CRIS Current Research Information System

LIGUORI, ROCCO
 Distribuzione geografica
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Continente #
NA - Nord America 24.126
AS - Asia 20.178
EU - Europa 14.843
Continente sconosciuto - Info sul continente non disponibili 1.240
SA - Sud America 1.179
AF - Africa 1.059
OC - Oceania 51
Totale 62.676
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Nazione #
US - Stati Uniti d'America 23.614
SG - Singapore 5.364
VN - Vietnam 5.109
CN - Cina 4.967
IT - Italia 3.803
GB - Regno Unito 2.840
DE - Germania 2.150
HK - Hong Kong 1.531
SE - Svezia 1.230
FR - Francia 942
IN - India 892
BR - Brasile 807
NL - Olanda 783
RU - Federazione Russa 683
KR - Corea 519
IE - Irlanda 486
UA - Ucraina 444
BD - Bangladesh 428
CI - Costa d'Avorio 373
JP - Giappone 338
FI - Finlandia 313
ZA - Sudafrica 295
CA - Canada 264
EE - Estonia 196
TG - Togo 180
AT - Austria 168
ID - Indonesia 154
CH - Svizzera 132
AR - Argentina 129
PH - Filippine 129
BG - Bulgaria 120
JO - Giordania 115
MX - Messico 101
TR - Turchia 97
ES - Italia 96
PL - Polonia 95
BE - Belgio 83
SC - Seychelles 81
IQ - Iraq 78
TH - Thailandia 76
PK - Pakistan 66
EC - Ecuador 61
CO - Colombia 53
TW - Taiwan 48
AU - Australia 43
GR - Grecia 42
SA - Arabia Saudita 41
UZ - Uzbekistan 41
CL - Cile 36
LT - Lituania 35
VE - Venezuela 33
JM - Giamaica 32
IR - Iran 30
LB - Libano 30
MY - Malesia 27
RO - Romania 27
MA - Marocco 23
DK - Danimarca 22
CR - Costa Rica 21
PE - Perù 21
PT - Portogallo 21
PY - Paraguay 21
HR - Croazia 18
KE - Kenya 18
EU - Europa 16
NG - Nigeria 16
CZ - Repubblica Ceca 15
BY - Bielorussia 14
TT - Trinidad e Tobago 14
EG - Egitto 13
IL - Israele 13
NI - Nicaragua 13
KZ - Kazakistan 12
AL - Albania 11
ET - Etiopia 11
GT - Guatemala 11
HN - Honduras 11
HU - Ungheria 11
SK - Slovacchia (Repubblica Slovacca) 11
TN - Tunisia 11
AZ - Azerbaigian 10
DZ - Algeria 10
PR - Porto Rico 10
AE - Emirati Arabi Uniti 9
DO - Repubblica Dominicana 9
NO - Norvegia 8
OM - Oman 8
PS - Palestinian Territory 8
NP - Nepal 7
NZ - Nuova Zelanda 7
UY - Uruguay 7
MK - Macedonia 6
RS - Serbia 6
SM - San Marino 6
SN - Senegal 6
SV - El Salvador 6
A2 - ???statistics.table.value.countryCode.A2??? 5
KW - Kuwait 5
LV - Lettonia 5
MT - Malta 5
Totale 61.361
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Città #
Singapore 3.616
Ashburn 2.418
Southend 2.393
Fairfield 2.018
San Jose 1.521
Hong Kong 1.425
Chandler 1.298
Hefei 1.115
Ho Chi Minh City 1.096
Bologna 953
Seattle 913
Hanoi 908
Houston 900
Woodbridge 898
Wilmington 827
Santa Clara 748
Cambridge 716
Ann Arbor 669
Dong Ket 662
Council Bluffs 619
Princeton 618
Beijing 587
Boardman 514
Los Angeles 493
Dublin 483
Frankfurt am Main 467
Seoul 466
New York 391
Dallas 387
Abidjan 373
Lauterbourg 351
Eygelshoven 338
Tokyo 276
Milan 273
Jacksonville 264
Nanjing 243
Westminster 241
Helsinki 217
Padova 202
Buffalo 194
Berlin 187
Lomé 180
Turin 171
Rome 159
Munich 153
Haiphong 151
Da Nang 148
São Paulo 135
Redmond 133
Saint Petersburg 127
Redondo Beach 125
San Diego 124
Sofia 120
Bengaluru 118
Amman 113
Guangzhou 108
Jinan 107
Shanghai 107
Chicago 106
Phoenix 103
Shenyang 103
Vienna 101
Changsha 93
Florence 93
San Francisco 88
Bern 82
Hebei 82
London 79
Tianjin 78
Atlanta 77
Montreal 76
Medford 74
Brussels 73
Jakarta 73
Nanchang 72
Orem 70
Johannesburg 68
Dearborn 65
Warsaw 65
Des Moines 62
Nuremberg 62
Redwood City 60
Paris 59
Hangzhou 58
Zhengzhou 57
Amsterdam 56
Piscataway 55
Toronto 54
Denver 53
Falls Church 53
Hải Dương 53
Modena 52
Falkenstein 51
Lappeenranta 51
Boston 49
Mülheim 49
Biên Hòa 48
Newark 48
Yubileyny 48
Brooklyn 45
Totale 38.401
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Nome #
A new potential biomarker for dementia with Lewy bodies 913
Nutraceutical Approach to Peripheral Neuropathies: Evidence from Clinical Trials 603
Hypnic jerks: neurophysiological characterization of a new motor pattern. 541
Comparative assessment of MScanFit MUNE and quantitative EMG in amyotrophic lateral sclerosis diagnosis: A prospective study 414
The role of antibodies in small fiber neuropathy: a review of currently available evidence 381
Skin biopsy and microneurography disclose selective noradrenergic dysfunction due to dopamine-β-hydroxylase deficiency 317
Altered globotriaosylceramide accumulation and mucosal neuronal fiber density in the colon of the Fabry disease mouse model 295
Small fiber neuropathy associated with COVID-19 infection and vaccination: A prospective case-control study 287
