IRIS
RUFA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 21.295
EU - Europa 14.039
AS - Asia 7.465
SA - Sud America 1.202
AF - Africa 480
OC - Oceania 26
Continente sconosciuto - Info sul continente non disponibili 21
Totale 44.528
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Nazione #
US - Stati Uniti d'America 21.045
GB - Regno Unito 3.703
CN - Cina 2.795
RU - Federazione Russa 2.671
SG - Singapore 2.325
IE - Irlanda 1.723
IT - Italia 1.273
UA - Ucraina 1.106
BR - Brasile 1.013
SE - Svezia 1.008
FR - Francia 785
DE - Germania 774
VN - Vietnam 614
HK - Hong Kong 524
FI - Finlandia 460
KR - Corea 397
ZA - Sudafrica 275
IN - India 178
CA - Canada 142
TR - Turchia 116
ES - Italia 98
NL - Olanda 98
BD - Bangladesh 96
IQ - Iraq 78
NG - Nigeria 71
MX - Messico 63
PL - Polonia 59
BE - Belgio 56
JP - Giappone 55
AR - Argentina 53
PK - Pakistan 53
CI - Costa d'Avorio 31
EC - Ecuador 31
CL - Cile 29
CZ - Repubblica Ceca 28
SA - Arabia Saudita 28
BG - Bulgaria 27
CO - Colombia 25
UZ - Uzbekistan 25
AT - Austria 24
AU - Australia 23
MA - Marocco 23
RO - Romania 23
LT - Lituania 21
KE - Kenya 19
EU - Europa 17
ID - Indonesia 17
IR - Iran 15
PH - Filippine 15
EG - Egitto 14
IL - Israele 14
VE - Venezuela 14
GR - Grecia 12
HU - Ungheria 11
JO - Giordania 11
NO - Norvegia 11
PY - Paraguay 11
TN - Tunisia 11
UY - Uruguay 11
DZ - Algeria 10
KG - Kirghizistan 10
AZ - Azerbaigian 9
DK - Danimarca 9
MY - Malesia 9
AE - Emirati Arabi Uniti 8
BO - Bolivia 8
DO - Repubblica Dominicana 8
ET - Etiopia 8
JM - Giamaica 8
NP - Nepal 8
EE - Estonia 7
OM - Oman 7
PS - Palestinian Territory 7
PT - Portogallo 7
KZ - Kazakistan 6
PE - Perù 6
TW - Taiwan 6
AL - Albania 5
CH - Svizzera 5
HN - Honduras 5
LB - Libano 5
LV - Lettonia 5
SI - Slovenia 5
SN - Senegal 5
TT - Trinidad e Tobago 5
GE - Georgia 4
KW - Kuwait 4
LK - Sri Lanka 4
MD - Moldavia 4
PA - Panama 4
RS - Serbia 4
SK - Slovacchia (Repubblica Slovacca) 4
SY - Repubblica araba siriana 4
AM - Armenia 3
AO - Angola 3
CR - Costa Rica 3
HR - Croazia 3
LA - Repubblica Popolare Democratica del Laos 3
LU - Lussemburgo 3
MK - Macedonia 3
Totale 44.482
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Città #
Menlo Park 4.450
Southend 3.333
Dallas 2.821
Dublin 1.716
Fairfield 1.363
Singapore 1.284
Ashburn 1.218
Chandler 1.127
Jacksonville 916
Santa Clara 815
Moscow 680
Beijing 661
Houston 654
San Jose 636
Wilmington 622
Woodbridge 622
Hong Kong 497
Hefei 488
Seattle 487
Cambridge 457
Ann Arbor 437
Seoul 396
Princeton 351
Nanjing 286
Siena 267
Johannesburg 247
The Dalles 240
Los Angeles 228
Helsinki 220
New York 204
Ho Chi Minh City 186
Lauterbourg 182
Boardman 152
San Mateo 150
Hanoi 147
Nanchang 119
Buffalo 116
Munich 111
Council Bluffs 107
São Paulo 104
Milan 86
Shenyang 86
Rome 79
Orem 78
San Diego 77
Florence 75
Venezia 68
Izmir 67
Abuja 66
Düsseldorf 66
Shanghai 64
Málaga 62
Dong Ket 60
Tianjin 56
Turku 55
Frankfurt am Main 54
Kunming 54
London 54
Tokyo 53
Toronto 49
Chennai 45
Jiaxing 45
Columbus 44
Hebei 44
Warsaw 44
Bengaluru 40
Changsha 40
San Francisco 40
Rio de Janeiro 39
Brooklyn 38
Dearborn 38
Brussels 36
Atlanta 32
Abidjan 31
Washington 31
Manchester 30
Belo Horizonte 29
Fremont 29
Jinan 29
Mestre 29
Montreal 29
Phoenix 29
Redondo Beach 29
Bologna 28
Chicago 28
Norwalk 28
Amsterdam 27
Lancaster 27
Naples 26
Sofia 26
Redwood City 25
Brasília 24
Denver 24
Haiphong 24
Tashkent 24
Hangzhou 23
Stockholm 23
Curitiba 22
Da Nang 22
Dhaka 21
Totale 31.648
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Nome #
A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE 395
A case of bilateral facial palsy with detection of herpes simplex virus type 1 DNA in the cerebrospinal fluid and serum anti-gm1 antibodies. 370
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case 369
A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778 360
A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes. 357
Hemodynamic evaluation of the optic nerve head in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 353
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 344
AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases 338
