IRIS
MANGANELLI, FIORE
 Distribuzione geografica
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Continente #
AS - Asia 10.088
NA - Nord America 9.756
EU - Europa 7.182
SA - Sud America 1.385
Continente sconosciuto - Info sul continente non disponibili 599
AF - Africa 265
OC - Oceania 23
Totale 29.298
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Nazione #
US - Stati Uniti d'America 9.267
SG - Singapore 4.336
RU - Federazione Russa 3.079
CN - Cina 1.991
IT - Italia 1.907
VN - Vietnam 1.690
BR - Brasile 1.100
HK - Hong Kong 829
DE - Germania 405
NL - Olanda 374
FR - Francia 332
CA - Canada 276
BD - Bangladesh 270
FI - Finlandia 265
JP - Giappone 185
GB - Regno Unito 183
IN - India 174
AR - Argentina 122
UA - Ucraina 122
SE - Svezia 113
IE - Irlanda 111
KR - Corea 110
MX - Messico 102
ZA - Sudafrica 65
CI - Costa d'Avorio 64
PL - Polonia 57
IQ - Iraq 50
PH - Filippine 48
ID - Indonesia 47
TH - Thailandia 47
PK - Pakistan 46
TR - Turchia 46
ES - Italia 40
AT - Austria 37
EC - Ecuador 34
CO - Colombia 30
MA - Marocco 26
TW - Taiwan 26
VE - Venezuela 25
CL - Cile 23
JO - Giordania 22
BE - Belgio 21
LT - Lituania 20
MY - Malesia 20
JM - Giamaica 19
UZ - Uzbekistan 19
PY - Paraguay 18
TN - Tunisia 17
DZ - Algeria 16
AU - Australia 15
KE - Kenya 15
SA - Arabia Saudita 15
EG - Egitto 14
PE - Perù 14
UY - Uruguay 13
CR - Costa Rica 12
TT - Trinidad e Tobago 11
CH - Svizzera 10
DK - Danimarca 10
IR - Iran 10
LB - Libano 10
NO - Norvegia 10
PA - Panama 10
AL - Albania 9
GT - Guatemala 9
KZ - Kazakistan 9
NP - Nepal 9
OM - Oman 9
RS - Serbia 9
DO - Repubblica Dominicana 8
HN - Honduras 8
PS - Palestinian Territory 8
AE - Emirati Arabi Uniti 7
BG - Bulgaria 7
BH - Bahrain 7
CZ - Repubblica Ceca 7
GR - Grecia 7
RO - Romania 7
BB - Barbados 6
IL - Israele 6
BA - Bosnia-Erzegovina 5
HR - Croazia 5
HU - Ungheria 5
NG - Nigeria 5
PT - Portogallo 5
QA - Qatar 5
SY - Repubblica araba siriana 5
AZ - Azerbaigian 4
ET - Etiopia 4
KG - Kirghizistan 4
NZ - Nuova Zelanda 4
SI - Slovenia 4
SN - Senegal 4
SV - El Salvador 4
BO - Bolivia 3
CW - ???statistics.table.value.countryCode.CW??? 3
HT - Haiti 3
KW - Kuwait 3
LA - Repubblica Popolare Democratica del Laos 3
LV - Lettonia 3
Totale 28.608
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Città #
Singapore 2.132
San Jose 1.546
Ashburn 853
Hong Kong 779
Moscow 715
Chandler 708
Beijing 560
Ho Chi Minh City 492
Hefei 485
Naples 449
Santa Clara 442
Hanoi 397
Council Bluffs 304
Amsterdam 286
Los Angeles 265
Dallas 243
Lauterbourg 215
The Dalles 206
Millbury 169
New York 164
Boston 162
Tokyo 161
Napoli 136
Buffalo 125
Des Moines 114
São Paulo 110
Princeton 106
Nanjing 99
Phoenix 97
Redondo Beach 96
Seattle 90
Lawrence 89
Munich 86
Jacksonville 84
Seoul 83
Ottawa 80
Milan 77
Chicago 76
Frankfurt am Main 71
Helsinki 71
Lappeenranta 70
Wilmington 67
Orem 66
Haiphong 64
Rome 63
Atlanta 55
Da Nang 54
Houston 52
Brooklyn 50
Montreal 47
Denver 46
Toronto 46
Warsaw 43
Mexico City 42
Stockholm 40
London 36
Falkenstein 34
Woodbridge 34
Hải Dương 32
Nuremberg 32
Chennai 31
Johannesburg 31
Biên Hòa 30
Shenyang 30
Turku 30
Brasília 29
Poplar 29
Rio de Janeiro 29
Dublin 28
Tianjin 28
Can Tho 27
Nanchang 27
Boardman 26
Dearborn 26
Kronberg 25
Charlotte 24
Dong Ket 24
Hebei 23
Washington 23
Belo Horizonte 22
Redwood City 22
Florence 21
Querétaro 20
Baghdad 19
Mumbai 19
Amman 18
Ankara 18
Manchester 18
San Francisco 18
Bangkok 17
Campinas 17
Columbus 17
Fairfield 17
Jiaxing 17
Lahore 17
Pune 17
Shanghai 17
Tashkent 17
Thái Bình 17
Porto Alegre 16
Totale 15.297
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Nome #
A case report of limbic encephalitis in a metastatic colon cancer patient during first-line bevacizumab-combined chemotherapy 242
Proximal weakness involvement in the first Italian case of Charcot-Marie-Tooth 2CC harboring a novel frameshift variant in NEFH 215
Vein wall thickness and severity of pulmonary involvement due to sars n-cov2 virus infection 202
Anodal transcranial direct current stimulation of motor cortex does not ameliorate spasticity in multiple sclerosis 194
Multiple cranial neuropathy due to varicella zoster virus reactivation without vesicular rash: a challenging diagnosis 191
Early predictive factors of disability in CIDP 189
Electrophysiological comparison between males and females in HNPP. 186
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 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
Chronic inflammatory demyelinating polyneuropathy mimicking an acute painful diabetic neuropathy. 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 177
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
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
Acute leukocytosis during alemtuzumab treatment in patients with active relapsing-remitting multiple sclerosis 165
Motor performance deterioration accelerates after 50 years of age in Charcot-Marie-Tooth type 1a patients 164
Skin innervation across amyotrophic lateral sclerosis clinical stages: new prognostic biomarkers 163
Global longitudinal strain in pre-symptomatic patients with mutation for transthyretin amyloidosis 163
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 161
Postural instability in Charcot-Marie-Tooth 1A disease 158
Long-term therapy with miglustat and cognitive decline in the adult form of Niemann-Pick disease type C: a case report 157
Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathy 155
Isolated intracranial Mycobacterium avium complex granulomas in an immune-competent man 154
