CRIS Current Research Information System

LIGUORI, ROCCO
 Distribuzione geografica
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Continente #
NA - Nord America 20.385
AS - Asia 19.535
EU - Europa 14.028
SA - Sud America 1.053
AF - Africa 1.050
OC - Oceania 46
Continente sconosciuto - Info sul continente non disponibili 25
Totale 56.122
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Nazione #
US - Stati Uniti d'America 20.121
SG - Singapore 5.272
VN - Vietnam 5.092
CN - Cina 4.890
IT - Italia 3.143
GB - Regno Unito 2.813
DE - Germania 2.146
HK - Hong Kong 1.480
SE - Svezia 1.199
FR - Francia 932
IN - India 885
NL - Olanda 763
BR - Brasile 747
RU - Federazione Russa 682
KR - Corea 519
IE - Irlanda 485
UA - Ucraina 443
CI - Costa d'Avorio 373
JP - Giappone 336
FI - Finlandia 312
ZA - Sudafrica 295
EE - Estonia 196
TG - Togo 180
AT - Austria 168
CA - Canada 141
ID - Indonesia 137
PH - Filippine 124
AR - Argentina 121
CH - Svizzera 120
BG - Bulgaria 119
JO - Giordania 115
PL - Polonia 93
BD - Bangladesh 91
TR - Turchia 84
ES - Italia 83
MX - Messico 82
BE - Belgio 80
SC - Seychelles 77
IQ - Iraq 76
TH - Thailandia 76
PK - Pakistan 64
EC - Ecuador 50
TW - Taiwan 48
GR - Grecia 41
UZ - Uzbekistan 41
AU - Australia 38
SA - Arabia Saudita 35
LT - Lituania 34
CL - Cile 31
CO - Colombia 30
IR - Iran 30
LB - Libano 29
RO - Romania 25
MA - Marocco 23
MY - Malesia 21
PY - Paraguay 20
VE - Venezuela 20
PT - Portogallo 19
PE - Perù 18
DK - Danimarca 17
HR - Croazia 17
EU - Europa 16
KE - Kenya 16
NG - Nigeria 16
BY - Bielorussia 14
EG - Egitto 13
IL - Israele 13
AL - Albania 11
ET - Etiopia 11
KZ - Kazakistan 11
SK - Slovacchia (Repubblica Slovacca) 11
TN - Tunisia 11
AZ - Azerbaigian 10
CZ - Repubblica Ceca 10
DZ - Algeria 10
AE - Emirati Arabi Uniti 9
DO - Repubblica Dominicana 9
JM - Giamaica 7
NZ - Nuova Zelanda 7
PS - Palestinian Territory 7
UY - Uruguay 7
MK - Macedonia 6
NP - Nepal 6
OM - Oman 6
SM - San Marino 6
SN - Senegal 6
A2 - ???statistics.table.value.countryCode.A2??? 5
CR - Costa Rica 5
HU - Ungheria 5
LV - Lettonia 5
MT - Malta 5
QA - Qatar 5
RS - Serbia 5
BO - Bolivia 4
GE - Georgia 4
KW - Kuwait 4
NO - Norvegia 4
PA - Panama 4
AO - Angola 3
BA - Bosnia-Erzegovina 3
Totale 56.052
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Città #
Singapore 3.541
Southend 2.393
Ashburn 2.185
Fairfield 2.017
Hong Kong 1.381
Chandler 1.297
Hefei 1.115
Ho Chi Minh City 1.090
San Jose 1.053
Hanoi 904
Seattle 904
Woodbridge 895
Houston 889
Bologna 857
Wilmington 826
Cambridge 715
Ann Arbor 669
Santa Clara 665
Dong Ket 662
Princeton 618
Beijing 558
Dublin 481
Frankfurt am Main 466
Seoul 466
Boardman 401
Los Angeles 395
Abidjan 373
Lauterbourg 351
Eygelshoven 338
Dallas 287
Tokyo 274
New York 261
Jacksonville 256
Council Bluffs 244
Nanjing 243
Westminster 241
Helsinki 217
Milan 214
Padova 202
Berlin 187
Lomé 180
Turin 164
Buffalo 157
Munich 152
Haiphong 149
Da Nang 148
Redmond 133
Saint Petersburg 127
Redondo Beach 125
Rome 121
San Diego 121
Sofia 119
Bengaluru 117
Amman 113
Guangzhou 107
Jinan 107
São Paulo 107
Shenyang 103
Vienna 101
Shanghai 97
Changsha 93
Bern 82
Hebei 82
Tianjin 78
Florence 77
Jakarta 73
Medford 73
Nanchang 72
Brussels 71
Chicago 70
London 70
Johannesburg 68
Phoenix 66
Dearborn 64
Warsaw 64
Nuremberg 62
Des Moines 60
Redwood City 59
Hangzhou 58
Paris 58
Amsterdam 55
Hải Dương 53
Zhengzhou 53
Falls Church 52
Falkenstein 51
Lappeenranta 51
Mülheim 49
Biên Hòa 48
Piscataway 48
Yubileyny 48
Atlanta 46
Montreal 46
Can Tho 44
Orem 44
Tongling 44
Toronto 43
Modena 41
Norwalk 41
San Francisco 40
Newark 39
Totale 36.015
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Nome #
A new potential biomarker for dementia with Lewy bodies 910
Hypnic jerks: neurophysiological characterization of a new motor pattern. 488
Comparative assessment of MScanFit MUNE and quantitative EMG in amyotrophic lateral sclerosis diagnosis: A prospective study 404
Skin biopsy and microneurography disclose selective noradrenergic dysfunction due to dopamine-β-hydroxylase deficiency 313
Altered globotriaosylceramide accumulation and mucosal neuronal fiber density in the colon of the Fabry disease mouse model 276
Autonomic innervation in multiple system atrophy and pure autonomic failure. 272
Mitochondrial dysfunction in myotonic dystrophy type 1 270
