IRIS PubliCatt

Luigetti, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 7.372
EU - Europa 7.282
AS - Asia 2.130
AF - Africa 82
SA - Sud America 20
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 8
Totale 16.909
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Nazione #
US - Stati Uniti d'America 7.284
DE - Germania 3.006
SE - Svezia 1.107
CN - Cina 931
UA - Ucraina 688
SG - Singapore 601
IT - Italia 591
IE - Irlanda 380
GB - Regno Unito 365
FR - Francia 351
PL - Polonia 257
ID - Indonesia 224
FI - Finlandia 166
IN - India 147
RU - Federazione Russa 141
BE - Belgio 86
CA - Canada 83
TR - Turchia 80
NL - Olanda 49
CI - Costa d'Avorio 45
JP - Giappone 36
ZA - Sudafrica 34
HK - Hong Kong 19
IR - Iran 19
RO - Romania 17
AU - Australia 15
CH - Svizzera 15
ES - Italia 15
KR - Corea 15
VN - Vietnam 14
PH - Filippine 10
AT - Austria 7
BR - Brasile 7
AE - Emirati Arabi Uniti 6
PT - Portogallo 6
TH - Thailandia 6
A2 - ???statistics.table.value.countryCode.A2??? 5
CZ - Repubblica Ceca 5
DK - Danimarca 5
CO - Colombia 4
HR - Croazia 4
IL - Israele 4
NO - Norvegia 4
AR - Argentina 3
CL - Cile 3
EU - Europa 3
MD - Moldavia 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
BD - Bangladesh 2
GR - Grecia 2
JO - Giordania 2
KZ - Kazakistan 2
LK - Sri Lanka 2
MX - Messico 2
PK - Pakistan 2
PR - Porto Rico 2
SA - Arabia Saudita 2
AL - Albania 1
BO - Bolivia 1
BZ - Belize 1
DZ - Algeria 1
EC - Ecuador 1
EG - Egitto 1
HU - Ungheria 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
LU - Lussemburgo 1
LV - Lettonia 1
MA - Marocco 1
MC - Monaco 1
MM - Myanmar 1
MY - Malesia 1
OM - Oman 1
PE - Perù 1
TW - Taiwan 1
Totale 16.909
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Città #
Chandler 1.414
Ashburn 536
Singapore 470
Redmond 404
Dublin 371
Jacksonville 339
San Mateo 333
Ann Arbor 303
New York 276
Nanjing 240
Nürnberg 231
Jakarta 223
Wilmington 197
Warsaw 194
Boston 157
Woodbridge 151
Dearborn 128
Moscow 115
Houston 114
Lawrence 112
Nanchang 99
Milan 95
Beijing 90
Redwood City 87
Cattolica 82
Seattle 80
Fairfield 79
Princeton 73
Marseille 72
Munich 70
Rome 70
Brussels 68
Chicago 67
Bremen 66
Izmir 66
Detroit 61
Kraków 57
Norwalk 56
Shenyang 49
Boardman 46
Abidjan 45
Hebei 45
Changsha 40
Los Angeles 40
Leawood 34
Guangzhou 33
Jiaxing 32
Ottawa 32
Kunming 30
University Park 29
Hangzhou 26
London 25
Mountain View 25
Pune 25
Cambridge 24
Zhengzhou 23
Phoenix 22
Tianjin 22
Fremont 21
Philadelphia 21
Helsinki 20
Lancaster 18
Waanrode 18
Auburn Hills 17
Hong Kong 17
Washington 17
Santa Clara 16
Simi Valley 16
Trieste 16
Millbury 15
Toronto 15
Cape Town 14
Hefei 14
Birmingham 13
Seoul 13
Busto Arsizio 12
Las Vegas 12
Shanghai 12
Stockholm 11
Buffalo 10
Hanoi 10
Jinan 10
Paris 10
San Diego 10
San Francisco 10
Chengdu 9
Florence 9
Leeds 9
Nashville 9
Amsterdam 8
Augusta 8
Lappeenranta 8
Manchester 8
Monza 8
The Bronx 8
Tokyo 8
Andover 7
Berlin 7
Liverpool 7
Miami 7
Totale 8.801
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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 677
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 323
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 303
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 281
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 263
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 204
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 198
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 197
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 191
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 181
Retinal detachment with an unusual shape. 168
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 165
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 163
Persistence of abnormal electrophysiological findings after carpal tunnel release 155
Distinctive clinical and neuroimaging characteristics of longitudinally extensive transverse myelitis associated with aquaporin-4 autoantibodies 146
Bilateral thalamic stroke transiently reduces arousals and NREM sleep instability. 140
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 136
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 134
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 132
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 130
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 128
A Case of Hemiabdominal Myoclonus 125
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 119
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 117
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 116
Assessment of neurological manifestations in hospitalized patients with COVID-19 116
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 114
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 113
Mitochondrial neuropathy: considerations on pathogenesis 113
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 112
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 110
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 108
