IRIS
RUFA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 22.265
EU - Europa 15.043
AS - Asia 7.510
SA - Sud America 1.218
AF - Africa 486
Continente sconosciuto - Info sul continente non disponibili 403
OC - Oceania 30
Totale 46.955
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Nazione #
US - Stati Uniti d'America 21.990
GB - Regno Unito 3.710
CN - Cina 2.802
RU - Federazione Russa 2.671
SG - Singapore 2.343
IT - Italia 2.208
IE - Irlanda 1.723
UA - Ucraina 1.106
SE - Svezia 1.038
BR - Brasile 1.022
FR - Francia 787
DE - Germania 783
VN - Vietnam 614
HK - Hong Kong 529
FI - Finlandia 462
KR - Corea 397
ZA - Sudafrica 276
IN - India 180
CA - Canada 154
TR - Turchia 116
NL - Olanda 103
BD - Bangladesh 102
ES - Italia 100
IQ - Iraq 78
NG - Nigeria 71
MX - Messico 65
PL - Polonia 63
JP - Giappone 57
AR - Argentina 56
BE - Belgio 56
PK - Pakistan 53
EC - Ecuador 33
CI - Costa d'Avorio 31
CL - Cile 30
CZ - Repubblica Ceca 30
BG - Bulgaria 28
SA - Arabia Saudita 28
AU - Australia 27
CO - Colombia 26
UZ - Uzbekistan 25
AT - Austria 24
MA - Marocco 23
RO - Romania 23
LT - Lituania 21
KE - Kenya 19
ID - Indonesia 18
EU - Europa 17
IR - Iran 15
PH - Filippine 15
EG - Egitto 14
IL - Israele 14
VE - Venezuela 14
GR - Grecia 12
HU - Ungheria 11
JM - Giamaica 11
JO - Giordania 11
NO - Norvegia 11
PY - Paraguay 11
TN - Tunisia 11
UY - Uruguay 11
DZ - Algeria 10
KG - Kirghizistan 10
MY - Malesia 10
AZ - Azerbaigian 9
DK - Danimarca 9
AE - Emirati Arabi Uniti 8
BO - Bolivia 8
DO - Repubblica Dominicana 8
ET - Etiopia 8
NP - Nepal 8
PT - Portogallo 8
EE - Estonia 7
HN - Honduras 7
OM - Oman 7
PS - Palestinian Territory 7
TW - Taiwan 7
KZ - Kazakistan 6
PE - Perù 6
SK - Slovacchia (Repubblica Slovacca) 6
AL - Albania 5
CH - Svizzera 5
LB - Libano 5
LV - Lettonia 5
RS - Serbia 5
SI - Slovenia 5
SN - Senegal 5
TT - Trinidad e Tobago 5
CR - Costa Rica 4
GE - Georgia 4
HR - Croazia 4
KW - Kuwait 4
LK - Sri Lanka 4
MD - Moldavia 4
PA - Panama 4
PR - Porto Rico 4
SC - Seychelles 4
SY - Repubblica araba siriana 4
AM - Armenia 3
AO - Angola 3
BB - Barbados 3
Totale 46.517
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Città #
Menlo Park 4.450
Southend 3.333
Dallas 2.823
Dublin 1.716
Ashburn 1.366
Fairfield 1.363
Singapore 1.293
Chandler 1.127
Jacksonville 916
Santa Clara 878
San Jose 701
Moscow 680
Beijing 664
Houston 656
Wilmington 623
Woodbridge 623
Milan 582
Hong Kong 501
Seattle 491
Hefei 488
Cambridge 457
Ann Arbor 437
Council Bluffs 436
Seoul 396
Princeton 351
Nanjing 286
Siena 267
Rome 254
Johannesburg 247
The Dalles 240
Los Angeles 229
Helsinki 221
New York 213
Ho Chi Minh City 186
Lauterbourg 182
Boardman 152
San Mateo 150
Hanoi 147
Nanchang 119
Buffalo 118
Munich 111
São Paulo 107
Columbus 93
Shenyang 86
Florence 83
Orem 80
San Diego 78
Venezia 68
Izmir 67
Abuja 66
Düsseldorf 66
Shanghai 65
Málaga 62
Dong Ket 60
Frankfurt am Main 58
Tianjin 56
Tokyo 55
Turku 55
Kunming 54
London 54
North Bergen 53
Toronto 50
Figino 48
Chennai 45
Jiaxing 45
Hebei 44
Warsaw 44
Brooklyn 41
Bengaluru 40
Changsha 40
Naples 40
San Francisco 40
Turin 40
Rio de Janeiro 39
Dearborn 38
Atlanta 36
Brussels 36
Bologna 35
Phoenix 33
Chicago 32
Abidjan 31
Washington 31
Manchester 30
Belo Horizonte 29
Fremont 29
Jinan 29
Mestre 29
Montreal 29
Redondo Beach 29
Norwalk 28
Amsterdam 27
Lancaster 27
Sofia 26
Brasília 25
Redwood City 25
Denver 24
Haiphong 24
Tashkent 24
Hangzhou 23
Stockholm 23
Totale 33.147
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Nome #
A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE 410
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case 384
A case of bilateral facial palsy with detection of herpes simplex virus type 1 DNA in the cerebrospinal fluid and serum anti-gm1 antibodies 374
A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes. 365
A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778 364
Hemodynamic evaluation of the optic nerve head in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 364
AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases 349
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 347
Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias. 346
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: Update on clinical, diagnostic, and management aspects 346
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene 339
A two-layered diffusion model traces the dynamics of information processing in the valuation-and-choice circuit of decision making 334
Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene 331
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. 329
Cerebellum and neuropsychiatric disorders: insights from ARSACS 323
Two novel HTRA1 mutations in a European CARASIL patient. 313
Cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies: a case report 312
Transient supranuclear paresis of the abduction in viral encephalitis of the brainstem 310
A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features 308
A case report of transient posterior internuclear ophthalmoplegia (PINO) associated with encephalitis of ponto-mesencephalic junction 306
A case of ovarioleukodystrophy without elF2B mutations 300
Visual impairment in FOXG1-mutated individuals and mice 300
Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 298
Frequency of OPA1 and OPTN gene variations in 18 patients with normal tension glaucoma 297
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 295
Automatic eye fixations identification based on analysis of variance and covariance, 295
Typical pathological changes of CADASIL in the optic nerve 295
Eye movement abnormalities in a patient with Zellweger spectrum disorder 294
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 290
The role of dentate nuclei in human oculomotor control: Insights from cerebrotendinous xanthomatosis 285
Homozygosity and severity of phenotypic presentation in a CADASIL family 282
Anti-saccades in cerebellar ataxias reveal a contribution of the cerebellum in executive functions 282
Systemic blood pressure profile in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 281
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence? 279
Clinical and MRI improvement in a case of progressive multifocal leukoencephalopathy 279
Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 279
Blinking Rate Comparison Between Patients with Chronic Pain and Parkinson's Disease 278
Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL) 277
Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) 276
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy. 273
A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis 268
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 267
Spatial ranking strategy and enhanced peripheral vision discrimination optimize performance and efficiency of visual sequential search. 267
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 264
Toscana itaca (Italian CADASIL) registry: an implementable online database for CADASIL (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy). 263
Impairment of vertical saccades from an acute pontine lesion in multiple sclerosis 262
Vertical supranuclear gaze palsy in Niemann-Pick type C disease 262
GABAAergic dysfunction in the olivary-cerebellar-brainstem network may cause eye oscillations and body tremor 262
Visual System Involvement in CADASIL. 261
Alu-element insertion in the OPA1 intron sequence associated with ADOA 258
Characteristic eye movements in ataxia-telangiectasia-like disorder: An explanatory hypothesis 258
Sixth nerve and superior division of third nerve palsy due to intracranial extension of multiple myeloma. A diagnostic challenge and differential diagnosis 256
Ocular-motor profile and effects of memantine in a familial form of adult cerebellar ataxia with slow saccades and square wave saccadic intrusions. 256
CADASIL and cerebrovascular diseases 254
Evaluating the human ongoing visual search performance by eye tracking application and sequencing tests 253
Evaluating gaze control on a multi-target sequencing task: The distribution of fixations is evidence of exploration optimisation. 253
Genetic leukoencephalopaties with unknown metabolic pathogenesis 252