Electrophysiological characterisation in hereditary spastic paraplegia type 5. 154
Subclinical neurological involvement does not develop if Wilson's disease is treated early 154
Telemedicine application to headache: a critical review 152
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
The Treatment of Hypersalivation in Rett Syndrome with Botulinum Toxin: Efficacy and Clinical Implications 150
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs 149
Upper motor neuron evaluation in multiple sclerosis patients treated with Sativex(®) 148
Diffuse brain connectivity changes in Charcot-Marie-tooth type 1A patients: A resting-state functional MRI study 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 146
Teaching Video NeuroImage: Delayed Radiation-Induced Unilateral Myokymia of the Tongue 145
Multimodal evoked potentials follow up in multiple sclerosis patients under fingolimod therapy 145
A rare mutation in MYH7 gene occurs with overlapping phenotype. 144
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late-onset axonal neuropathies 143
Inherited neuromyotonia: A clinical and genetic study of a family. 143
Executive functions are impaired in heterozygote patients with oculopharyngeal muscular dystrophy 142
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 142
Adult normative values for the PATA Rate Test 142
Efficacy of recanalization therapy for ischemic stroke: multicenter hospital network experience 141
25-Hydroxy-Vitamin D and Risk of Recurrent Stroke: A Dose Response Meta-Analysis 140
A Novel mutat of melin protein zero associated with an axonal form of Charcot-Marie.Tooth disease 139
The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease 139
Different cortical excitability profiles in hereditary brain iron and copper accumulation 139
Correction to: Frequency and clinical correlates of anti-nerve antibodies in a large population of CIDP patients included in the Italian database 138
Clinical utility of electrophysiological evaluation in Crigler-Najjar syndrome. 138
The analysis of epidermal nerve fibre spatial distribution improves the diagnostic yield of skin biopsy 137
Alemtuzumab in Covid era 137
Postganglionic Sudomotor Assessment in Early Stage of Multiple System Atrophy and Parkinson Disease: A Morpho-functional Study 137
A review of current rehabilitation practices and their benefits in patients with multiple sclerosis 137
Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease 135
Pseudo-orthostatic tremor: description of a not typical case 135
Brain Plasticity in Charcot-Marie-Tooth Type 1A Patients? A Combined Structural and Diffusion MRI Study 135
Can we identify hereditary TTR amyloidosis by the screening of carpal tunnel syndrome patients? 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
Spinocerebellar ataxia type 2-neuronopathy or neuropathy? 133
Seronegative occult HBV reactivation complicated with fulminant acute liver failure after rituximab for chronic inflammatory demyelinating polyneuropathy 133
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 133
How to manage with telemedicine people with neuromuscular diseases? 133
Pregnancy experience in women with spinal muscular atrophy: a case series 132
Dissective tandem stroke: an endovascular approach 132
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
Loss of cutaneous large and small fibers in naive and l-dopa-treated PD patients 131
Small fiber pathology parallels disease progression in Parkinson disease: a longitudinal study 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
Comparison of the diagnostic accuracy of the 2021 EAN/PNS and 2010 EFNS/PNS diagnostic criteria for chronic inflammatory demyelinating polyradiculoneuropathy 129
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial 128
Frequency and clinical correlates of anti-nerve antibodies in a large population of CIDP patients included in the Italian database 128
Assessment of diagnostic criteria for multifocal motor neuropathy in patients included in the Italian database 127
A case of severe increase of liver enzymes in a ATTRv patient after one year of inotersen treatment 127
Value of Antibody Determinations in Chronic Dysimmune Neuropathies 127
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers 127
Expanding the spectrum of genes responsible for hereditary motor neuropathies 127
The emotional impact of COVID-19 outbreak in amyotrophic lateral sclerosis patients: evaluation of depression, anxiety and interoceptive awareness 127
Neuropathic pain experience in symptomatic and presymptomatic subjects carrying a transthyretin gene mutation 126
A novel family with axonal Charcot-Marie-Tooth disease caused by a mutation in the EGR2 gene 126
GABAergic dysfunction mediates motor impairment in Rett syndrome 126
Charcot-Marie-Tooth type 2CC misdiagnosed as Chronic Inflammatory Demyelinating Polyradiculoneuropathy 125
Small-fiber involvement in spinobulbar muscular atrophy (Kennedy's disease). 125
Autonomic nervous system involvement in a new CMT2B family. 125
Charcot-Marie-Tooth disease: New insights from skin biopsy 125
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL. 124
Totale 14.815
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Categoria #
all - tutte 95.267
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 95.267
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.004 0 0 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
2025/202614.507 1.440 1.191 1.585 1.506 2.314 609 1.462 861 1.556 1.027 490 466
2026/20271.357 433 592 332 0 0 0 0 0 0 0 0 0
Totale 29.298