CRIS Current Research Information System

LIGUORI, ROCCO
 Distribuzione geografica
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Continente #
NA - Nord America 17.831
AS - Asia 14.503
EU - Europa 12.567
AF - Africa 941
SA - Sud America 900
OC - Oceania 43
Continente sconosciuto - Info sul continente non disponibili 24
Totale 46.809
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Nazione #
US - Stati Uniti d'America 17.633
SG - Singapore 4.588
CN - Cina 4.135
IT - Italia 2.829
GB - Regno Unito 2.762
VN - Vietnam 2.536
DE - Germania 2.082
HK - Hong Kong 1.264
SE - Svezia 1.197
IN - India 779
RU - Federazione Russa 670
BR - Brasile 654
FR - Francia 537
KR - Corea 476
IE - Irlanda 466
UA - Ucraina 434
NL - Olanda 383
CI - Costa d'Avorio 373
ZA - Sudafrica 244
FI - Finlandia 226
EE - Estonia 196
JP - Giappone 193
TG - Togo 180
AT - Austria 159
BG - Bulgaria 119
ID - Indonesia 118
CH - Svizzera 114
CA - Canada 112
AR - Argentina 108
JO - Giordania 104
PL - Polonia 78
SC - Seychelles 77
BE - Belgio 70
MX - Messico 61
ES - Italia 58
TR - Turchia 47
EC - Ecuador 42
GR - Grecia 37
AU - Australia 35
PK - Pakistan 35
PH - Filippine 34
BD - Bangladesh 32
IR - Iran 30
LT - Lituania 27
UZ - Uzbekistan 26
LB - Libano 24
CL - Cile 20
CO - Colombia 20
RO - Romania 20
EU - Europa 16
PY - Paraguay 16
PE - Perù 15
PT - Portogallo 15
NG - Nigeria 14
HR - Croazia 13
VE - Venezuela 13
BY - Bielorussia 12
DK - Danimarca 12
IL - Israele 12
IQ - Iraq 11
MA - Marocco 11
CZ - Repubblica Ceca 10
KE - Kenya 9
KZ - Kazakistan 9
SA - Arabia Saudita 9
DO - Repubblica Dominicana 8
MY - Malesia 7
NZ - Nuova Zelanda 7
TN - Tunisia 7
MK - Macedonia 6
SM - San Marino 6
TW - Taiwan 6
UY - Uruguay 6
A2 - ???statistics.table.value.countryCode.A2??? 5
DZ - Algeria 5
SK - Slovacchia (Repubblica Slovacca) 5
SN - Senegal 5
TH - Thailandia 5
AE - Emirati Arabi Uniti 4
AL - Albania 4
EG - Egitto 4
PA - Panama 4
GF - Guiana Francese 3
KW - Kuwait 3
LU - Lussemburgo 3
NO - Norvegia 3
QA - Qatar 3
BA - Bosnia-Erzegovina 2
CR - Costa Rica 2
GT - Guatemala 2
HU - Ungheria 2
JM - Giamaica 2
KG - Kirghizistan 2
LK - Sri Lanka 2
MC - Monaco 2
MT - Malta 2
PR - Porto Rico 2
PS - Palestinian Territory 2
TT - Trinidad e Tobago 2
XK - ???statistics.table.value.countryCode.XK??? 2
Totale 46.776
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Città #
Singapore 2.943
Southend 2.393
Fairfield 2.017
Ashburn 2.005
Chandler 1.297
Hong Kong 1.245
Hefei 1.105
Seattle 904
Woodbridge 895
Houston 886
Wilmington 826
Bologna 767
Cambridge 680
Ann Arbor 669
Dong Ket 662
Santa Clara 632
Princeton 618
Beijing 543
Seoul 464
Dublin 462
Frankfurt am Main 423
Boardman 396
Ho Chi Minh City 391
Abidjan 373
Hanoi 320
Dallas 273
Los Angeles 273
Jacksonville 254
Westminster 241
Nanjing 234
New York 223
Padova 202
Milan 200
Berlin 187
Lomé 180
Tokyo 164
Turin 161
Munich 152
Buffalo 146
Helsinki 141
Redmond 133
Saint Petersburg 127
Redondo Beach 125
San Diego 119
Sofia 119
Bengaluru 115
Amman 104
Jinan 103
Shenyang 103
Rome 102
Vienna 94
Changsha 87
São Paulo 85
Bern 82
Hebei 82
Florence 77
Guangzhou 74
Medford 73
Jakarta 71
Nanchang 71
Tianjin 68
Shanghai 67
Dearborn 64
Brussels 62
London 60
Redwood City 59
Nuremberg 58
Phoenix 58
Chicago 54
Falls Church 52
Warsaw 52
Mülheim 49
Yubileyny 48
Zhengzhou 48
Des Moines 47
Hangzhou 46
Haiphong 44
Falkenstein 43
Tongling 43
Lappeenranta 42
Norwalk 41
Paris 41
Toronto 39
Amsterdam 38
Da Nang 38
Olalla 36
Verona 36
Jiaxing 35
Bremen 34
Turku 34
Mahé 33
Parma 33
San Francisco 33
Taizhou 33
Atlanta 32
Forlì 31
Montreal 31
Moscow 31
Boston 30
Chennai 30
Totale 30.646
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Nome #
A new potential biomarker for dementia with Lewy bodies 528
Hypnic jerks: neurophysiological characterization of a new motor pattern. 436
Skin biopsy and microneurography disclose selective noradrenergic dysfunction due to dopamine-β-hydroxylase deficiency 289
Altered globotriaosylceramide accumulation and mucosal neuronal fiber density in the colon of the Fabry disease mouse model 254
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis 249
Mitochondrial dysfunction in myotonic dystrophy type 1 241
