statistiche ricercatore

statistiche per LIGUORI, ROCCO

Distribuzione geografica
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Continente #
NA - Nord America 6487
EU - Europa 3858
AS - Asia 988
Continente sconosciuto - Info sul continente non disponibili 15
AF - Africa 3
OC - Oceania 1
SA - Sud America 1
Totale 11353
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Nazione #
US - Stati Uniti d'America 6483
GB - Regno Unito 1746
CN - Cina 955
IT - Italia 654
UA - Ucraina 350
FR - Francia 332
DE - Germania 306
RU - Federazione Russa 225
EE - Estonia 194
LB - Libano 16
EU - Europa 15
GR - Grecia 13
BG - Bulgaria 10
JP - Giappone 7
SE - Svezia 6
CA - Canada 4
CH - Svizzera 4
IN - India 4
NL - Olanda 3
SC - Seychelles 3
BE - Belgio 2
ES - Italia 2
IR - Iran 2
MC - Monaco 2
MK - Macedonia 2
PT - Portogallo 2
AU - Australia 1
BR - Brasile 1
HR - Croazia 1
IL - Israele 1
KR - Corea 1
LU - Lussemburgo 1
PL - Polonia 1
RO - Romania 1
SI - Slovenia 1
TW - Taiwan 1
VN - Vietnam 1
Totale 11353
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Città #
Southend 1588
Fairfield 1435
Woodbridge 729
Seattle 716
Houston 697
Ashburn 662
Wilmington 544
Cambridge 530
Ann Arbor 363
Westminster 241
Nanjing 216
Bologna 195
Padova 192
Jacksonville 170
Saint Petersburg 108
Shenyang 87
Hebei 76
Jinan 72
Nanchang 68
Changsha 66
Dearborn 64
Redmond 58
Beijing 54
Redwood City 53
Milan 41
Tianjin 41
Hangzhou 33
Jiaxing 31
Zhengzhou 23
Haikou 22
Ningbo 20
Phoenix 20
Guangzhou 18
Taizhou 17
Kunming 16
Lanzhou 15
Verona 14
Costa Mesa 12
Hefei 10
Sofia 10
Fuzhou 9
Taiyuan 9
Frankfurt Am Main 8
Tokyo 7
Wuhan 7
Shanghai 6
Wayne 6
Forlì 5
Garbagnate Milanese 5
Munich 5
San Venanzo 5
Faenza 4
Ferrara 4
Parma 4
Rome 4
San Jose 4
Centro 3
Chongqing 3
Lausanne 3
Mumbai 3
North Bergen 3
Orange 3
Plauen 3
Radcliffe 3
Alicante 2
Atlanta 2
Benevento 2
Brooklyn 2
Buffalo Grove 2
Chengdu 2
Cittadella 2
Foggia 2
Gosselies 2
Huzhou 2
Kiev 2
Macon 2
Modena 2
Montréal 2
Muenster 2
New York 2
Portici 2
Reggio Nell'emilia 2
Shenzhen 2
Skopje 2
Torino 2
Waltham 2
Xian 2
Yekaterinburg 2
Amiens 1
Aversa 1
Belo Horizonte 1
Belvedere Spinello 1
Bermatingen 1
Brembilla 1
Buffalo 1
Buggiano 1
Cadelbosco Di Sopra 1
Cardiff 1
Carol Stream 1
Castel Bolognese 1
Totale 9503
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Nome #
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy. 86
Defective Mitochondrial Adenosine Triphosphate Production in Skeletal Muscle From Patients With Dominant Optic Atrophy Due to OPA1 Mutations 84
Nocturnal Sleep Dynamics Identify Narcolepsy Type 1. 82
null 77
Mitochondrial dysfunction in myotonic dystrophy type 1 77
Generalised anhidrosis: different lesion sites demonstrated by microneurography and skin biopsy. 75
Intermittent head drops: the differential spectrum 73
Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy. 73
Habituation of sympathetic sudomotor and vasomotor skin responses: neural and non-neural components in healthy subjects. 72
Preganglionic sudomotor nerve fiber lesion in a patient with Multiple System Atrophy and generalized anhidrosis. 72
Anti-ganglioside antibodies in coeliac disease with neurological disorders. 71
Narcolepsy is a common phenotype in HSAN IE and ADCA-DN 71
Increased expression of Trpv1 in peripheral terminals mediates thermal nociception in Fabry disease mouse model 70
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 70
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 69
Sleep-related stridor due to dystonic vocal cord motion and neurogenic tachypnea/tachycardia in multiple system atrophy. 68
A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype 67
Sleep-related periodic respiration with central sleep apnea in Leber Hereditary Optic Neuropathy (LHON). 66
Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1 66
null 66
Sympathetic and cardiovascular activity during cataplexy in narcolepsy. 65
A case of fatal familial insomnia in Africa. 65
Continuous motor unit activity syndromes: A video-polysomnographic study. 65
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. 64
Variation in the neurophysiological examination of amyotrophic lateral sclerosis in Europe. 64
Somatic and autonomic small fiber neuropathy induced by bortezomib therapy: an immunofluorescence study. 64
Paraneoplastic cerebellar degeneration and lambert-eaton myasthenia in a patient with merkel cell carcinoma and voltage-gated calcium channel antibodies 64
Color choice preference in cognitively impaired patients: A look inside alzheimer’s disease through the use of lüscher color diagnostic 64
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 63
Pain Related Channels Are Differentially Expressed in Neuronal and Non-Neuronal Cells of Glabrous Skin of Fabry Knockout Male Mice 63
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy 63
Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing 63
Daytime sympathetic hyperactivity in OSAS is related to excessive daytime sleepiness. 63
Anhidrosis in multiple system atrophy: a preganglionic sudomotor dysfunction? 62
Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes. 62
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy. 62
Immunotherapy of oneiric stupor in Morvan syndrome: Efficacy documented by actigraphy 62
Skin biopsy and I-123 MIBG scintigraphy findings in idiopathic Parkinson's disease and parkinsonism: A comparative study 62