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 107
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 107
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 104
Ultrasound evaluation in transthyretin-related amyloid neuropathy 103
A novel L67P SOD1 mutation in an Italian ALS patient. 102
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? 101
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 101
Neurologic improvement after peripheral blood stem cell transplantation in poems 98
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 98
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 97
Posterior interosseous nerve syndrome due to radioulnar joint cyst 97
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 97
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 96
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 96
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 96
Vertebral artery dissection presenting with isolated occipital headache 96
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 95
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 95
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 95
Somatosensory Evoked Potentials of Inferior Alveolar Nerve: confirmation of a possible non-invasive neurophysiological approach 95
Mycosis fungoides as a cause of severe obstructive sleep apnea 94
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 93
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 92
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 92
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 91
Wernicke's encephalopathy following chronic diarrhoea 91
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 91
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 90
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 88
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 88
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 88
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 88
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 86
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 86
Nerve ultrasound in CMT2E/CMT1F due to NEFL mutation: Confirmation of an axonal pathology 86
Teaching NeuroImages: Transient mutism associated with splenium lesion in capecitabine-induced leukoencephalopathy 86
HFE p.H63D polymorphism does not influence ALS phenotype and survival 84
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 84
Sural nerve pathology in ALS patients: a single-centre experience 83
Restless Legs Syndrome and lateralized periodic movements due to a spinal schwannoma 83
Improvement of obstructive sleep apneas caused by hydrocephalus associated with Chiari malformation Type II following surgery. 80
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 80
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 80
A Case of Hemiabdominal Myoclonus 79
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review 79
Nerve conduction studies of the sural nerve: Normative data from a single-center experience 78
Benedictine hand of 'central' origin 78
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 78
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 77
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 77
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 76
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 76
An uncommon cause of headache resolution: spontaneous ventriculostomy in obstructive hydrocephalus 76
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 75
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 75
Nerve ultrasound in patients with CMT1C: Description of three cases 75
Low rate repetitive nerve stimulation in Lambert-Eaton myasthenic syndrome: Peculiar characteristics of decremental pattern from a single-centre experience 74
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease 74
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 74
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 74
Gadolinium enhancement of the lumbar leptomeninges and roots in a case of ALS 73
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features 73
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 72
Ultrasound evaluation in transthyretin-related amyloid neuropathy 72
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 72
Lower motor neuron involvement in longitudinally extensive transverse myelitis with and without aquaporin-4 antibodies 71
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive cases 71
Sjögren's syndrome presenting with isolated sensory axonal polyneuropathy 71
Totale 11.528
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Categoria #
all - tutte 68.753
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 68.753
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.295 0 0 0 0 168 179 212 67 111 151 223 184
2020/20211.489 61 161 55 209 211 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
2024/2025959 99 126 321 192 221 0 0 0 0 0 0 0
Totale 17.254