IRIS UniCatt

Luigetti, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 9.217
EU - Europa 8.269
AS - Asia 6.101
SA - Sud America 1.438
AF - Africa 227
OC - Oceania 23
Continente sconosciuto - Info sul continente non disponibili 9
Totale 25.284
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Nazione #
US - Stati Uniti d'America 8.981
DE - Germania 3.224
SG - Singapore 2.942
CN - Cina 1.656
BR - Brasile 1.223
SE - Svezia 1.144
IT - Italia 753
UA - Ucraina 705
GB - Regno Unito 480
FR - Francia 466
IE - Irlanda 385
VN - Vietnam 329
PL - Polonia 305
FI - Finlandia 249
ID - Indonesia 246
IN - India 246
RU - Federazione Russa 191
CA - Canada 148
TR - Turchia 104
BD - Bangladesh 90
BE - Belgio 87
ZA - Sudafrica 87
AR - Argentina 81
HK - Hong Kong 75
JP - Giappone 71
NL - Olanda 67
IQ - Iraq 59
MX - Messico 52
CI - Costa d'Avorio 46
ES - Italia 44
KR - Corea 40
EC - Ecuador 37
AT - Austria 34
SA - Arabia Saudita 28
MA - Marocco 27
PK - Pakistan 26
PY - Paraguay 25
IR - Iran 23
AU - Australia 22
AE - Emirati Arabi Uniti 21
JO - Giordania 21
CL - Cile 20
CO - Colombia 20
RO - Romania 19
KE - Kenya 18
CH - Svizzera 17
LT - Lituania 15
PT - Portogallo 14
IL - Israele 13
PH - Filippine 13
UZ - Uzbekistan 13
CZ - Repubblica Ceca 11
DK - Danimarca 10
KZ - Kazakistan 10
VE - Venezuela 10
DZ - Algeria 9
AZ - Azerbaigian 8
TH - Thailandia 8
TN - Tunisia 8
UY - Uruguay 8
DO - Repubblica Dominicana 7
EG - Egitto 7
KG - Kirghizistan 7
PS - Palestinian Territory 7
SN - Senegal 7
BO - Bolivia 6
LK - Sri Lanka 6
PE - Perù 6
A2 - ???statistics.table.value.countryCode.A2??? 5
BY - Bielorussia 5
HR - Croazia 5
NO - Norvegia 5
NP - Nepal 5
OM - Oman 5
SI - Slovenia 5
TT - Trinidad e Tobago 5
AM - Armenia 4
JM - Giamaica 4
LA - Repubblica Popolare Democratica del Laos 4
MD - Moldavia 4
NI - Nicaragua 4
AO - Angola 3
ET - Etiopia 3
EU - Europa 3
GE - Georgia 3
GM - Gambi 3
GR - Grecia 3
HN - Honduras 3
IS - Islanda 3
LB - Libano 3
LV - Lettonia 3
MM - Myanmar 3
PR - Porto Rico 3
QA - Qatar 3
SK - Slovacchia (Repubblica Slovacca) 3
AL - Albania 2
BB - Barbados 2
BG - Bulgaria 2
BZ - Belize 2
CR - Costa Rica 2
Totale 25.249
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Città #
Chandler 1.414
Singapore 1.314
Ashburn 820
Redmond 404
Dublin 374
Beijing 355
New York 346
Jacksonville 343
San Mateo 333
Ann Arbor 303
Nanjing 240
Nürnberg 231
Warsaw 231
Jakarta 225
Wilmington 198
Los Angeles 181
Boston 172
Hefei 151
Woodbridge 151
Munich 138
Dearborn 128
Houston 128
Moscow 119
Ho Chi Minh City 116
São Paulo 113
Lawrence 112
Rome 109
Milan 108
Dallas 102
Hanoi 99
Nanchang 99
Chicago 98
Seattle 98
Redwood City 87
Frankfurt am Main 86
Cattolica 82
Fairfield 79
Buffalo 73
Princeton 73
Marseille 72
Hong Kong 71
Brussels 69
Bremen 68
Izmir 68
Detroit 66
Kraków 57
Norwalk 56
Helsinki 49
Shenyang 49
Abidjan 46
Boardman 46
Hebei 45
Santa Clara 45
Kent 44
Tokyo 43
Changsha 42
The Dalles 42
London 39
Seoul 38
Ottawa 37
Rio de Janeiro 37
San Francisco 36
Brooklyn 35
Guangzhou 35
Phoenix 35
Hangzhou 34
Leawood 34
Jiaxing 33
Lappeenranta 33
Johannesburg 31
Nuremberg 31
Stockholm 31
Kunming 30
University Park 29
Philadelphia 28
Pune 28
Turku 28
Belo Horizonte 27
Montreal 26
Toronto 26
Zhengzhou 26
Denver 25
Mountain View 25
Atlanta 24
Cambridge 24
Dhaka 24
Tianjin 24
Baghdad 23
Brasília 23
Cape Town 23
Düsseldorf 23
Chennai 21
Fremont 21
Curitiba 20
North Bergen 20
Amman 19
Guarulhos 18
Lancaster 18
Poplar 18
Shanghai 18
Totale 11.989
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Nome #
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: Data from an early-access program in Italy 720
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 353
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 334
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 311
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 290
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 243
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 239
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 239
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 229
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 225
Retinal detachment with an unusual shape. 200
Persistence of abnormal electrophysiological findings after carpal tunnel release 197
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 189
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 187
Distinctive clinical and neuroimaging characteristics of longitudinally extensive transverse myelitis associated with aquaporin-4 autoantibodies 185
Bilateral thalamic stroke transiently reduces arousals and NREM sleep instability. 183
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 177
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 175
Assessment of neurological manifestations in hospitalized patients with COVID-19 170
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 167
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 161
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 159
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 159
A Case of Hemiabdominal Myoclonus 156
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 156
Mitochondrial neuropathy: considerations on pathogenesis 151
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 150
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 150
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 148
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 147
