IRIS
MANGANELLI, FIORE
 Distribuzione geografica
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Continente #
AS - Asia 7.475
EU - Europa 6.362
NA - Nord America 5.990
SA - Sud America 1.252
AF - Africa 218
OC - Oceania 17
Continente sconosciuto - Info sul continente non disponibili 6
Totale 21.320
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Nazione #
US - Stati Uniti d'America 5.687
SG - Singapore 4.047
RU - Federazione Russa 3.075
CN - Cina 1.739
IT - Italia 1.526
BR - Brasile 1.028
HK - Hong Kong 670
VN - Vietnam 488
DE - Germania 362
NL - Olanda 350
FI - Finlandia 257
CA - Canada 167
GB - Regno Unito 148
UA - Ucraina 113
IN - India 110
SE - Svezia 110
AR - Argentina 104
IE - Irlanda 100
FR - Francia 90
KR - Corea 86
MX - Messico 86
CI - Costa d'Avorio 63
ZA - Sudafrica 53
PL - Polonia 51
BD - Bangladesh 46
JP - Giappone 43
ID - Indonesia 34
ES - Italia 33
TR - Turchia 33
AT - Austria 32
EC - Ecuador 30
IQ - Iraq 24
PK - Pakistan 21
CO - Colombia 18
LT - Lituania 18
MA - Marocco 17
VE - Venezuela 17
BE - Belgio 16
CL - Cile 16
UZ - Uzbekistan 15
PY - Paraguay 14
PE - Perù 12
TN - Tunisia 12
JO - Giordania 11
KE - Kenya 11
AU - Australia 10
DZ - Algeria 10
EG - Egitto 10
IR - Iran 10
UY - Uruguay 10
PA - Panama 9
DK - Danimarca 7
DO - Repubblica Dominicana 7
KZ - Kazakistan 7
LB - Libano 7
MY - Malesia 7
PS - Palestinian Territory 7
RS - Serbia 7
SA - Arabia Saudita 7
AE - Emirati Arabi Uniti 6
CH - Svizzera 6
GR - Grecia 6
IL - Israele 6
PH - Filippine 6
AL - Albania 5
BA - Bosnia-Erzegovina 5
BG - Bulgaria 5
CZ - Repubblica Ceca 5
HU - Ungheria 5
JM - Giamaica 5
NP - Nepal 5
AZ - Azerbaigian 4
BH - Bahrain 4
CR - Costa Rica 4
GT - Guatemala 4
NG - Nigeria 4
NO - Norvegia 4
RO - Romania 4
TT - Trinidad e Tobago 4
BB - Barbados 3
CW - ???statistics.table.value.countryCode.CW??? 3
ET - Etiopia 3
HN - Honduras 3
HR - Croazia 3
HT - Haiti 3
KG - Kirghizistan 3
MU - Mauritius 3
NZ - Nuova Zelanda 3
OM - Oman 3
PT - Portogallo 3
QA - Qatar 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
SY - Repubblica araba siriana 3
TH - Thailandia 3
TJ - Tagikistan 3
TW - Taiwan 3
BW - Botswana 2
BY - Bielorussia 2
CY - Cipro 2
Totale 21.255
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Città #
Singapore 1.965
Moscow 713
Chandler 708
Hong Kong 666
Beijing 532
Ashburn 530
Hefei 485
Santa Clara 403
Naples 393
Amsterdam 275
Dallas 218
Los Angeles 179
Ho Chi Minh City 172
Millbury 169
Boston 155
Napoli 136
Buffalo 108
Princeton 106
New York 101
Des Moines 100
Nanjing 99
Hanoi 97
Redondo Beach 96
São Paulo 95
Lawrence 89
Munich 85
Seattle 83
Seoul 83
Ottawa 79
Jacksonville 78
Helsinki 69
Wilmington 66
Lappeenranta 64
Chicago 52
Milan 45
Frankfurt am Main 43
The Dalles 43
Houston 41
Warsaw 41
Atlanta 40
Brooklyn 40
Mexico City 40
Denver 39
Stockholm 39
Orem 38
Tokyo 36
Rome 35
Woodbridge 33
Montreal 32
Shenyang 30
Turku 30
Falkenstein 29
Brasília 28
London 28
Nuremberg 28
Nanchang 27
Rio de Janeiro 27
Tianjin 27
Dearborn 26
Poplar 26
Kronberg 25
Boardman 24
Chennai 24
Dong Ket 24
Johannesburg 24
Hebei 23
Toronto 23
Redwood City 22
Belo Horizonte 21
Phoenix 21
Querétaro 19
Biên Hòa 18
Haiphong 18
Ankara 17
Campinas 17
Jiaxing 17
Washington 17
Dublin 16
Fairfield 16
Mumbai 16
Porto Alegre 16
Manchester 15
Norwalk 15
Ann Arbor 14
Düsseldorf 14
Florence 14
Casoria 13
Columbus 13
Da Nang 13
Pune 13
Salvador 13
Shenzhen 13
Tashkent 13
Wuhan 13
Baghdad 12
Charlotte 12
Guayaquil 12
Hangzhou 12
Manaus 12
Vienna 12
Totale 10.806
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Nome #
A case report of limbic encephalitis in a metastatic colon cancer patient during first-line bevacizumab-combined chemotherapy 188
Proximal weakness involvement in the first Italian case of Charcot-Marie-Tooth 2CC harboring a novel frameshift variant in NEFH 188
Chronic inflammatory demyelinating polyneuropathy mimicking an acute painful diabetic neuropathy. 159
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
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
Motor performance deterioration accelerates after 50 years of age in Charcot-Marie-Tooth type 1a patients 134
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
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 130
Skin innervation across amyotrophic lateral sclerosis clinical stages: new prognostic biomarkers 128
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
Acute leukocytosis during alemtuzumab treatment in patients with active relapsing-remitting multiple sclerosis 121
A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder 120
Telemedicine application to headache: a critical review 120
Different cortical excitability profiles in hereditary brain iron and copper accumulation 119
Diffuse brain connectivity changes in Charcot-Marie-tooth type 1A patients: A resting-state functional MRI study 119
A rare mutation in MYH7 gene occurs with overlapping phenotype. 118
Multiple cranial neuropathy due to varicella zoster virus reactivation without vesicular rash: a challenging diagnosis 116