Video-based eye tracking: our experience with advanced stimuli design for eye tracking software 252
Fast versus slow: different saccadic behavior in cerebellar ataxias 250
A novel OPA1 mutation resulting in atypical dominant optic atrophy with NTG “Like” phenotype. 250
Molecular genetic study of Leber’s hereditary optic neurophaty (LHON): mutation screening by sequencing of ND1, ND4, ND%, ND6 genes 249
Trigeminal-Nociceptive Activation And Pupillary Changes In Two Patients With Wernicke’s Encephalopathy 249
Acute visual loss due to anterior ischemic optic neuropathy as first symptom in a patient with CADASIL 248
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation 248
Type I sialidosis: a clinical, biochemical and neuroradiological study 245
Sindrome di Goldman-Favre: descrizione di un caso 244
Transient periodic lateralised epileptiform discharges (PLEDs) following internal carotid artery stenting 243
Eight and a Half Syndrome with Hemiparesis and Hemihypesthesia: The Nine Syndrome? 241
Using a simplified trail making test B to assess visuo-spatial and sequencing abilities in hereditary spinocerebellar ataxias (SCA) 239
Photophobia and bilateral pulvinar involvement in non-alcoholic Wernicke's encephalopathy. 238
Eye movement recording and nonlinear dynamics analysis - The case of saccades 237
Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene 237
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy 236
Adult-onset phenylketonuria revealed by acute reversible dementia, prosopagnosia and parkinsonism. 236
Cognitive Biases and Gaze Direction: An Experimental Study 233
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay. 232
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption 232
Vitamin-E serum level in LHON patients 232
High energy efficiency biped robot controlled by the human brain for people with ALS disease 229
Hemodynamic evaluation at the papilla in CADASIL 227
High-Dose Methylprednisolone For Bickerstaff’s Brainstem Encephalitis. 227
The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene. 227
Analisi quantitativa di saccadi orizzontali in disordini atassici degenerative 227
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 226
Evaluating human visual search performance by Monte Carlo methods and heuristic model 225
Lateral Medullary Ischemia Presenting with Persistent Hiccups and Vertigo 223
Cognitive Biases And Gaze Direction. An Experimental Study. 222
Visual Sequencing Search Strategy in Parkinson's Disease 221
Velocity profile and trajectory of saccades in different forms of cerebellar ataxia 221
Heterogeneity of retinal manifestations in mitochondrial myopathy: genotype/phenotype correlation in our experience. 220
Pulsating enophthalmos in an adult patient with type 1 neurofibromatosis 220
Valutazione delle associazioni tra polimorfismi del gene OPA 1 e glaucoma normotensivo in Italia 220
Lithium neurotoxicity mimicking rapidly progressive dementia 218
EVA:Eye Tracking Stimulus Integrated Semi Automated Case Base System. 218
Dynamical complexity analysis of saccadic eye movements in two different psychological conditions 218
Ischemic stroke as first clinical manifestation in alagille syndrome : a case report. 217
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation between eye-tracking and neuroosychological studies. 217
Influences of data filtering on human-computer interaction by gaze-contingent display and eyetracking applications 217
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telythromicin consumption 217
Plasma levels of asymmetric dimethylarginine (ADMA) in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarct and Leukoencephalopathy (CADASIL) 215
Totale 26.948
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Categoria #
all - tutte 128.569
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 128.569
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.219 0 295 201 189 128 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
2025/202614.186 1.021 2.214 1.968 1.403 2.620 457 1.388 466 423 775 278 1.173
2026/20271.072 632 440 0 0 0 0 0 0 0 0 0 0
Totale 46.955