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome 267
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis 264
Cognitive rehabilitation and transcranial direct current stimulation in a patient with posterior cortical atrophy: An fMRI study 262
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 262
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 261
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 246
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome b (MT-CYB) Gene 244
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 242
Defective Mitochondrial Adenosine Triphosphate Production in Skeletal Muscle From Patients With Dominant Optic Atrophy Due to OPA1 Mutations 241
Anti-ganglioside antibodies in coeliac disease with neurological disorders. 239
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. 238
A case of fatal familial insomnia in Africa. 237
Small fiber neuropathy in female patients with fabry disease. 237
A further Rasch study confirms that ALSFRS-R does not conform to fundamental measurement requirements 230
Volumetric absorptive microsampling coupled with UHPLC-MS/MS for the determination of Lyso-Gb3 as Fabry disease diagnostic biomarker 228
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 228
Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases 223
Biomarkers for REM sleep behavior disorder in idiopathic and narcoleptic patients 222
Intravenous immunoglobulin therapy in COVID-19-related encephalopathy 222
Diagnostic-prognostic value and electrophysiological correlates of CSF biomarkers of neurodegeneration and neuroinflammation in amyotrophic lateral sclerosis 221
Generalised anhidrosis: different lesion sites demonstrated by microneurography and skin biopsy. 217
A 36-Year-Old Woman With Right Eye Ptosis 217
Color choice preference in cognitively impaired patients: A look inside alzheimer’s disease through the use of lüscher color diagnostic 216
Case Report: Optic Atrophy and Nephropathy With m.13513G>A/MT-ND5 mtDNA Pathogenic Variant 215
Increased expression of Trpv1 in peripheral terminals mediates thermal nociception in Fabry disease mouse model 213
Amyotrophic lateral sclerosis: a comparison of two staging systems in a population-based study 213
Skin globotriaosylceramide 3 deposits are specific to Fabry disease with classical mutations and associated with small fibre neuropathy. 213
Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern? 209
A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations. 208
A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings 208
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells. 207
A case report of IgG4-related disease: an insidious path to the diagnosis through kidney, heart and brain 206
Anhidrosis in multiple system atrophy: a preganglionic sudomotor dysfunction? 205
In Vivo Parieto-Occipital White Matter Metabolism Is Correlated with Visuospatial Deficits in Adult DM1 Patients 204
Intermittent head drops: the differential spectrum 204
Difference in safety and humoral response to mRNA SARS-CoV-2 vaccines in patients with autoimmune neurological disorders: the ANCOVAX study 202
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 202
Brain & Skeletal Muscle MRS Study in Patients with Myotonic Dystrophy Type 1 201
Antibodies against hypocretin receptor 2 are rare in narcolepsy 201
Human figure drawing distinguishes Alzheimer’s patients: a cognitive screening test study 199
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 198
Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases 198
Autosomal dominant adult spinal muscular atrophy associated with alacrimia and achalasia. 196
Cervical demyelinating lesion presenting with choreoathetoid movements and dystonia 196
Absent cardiac and muscle sympathetic nerve activities involvement in Ross syndrome: A follow-up study 196
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation 196
Attività nervosa simpatica ed ipersonnia in pazienti con Sindrome delle Apnee Ostruttive nel Sonno. 194
An inflammatory myopathy unmasks a case of leprosy in an Italian patient 194
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 194
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations 194
Paroxysmal kinesigenic dyskinesia and focal epilepsy in childhood: A case report 194
