IRIS PubliCatt

Luigetti, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 7.212
EU - Europa 7.004
AS - Asia 1.191
AF - Africa 80
SA - Sud America 19
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 8
Totale 15.529
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Nazione #
US - Stati Uniti d'America 7.140
DE - Germania 2.980
SE - Svezia 1.106
CN - Cina 819
UA - Ucraina 688
IT - Italia 518
IE - Irlanda 378
GB - Regno Unito 359
FR - Francia 341
PL - Polonia 256
FI - Finlandia 160
IN - India 144
BE - Belgio 82
TR - Turchia 78
CA - Canada 67
CI - Costa d'Avorio 45
NL - Olanda 44
JP - Giappone 36
ZA - Sudafrica 33
IR - Iran 19
HK - Hong Kong 18
AU - Australia 15
CH - Svizzera 15
RO - Romania 15
KR - Corea 14
RU - Federazione Russa 14
ES - Italia 12
VN - Vietnam 12
PH - Filippine 10
SG - Singapore 10
BR - Brasile 7
AE - Emirati Arabi Uniti 6
PT - Portogallo 6
TH - Thailandia 6
A2 - ???statistics.table.value.countryCode.A2??? 5
DK - Danimarca 5
AT - Austria 4
CO - Colombia 4
NO - Norvegia 4
CL - Cile 3
CZ - Repubblica Ceca 3
EU - Europa 3
HR - Croazia 3
IL - Israele 3
MD - Moldavia 3
AR - Argentina 2
GR - Grecia 2
ID - Indonesia 2
JO - Giordania 2
KZ - Kazakistan 2
MX - Messico 2
PK - Pakistan 2
PR - Porto Rico 2
SA - Arabia Saudita 2
SI - Slovenia 2
AL - Albania 1
BO - Bolivia 1
BZ - Belize 1
DZ - Algeria 1
EC - Ecuador 1
EG - Egitto 1
HU - Ungheria 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LV - Lettonia 1
MC - Monaco 1
MM - Myanmar 1
MY - Malesia 1
OM - Oman 1
PE - Perù 1
TW - Taiwan 1
Totale 15.529
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Città #
Chandler 1.414
Ashburn 532
Redmond 404
Dublin 369
Jacksonville 339
San Mateo 333
Ann Arbor 303
New York 276
Nanjing 240
Nürnberg 231
Wilmington 197
Warsaw 194
Boston 157
Woodbridge 151
Dearborn 128
Houston 114
Lawrence 112
Nanchang 99
Milan 90
Beijing 87
Redwood City 87
Cattolica 80
Seattle 80
Fairfield 79
Princeton 73
Marseille 72
Chicago 67
Bremen 66
Izmir 66
Brussels 64
Detroit 61
Kraków 57
Norwalk 56
Shenyang 49
Munich 48
Abidjan 45
Hebei 45
Rome 44
Changsha 40
Boardman 39
Leawood 34
Guangzhou 33
Jiaxing 32
Kunming 29
University Park 29
Hangzhou 26
Mountain View 25
Ottawa 25
Pune 25
Cambridge 24
London 23
Tianjin 22
Zhengzhou 22
Fremont 21
Philadelphia 21
Los Angeles 20
Phoenix 19
Lancaster 18
Waanrode 18
Auburn Hills 17
Washington 17
Helsinki 16
Hong Kong 16
Simi Valley 16
Trieste 16
Millbury 15
Hefei 14
Birmingham 13
Cape Town 13
Las Vegas 12
Seoul 12
Shanghai 12
Buffalo 10
Hanoi 10
Jinan 10
San Diego 10
San Francisco 10
Stockholm 10
Toronto 10
Leeds 9
Nashville 9
Augusta 8
Manchester 8
The Bronx 8
Tokyo 8
Amsterdam 7
Andover 7
Berlin 7
Chengdu 7
Liverpool 7
Miami 7
Plantation 7
San Antonio 7
Bologna 6
Changchun 6
Columbus 6
Costa Mesa 6
Dallas 6
Dubai 6
Edinburgh 6
Totale 7.861
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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 669
Clinical–neurophysiological correlations in a series of patients with IgM-related neuropathy 317
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 297
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 274
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 258
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child. 199
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 192
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 189
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations 182
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 174
Retinal detachment with an unusual shape. 164
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 161
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease 158
Persistence of abnormal electrophysiological findings after carpal tunnel release 148
Distinctive clinical and neuroimaging characteristics of longitudinally extensive transverse myelitis associated with aquaporin-4 autoantibodies 141
Bilateral thalamic stroke transiently reduces arousals and NREM sleep instability. 132
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else? 126
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 126
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 125
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantation 122
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 122
A Case of Hemiabdominal Myoclonus 118
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Amyotrophic Lateral 115
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 112
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 108
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 108
Assessment of neurological manifestations in hospitalized patients with COVID-19 108
Mitochondrial neuropathy: considerations on pathogenesis 107
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 106
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience 105
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 104
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot study 104
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 102
Ultrasound evaluation in transthyretin-related amyloid neuropathy 101
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience 100