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene 334
Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene 328
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: Update on clinical, diagnostic, and management aspects 328
A two-layered diffusion model traces the dynamics of information processing in the valuation-and-choice circuit of decision making 323
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. 321
Cerebellum and neuropsychiatric disorders: insights from ARSACS 315
Cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies: a case report 309
Transient supranuclear paresis of the abduction in viral encephalitis of the brainstem 303
A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features 298
Visual impairment in FOXG1-mutated individuals and mice 294
A case report of transient posterior internuclear ophthalmoplegia (PINO) associated with encephalitis of ponto-mesencephalic junction 294
Two novel HTRA1 mutations in a European CARASIL patient. 290
Frequency of OPA1 and OPTN gene variations in 18 patients with normal tension glaucoma 289
Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias. 289
Eye movement abnormalities in a patient with Zellweger spectrum disorder 289
Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 289
Automatic eye fixations identification based on analysis of variance and covariance, 286
A case of ovarioleukodystrophy without elF2B mutations 285
Typical pathological changes of CADASIL in the optic nerve 279
The role of dentate nuclei in human oculomotor control: Insights from cerebrotendinous xanthomatosis 278
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 278
Systemic blood pressure profile in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 275
Clinical and MRI improvement in a case of progressive multifocal leukoencephalopathy 274
Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 274
Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study 271
Homozygosity and severity of phenotypic presentation in a CADASIL family 271
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy. 269
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence? 268
Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL) 268
Anti-saccades in cerebellar ataxias reveal a contribution of the cerebellum in executive functions 268
Blinking Rate Comparison Between Patients with Chronic Pain and Parkinson's Disease 265
Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). 261
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 260
Spatial ranking strategy and enhanced peripheral vision discrimination optimize performance and efficiency of visual sequential search. 260
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 259
Vertical supranuclear gaze palsy in Niemann-Pick type C disease 257
A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis 255
Toscana itaca (Italian CADASIL) registry: an implementable online database for CADASIL (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy). 254
GABAAergic dysfunction in the olivary-cerebellar-brainstem network may cause eye oscillations and body tremor 254
Alu-element insertion in the OPA1 intron sequence associated with ADOA 252
Impairment of vertical saccades from an acute pontine lesion in multiple sclerosis 249
Visual System Involvement in CADASIL. 249
Genetic leukoencephalopaties with unknown metabolic pathogenesis 248
A novel OPA1 mutation resulting in atypical dominant optic atrophy with NTG “Like” phenotype. 247
Characteristic eye movements in ataxia-telangiectasia-like disorder: An explanatory hypothesis 246
CADASIL and cerebrovascular diseases 245
Evaluating the human ongoing visual search performance by eye tracking application and sequencing tests 245
Trigeminal-Nociceptive Activation And Pupillary Changes In Two Patients With Wernicke’s Encephalopathy 244
Evaluating gaze control on a multi-target sequencing task: The distribution of fixations is evidence of exploration optimisation. 243
Molecular genetic study of Leber’s hereditary optic neurophaty (LHON): mutation screening by sequencing of ND1, ND4, ND%, ND6 genes 243
