IRIS
MIGNARRI, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 6.269
EU - Europa 4.016
AS - Asia 1.924
SA - Sud America 333
AF - Africa 132
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 3
Totale 12.683
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Nazione #
US - Stati Uniti d'America 6.205
GB - Regno Unito 1.268
RU - Federazione Russa 777
CN - Cina 680
SG - Singapore 619
IE - Irlanda 477
BR - Brasile 284
IT - Italia 282
UA - Ucraina 278
SE - Svezia 239
DE - Germania 213
FR - Francia 196
VN - Vietnam 176
HK - Hong Kong 153
FI - Finlandia 100
ZA - Sudafrica 81
KR - Corea 73
ES - Italia 58
TR - Turchia 53
IN - India 34
CA - Canada 31
NL - Olanda 27
PL - Polonia 26
BE - Belgio 23
PK - Pakistan 20
BD - Bangladesh 19
IQ - Iraq 19
MX - Messico 19
JP - Giappone 15
AR - Argentina 13
LT - Lituania 11
MA - Marocco 10
SA - Arabia Saudita 10
IL - Israele 9
CO - Colombia 8
DZ - Algeria 8
EG - Egitto 8
ID - Indonesia 8
NG - Nigeria 7
VE - Venezuela 7
EC - Ecuador 6
EU - Europa 6
PE - Perù 6
SK - Slovacchia (Repubblica Slovacca) 6
CI - Costa d'Avorio 5
CZ - Repubblica Ceca 5
GR - Grecia 5
KE - Kenya 4
KZ - Kazakistan 4
PT - Portogallo 4
TN - Tunisia 4
AT - Austria 3
AZ - Azerbaigian 3
BG - Bulgaria 3
BO - Bolivia 3
IR - Iran 3
MD - Moldavia 3
PH - Filippine 3
SV - El Salvador 3
UY - Uruguay 3
UZ - Uzbekistan 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
AU - Australia 2
ET - Etiopia 2
HN - Honduras 2
JM - Giamaica 2
JO - Giordania 2
KW - Kuwait 2
LB - Libano 2
MK - Macedonia 2
MY - Malesia 2
NP - Nepal 2
PA - Panama 2
PY - Paraguay 2
RO - Romania 2
SI - Slovenia 2
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BH - Bahrain 1
CG - Congo 1
CL - Cile 1
CR - Costa Rica 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GD - Grenada 1
HU - Ungheria 1
KG - Kirghizistan 1
LV - Lettonia 1
LY - Libia 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
OM - Oman 1
PS - Palestinian Territory 1
RS - Serbia 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TJ - Tagikistan 1
Totale 12.683
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Città #
Southend 1.131
Dallas 1.092
Fairfield 675
Menlo Park 504
Dublin 475
Ashburn 400
Woodbridge 337
Singapore 327
Chandler 273
Wilmington 253
Seattle 249
Houston 245
Jacksonville 243
Moscow 241
Cambridge 228
Santa Clara 218
Beijing 197
Ann Arbor 190
Hong Kong 149
San Jose 130
Siena 95
Princeton 93
Hefei 79
Johannesburg 79
Los Angeles 71
Seoul 71
Nanjing 70
The Dalles 60
New York 58
Ho Chi Minh City 55
Munich 54
Málaga 52
Helsinki 44
Lauterbourg 44
Boardman 42
Lancaster 41
San Diego 40
Council Bluffs 34
Izmir 33
Hanoi 31
Dong Ket 29
Buffalo 26
San Mateo 26
Orem 24
Changsha 22
Nanchang 22
Warsaw 22
London 21
Hebei 20
Tianjin 19
Shenyang 18
São Paulo 17
Brussels 16
Shanghai 16
Dearborn 15
Florence 14
Jiaxing 14
Milan 14
San Francisco 14
Tokyo 14
Turku 14
Columbus 13
Redondo Beach 13
Düsseldorf 12
Norwalk 12
Toronto 12
Frankfurt am Main 11
Montreal 11
Kunming 10
Belo Horizonte 9
Brooklyn 9
Chicago 9
Stockholm 9
Atlanta 8
Guangzhou 8
Hangzhou 8
Jinan 8
Bengaluru 7
Da Nang 7
Denver 7
Rome 7
Waanrode 7
Washington 7
Abuja 6
Baghdad 6
Bologna 6
Boston 6
Brasília 6
Bratislava 6
Lahore 6
Mestre 6
Mumbai 6
Nuremberg 6
Phoenix 6
Richland 6
Rio de Janeiro 6
Abidjan 5