Cognitive rehabilitation and transcranial direct current stimulation in a patient with posterior cortical atrophy: An fMRI study 237
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome 236
Anti-ganglioside antibodies in coeliac disease with neurological disorders. 231
Autonomic innervation in multiple system atrophy and pure autonomic failure. 227
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 227
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 224
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 223
A case of fatal familial insomnia in Africa. 220
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 214
Defective Mitochondrial Adenosine Triphosphate Production in Skeletal Muscle From Patients With Dominant Optic Atrophy Due to OPA1 Mutations 207
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome b (MT-CYB) Gene 204
Generalised anhidrosis: different lesion sites demonstrated by microneurography and skin biopsy. 202
Intermittent head drops: the differential spectrum 201
A further Rasch study confirms that ALSFRS-R does not conform to fundamental measurement requirements 199
Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases 197
Intravenous immunoglobulin therapy in COVID-19-related encephalopathy 197
Anhidrosis in multiple system atrophy: a preganglionic sudomotor dysfunction? 194
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. 193
Amyotrophic lateral sclerosis: a comparison of two staging systems in a population-based study 193
Biomarkers for REM sleep behavior disorder in idiopathic and narcoleptic patients 193
A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations. 190
Paroxysmal kinesigenic dyskinesia and focal epilepsy in childhood: A case report 189
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 188
Skin globotriaosylceramide 3 deposits are specific to Fabry disease with classical mutations and associated with small fibre neuropathy. 188
A 36-Year-Old Woman With Right Eye Ptosis 188
Nocturnal Sleep Dynamics Identify Narcolepsy Type 1. 187
Volumetric absorptive microsampling coupled with UHPLC-MS/MS for the determination of Lyso-Gb3 as Fabry disease diagnostic biomarker 186
Increased expression of Trpv1 in peripheral terminals mediates thermal nociception in Fabry disease mouse model 186
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells. 185
Color choice preference in cognitively impaired patients: A look inside alzheimer’s disease through the use of lüscher color diagnostic 184
Case Report: Optic Atrophy and Nephropathy With m.13513G>A/MT-ND5 mtDNA Pathogenic Variant 182
Antibodies against hypocretin receptor 2 are rare in narcolepsy 182
Absent cardiac and muscle sympathetic nerve activities involvement in Ross syndrome: A follow-up study 181
A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings 180
Autonomic disturbances in narcolepsy. 180
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 179
An inflammatory myopathy unmasks a case of leprosy in an Italian patient 179
A comparative blind study between skin biopsy and seed amplification assay to disclose pathological α-synuclein in RBD 178
Autosomal dominant adult spinal muscular atrophy associated with alacrimia and achalasia. 178
In Vivo Parieto-Occipital White Matter Metabolism Is Correlated with Visuospatial Deficits in Adult DM1 Patients 177
Brachial amyotrophic diplegia associated with the a140a superoxide dismutase 1 mutation. 177
Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases 174
Attività nervosa simpatica ed ipersonnia in pazienti con Sindrome delle Apnee Ostruttive nel Sonno. 173
Cervical demyelinating lesion presenting with choreoathetoid movements and dystonia 173
Agrypnia Excitata: a microneurographic study of muscle sympathetic nerve activity. 172
Idebenone treatment in Leber's hereditary optic neuropathy. 172
Acute rhabdomyolysis induced by tonic-clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency. 172
Somatic and autonomic small fiber neuropathy induced by bortezomib therapy: an immunofluorescence study. 171
Brain & Skeletal Muscle MRS Study in Patients with Myotonic Dystrophy Type 1 169
Cataplectic attacks during rapid eye movement sleep behavior disorder episodes in a narcoleptic patient. 169
Cerebrospinal fluid biomarkers in patients with frontotemporal dementia spectrum: A single-center study 169
