IRIS
RUFA, ALESSANDRA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 19.935
EU - Europa 13.537
AS - Asia 6.191
SA - Sud America 1.081
AF - Africa 131
Continente sconosciuto - Info sul continente non disponibili 20
OC - Oceania 18
Totale 40.913
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 19.737
GB - Regno Unito 3.664
RU - Federazione Russa 2.683
CN - Cina 2.544
SG - Singapore 1.991
IE - Irlanda 1.731
IT - Italia 1.154
UA - Ucraina 1.104
SE - Svezia 1.007
BR - Brasile 944
DE - Germania 744
FR - Francia 576
HK - Hong Kong 465
KR - Corea 400
FI - Finlandia 397
VN - Vietnam 242
CA - Canada 124
IN - India 121
TR - Turchia 109
ES - Italia 91
NL - Olanda 77
BD - Bangladesh 60
BE - Belgio 56
PL - Polonia 51
AR - Argentina 49
JP - Giappone 47
MX - Messico 46
ZA - Sudafrica 43
IQ - Iraq 37
CI - Costa d'Avorio 30
CZ - Repubblica Ceca 28
BG - Bulgaria 26
PK - Pakistan 23
UZ - Uzbekistan 23
AT - Austria 22
EC - Ecuador 21
LT - Lituania 20
CO - Colombia 19
EU - Europa 17
MA - Marocco 17
RO - Romania 17
SA - Arabia Saudita 17
AU - Australia 15
IR - Iran 15
IL - Israele 12
GR - Grecia 11
CL - Cile 10
ID - Indonesia 10
PT - Portogallo 10
UY - Uruguay 10
VE - Venezuela 10
DK - Danimarca 9
HU - Ungheria 9
KG - Kirghizistan 8
AE - Emirati Arabi Uniti 7
EE - Estonia 7
EG - Egitto 7
KE - Kenya 7
PY - Paraguay 7
TN - Tunisia 7
DO - Repubblica Dominicana 6
PH - Filippine 6
TW - Taiwan 6
AL - Albania 5
AZ - Azerbaigian 5
BO - Bolivia 5
CH - Svizzera 5
JO - Giordania 5
KZ - Kazakistan 5
PE - Perù 5
SI - Slovenia 5
SN - Senegal 5
LK - Sri Lanka 4
LV - Lettonia 4
MD - Moldavia 4
NO - Norvegia 4
PS - Palestinian Territory 4
TT - Trinidad e Tobago 4
AM - Armenia 3
DZ - Algeria 3
ET - Etiopia 3
GE - Georgia 3
HN - Honduras 3
JM - Giamaica 3
LA - Repubblica Popolare Democratica del Laos 3
LB - Libano 3
LU - Lussemburgo 3
MK - Macedonia 3
NG - Nigeria 3
NP - Nepal 3
NZ - Nuova Zelanda 3
PA - Panama 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
BS - Bahamas 2
BY - Bielorussia 2
KW - Kuwait 2
MU - Mauritius 2
MY - Malesia 2
OM - Oman 2
Totale 40.892
Salva come PNG Salva come JPEG
Città #
Menlo Park 4.486
Southend 3.349
Dallas 2.831
Dublin 1.725
Fairfield 1.366
Singapore 1.155
Chandler 1.129
Ashburn 1.082
Jacksonville 919
Santa Clara 787
Moscow 683
Beijing 663
Houston 652
Wilmington 624
Woodbridge 621
Seattle 487
Hong Kong 458
Cambridge 456
Ann Arbor 438
Seoul 399
Hefei 390
Princeton 351
Nanjing 287
Siena 260
Los Angeles 209
New York 179
Helsinki 157
Boardman 152
San Mateo 150
Nanchang 119
The Dalles 116
Munich 112
Buffalo 109
São Paulo 96
Shenyang 85
San Diego 77
Rome 75
Florence 71
Milan 69
Izmir 68
Venezia 68
Düsseldorf 66
Málaga 62
Dong Ket 60
Council Bluffs 59
Shanghai 59
Tianjin 57
Turku 55
Kunming 54
Ho Chi Minh City 53
Tokyo 47
Hanoi 46
Hebei 45
Jiaxing 45
London 45
Toronto 45
Columbus 41
Changsha 40
Warsaw 39
Bengaluru 38
Dearborn 38
Brussels 36
Rio de Janeiro 35
San Francisco 35
Brooklyn 32
Frankfurt am Main 32
Washington 31
Abidjan 30
Fremont 29
Jinan 29
Mestre 29
Redondo Beach 29
Belo Horizonte 28
Norwalk 28
Lancaster 27
Chennai 26
Phoenix 26
Sofia 26
Atlanta 25
Johannesburg 25
Naples 25
Redwood City 25
Chicago 24
Montreal 24
Denver 23
Tashkent 23
Bologna 22
Stockholm 22
Brasília 21
Hangzhou 21
Orem 20
Amsterdam 19
Curitiba 19
Manchester 19
Ningbo 19
Boston 18
Renton 18
Poplar 17
St Louis 17
Waanrode 17
Totale 29.475
Salva come PNG Salva come JPEG
Nome #
A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE 368
A case of bilateral facial palsy with detection of herpes simplex virus type 1 DNA in the cerebrospinal fluid and serum anti-gm1 antibodies. 346
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case 346
A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes. 337
Hemodynamic evaluation of the optic nerve head in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 336
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 330
A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778 328
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene 314
Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene 306
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. 306