A Novel mutat of melin protein zero associated with an axonal form of Charcot-Marie.Tooth disease 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
25-Hydroxy-Vitamin D and Risk of Recurrent Stroke: A Dose Response Meta-Analysis 114
Multimodal evoked potentials follow up in multiple sclerosis patients under fingolimod therapy 114
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs 114
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease 113
The Treatment of Hypersalivation in Rett Syndrome with Botulinum Toxin: Efficacy and Clinical Implications 113
Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathy 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
Teaching Video NeuroImage: Delayed Radiation-Induced Unilateral Myokymia of the Tongue 111
The Effect of Cerebellar Degeneration on Human Sensori-motor Plasticity 111
Upper motor neuron evaluation in multiple sclerosis patients treated with Sativex(®) 111
Adult normative values for the PATA Rate Test 111
Alemtuzumab in Covid era 111
Inherited neuromyotonia: A clinical and genetic study of a family. 110
The emotional impact of COVID-19 outbreak in amyotrophic lateral sclerosis patients: evaluation of depression, anxiety and interoceptive awareness 110
Correction to: Frequency and clinical correlates of anti-nerve antibodies in a large population of CIDP patients included in the Italian database 109
Efficacy of recanalization therapy for ischemic stroke: multicenter hospital network experience 109
Clinical utility of electrophysiological evaluation in Crigler-Najjar syndrome. 109
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
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
Pseudo-orthostatic tremor: description of a not typical case 107
A case of severe increase of liver enzymes in a ATTRv patient after one year of inotersen treatment 106
Anti-GAD antibody ocular flutter: expanding the spectrum of autoimmune ocular motor disorders 106
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 106
The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease 106
How to manage with telemedicine people with neuromuscular diseases? 106
GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features. 105
Primary Progressive Multiple Sclerosis Under Anti-TNFα Treatment: A Case Report 105
Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease 104
Somatosensory Temporal Discrimination Threshold Is Increased in Patients with Cerebellar Atrophy. 104
Charcot-Marie-Tooth disease: New insights from skin biopsy 104
Normalization of timed neuropsychological tests with the PATA rate and nine-hole pegboard tests 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
A Novel CAPN1 Mutation Causes a Pure Hereditary Spastic Paraplegia in an Italian Family 103
Mutilating fingertip ulcers in uncontrolled type 1 diabetes mellitus. 103
Seronegative occult HBV reactivation complicated with fulminant acute liver failure after rituximab for chronic inflammatory demyelinating polyneuropathy 103
In vivo evidence of cortical amyloid deposition in the adult form of Niemann Pick type C 103
Brain Plasticity in Charcot-Marie-Tooth Type 1A Patients? A Combined Structural and Diffusion MRI Study 103
The first two-year follow-up in a patient with isolated sensory neuronopathy due to biallelic expansion in RFC1 gene 102
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers 102
Dissective tandem stroke: an endovascular approach 102
Autonomic nervous system involvement in a new CMT2B family. 102
Vein wall thickness and severity of pulmonary involvement due to sars n-cov2 virus infection 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
GABAergic dysfunction mediates motor impairment in Rett syndrome 101
Postganglionic Sudomotor Assessment in Early Stage of Multiple System Atrophy and Parkinson Disease: A Morpho-functional Study 101
Machine Learning for Early Diagnosis of ATTRv Amyloidosis in Non-Endemic Areas: A Multicenter Study from Italy 100
Neuropathic pain experience in symptomatic and presymptomatic subjects carrying a transthyretin gene mutation 100
Comparison of the diagnostic accuracy of the 2021 EAN/PNS and 2010 EFNS/PNS diagnostic criteria for chronic inflammatory demyelinating polyradiculoneuropathy 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
Expanding the spectrum of genes responsible for hereditary motor neuropathies 99
Lichenoid rash: A new side effect of oral Cladribine 99
Quantitative Sensory Testing in Late-Onset ATTRv Presymptomatic Subjects: A Single Center Experience 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 11.533
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Categoria #
all - tutte 71.204
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 71.204
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021291 0 0 0 0 0 68 36 38 44 18 59 28
2021/20221.031 25 2 5 4 12 11 2 25 109 171 194 471
2022/20231.815 222 168 38 120 229 194 17 154 234 259 96 84
2023/20241.344 53 178 290 77 60 168 45 148 19 28 196 82
2024/20257.227 345 337 47 42 284 343 901 513 482 749 2.558 626
2025/20268.456 1.440 1.191 1.585 1.506 2.314 420 0 0 0 0 0 0
Totale 21.890