Non-paraneoplastic ataxia in a patient with contactin-associated protein-2 antibodies and benign course 61
A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings 61
Skin globotriaosylceramide 3 deposits are specific to Fabry disease with classical mutations and associated with small fibre neuropathy. 61
A prospective multicentre study on sural nerve action potentials in ALS. 60
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation. 60
Quality of life in patients with craniocervical dystonia: Italian validation of the "Cervical Dystonia Impact Profile (CDIP-58)" and the "Craniocervical Dystonia Questionnaire (CDQ-24)". 60
Skin nerve misfolded α-synuclein in pure autonomic failure and Parkinson disease 60
Riluzole and other prognostic factors in ALS: a population-based registry study in Italy 60
null 60
Skin sympathetic adrenergic innervation: an immunofluorescence confocal study. 60
Erythematous papules on the parasternal region in a 76-year-old man. 59
Skin biopsy and microneurography disclose selective noradrenergic dysfunction due to dopamine-β-hydroxylase deficiency 59
Amyotrophic lateral sclerosis: a comparison of two staging systems in a population-based study 59
Molecular biology of channelopathies: impact on diagnosis and treatment. 59
The empowerment of translational research: lessons from laminopathies. 58
Modulation of the muscle activity during sleep in cervical dystonia 58
Absent cardiac and muscle sympathetic nerve activities involvement in Ross syndrome: A follow-up study 58
Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations 57
Sympathetic and cardiovascular changes during sleep in narcolepsy with cataplexy patients. 57
An inflammatory myopathy unmasks a case of leprosy in an Italian patient 57
Antibodies against hypocretin receptor 2 are rare in narcolepsy 57
Post-ganglionic autonomic neuropathy associated with anti-glutamic acid decarboxylase antibodies 57
Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature 57
Autonomic disturbances in narcolepsy. 56
null 56
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 56
Impaired eye blink classical conditioning distinguishes dystonic patients with and without tremor 56
The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance 56
A defective SERCA1 protein is responsible for congenital Pseudo-Myotonia in Chianina cattle 55
Idiopathic central sleep apnoea syndrome treated with zolpidem. 55
Isolated generalised anhidrosis induced by postganglionic sympathetic skin nerve fibre degeneration: an incomplete Ross syndrome? 55
Acute rhabdomyolysis induced by tonic-clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency. 55
Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene. 55
Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1. 55
Parkinsonian tremor persisting during cataplexy 55
Cervical demyelinating lesion presenting with choreoathetoid movements and dystonia 55
The Italian Dystonia Registry: rationale, design and preliminary findings 55
Influence of medical audit on electrodiagnostic evaluation of polyneuropathy. A multicentre study. 55
Skin sympathetic fiber α-synuclein deposits: a potential biomarker for pure autonomic failure. 54
Brachial amyotrophic diplegia associated with the a140a superoxide dismutase 1 mutation. 54
Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations. 54
LOPED study: Looking for an early diagnosis in a late-onset Pompe disease high-risk population 54
null 54
The spectrum of REM sleep-related episodes in children with type 1 narcolepsy 54
Spine Topographical Distribution of Skin α-Synuclein Deposits in Idiopathic Parkinson Disease 54
null 54
Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine. 54
Agrypnia Excitata: a microneurographic study of muscle sympathetic nerve activity. 53
Impact of medical audit on electrodiagnostic medicine in polyneuropathy. 53
Muscle sympathetic response to arousal predicts neurovascular reactivity during mental stress. 53
Cataplectic attacks during rapid eye movement sleep behavior disorder episodes in a narcoleptic patient. 53
Visual system involvement in patients with Friedreich's ataxia 53
A multi-center, multinational age- and gender-adjusted normative dataset for immunofluorescent intraepidermal nerve fiber density at the distal leg 53
Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction 53
High frequency somatosensory stimulation increases sensori-motor inhibition and leads to perceptual improvement in healthy subjects 53
null 53
Arousal elicits exaggerated inhibition of sympathetic nerve activity in phobic syncope patients. 53
Characterization of Human Dermal Fibroblasts in Fabry Disease 53
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. 53
Axial myoclonus in paraproteinemic polyneuropathy. 52
Small fiber neuropathy in female patients with fabry disease. 52
Autonomic innervation in multiple system atrophy and pure autonomic failure. 52
Totale 6058
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Categoria #
all - tutte 11651
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 11651
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2015/201655 0000 00 2513 9044
2016/201753 32419 93 00 2065
2017/2018506 3290 1510 1910 4639038
2018/20191532 682019167 15188 6377 13924691268
2019/20207579 101119866405 764770 936970 1243479392345
2020/20211887 838289107202 197206 480 0000
Totale 11651
 
 
 
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