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: Update on clinical, diagnostic, and management aspects 305
AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases 305
A two-layered diffusion model traces the dynamics of information processing in the valuation-and-choice circuit of decision making 301
Cerebellum and neuropsychiatric disorders: insights from ARSACS 296
Cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies: a case report 291
Transient supranuclear paresis of the abduction in viral encephalitis of the brainstem 288
Visual impairment in FOXG1-mutated individuals and mice 278
Two novel HTRA1 mutations in a European CARASIL patient. 276
Eye movement abnormalities in a patient with Zellweger spectrum disorder 274
A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features 271
A case report of transient posterior internuclear ophthalmoplegia (PINO) associated with encephalitis of ponto-mesencephalic junction 271
Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 267
The role of dentate nuclei in human oculomotor control: Insights from cerebrotendinous xanthomatosis 266
A case of ovarioleukodystrophy without elF2B mutations 264
Frequency of OPA1 and OPTN gene variations in 18 patients with normal tension glaucoma 261
Clinical and MRI improvement in a case of progressive multifocal leukoencephalopathy 259
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence? 257
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 256
Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL) 253
Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias. 252
Systemic blood pressure profile in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 251
Homozygosity and severity of phenotypic presentation in a CADASIL family 251
Typical pathological changes of CADASIL in the optic nerve 249
Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 247
Automatic eye fixations identification based on analysis of variance and covariance, 243
GABAAergic dysfunction in the olivary-cerebellar-brainstem network may cause eye oscillations and body tremor 241
Anti-saccades in cerebellar ataxias reveal a contribution of the cerebellum in executive functions 241
Spatial ranking strategy and enhanced peripheral vision discrimination optimize performance and efficiency of visual sequential search. 240
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 239
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy. 239
Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). 238
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 238
Blinking Rate Comparison Between Patients with Chronic Pain and Parkinson's Disease 237
Vertical supranuclear gaze palsy in Niemann-Pick type C disease 233
Video-based eye tracking: our experience with advanced stimuli design for eye tracking software 232
A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis 230
Toscana itaca (Italian CADASIL) registry: an implementable online database for CADASIL (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy). 230
Type I sialidosis: a clinical, biochemical and neuroradiological study 230
Visual System Involvement in CADASIL. 230
Evaluating gaze control on a multi-target sequencing task: The distribution of fixations is evidence of exploration optimisation. 228
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 227
Characteristic eye movements in ataxia-telangiectasia-like disorder: An explanatory hypothesis 227
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation 226
A novel OPA1 mutation resulting in atypical dominant optic atrophy with NTG “Like” phenotype. 225
CADASIL and cerebrovascular diseases 224
Genetic leukoencephalopaties with unknown metabolic pathogenesis 224
Sixth nerve and superior division of third nerve palsy due to intracranial extension of multiple myeloma. A diagnostic challenge and differential diagnosis 224
Ocular-motor profile and effects of memantine in a familial form of adult cerebellar ataxia with slow saccades and square wave saccadic intrusions. 223
Trigeminal-Nociceptive Activation And Pupillary Changes In Two Patients With Wernicke’s Encephalopathy 223