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 99
A novel L67P SOD1 mutation in an Italian ALS patient. 97
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant 94
Posterior interosseous nerve syndrome due to radioulnar joint cyst 94
Vertebral artery dissection presenting with isolated occipital headache 93
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? 93
Clinical-neurophysiological correlations in a series of patients with IgM-related neuropathy 93
Usefulness of F-18 FDG PET/CT in the follow-up of POEMS syndrome after autologous peripheral blood stem cell transplantation 90
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation 90
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 90
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 88
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 88
Mycosis fungoides as a cause of severe obstructive sleep apnea 88
Neurologic improvement after peripheral blood stem cell transplantation in poems 88
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 88
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion 87
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 87
Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature 86
Somatosensory Evoked Potentials of Inferior Alveolar Nerve: confirmation of a possible non-invasive neurophysiological approach 86
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 84
Wernicke's encephalopathy following chronic diarrhoea 84
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis 84
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 84
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 83
Nerve ultrasound in CMT2E/CMT1F due to NEFL mutation: Confirmation of an axonal pathology 83
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 82
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 81
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 81
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients 80
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 79
Teaching NeuroImages: Transient mutism associated with splenium lesion in capecitabine-induced leukoencephalopathy 79
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 78
Improvement of obstructive sleep apneas caused by hydrocephalus associated with Chiari malformation Type II following surgery. 77
HFE p.H63D polymorphism does not influence ALS phenotype and survival 77
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 77
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 77
Sural nerve pathology in ALS patients: a single-centre experience 76
Restless Legs Syndrome and lateralized periodic movements due to a spinal schwannoma 74
Nerve ultrasound in patients with CMT1C: Description of three cases 73
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review 73
ANCA-related vasculitic neuropathy mimicking motor neuron disease. 72
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. 72
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 72
Post-Encephalitic Parkinsonism and Sleep Disorder Responsive to Immunological Treatment: A Case Report 72
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 71
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease 71
A Case of Hemiabdominal Myoclonus 71
Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations 71
Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 70
Nerve conduction studies of the sural nerve: Normative data from a single-center experience 70
Benedictine hand of 'central' origin 70
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma. 70
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 70
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features 69
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience 69
Ultrasound evaluation in transthyretin-related amyloid neuropathy 68
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 68
Low rate repetitive nerve stimulation in Lambert-Eaton myasthenic syndrome: Peculiar characteristics of decremental pattern from a single-centre experience 67
Erratum to “Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience” (Clinical Neurology and Neurosurgery (2016) 147 (117–118) (S030384671630097X) (10.1016/j.clineuro.2016.03.007)) 67
An uncommon cause of headache resolution: spontaneous ventriculostomy in obstructive hydrocephalus 66
Ultrasound visualization of nerve morphological alteration at the site of conduction block. 65
Proximal basilar artery fenestration with bridging artery appearance. 65
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs 64
Teaching neuroimages: Peroneal intraneural ganglion cyst: a rare cause of drop foot in a child 64
Lower motor neuron involvement in longitudinally extensive transverse myelitis with and without aquaporin-4 antibodies 64
Totale 10.877
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Categoria #
all - tutte 52.463
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 52.463
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019264 0 0 0 0 0 0 0 0 0 0 143 121
2019/20202.055 424 121 112 103 168 179 212 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
2023/20241.524 95 572 56 127 61 361 100 60 13 78 1 0
Totale 15.872