CRIS Current Research Information System

LIGUORI, ROCCO
 Distribuzione geografica
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Continente #
NA - Nord America 14.415
EU - Europa 9.764
AS - Asia 5.025
AF - Africa 572
SA - Sud America 32
OC - Oceania 29
Continente sconosciuto - Info sul continente non disponibili 21
Totale 29.858
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Nazione #
US - Stati Uniti d'America 14.368
GB - Regno Unito 2.660
IT - Italia 2.047
CN - Cina 1.651
DE - Germania 1.413
VN - Vietnam 1.341
SE - Svezia 1.175
SG - Singapore 1.021
IN - India 607
IE - Irlanda 446
UA - Ucraina 419
FR - Francia 407
RU - Federazione Russa 356
ZA - Sudafrica 198
EE - Estonia 195
TG - Togo 180
CI - Costa d'Avorio 142
BG - Bulgaria 119
CH - Svizzera 100
JO - Giordania 98
FI - Finlandia 82
AT - Austria 73
ID - Indonesia 66
NL - Olanda 54
BE - Belgio 47
CA - Canada 40
JP - Giappone 38
SC - Seychelles 36
GR - Grecia 31
PH - Filippine 30
HK - Hong Kong 29
PL - Polonia 28
AU - Australia 24
ES - Italia 24
IR - Iran 24
TR - Turchia 24
LB - Libano 20
UZ - Uzbekistan 20
RO - Romania 18
BR - Brasile 17
EU - Europa 16
PK - Pakistan 14
PT - Portogallo 13
DK - Danimarca 11
NG - Nigeria 11
CZ - Repubblica Ceca 10
KR - Corea 10
CL - Cile 8
HR - Croazia 7
IL - Israele 7
A2 - ???statistics.table.value.countryCode.A2??? 5
KZ - Kazakistan 5
LT - Lituania 5
NZ - Nuova Zelanda 5
TH - Thailandia 5
MK - Macedonia 4
KW - Kuwait 3
MX - Messico 3
TW - Taiwan 3
AL - Albania 2
AR - Argentina 2
CO - Colombia 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
HU - Ungheria 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 29.858
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Città #
Southend 2.393
Fairfield 2.017
Chandler 1.297
Ashburn 1.206
Woodbridge 895
Seattle 885
Houston 878
Singapore 851
Wilmington 823
Cambridge 680
Ann Arbor 669
Dong Ket 662
Princeton 618
Bologna 545
Dublin 444
Jacksonville 254
Westminster 241
Nanjing 232
Padova 201
Berlin 182
Lomé 180
Santa Clara 173
New York 159
Turin 154
Abidjan 142
Redmond 133
Saint Petersburg 127
Sofia 119
San Diego 118
Milan 117
Jinan 101
Amman 98
Shenyang 97
Beijing 92
Bern 82
Hebei 82
Changsha 78
Medford 73
Nanchang 69
Dearborn 64
Jakarta 63
Florence 60
Guangzhou 59
Helsinki 59
Redwood City 59
Tianjin 59
Rome 53
Falls Church 52
Los Angeles 52
Mülheim 49
Shanghai 47
Des Moines 45
Hangzhou 45
Vienna 45
Brussels 44
Norwalk 41
Zhengzhou 41
Olalla 36
Bremen 34
Jiaxing 34
Mahé 33
Frankfurt am Main 32
Paris 31
Taizhou 31
Braunschweig 29
London 29
Forlì 27
Verona 27
Ningbo 26
Washington 26
Boardman 25
Haikou 25
Phoenix 24
Bühl 23
Toronto 22
Lappeenranta 21
Pune 19
Tokyo 19
Kuban 18
Wuhan 18
Boydton 17
Fuzhou 17
Kunming 17
San Francisco 17
Hong Kong 16
Nijmegen 16
Chicago 15
Lanzhou 15
Modena 15
Warsaw 15
Ancona 14
Monzuno 14
Mountain View 14
Shenzhen 14
Taiyuan 14
Chengdu 13
Xi'an 13
Costa Mesa 12
Parma 12
Foshan 11
Totale 20.004
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Nome #
Hypnic jerks: neurophysiological characterization of a new motor pattern. 295
Altered globotriaosylceramide accumulation and mucosal neuronal fiber density in the colon of the Fabry disease mouse model 211
Cognitive rehabilitation and transcranial direct current stimulation in a patient with posterior cortical atrophy: An fMRI study 199
Anti-ganglioside antibodies in coeliac disease with neurological disorders. 197
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 196
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome 193
Mitochondrial dysfunction in myotonic dystrophy type 1 183
A case of fatal familial insomnia in Africa. 180
Autonomic innervation in multiple system atrophy and pure autonomic failure. 176
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 173
Defective Mitochondrial Adenosine Triphosphate Production in Skeletal Muscle From Patients With Dominant Optic Atrophy Due to OPA1 Mutations 163