Acute visual loss due to anterior ischemic optic neuropathy as first symptom in a patient with CADASIL 242
Sixth nerve and superior division of third nerve palsy due to intracranial extension of multiple myeloma. A diagnostic challenge and differential diagnosis 242
Ocular-motor profile and effects of memantine in a familial form of adult cerebellar ataxia with slow saccades and square wave saccadic intrusions. 242
Type I sialidosis: a clinical, biochemical and neuroradiological study 240
Video-based eye tracking: our experience with advanced stimuli design for eye tracking software 240
Fast versus slow: different saccadic behavior in cerebellar ataxias 239
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation 237
Transient periodic lateralised epileptiform discharges (PLEDs) following internal carotid artery stenting 233
Using a simplified trail making test B to assess visuo-spatial and sequencing abilities in hereditary spinocerebellar ataxias (SCA) 233
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy 230
Eight and a Half Syndrome with Hemiparesis and Hemihypesthesia: The Nine Syndrome? 229
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption 229
Sindrome di Goldman-Favre: descrizione di un caso 228
Eye movement recording and nonlinear dynamics analysis - The case of saccades 227
Adult-onset phenylketonuria revealed by acute reversible dementia, prosopagnosia and parkinsonism. 227
Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene 224
Cognitive Biases and Gaze Direction: An Experimental Study 224
Analisi quantitativa di saccadi orizzontali in disordini atassici degenerative 223
High energy efficiency biped robot controlled by the human brain for people with ALS disease 222
Vitamin-E serum level in LHON patients 222
Hemodynamic evaluation at the papilla in CADASIL 221
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 221
Photophobia and bilateral pulvinar involvement in non-alcoholic Wernicke's encephalopathy. 221
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay. 220
High-Dose Methylprednisolone For Bickerstaff’s Brainstem Encephalitis. 219
The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene. 218
Evaluating human visual search performance by Monte Carlo methods and heuristic model 218
Valutazione delle associazioni tra polimorfismi del gene OPA 1 e glaucoma normotensivo in Italia 216
Visual Sequencing Search Strategy in Parkinson's Disease 213
Velocity profile and trajectory of saccades in different forms of cerebellar ataxia 213
Heterogeneity of retinal manifestations in mitochondrial myopathy: genotype/phenotype correlation in our experience. 210
Pulsating enophthalmos in an adult patient with type 1 neurofibromatosis 210
Lateral Medullary Ischemia Presenting with Persistent Hiccups and Vertigo 209
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation between eye-tracking and neuroosychological studies. 209
Cognitive Biases And Gaze Direction. An Experimental Study. 209
Ischemic stroke as first clinical manifestation in alagille syndrome : a case report. 208
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telythromicin consumption 207
Dynamical complexity analysis of saccadic eye movements in two different psychological conditions 207
Influences of data filtering on human-computer interaction by gaze-contingent display and eyetracking applications 205
Lithium neurotoxicity mimicking rapidly progressive dementia 205
Effect of memantine on saccadic intrusion in a case of hereditary spinocerebellar ataxia 205
Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 204
Totale 25.960
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Categoria #
all - tutte 122.468
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 122.468
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021223 0 0 0 0 0 0 0 0 0 0 0 223
2021/20222.365 146 295 201 189 128 59 100 78 110 251 260 548
2022/20233.901 233 254 541 507 466 736 67 339 434 93 161 70
2023/20242.645 122 78 217 107 104 712 884 114 43 40 36 188
2024/20255.353 92 346 437 294 738 273 192 328 405 189 541 1.518
2025/202613.213 1.021 2.214 1.968 1.403 2.620 457 1.388 466 423 775 278 200
Totale 44.910