CRIS Current Research Information System

LIGUORI, ROCCO
 Distribuzione geografica
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Continente #
NA - Nord America 15.263
EU - Europa 9.943
AS - Asia 5.627
AF - Africa 574
SA - Sud America 34
OC - Oceania 30
Continente sconosciuto - Info sul continente non disponibili 21
Totale 31.492
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Nazione #
US - Stati Uniti d'America 15.213
GB - Regno Unito 2.666
IT - Italia 2.118
CN - Cina 1.817
SG - Singapore 1.432
DE - Germania 1.428
VN - Vietnam 1.341
SE - Svezia 1.175
IN - India 611
IE - Irlanda 449
UA - Ucraina 421
FR - Francia 408
RU - Federazione Russa 397
ZA - Sudafrica 200
EE - Estonia 195
TG - Togo 180
CI - Costa d'Avorio 142
BG - Bulgaria 119
CH - Svizzera 109
JO - Giordania 98
FI - Finlandia 93
AT - Austria 73
ID - Indonesia 67
NL - Olanda 62
BE - Belgio 53
CA - Canada 43
JP - Giappone 40
HK - Hong Kong 37
SC - Seychelles 36
GR - Grecia 31
PH - Filippine 30
PL - Polonia 29
ES - Italia 26
TR - Turchia 26
AU - Australia 25
IR - Iran 24
PK - Pakistan 21
LB - Libano 20
UZ - Uzbekistan 20
BR - Brasile 19
RO - Romania 18
EU - Europa 16
PT - Portogallo 13
DK - Danimarca 12
NG - Nigeria 11
CZ - Repubblica Ceca 10
KR - Corea 10
CL - Cile 8
HR - Croazia 7
IL - Israele 7
LT - Lituania 6
A2 - ???statistics.table.value.countryCode.A2??? 5
KZ - Kazakistan 5
NZ - Nuova Zelanda 5
TH - Thailandia 5
MK - Macedonia 4
TW - Taiwan 4
KW - Kuwait 3
MX - Messico 3
AL - Albania 2
AR - Argentina 2
CO - Colombia 2
HU - Ungheria 2
JM - Giamaica 2
LU - Lussemburgo 2
MC - Monaco 2
MT - Malta 2
NO - Norvegia 2
PA - Panama 2
QA - Qatar 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
SM - San Marino 2
TN - Tunisia 2
BN - Brunei Darussalam 1
EC - Ecuador 1
EG - Egitto 1
FK - Isole Falkland (Malvinas) 1
IM - Isola di Man 1
LK - Sri Lanka 1
LV - Lettonia 1
MA - Marocco 1
MD - Moldavia 1
MM - Myanmar 1
MN - Mongolia 1
MU - Mauritius 1
MY - Malesia 1
PE - Perù 1
RS - Serbia 1
SI - Slovenia 1
Totale 31.492
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Città #
Southend 2.393
Fairfield 2.017
Chandler 1.297
Singapore 1.246
Ashburn 1.221
Woodbridge 895
Seattle 885
Houston 878
Wilmington 823
Cambridge 680
Ann Arbor 669
Dong Ket 662
Princeton 618
Santa Clara 598
Bologna 558
Dublin 446
Boardman 388
Jacksonville 254
Westminster 241
Nanjing 234
Padova 201
Berlin 182
Lomé 180
New York 159
Turin 154
Abidjan 142
Redmond 133
Saint Petersburg 127
Milan 119
Sofia 119
San Diego 118
Jinan 102
Amman 98
Shenyang 98
Beijing 94
Bern 82
Hebei 82
Changsha 80
Medford 73
Nanchang 69
Helsinki 68
Guangzhou 67
Dearborn 64
Florence 63
Jakarta 63
Tianjin 61
Redwood City 59
Shanghai 58
Rome 56
Falls Church 52
Los Angeles 52
Mülheim 49
Brussels 47
Hangzhou 46
Des Moines 45
Vienna 45
Zhengzhou 43
Norwalk 41
Phoenix 37
Olalla 36
Jiaxing 35
Bremen 34
Mahé 33
Frankfurt am Main 32
Taizhou 32
London 31
Paris 31
Braunschweig 29
Forlì 27
Verona 27
Ningbo 26
Washington 26
Haikou 25
Hong Kong 24
Moscow 24
Bühl 23
Lappeenranta 23
Toronto 23
Wuhan 21
Modena 20
Tokyo 20
Pune 19
San Francisco 19
Fuzhou 18
Kuban 18
Kunming 18
Boydton 17
Lanzhou 16
Nijmegen 16
Shenzhen 16
Chicago 15
Falkenstein 15
Warsaw 15
Ancona 14
Monzuno 14
Mountain View 14
Taiyuan 14
Xi'an 14
Chengdu 13
Parma 13
Totale 21.331
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Nome #
Hypnic jerks: neurophysiological characterization of a new motor pattern. 333
Altered globotriaosylceramide accumulation and mucosal neuronal fiber density in the colon of the Fabry disease mouse model 217
Cognitive rehabilitation and transcranial direct current stimulation in a patient with posterior cortical atrophy: An fMRI study 207
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 201
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome 200
Anti-ganglioside antibodies in coeliac disease with neurological disorders. 198
Mitochondrial dysfunction in myotonic dystrophy type 1 191
A case of fatal familial insomnia in Africa. 188
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 181