Using a simplified trail making test B to assess visuo-spatial and sequencing abilities in hereditary spinocerebellar ataxias (SCA) 222
Acute visual loss due to anterior ischemic optic neuropathy as first symptom in a patient with CADASIL 221
Alu-element insertion in the OPA1 intron sequence associated with ADOA. 221
Molecular genetic study of Leber’s hereditary optic neurophaty (LHON): mutation screening by sequencing of ND1, ND4, ND%, ND6 genes 221
Evaluating the human ongoing visual search performance by eye tracking application and sequencing tests 220
Fast versus slow: different saccadic behavior in cerebellar ataxias 219
Sindrome di Goldman-Favre: descrizione di un caso 216
Impairment of vertical saccades from an acute pontine lesion in multiple sclerosis 216
Transient periodic lateralised epileptiform discharges (PLEDs) following internal carotid artery stenting 216
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption 214
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay. 213
High energy efficiency biped robot controlled by the human brain for people with ALS disease 212
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy 209
Adult-onset phenylketonuria revealed by acute reversible dementia, prosopagnosia and parkinsonism. 209
The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene. 208
Eight and a Half Syndrome with Hemiparesis and Hemihypesthesia: The Nine Syndrome? 207
Vitamin-E serum level in LHON patients 207
Hemodynamic evaluation at the papilla in CADASIL 205
Eye movement recording and nonlinear dynamics analysis - The case of saccades 205
Pulsating enophthalmos in an adult patient with type 1 neurofibromatosis 205
Photophobia and bilateral pulvinar involvement in non-alcoholic Wernicke's encephalopathy. 205
High-Dose Methylprednisolone For Bickerstaff’s Brainstem Encephalitis. 204
Velocity profile and trajectory of saccades in different forms of cerebellar ataxia 204
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 201
Evaluating human visual search performance by Monte Carlo methods and heuristic model 199
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation between eye-tracking and neuroosychological studies. 197
Analisi quantitativa di saccadi orizzontali in disordini atassici degenerative 197
Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene 196
Valutazione delle associazioni tra polimorfismi del gene OPA 1 e glaucoma normotensivo in Italia 196
Idiopathic bilateral facial palsy: is a causative role of anti-GM1 ganglioside and herpes simplex type 1 possible? 195
Heterogeneity of retinal manifestations in mitochondrial myopathy: genotype/phenotype correlation in our experience. 195
Plasma levels of asymmetric dimethylarginine (ADMA) in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarct and Leukoencephalopathy (CADASIL) 195
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telythromicin consumption 194
Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. 192
Lateral Medullary Ischemia Presenting with Persistent Hiccups and Vertigo 191
Spike removal through multiscale wavelet and entropy analysis of ocular motor noise: a case study in patients with cerebellar disease. 191
Cognitive Biases And Gaze Direction. An Experimental Study. 190
High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiarities. 190
Using simplified trial macking test B to evacuate ongoing learning capabilities on visual search. 189
Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency 189
Cognitive Biases and Gaze Direction: An Experimental Study 188
Totale 23.962
Salva come PNG Salva come JPEG
Categoria #
all - tutte 111.129
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 111.129
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.288 0 0 0 0 0 391 131 588 384 169 401 224
2021/20222.372 147 296 201 191 128 59 100 78 111 252 260 549
2022/20233.914 233 255 545 509 466 740 67 340 434 94 161 70
2023/20242.670 122 79 218 108 105 716 901 114 43 40 36 188
2024/20255.401 92 348 448 305 741 274 192 329 408 191 543 1.530
2025/20269.410 1.028 2.224 1.983 1.414 2.657 104 0 0 0 0 0 0
Totale 41.278