Predicting conversion from mild cognitive impairment to Alzheimer's disease using brain 1 H-MRS and volumetric changes: A two- year retrospective follow-up study 286
Mitochondrial dysfunction in myotonic dystrophy type 1 282
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 277
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome 277
Autonomic innervation in multiple system atrophy and pure autonomic failure. 276
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis 270
Cognitive rehabilitation and transcranial direct current stimulation in a patient with posterior cortical atrophy: An fMRI study 269
Diagnostic-prognostic value and electrophysiological correlates of CSF biomarkers of neurodegeneration and neuroinflammation in amyotrophic lateral sclerosis 266
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome b (MT-CYB) Gene 265
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 254
Defective Mitochondrial Adenosine Triphosphate Production in Skeletal Muscle From Patients With Dominant Optic Atrophy Due to OPA1 Mutations 249
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. 246
Anti-ganglioside antibodies in coeliac disease with neurological disorders. 245
A case of fatal familial insomnia in Africa. 245
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 245
Bando Progetti di Ricerca Giovani Ricercatori – Ricerca Finalizzata 2010 Project Title:Biomolecular and functional analysis of pathogenetic mechanisms of neuropathic pain in genetic and acquired small fibre neuropathies. Project Code:RF-2010-2313899 244
Small fiber neuropathy in female patients with fabry disease. 244
Case Report: Optic Atrophy and Nephropathy With m.13513G>A/MT-ND5 mtDNA Pathogenic Variant 236
A further Rasch study confirms that ALSFRS-R does not conform to fundamental measurement requirements 235
Conformational Antibodies to Proteolipid Protein-1 and Its Peripheral Isoform DM20 in Patients With CNS Autoimmune Demyelinating Disorders 234
Amyotrophic lateral sclerosis: a comparison of two staging systems in a population-based study 234
Skin globotriaosylceramide 3 deposits are specific to Fabry disease with classical mutations and associated with small fibre neuropathy. 234
Intravenous immunoglobulin therapy in COVID-19-related encephalopathy 233
Biomarkers for REM sleep behavior disorder in idiopathic and narcoleptic patients 232
Volumetric absorptive microsampling coupled with UHPLC-MS/MS for the determination of Lyso-Gb3 as Fabry disease diagnostic biomarker 231
Increased expression of Trpv1 in peripheral terminals mediates thermal nociception in Fabry disease mouse model 231
Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases 230
A 36-Year-Old Woman With Right Eye Ptosis 226
Color choice preference in cognitively impaired patients: A look inside alzheimer’s disease through the use of lüscher color diagnostic 224
Generalised anhidrosis: different lesion sites demonstrated by microneurography and skin biopsy. 222
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 222
Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern? 219
Human figure drawing distinguishes Alzheimer’s patients: a cognitive screening test study 219
Comparison of ice pack test and single-fiber EMG diagnostic accuracy in patients referred for myasthenic ptosis 219
Difference in safety and humoral response to mRNA SARS-CoV-2 vaccines in patients with autoimmune neurological disorders: the ANCOVAX study 218
In Vivo Parieto-Occipital White Matter Metabolism Is Correlated with Visuospatial Deficits in Adult DM1 Patients 216
A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations. 216
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 216
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome (Scientific Reports, (2020), 10, 1, (4785), 10.1038/s41598-020-61735-3) 213
A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings 213
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells. 213
Anhidrosis in multiple system atrophy: a preganglionic sudomotor dysfunction? 212
The Distinguishing Motor Features of Cataplexy: A Study from Video Recorded Attacks 212
A case report of IgG4-related disease: an insidious path to the diagnosis through kidney, heart and brain 211
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation 211
Intermittent head drops: the differential spectrum 208
Brain & Skeletal Muscle MRS Study in Patients with Myotonic Dystrophy Type 1 208
Autosomal dominant adult spinal muscular atrophy associated with alacrimia and achalasia. 207
Antibodies against hypocretin receptor 2 are rare in narcolepsy 207