Acute rhabdomyolysis induced by tonic-clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency. 193
Disruption of the microbiota-gut-brain axis is a defining characteristic of the α-Gal A (-/0) mouse model of Fabry disease 192
Nocturnal Sleep Dynamics Identify Narcolepsy Type 1. 192
Brachial amyotrophic diplegia associated with the a140a superoxide dismutase 1 mutation. 192
Cataplectic attacks during rapid eye movement sleep behavior disorder episodes in a narcoleptic patient. 192
Comparison of ice pack test and single-fiber EMG diagnostic accuracy in patients referred for myasthenic ptosis 192
A comparative blind study between skin biopsy and seed amplification assay to disclose pathological α-synuclein in RBD 191
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) 189
Somatic and autonomic small fiber neuropathy induced by bortezomib therapy: an immunofluorescence study. 189
Autonomic disturbances in narcolepsy. 188
Idebenone treatment in Leber's hereditary optic neuropathy. 188
Neurophysiological correlates of abnormal somatosensory temporal discrimination in dystonia 188
Neurological Manifestations of Long {COVID}: A Single-Center One-Year Experience 187
Cerebrospinal fluid biomarkers in patients with frontotemporal dementia spectrum: A single-center study 186
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 186
Discinesia parossistica chinesigenica ed epilessia focale: descrizione di caso in età evolutiva 185
The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance 185
Added value of electromyography in the diagnosis of myopathy: A consensus exercise 184
Agrypnia Excitata: a microneurographic study of muscle sympathetic nerve activity. 184
Characterization of Human Dermal Fibroblasts in Fabry Disease 184
The Distinguishing Motor Features of Cataplexy: A Study from Video Recorded Attacks 184
Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy. 182
Correlations Between Cardiac Magnetic Resonance and Myocardial Histologic Findings in Fabry Disease 181
Conformational Antibodies to Proteolipid Protein-1 and Its Peripheral Isoform DM20 in Patients With CNS Autoimmune Demyelinating Disorders 181
Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing 181
Epilepsy in MT-ATP6 - related mils/NARP: correlation of elettroclinical features with heteroplasmy 181
Blood neurofilament light chain and S100B as biomarkers of neurological involvement and functional prognosis in COVID-19: a multicenter study 179
Elevated plasma p-tau181 levels unrelated to Alzheimer's disease pathology in amyotrophic lateral sclerosis 179
AUTOSOMAL DOMINANT EARLY-ONSET CORTICAL MYOCLONUS, PHOTIC - INDUCED MYOCLONUS, AND EPILEPSY IN A LARGE PEDIGREE 179
The Effect of Curcumin on Idiopathic Parkinson Disease: A Clinical and Skin Biopsy Study 178
Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1 178
Axial myoclonus in paraproteinemic polyneuropathy. 178
Type 1 narcolepsy in anti-Hu antibodies mediated encephalitis: a case report 178
Multimodal investigation of melanopsin retinal ganglion cells in Alzheimer's disease 177
Habituation of sympathetic sudomotor and vasomotor skin responses: neural and non-neural components in healthy subjects. 177
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. 177
Fabry Disease Nephropathy: Histological Changes With Nonclassical Mutations and Genetic Variants of Unknown Significance 176
Preganglionic sudomotor nerve fiber lesion in a patient with Multiple System Atrophy and generalized anhidrosis. 176
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. 176
Anidrosi generalizzata: differenti sedi lesionali evidenziate attraverso la biopsia cutanea e la microneurografia. 176
Sulcal Morphometry Predicts Mild Cognitive Impairment Conversion to Alzheimer’s Disease 175
The empowerment of translational research: lessons from laminopathies. 175
Totale 21.748
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Categoria #
all - tutte 151.686
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 151.686
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.951 0 0 0 0 0 0 0 0 0 277 187 1.487
2021/20225.630 512 180 330 294 472 253 150 507 274 498 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
2025/202620.552 1.839 2.046 1.982 1.703 2.213 1.492 2.731 1.030 4.163 1.353 0 0
Totale 57.324