Small fiber neuropathy in female patients with fabry disease. 169
A case report of IgG4-related disease: an insidious path to the diagnosis through kidney, heart and brain 168
Human figure drawing distinguishes Alzheimer’s patients: a cognitive screening test study 168
Disruption of the microbiota-gut-brain axis is a defining characteristic of the α-Gal A (-/0) mouse model of Fabry disease 167
Habituation of sympathetic sudomotor and vasomotor skin responses: neural and non-neural components in healthy subjects. 167
Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy. 167
The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance 167
AUTOSOMAL DOMINANT EARLY-ONSET CORTICAL MYOCLONUS, PHOTIC - INDUCED MYOCLONUS, AND EPILEPSY IN A LARGE PEDIGREE 166
Added value of electromyography in the diagnosis of myopathy: A consensus exercise 166
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 166
Discinesia parossistica chinesigenica ed epilessia focale: descrizione di caso in età evolutiva 165
Comparison of ice pack test and single-fiber EMG diagnostic accuracy in patients referred for myasthenic ptosis 165
Preganglionic sudomotor nerve fiber lesion in a patient with Multiple System Atrophy and generalized anhidrosis. 164
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation 164
Methods of sudomotor innervation quantification. 162
Axial myoclonus in paraproteinemic polyneuropathy. 162
Accuracy of clinical diagnosis of dementia with Lewy bodies: a systematic review and meta-analysis 162
Diagnostic-prognostic value and electrophysiological correlates of CSF biomarkers of neurodegeneration and neuroinflammation in amyotrophic lateral sclerosis 162
Characterization of Human Dermal Fibroblasts in Fabry Disease 161
Neurological Manifestations of Long {COVID}: A Single-Center One-Year Experience 160
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. 160
Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing 160
Anidrosi generalizzata: differenti sedi lesionali evidenziate attraverso la biopsia cutanea e la microneurografia. 159
A defective SERCA1 protein is responsible for congenital Pseudo-Myotonia in Chianina cattle 158
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 158
Continuous motor unit activity syndromes: A video-polysomnographic study. 157
Daytime sympathetic hyperactivity in OSAS is related to excessive daytime sleepiness. 156
Post-ganglionic autonomic neuropathy associated with anti-glutamic acid decarboxylase antibodies 156
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations 156
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy. 155
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 155
A prospective multicentre study on sural nerve action potentials in ALS. 154
The empowerment of translational research: lessons from laminopathies. 154
Type 1 narcolepsy in anti-Hu antibodies mediated encephalitis: a case report 154
Neurophysiological correlates of abnormal somatosensory temporal discrimination in dystonia 154
Correlations Between Cardiac Magnetic Resonance and Myocardial Histologic Findings in Fabry Disease 153
Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1 153
The Distinguishing Motor Features of Cataplexy: A Study from Video Recorded Attacks 153
Fabry Disease Nephropathy: Histological Changes With Nonclassical Mutations and Genetic Variants of Unknown Significance 152
Difference in safety and humoral response to mRNA SARS-CoV-2 vaccines in patients with autoimmune neurological disorders: the ANCOVAX study 152
Age at onset and symptom spread in primary adult-onset blepharospasm and cervical dystonia. 152
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. 152
Attività nervosa simpatico muscolare in un paziente affetto da sindrome di Eaton-Lambert ed ipertensione arteriosa. 151
Totale 18.636
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Categoria #
all - tutte 137.401
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 137.401
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.934 0 0 0 0 0 206 162 269 346 277 187 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
2025/202611.102 1.839 2.046 1.982 1.703 2.213 1.319 0 0 0 0 0 0
Totale 47.874