IRIS
MANGANELLI, FIORE
 Distribuzione geografica
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Continente #
AS - Asia 9.910
NA - Nord America 8.345
EU - Europa 6.997
SA - Sud America 1.358
AF - Africa 264
OC - Oceania 23
Continente sconosciuto - Info sul continente non disponibili 6
Totale 26.903
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Nazione #
US - Stati Uniti d'America 7.966
SG - Singapore 4.329
RU - Federazione Russa 3.079
CN - Cina 1.966
IT - Italia 1.754
VN - Vietnam 1.686
BR - Brasile 1.085
HK - Hong Kong 825
DE - Germania 405
NL - Olanda 368
FR - Francia 326
FI - Finlandia 265
CA - Canada 212
JP - Giappone 181
GB - Regno Unito 179
IN - India 170
BD - Bangladesh 156
UA - Ucraina 120
AR - Argentina 118
SE - Svezia 112
IE - Irlanda 111
KR - Corea 110
MX - Messico 101
ZA - Sudafrica 65
CI - Costa d'Avorio 64
PL - Polonia 55
IQ - Iraq 50
PH - Filippine 46
PK - Pakistan 46
TH - Thailandia 46
TR - Turchia 45
ID - Indonesia 42
ES - Italia 40
AT - Austria 35
EC - Ecuador 34
MA - Marocco 26
TW - Taiwan 26
CO - Colombia 24
VE - Venezuela 24
CL - Cile 22
JO - Giordania 22
LT - Lituania 20
BE - Belgio 19
UZ - Uzbekistan 19
PY - Paraguay 18
TN - Tunisia 17
DZ - Algeria 16
AU - Australia 15
KE - Kenya 15
MY - Malesia 15
SA - Arabia Saudita 15
EG - Egitto 14
PE - Perù 14
UY - Uruguay 13
JM - Giamaica 11
DK - Danimarca 10
IR - Iran 10
LB - Libano 10
PA - Panama 10
AL - Albania 9
CH - Svizzera 9
KZ - Kazakistan 9
NP - Nepal 9
OM - Oman 9
RS - Serbia 9
DO - Repubblica Dominicana 8
PS - Palestinian Territory 8
BG - Bulgaria 7
BH - Bahrain 7
GR - Grecia 7
RO - Romania 7
AE - Emirati Arabi Uniti 6
CR - Costa Rica 6
CZ - Repubblica Ceca 6
IL - Israele 6
BA - Bosnia-Erzegovina 5
HR - Croazia 5
HU - Ungheria 5
NG - Nigeria 5
NO - Norvegia 5
PT - Portogallo 5
QA - Qatar 5
SY - Repubblica araba siriana 5
AZ - Azerbaigian 4
BB - Barbados 4
ET - Etiopia 4
GT - Guatemala 4
HN - Honduras 4
KG - Kirghizistan 4
NZ - Nuova Zelanda 4
SI - Slovenia 4
SN - Senegal 4
TT - Trinidad e Tobago 4
BO - Bolivia 3
CW - ???statistics.table.value.countryCode.CW??? 3
HT - Haiti 3
KW - Kuwait 3
LV - Lettonia 3
MN - Mongolia 3
MU - Mauritius 3
Totale 26.820
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Città #
Singapore 2.130
San Jose 1.134
Hong Kong 777
Ashburn 740
Moscow 715
Chandler 708
Beijing 559
Ho Chi Minh City 490
Hefei 485
Naples 434
Santa Clara 419
Hanoi 395
Amsterdam 286
Los Angeles 242
Dallas 233
Lauterbourg 215
The Dalles 206
Millbury 169
Boston 159
Tokyo 157
New York 145
Napoli 136
Buffalo 117
Des Moines 113
Princeton 106
São Paulo 103
Nanjing 99
Council Bluffs 96
Redondo Beach 96
Lawrence 89
Munich 86
Seattle 84
Seoul 83
Jacksonville 82
Ottawa 80
Frankfurt am Main 71
Helsinki 71
Lappeenranta 70
Wilmington 67
Chicago 65
Haiphong 64
Orem 63
Milan 61
Da Nang 54
Rome 51
Atlanta 47
Houston 47
Brooklyn 45
Warsaw 43
Denver 42
Mexico City 42
Montreal 41
Stockholm 40
Toronto 36
Falkenstein 34
London 34
Woodbridge 33
Hải Dương 32
Nuremberg 32
Chennai 31
Johannesburg 31
Phoenix 31
Biên Hòa 30
Shenyang 30
Turku 30
Poplar 29
Brasília 28
Dublin 28
Rio de Janeiro 28
Tianjin 28
Can Tho 27
Nanchang 27
Dearborn 26
Boardman 25
Kronberg 25
Dong Ket 24
Hebei 23
Redwood City 22
Belo Horizonte 21
Florence 21
Querétaro 20
Washington 20
Baghdad 19
Charlotte 19
Amman 18
Ankara 18
Manchester 18
Bangkok 17
Campinas 17
Columbus 17
Jiaxing 17
Lahore 17
Mumbai 17
Pune 17
Shanghai 17
Tashkent 17
Thái Bình 17
Fairfield 16
Porto Alegre 16
Norwalk 15
Totale 14.267
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Nome #
A case report of limbic encephalitis in a metastatic colon cancer patient during first-line bevacizumab-combined chemotherapy 234
Proximal weakness involvement in the first Italian case of Charcot-Marie-Tooth 2CC harboring a novel frameshift variant in NEFH 211
Anodal transcranial direct current stimulation of motor cortex does not ameliorate spasticity in multiple sclerosis 187
Early predictive factors of disability in CIDP 186
Electrophysiological comparison between males and females in HNPP. 182
Multiple cranial neuropathy due to varicella zoster virus reactivation without vesicular rash: a challenging diagnosis 181
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
Vein wall thickness and severity of pulmonary involvement due to sars n-cov2 virus infection 169
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 169
Six-minute walk test is reliable and sensitive in detecting response to therapy in CIDP 168
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 168
Small nerve fiber involvement in CMT1A 167
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability. 164
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 160
Motor performance deterioration accelerates after 50 years of age in Charcot-Marie-Tooth type 1a patients 160
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease 157
Global longitudinal strain in pre-symptomatic patients with mutation for transthyretin amyloidosis 157
Postural instability in Charcot-Marie-Tooth 1A disease 156
Skin innervation across amyotrophic lateral sclerosis clinical stages: new prognostic biomarkers 155
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 154
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. 150
Subclinical neurological involvement does not develop if Wilson's disease is treated early 150
Central cholinergic dysfunction in the adult form of Niemann Pick disease type C: a further link with Alzheimer's disease? 147
Case of acute motor conduction block neuropathy (AMCBN) 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