Cervical demyelinating lesion presenting with choreoathetoid movements and dystonia 206
Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases 206
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations 206
Attività nervosa simpatica ed ipersonnia in pazienti con Sindrome delle Apnee Ostruttive nel Sonno. 204
Disruption of the microbiota-gut-brain axis is a defining characteristic of the α-Gal A (-/0) mouse model of Fabry disease 203
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 203
A comparative blind study between skin biopsy and seed amplification assay to disclose pathological α-synuclein in RBD 201
Impaired plasma membrane calcium ATPase activity and mitochondrial dysfunction contribute to calcium dysregulation in Fabry disease-related painful neuropathy 201
An inflammatory myopathy unmasks a case of leprosy in an Italian patient 201
Acute rhabdomyolysis induced by tonic-clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency. 200
The autonomic innervation of hairy skin in humans: an in vivo confocal study 200
Absent cardiac and muscle sympathetic nerve activities involvement in Ross syndrome: A follow-up study 199
Idebenone treatment in Leber's hereditary optic neuropathy. 199
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 199
Brachial amyotrophic diplegia associated with the a140a superoxide dismutase 1 mutation. 198
Paroxysmal kinesigenic dyskinesia and focal epilepsy in childhood: A case report 198
Discinesia parossistica chinesigenica ed epilessia focale: descrizione di caso in età evolutiva 197
Cerebrospinal fluid biomarkers in patients with frontotemporal dementia spectrum: A single-center study 197
Sulcal Morphometry Predicts Mild Cognitive Impairment Conversion to Alzheimer’s Disease 196
Nocturnal Sleep Dynamics Identify Narcolepsy Type 1. 196
Somatic and autonomic small fiber neuropathy induced by bortezomib therapy: an immunofluorescence study. 196
Cataplectic attacks during rapid eye movement sleep behavior disorder episodes in a narcoleptic patient. 196
Blood neurofilament light chain and S100B as biomarkers of neurological involvement and functional prognosis in COVID-19: a multicenter study 195
The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance 194
Neurophysiological correlates of abnormal somatosensory temporal discrimination in dystonia 194
Epilepsy in MT-ATP6 - related mils/NARP: correlation of elettroclinical features with heteroplasmy 194
Neurological Manifestations of Long {COVID}: A Single-Center One-Year Experience 192
Habituation of sympathetic sudomotor and vasomotor skin responses: neural and non-neural components in healthy subjects. 192
Characterization of Human Dermal Fibroblasts in Fabry Disease 191
Correlations Between Cardiac Magnetic Resonance and Myocardial Histologic Findings in Fabry Disease 190
COVID-19 and the Brain: The Neuropathological Italian Experience on 33 Adult Autopsies 190
Autonomic disturbances in narcolepsy. 190
Multimodal investigation of melanopsin retinal ganglion cells in Alzheimer's disease 189
Added value of electromyography in the diagnosis of myopathy: A consensus exercise 189
Agrypnia Excitata: a microneurographic study of muscle sympathetic nerve activity. 189
Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy. 188
Preganglionic sudomotor nerve fiber lesion in a patient with Multiple System Atrophy and generalized anhidrosis. 187
AUTOSOMAL DOMINANT EARLY-ONSET CORTICAL MYOCLONUS, PHOTIC - INDUCED MYOCLONUS, AND EPILEPSY IN A LARGE PEDIGREE 187
The empowerment of translational research: lessons from laminopathies. 187
Axial myoclonus in paraproteinemic polyneuropathy. 187
The Effect of Curcumin on Idiopathic Parkinson Disease: A Clinical and Skin Biopsy Study 186
Anidrosi generalizzata: differenti sedi lesionali evidenziate attraverso la biopsia cutanea e la microneurografia. 186
Elevated plasma p-tau181 levels unrelated to Alzheimer's disease pathology in amyotrophic lateral sclerosis 185
Totale 23.637
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Categoria #
all - tutte 173.227
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 173.227
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20224.938 0 0 330 294 472 253 150 507 274 498 1.245 915
2022/20236.021 623 826 309 751 347 466 252 446 990 221 472 318
2023/20242.273 117 314 202 211 174 465 158 153 64 191 115 109
2024/20258.517 324 1.171 693 535 1.128 441 747 297 164 565 493 1.959
2025/202622.900 1.839 2.046 1.982 1.703 2.213 1.492 2.731 1.029 4.151 1.663 1.108 943
2026/20273.004 1.127 1.333 544 0 0 0 0 0 0 0 0 0
Totale 62.676