Generalised anhidrosis: different lesion sites demonstrated by microneurography and skin biopsy. 162
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 161
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. 160
A 36-Year-Old Woman With Right Eye Ptosis 160
A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations. 158
Anhidrosis in multiple system atrophy: a preganglionic sudomotor dysfunction? 156
Agrypnia Excitata: a microneurographic study of muscle sympathetic nerve activity. 156
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 156
An inflammatory myopathy unmasks a case of leprosy in an Italian patient 155
Acute rhabdomyolysis induced by tonic-clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency. 155
Autonomic disturbances in narcolepsy. 153
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells. 151
Color choice preference in cognitively impaired patients: A look inside alzheimer’s disease through the use of lüscher color diagnostic 151
Biomarkers for REM sleep behavior disorder in idiopathic and narcoleptic patients 151
Antibodies against hypocretin receptor 2 are rare in narcolepsy 150
Absent cardiac and muscle sympathetic nerve activities involvement in Ross syndrome: A follow-up study 150
Increased expression of Trpv1 in peripheral terminals mediates thermal nociception in Fabry disease mouse model 148
Amyotrophic lateral sclerosis: a comparison of two staging systems in a population-based study 148
Accuracy of clinical diagnosis of dementia with Lewy bodies: a systematic review and meta-analysis 146
Autosomal dominant adult spinal muscular atrophy associated with alacrimia and achalasia. 145
Intermittent head drops: the differential spectrum 143
Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases 142
A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings 141
Intravenous immunoglobulin therapy in COVID-19-related encephalopathy 141
null 139
Cataplectic attacks during rapid eye movement sleep behavior disorder episodes in a narcoleptic patient. 138
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 138
Attività nervosa simpatica ed ipersonnia in pazienti con Sindrome delle Apnee Ostruttive nel Sonno. 137
A case report of IgG4-related disease: an insidious path to the diagnosis through kidney, heart and brain 137
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 135
Brachial amyotrophic diplegia associated with the a140a superoxide dismutase 1 mutation. 135
Axial myoclonus in paraproteinemic polyneuropathy. 135
Nocturnal Sleep Dynamics Identify Narcolepsy Type 1. 134
Added value of electromyography in the diagnosis of myopathy: A consensus exercise 134
A defective SERCA1 protein is responsible for congenital Pseudo-Myotonia in Chianina cattle 134
Brain & Skeletal Muscle MRS Study in Patients with Myotonic Dystrophy Type 1 133
The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance 133
Cerebrospinal fluid biomarkers in patients with frontotemporal dementia spectrum: A single-center study 133
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy. 132
Discinesia parossistica chinesigenica ed epilessia focale: descrizione di caso in età evolutiva 131
A prospective multicentre study on sural nerve action potentials in ALS. 131
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy. 131
Anidrosi generalizzata: differenti sedi lesionali evidenziate attraverso la biopsia cutanea e la microneurografia. 130
Cervical demyelinating lesion presenting with choreoathetoid movements and dystonia 130
Idebenone treatment in Leber's hereditary optic neuropathy. 130
AUTOSOMAL DOMINANT EARLY-ONSET CORTICAL MYOCLONUS, PHOTIC - INDUCED MYOCLONUS, AND EPILEPSY IN A LARGE PEDIGREE 129
Human figure drawing distinguishes Alzheimer’s patients: a cognitive screening test study 129
Preganglionic sudomotor nerve fiber lesion in a patient with Multiple System Atrophy and generalized anhidrosis. 128
Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy. 128
