IRIS UniCatt

Luigetti, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 10.998
EU - Europa 8.743
AS - Asia 7.650
SA - Sud America 1.576
AF - Africa 269
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 10
Totale 29.270
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Nazione #
US - Stati Uniti d'America 10.715
SG - Singapore 3.551
DE - Germania 3.261
CN - Cina 1.819
BR - Brasile 1.303
SE - Svezia 1.148
IT - Italia 850
VN - Vietnam 737
UA - Ucraina 711
FR - Francia 697
GB - Regno Unito 507
IE - Irlanda 388
PL - Polonia 310
IN - India 279
FI - Finlandia 276
ID - Indonesia 249
RU - Federazione Russa 192
JP - Giappone 176
CA - Canada 171
HK - Hong Kong 143
TR - Turchia 121
BD - Bangladesh 119
AR - Argentina 97
ZA - Sudafrica 96
BE - Belgio 90
IQ - Iraq 87
NL - Olanda 79
MX - Messico 66
ES - Italia 50
CI - Costa d'Avorio 46
EC - Ecuador 46
PK - Pakistan 46
KR - Corea 42
SA - Arabia Saudita 41
AT - Austria 35
CO - Colombia 32
PY - Paraguay 31
MA - Marocco 30
JO - Giordania 26
KE - Kenya 26
CL - Cile 25
PH - Filippine 25
IR - Iran 24
AU - Australia 23
AE - Emirati Arabi Uniti 22
RO - Romania 19
TN - Tunisia 19
UZ - Uzbekistan 19
LT - Lituania 18
CH - Svizzera 17
PT - Portogallo 15
IL - Israele 14
VE - Venezuela 13
CZ - Repubblica Ceca 12
KZ - Kazakistan 12
TH - Thailandia 12
AZ - Azerbaigian 10
DK - Danimarca 10
EG - Egitto 10
PE - Perù 10
UY - Uruguay 10
DO - Repubblica Dominicana 9
DZ - Algeria 9
SN - Senegal 9
JM - Giamaica 8
NP - Nepal 8
BO - Bolivia 7
BY - Bielorussia 7
KG - Kirghizistan 7
OM - Oman 7
PS - Palestinian Territory 7
ET - Etiopia 6
HR - Croazia 6
LB - Libano 6
LK - Sri Lanka 6
A2 - ???statistics.table.value.countryCode.A2??? 5
GR - Grecia 5
MY - Malesia 5
NI - Nicaragua 5
NO - Norvegia 5
SI - Slovenia 5
TT - Trinidad e Tobago 5
AM - Armenia 4
HN - Honduras 4
LA - Repubblica Popolare Democratica del Laos 4
MD - Moldavia 4
MM - Myanmar 4
QA - Qatar 4
RS - Serbia 4
AL - Albania 3
AO - Angola 3
EU - Europa 3
GE - Georgia 3
GM - Gambi 3
IS - Islanda 3
LV - Lettonia 3
PA - Panama 3
PR - Porto Rico 3
SK - Slovacchia (Repubblica Slovacca) 3
BA - Bosnia-Erzegovina 2
Totale 29.225
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Città #
Singapore 1.887
Chandler 1.414
Ashburn 1.092
San Jose 954
Redmond 404
Dublin 377
Beijing 363
New York 362
Jacksonville 344
San Mateo 333
Ann Arbor 303
Ho Chi Minh City 263
Nanjing 240
Warsaw 236
Nürnberg 231
Jakarta 226
Lauterbourg 199
Los Angeles 198
Wilmington 198
Hanoi 189
Boston 173
Hefei 151
Woodbridge 151
Tokyo 147
Munich 138
Houston 131
Hong Kong 130
Dearborn 128
São Paulo 122
Rome 120
Milan 119
Moscow 119
Frankfurt am Main 118
Lawrence 112
Chicago 110
Dallas 104
Seattle 103
Nanchang 99
Redwood City 87
Cattolica 82
Fairfield 79
Buffalo 77
Helsinki 74
Marseille 73
Princeton 73
The Dalles 71
Bremen 69
Brussels 69
Izmir 68
Santa Clara 67
Detroit 66
Kraków 57
Norwalk 56
Paris 52
Shenyang 50
Council Bluffs 49
Boardman 47
Abidjan 46
Hebei 45
Kent 44
Orem 44
Guangzhou 43
London 43
Changsha 42
Johannesburg 40
Baghdad 38
Brooklyn 38
Ottawa 38
Rio de Janeiro 38
Seoul 38
St Louis 38
Phoenix 37
San Francisco 36
Atlanta 35
Hangzhou 35
Lappeenranta 35
Stockholm 35
Da Nang 34
Leawood 34
Montreal 34
Jiaxing 33
Nuremberg 32
Pune 32
Denver 31
Kunming 31
Dhaka 29
Haiphong 29
Philadelphia 29
Shanghai 29
Toronto 29
University Park 29
Tianjin 28
Turku 28
Belo Horizonte 27
Zhengzhou 27
Brasília 26
Mountain View 25
Amman 24
Cambridge 24
Cape Town 23
Totale 14.809
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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 739
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 376
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 360
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 334
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 314
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 267
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 260
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 250
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 247
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 244
Retinal detachment with an unusual shape. 218
Persistence of abnormal electrophysiological findings after carpal tunnel release 218
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 213
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 205
Bilateral thalamic stroke transiently reduces arousals and NREM sleep instability. 204
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 195
Distinctive clinical and neuroimaging characteristics of longitudinally extensive transverse myelitis associated with aquaporin-4 autoantibodies 195
Assessment of neurological manifestations in hospitalized patients with COVID-19 194
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 188
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 184
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 183
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 183
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 180
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 172
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 172
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 169
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 168
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 166
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 166
A Case of Hemiabdominal Myoclonus 164
Mitochondrial neuropathy: considerations on pathogenesis 163
