-Marie-Tooth type 2B 47
Gender differences in non-motor symptoms in early, drug naïve Parkinson's disease 47
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 46
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2. 46
Case of acute motor conduction block neuropathy (AMCBN) 46
A 15-year molecular analysis of Duchenne/Becker muscular dystrophy: genetic features in a large cohort 46
Sural nerve and epidermal vascular abnormalities in a case of POEMS syndrome. 46
Central cholinergic dysfunction in the adult form of Niemann Pick disease type C: a further link with Alzheimer's disease? 46
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 46
Absent innervation of skin and sweat glands in congenital insensitivity to pain with anhidrosis 45
Axonal degeneration in systemic sclerosis can be reverted by factors improving tissue oxygenation 45
Evaluation of sudomotor function in diabetes using the dynamic sweat test. 45
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 45
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 45
Correlation between phenotype and CTG repeats in myotonic dystrophy patients from southern Italy. 45
Short-latency afferent inhibition in patients with Parkinson's disease and freezing of gait 45
Spinocerebellar ataxia type 2-neuronopathy or neuropathy? 45
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. 44
Congenital fiber type disproportion myopathy. Report of a case with late onset and myalgia. 44
Hirayama's disease: an Italian single center experience and review of the literature 44
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs 44
Cutaneous sensory and autonomic denervation in Progressive Supranuclear Palsy 44
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. 43
ALTERATIONS OF AUTOPHAGIC FLUX IN CHARCOT-MARIE-TOOTH 2B DISEASE 43
Is Ross sindrome a dysautonomic disorder only? An electrophysiologic and histologic study 42
Adult-onset Alexander disease : Report on a family. 42
GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features. 42
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability. 42
A new case of Ullrich's disease. 42
Disruption of GABA(A)-mediated intracortical inhibition in patients with chorea-acanthocytosis 42
Loss of cutaneous large and small fibers in naive and l-dopa-treated PD patients 42
The role of skin biopsy in differentiating small fiber neuropathy from ganglionopathy 42
Charcot-Marie-Tooth disease: New insights from skin biopsy 41
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial 41
Congenital myopathies: Clinical phenotypes and new diagnostic tools 41
A Quantitative Polymerase Chain Reaction (PCR) Assay Completely Discriminates between Duchenne and Becker Muscular Dystrophy Deletion Carriers and Normal Females. 40
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 40
Clinical and CT-scan study of a case of cerebellar ataxia and progressive hearing loss: Lichtenstein-Knorr disease? 40
A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family. 40
Somatosensory Temporal Discrimination Threshold Is Increased in Patients with Cerebellar Atrophy. 40
Frequency and time to relapse after discontinuing 6-month therapy with IVIg or pulsed methylprednisolone in CIDP 40
GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course 40
Interpreting Genetic Variants in Titin in Patients With Muscle Disorders 40
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise" 40
In vivo evidence of cortical amyloid deposition in the adult form of Niemann Pick type C 40
Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy. 39
Excitatory and inhibitory mechanisms in Wilson disease: investigation with magnetic motor cortex stimulation 39
Late recovery after traumatic, anoxic, or hemorrhagic long-lasting vegetative state. 39
Ross syndrome: a rare or a misknown disorder of thermoregulation? A skin innervation study on 12 subjects. 39
Age at onset and symptom spread in primary adult-onset blepharospasm and cervical dystonia 39
Atypical clinical and radiological presentation of cryptococcal choroid plexitis in an immunocompetent woman 39
Postganglionic sudomotor denervation in patients with multiple system atrophy 39
Clonus of the lower jaw: An old sign that comes back 39
Multimodal evoked potentials follow up in multiple sclerosis patients under fingolimod therapy 39
Totale 5.025
Salva come PNG Salva come JPEG
Categoria #
all - tutte 49.536
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 49.536
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020519 0 0 0 0 0 31 66 11 12 118 144 137
2020/2021903 35 60 98 61 84 129 74 46 84 37 156 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
2024/20251.517 426 423 48 91 261 268 0 0 0 0 0 0
Totale 10.344