The Distinguishing Motor Features of Cataplexy: A Study from Video Recorded Attacks 128
Somatic and autonomic small fiber neuropathy induced by bortezomib therapy: an immunofluorescence study. 127
Habituation of sympathetic sudomotor and vasomotor skin responses: neural and non-neural components in healthy subjects. 126
Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing 126
Characterization of Human Dermal Fibroblasts in Fabry Disease 126
Continuous motor unit activity syndromes: A video-polysomnographic study. 125
Post-ganglionic autonomic neuropathy associated with anti-glutamic acid decarboxylase antibodies 125
Comparison of ice pack test and single-fiber EMG diagnostic accuracy in patients referred for myasthenic ptosis 125
Daytime sympathetic hyperactivity in OSAS is related to excessive daytime sleepiness. 124
Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene. 124
Paraneoplastic cerebellar degeneration and lambert-eaton myasthenia in a patient with merkel cell carcinoma and voltage-gated calcium channel antibodies 124
Skin globotriaosylceramide 3 deposits are specific to Fabry disease with classical mutations and associated with small fibre neuropathy. 124
Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases 124
Narcolepsy is a common phenotype in HSAN IE and ADCA-DN 123
Attività nervosa simpatico muscolare e pressione arteriosa in pazienti Tilt positivi e Tilt negativi con sincope vasovagale. 122
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy 121
The empowerment of translational research: lessons from laminopathies. 120
Attività nervosa simpatico muscolare in un paziente affetto da sindrome di Eaton-Lambert ed ipertensione arteriosa. 119
Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1 118
Skin biopsy and microneurography disclose selective noradrenergic dysfunction due to dopamine-β-hydroxylase deficiency 118
Isolated generalised anhidrosis induced by postganglionic sympathetic skin nerve fibre degeneration: an incomplete Ross syndrome? 117
Methods of sudomotor innervation quantification. 116
Arousal elicits exaggerated inhibition of sympathetic nerve activity in phobic syncope patients. 115
Axial myoclonus in devic neuromyelitis optica. 115
Pearls & Oy-sters: rapidly progressive dementia: prions or immunomediated? 115
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 115
Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes. 114
Pain Related Channels Are Differentially Expressed in Neuronal and Non-Neuronal Cells of Glabrous Skin of Fabry Knockout Male Mice 114
LOPED study: Looking for an early diagnosis in a late-onset Pompe disease high-risk population 114
Type 1 narcolepsy in anti-Hu antibodies mediated encephalitis: a case report 114
Abnormal α-synuclein deposits in skin nerves: intra- and inter-laboratory reproducibility 114
Cerebellar and brainstem functional abnormalities in patients with primary orthostatic tremor 114
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 113
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions 113
Neurophysiological correlates of abnormal somatosensory temporal discrimination in dystonia 112
Sympathetic and cardiovascular activity during cataplexy in narcolepsy. 111
Variation in the neurophysiological examination of amyotrophic lateral sclerosis in Europe. 111
Cutaneous sensory and autonomic denervation in CADASIL 111
Development of a disability scale for myotonic dystrophy type 1. 111
Diagnostic-prognostic value and electrophysiological correlates of CSF biomarkers of neurodegeneration and neuroinflammation in amyotrophic lateral sclerosis 111
Totale 13.868
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Categoria #
all - tutte 85.157
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 85.157
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20206.304 0 0 0 405 764 770 936 970 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
2024/20252.512 324 1.171 693 324 0 0 0 0 0 0 0 0
Totale 30.767