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 161
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 161
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 160
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 160
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 159
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 158
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 156
Neurologic improvement after peripheral blood stem cell transplantation in poems 156
A novel L67P SOD1 mutation in an Italian ALS patient. 155
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 153
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 153
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 153
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 150
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 150
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 150
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 149
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 149
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 149
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 148
Somatosensory Evoked Potentials of Inferior Alveolar Nerve: confirmation of a possible non-invasive neurophysiological approach 148
Pathological findings in chronic inflammatory demyelinating polyradiculoneuropathy: A single-center experience 147
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 145
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? 145
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 145
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 145
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 144
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 143
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 143
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 143
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 142
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 142
Recurrent miller fisher: a new case report and a literature review 142
Ocular Morpho-Functional Evaluation in ATTRv Pre-Symptomatic Carriers: A Case Series 141
Vertebral artery dissection presenting with isolated occipital headache 141
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 141
Restless Legs Syndrome and lateralized periodic movements due to a spinal schwannoma 140
Ocular involvement in hereditary transthyretin amyloidosis: A case series describing novel potential biomarkers 139
Mycosis fungoides as a cause of severe obstructive sleep apnea 137
Longitudinal assessments in discordant twins with SMA 137
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 137
Ultrasound evaluation in transthyretin-related amyloid neuropathy 136
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review 136
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction 136
Guillain–Barré syndrome from an emergency department view: how to better predict the outcome? 136
Pupillometric findings in ATTRv patients and carriers: results from a single-centre experience 135
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 135
Sural nerve pathology in ALS patients: a single-centre experience 133
Wernicke's encephalopathy following chronic diarrhoea 133
Posterior interosseous nerve syndrome due to radioulnar joint cyst 133
Ocular Involvement in Hereditary Amyloidosis 133
Nerve conduction studies of the sural nerve: Normative data from a single-center experience 131
A Case of Hemiabdominal Myoclonus 130
Clinical features and outcome of patients with autoimmune cerebellar ataxia evaluated with the Scale for the Assessment and Rating of Ataxia 129
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 127
Sural nerve biopsy in peripheral neuropathies: 30-year experience from a single center 127
Improvement of obstructive sleep apneas caused by hydrocephalus associated with Chiari malformation Type II following surgery. 126
Benedictine hand of 'central' origin 126
HFE p.H63D polymorphism does not influence ALS phenotype and survival 126
Teaching NeuroImages: Transient mutism associated with splenium lesion in capecitabine-induced leukoencephalopathy 126
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 125
Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian Centre 125
Serum Neurofilament and Free Light Chain Levels in Patients Undergoing Treatment for Chronic Inflammatory Demyelinating Polyneuropathy 124
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 124
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 123
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 123
An uncommon cause of headache resolution: spontaneous ventriculostomy in obstructive hydrocephalus 123
Generation of an induced pluripotent stem cell line (UCSCi002-A) from a patient with a variant in TARDBP gene associated with familial amyotrophic lateral sclerosis and frontotemporal dementia 121
Nerve MR in the Differential Diagnosis of Neuropathies: A Case Series from a Single Center 121
Does albuterol have an effect on neuromuscular junction dysfunction in spinal muscular atrophy? 121
Totale 16.932
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Categoria #
all - tutte 115.215
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 115.215
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021275 0 0 0 0 0 0 0 0 0 0 248 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
2025/20269.670 1.680 303 601 1.189 1.738 496 1.799 508 581 764 11 0
Totale 29.716