Autonomic innervation in multiple system atrophy and pure autonomic failure. 178
Defective Mitochondrial Adenosine Triphosphate Production in Skeletal Muscle From Patients With Dominant Optic Atrophy Due to OPA1 Mutations 170
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. 168
Generalised anhidrosis: different lesion sites demonstrated by microneurography and skin biopsy. 164
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 164
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 164
A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations. 163
A 36-Year-Old Woman With Right Eye Ptosis 163
Anhidrosis in multiple system atrophy: a preganglionic sudomotor dysfunction? 161
Absent cardiac and muscle sympathetic nerve activities involvement in Ross syndrome: A follow-up study 159
An inflammatory myopathy unmasks a case of leprosy in an Italian patient 159
Agrypnia Excitata: a microneurographic study of muscle sympathetic nerve activity. 158
Acute rhabdomyolysis induced by tonic-clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency. 158
Color choice preference in cognitively impaired patients: A look inside alzheimer’s disease through the use of lüscher color diagnostic 157
Autonomic disturbances in narcolepsy. 155
Intermittent head drops: the differential spectrum 154
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells. 154
Biomarkers for REM sleep behavior disorder in idiopathic and narcoleptic patients 154
Increased expression of Trpv1 in peripheral terminals mediates thermal nociception in Fabry disease mouse model 153
Antibodies against hypocretin receptor 2 are rare in narcolepsy 152
Amyotrophic lateral sclerosis: a comparison of two staging systems in a population-based study 151
Autosomal dominant adult spinal muscular atrophy associated with alacrimia and achalasia. 150
Accuracy of clinical diagnosis of dementia with Lewy bodies: a systematic review and meta-analysis 147
Intravenous immunoglobulin therapy in COVID-19-related encephalopathy 146
Attività nervosa simpatica ed ipersonnia in pazienti con Sindrome delle Apnee Ostruttive nel Sonno. 145
A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings 145
Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases 145
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 144
Axial myoclonus in paraproteinemic polyneuropathy. 142
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 141
Cataplectic attacks during rapid eye movement sleep behavior disorder episodes in a narcoleptic patient. 140
Nocturnal Sleep Dynamics Identify Narcolepsy Type 1. 139
null 139
Cerebrospinal fluid biomarkers in patients with frontotemporal dementia spectrum: A single-center study 139
A case report of IgG4-related disease: an insidious path to the diagnosis through kidney, heart and brain 139
Human figure drawing distinguishes Alzheimer’s patients: a cognitive screening test study 139
Brachial amyotrophic diplegia associated with the a140a superoxide dismutase 1 mutation. 138
Cervical demyelinating lesion presenting with choreoathetoid movements and dystonia 138
The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance 138
Discinesia parossistica chinesigenica ed epilessia focale: descrizione di caso in età evolutiva 137
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy. 137
Brain & Skeletal Muscle MRS Study in Patients with Myotonic Dystrophy Type 1 137
Added value of electromyography in the diagnosis of myopathy: A consensus exercise 137
A defective SERCA1 protein is responsible for congenital Pseudo-Myotonia in Chianina cattle 137
Anidrosi generalizzata: differenti sedi lesionali evidenziate attraverso la biopsia cutanea e la microneurografia. 136
AUTOSOMAL DOMINANT EARLY-ONSET CORTICAL MYOCLONUS, PHOTIC - INDUCED MYOCLONUS, AND EPILEPSY IN A LARGE PEDIGREE 134
Idebenone treatment in Leber's hereditary optic neuropathy. 134
A prospective multicentre study on sural nerve action potentials in ALS. 133
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy. 133
Preganglionic sudomotor nerve fiber lesion in a patient with Multiple System Atrophy and generalized anhidrosis. 132
Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy. 132
The Distinguishing Motor Features of Cataplexy: A Study from Video Recorded Attacks 132
Somatic and autonomic small fiber neuropathy induced by bortezomib therapy: an immunofluorescence study. 131
Post-ganglionic autonomic neuropathy associated with anti-glutamic acid decarboxylase antibodies 131
Habituation of sympathetic sudomotor and vasomotor skin responses: neural and non-neural components in healthy subjects. 130
Paraneoplastic cerebellar degeneration and lambert-eaton myasthenia in a patient with merkel cell carcinoma and voltage-gated calcium channel antibodies 129
Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing 129
Characterization of Human Dermal Fibroblasts in Fabry Disease 129
Skin globotriaosylceramide 3 deposits are specific to Fabry disease with classical mutations and associated with small fibre neuropathy. 129
Comparison of ice pack test and single-fiber EMG diagnostic accuracy in patients referred for myasthenic ptosis 129
Continuous motor unit activity syndromes: A video-polysomnographic study. 127
Daytime sympathetic hyperactivity in OSAS is related to excessive daytime sleepiness. 126
Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene. 126
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy 126
Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases 126
Skin biopsy and microneurography disclose selective noradrenergic dysfunction due to dopamine-β-hydroxylase deficiency 125
Narcolepsy is a common phenotype in HSAN IE and ADCA-DN 125
Attività nervosa simpatico muscolare e pressione arteriosa in pazienti Tilt positivi e Tilt negativi con sincope vasovagale. 124
Isolated generalised anhidrosis induced by postganglionic sympathetic skin nerve fibre degeneration: an incomplete Ross syndrome? 124
Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1 124
The empowerment of translational research: lessons from laminopathies. 123
Attività nervosa simpatico muscolare in un paziente affetto da sindrome di Eaton-Lambert ed ipertensione arteriosa. 122
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 121
Neurophysiological correlates of abnormal somatosensory temporal discrimination in dystonia 121
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 120
Axial myoclonus in devic neuromyelitis optica. 119
Pain Related Channels Are Differentially Expressed in Neuronal and Non-Neuronal Cells of Glabrous Skin of Fabry Knockout Male Mice 119
Pearls & Oy-sters: rapidly progressive dementia: prions or immunomediated? 119
Methods of sudomotor innervation quantification. 118
Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes. 118
LOPED study: Looking for an early diagnosis in a late-onset Pompe disease high-risk population 118
Cerebellar and brainstem functional abnormalities in patients with primary orthostatic tremor 118
Arousal elicits exaggerated inhibition of sympathetic nerve activity in phobic syncope patients. 117
High frequency somatosensory stimulation increases sensori-motor inhibition and leads to perceptual improvement in healthy subjects 117
Type 1 narcolepsy in anti-Hu antibodies mediated encephalitis: a case report 117
Sympathetic and cardiovascular activity during cataplexy in narcolepsy. 116
A further Rasch study confirms that ALSFRS-R does not conform to fundamental measurement requirements 116
Development of a disability scale for myotonic dystrophy type 1. 116
From state dissociation to status dissociatus 116
Abnormal α-synuclein deposits in skin nerves: intra- and inter-laboratory reproducibility 116
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation 116
Totale 14.353
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Categoria #
all - tutte 91.301
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 91.301
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20205.135 0 0 0 0 0 770 936 970 1.243 479 392 345
2020/20214.567 838 289 107 202 197 206 162 269 346 277 187 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
2024/20254.150 324 1.171 693 535 1.128 299 0 0 0 0 0 0
Totale 32.405