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 146
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 146
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 145
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 141
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 139
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 137
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 137
A novel L67P SOD1 mutation in an Italian ALS patient. 136
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 136
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 134
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 134
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 133
Neurologic improvement after peripheral blood stem cell transplantation in poems 133
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 132
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 132
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 132
Is it the use of Non Invasive Ventilation for less than four hours in the day sufficient to prolong survival in patients with Amyotrophic Lateral Sclerosis? 131
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 129
Ultrasound evaluation in transthyretin-related amyloid neuropathy 129
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 128
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 128
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 128
Vertebral artery dissection presenting with isolated occipital headache 127
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 127
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 126
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 126
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 126
Somatosensory Evoked Potentials of Inferior Alveolar Nerve: confirmation of a possible non-invasive neurophysiological approach 126
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 126
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 125
Posterior interosseous nerve syndrome due to radioulnar joint cyst 122
Restless Legs Syndrome and lateralized periodic movements due to a spinal schwannoma 122
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 121
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 121
Pathological findings in chronic inflammatory demyelinating polyradiculoneuropathy: A single-center experience 121
Nerve conduction studies of the sural nerve: Normative data from a single-center experience 119
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review 119
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction 119
Longitudinal assessments in discordant twins with SMA 119
Mycosis fungoides as a cause of severe obstructive sleep apnea 118
Teaching NeuroImages: Transient mutism associated with splenium lesion in capecitabine-induced leukoencephalopathy 118
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 116
Wernicke's encephalopathy following chronic diarrhoea 116
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 116
Sural nerve pathology in ALS patients: a single-centre experience 115
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 115
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 114
Clinical features and outcome of patients with autoimmune cerebellar ataxia evaluated with the Scale for the Assessment and Rating of Ataxia 114
Benedictine hand of 'central' origin 113
A Case of Hemiabdominal Myoclonus 113
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 112
HFE p.H63D polymorphism does not influence ALS phenotype and survival 112
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 111
Nerve ultrasound in CMT2E/CMT1F due to NEFL mutation: Confirmation of an axonal pathology 111
Guillain–Barré syndrome from an emergency department view: how to better predict the outcome? 111
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 110
Improvement of obstructive sleep apneas caused by hydrocephalus associated with Chiari malformation Type II following surgery. 109
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 109
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 109
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 108
Ocular Involvement in Hereditary Amyloidosis 108
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 107
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 107
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 107
Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian Centre 107
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 106
An uncommon cause of headache resolution: spontaneous ventriculostomy in obstructive hydrocephalus 106
Sural nerve biopsy in peripheral neuropathies: 30-year experience from a single center 106
Ocular involvement in hereditary transthyretin amyloidosis: A case series describing novel potential biomarkers 106
Recurrent miller fisher: a new case report and a literature review 105
Totale 15.043
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Categoria #
all - tutte 105.600
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 105.600
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021792 0 0 0 0 0 63 155 43 170 86 248 27
2021/20221.828 197 130 20 180 56 55 45 284 90 109 296 366
2022/20234.453 439 516 298 601 250 505 156 303 483 731 110 61
2023/20241.947 95 572 56 127 61 361 100 60 13 78 207 217
2024/20253.751 99 126 321 192 257 115 136 163 516 364 788 674
2025/20265.614 1.680 303 601 1.189 1.738 103 0 0 0 0 0 0
Totale 25.660