Upper motor neuron evaluation in multiple sclerosis patients treated with Sativex(®) 145
Cervical dystonia patients display subclinical gait changes 145
The Treatment of Hypersalivation in Rett Syndrome with Botulinum Toxin: Efficacy and Clinical Implications 145
Multimodal evoked potentials follow up in multiple sclerosis patients under fingolimod therapy 142
Acute leukocytosis during alemtuzumab treatment in patients with active relapsing-remitting multiple sclerosis 141
Teaching Video NeuroImage: Delayed Radiation-Induced Unilateral Myokymia of the Tongue 140
Inherited neuromyotonia: A clinical and genetic study of a family. 140
A rare mutation in MYH7 gene occurs with overlapping phenotype. 139
Diffuse brain connectivity changes in Charcot-Marie-tooth type 1A patients: A resting-state functional MRI study 139
Cutaneous sensory and autonomic denervation in Progressive Supranuclear Palsy 139
Telemedicine application to headache: a critical review 139
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
Different cortical excitability profiles in hereditary brain iron and copper accumulation 137
The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease 136
Efficacy of recanalization therapy for ischemic stroke: multicenter hospital network experience 135
25-Hydroxy-Vitamin D and Risk of Recurrent Stroke: A Dose Response Meta-Analysis 134
Clinical utility of electrophysiological evaluation in Crigler-Najjar syndrome. 134
Adult normative values for the PATA Rate Test 133
Correction to: Frequency and clinical correlates of anti-nerve antibodies in a large population of CIDP patients included in the Italian database 132
The analysis of epidermal nerve fibre spatial distribution improves the diagnostic yield of skin biopsy 132
Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease 131
Two families with novel PMP22 point mutations: genotype-phenotype correlation. 130
Thermosensitive hereditary neuropathy with liability to pressure palsy. 130
Alemtuzumab in Covid era 130
Dissective tandem stroke: an endovascular approach 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
Loss of cutaneous large and small fibers in naive and l-dopa-treated PD patients 129
Pseudo-orthostatic tremor: description of a not typical case 129
Brain Plasticity in Charcot-Marie-Tooth Type 1A Patients? A Combined Structural and Diffusion MRI Study 129
Can we identify hereditary TTR amyloidosis by the screening of carpal tunnel syndrome patients? 129
Reply (Acute motor conduction block neuropathy or acute multifocal motor neuropathy: an attempt at a nosological systematization) 128
Seronegative occult HBV reactivation complicated with fulminant acute liver failure after rituximab for chronic inflammatory demyelinating polyneuropathy 128
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 128
Postganglionic Sudomotor Assessment in Early Stage of Multiple System Atrophy and Parkinson Disease: A Morpho-functional Study 128
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. 127
Spinocerebellar ataxia type 2-neuronopathy or neuropathy? 127
Short-latency afferent inhibition in patients with Parkinson's disease and freezing of gait 126
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 126
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial 126
In vivo evidence of cortical amyloid deposition in the adult form of Niemann Pick type C 126
A review of current rehabilitation practices and their benefits in patients with multiple sclerosis 125
Comparison of the diagnostic accuracy of the 2021 EAN/PNS and 2010 EFNS/PNS diagnostic criteria for chronic inflammatory demyelinating polyradiculoneuropathy 124
The Effect of Cerebellar Degeneration on Human Sensori-motor Plasticity 124
The emotional impact of COVID-19 outbreak in amyotrophic lateral sclerosis patients: evaluation of depression, anxiety and interoceptive awareness 124
A case of severe increase of liver enzymes in a ATTRv patient after one year of inotersen treatment 123
Autonomic nervous system involvement in a new CMT2B family. 123
GABAergic dysfunction mediates motor impairment in Rett syndrome 123
How to manage with telemedicine people with neuromuscular diseases? 123
Value of Antibody Determinations in Chronic Dysimmune Neuropathies 122
Small-fiber involvement in spinobulbar muscular atrophy (Kennedy's disease). 122
A novel family with axonal Charcot-Marie-Tooth disease caused by a mutation in the EGR2 gene 122
Expanding the spectrum of genes responsible for hereditary motor neuropathies 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
Charcot-Marie-Tooth disease: New insights from skin biopsy 121
Frequency and clinical correlates of anti-nerve antibodies in a large population of CIDP patients included in the Italian database 121
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers 120
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL. 120
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
The first two-year follow-up in a patient with isolated sensory neuronopathy due to biallelic expansion in RFC1 gene 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
Totale 14.128
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Categoria #
all - tutte 84.259
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 84.259
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202128 0 0 0 0 0 0 0 0 0 0 0 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
2025/202614.061 1.440 1.191 1.585 1.506 2.314 609 1.462 861 1.556 1.027 490 20
Totale 27.495