Amsterdam 5
Andover 5
Biên Hòa 5
Totale 9.402
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Nome #
An atypical case of Creutzfeldt-Jakob disease mimicking frontotemporal dementia: genotypic influence and clinical implications 473
A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE 390
Cerebellum and neuropsychiatric disorders: insights from ARSACS 314
Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia 310
A mimic of first dorsal interosseus atrophy revealed by ultrasound study 310
Eye movement abnormalities in a patient with Zellweger spectrum disorder 287
Zellweger Spectrum Disorder with Mild Phenotype Caused by PEX2 Gene Mutations 279
Clinical relevance of brain volume changes in patients with cerebrotendinous xanthomatosis 278
Cerebellar hypometabolism with normal structural findings in Cerebrotendinous xanthomatosis. A case report 277
The role of dentate nuclei in human oculomotor control: Insights from cerebrotendinous xanthomatosis 277
Mitochondrial dysfunction in hereditary spastic paraparesis with mutations in DDHD1/SPG28 273
Demyelinating polyneuropathy in a case of anti-LGI1 encephalitis 262
Cerebrotendinous xanthomatosis with progressive cerebellar vacuolation. Six-year MRI follow-up 255
Narcolepsy is a common phenotype in HSAN IE and ADCA-DN 254
Temporal lobe abnormalities in neurosyphilis 252
Two-year follow-up after chelating therapy in a patient with adult-onset parkinsonism and hypermanganesaemia due to SLC30A10 mutations 248
Imaging of the thymus in myotonic dystrophy type 1 244
The first Italian patient with oculopharyngodistal myopathy: Case report and considerations on differential diagnosis. 242
Polyneuropathy with demyelinating changes in Churg–Strauss syndrome: an unusual association 234
Brain metabolism changes after therapy with chenodeoxycholic acid in a case of cerebrotendinous xanthomatosis. 233
The spectrum of magnetic resonance findings in cerebrotendinous xanthomatosis: redefinition and evidence of new markers of disease progression 232
Primary familial brain calcification: Genetic analysis and clinical spectrum. 228
A suspicion index for early diagnosis and treatment of cerebrotendinous xanthomatosis. 226
Hereditary spastic paraplegia type 5: a potentially treatable disorder of cholesterol metabolism 222
Clinical Features and Outcome of the Guillain–Barre Syndrome: A Single-Center 11-Year Experience 219
Electrodiagnosis in cranial botulism 219
Neuroendocrine lung cancer in a patient with limbic encephalopathy due to anti-Hu antibodies: A rare association not to be missed 215
First report of an Iraqi Kurdish CADASIL patient. 214
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4. 213
Myoclonus epilepsy, retinitis pigmentosa, leukoencephalopathy and cerebral calcifications associated with a novel m.5513G>A mutation in the MT-TW gene 212
Parkinsonism as neurological presentation of late-onset cerebrotendinous xanthomatosis 210
Brachial plexopathy due to breast cancer metastases: electrophysiological and imaging findings 209
Lithium neurotoxicity mimicking rapidly progressive dementia 204
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 202
Discordant manifestations in Italian brothers with GNE myopathy 201
Long-Term Bone Density Evaluation in Cerebrotendinous Xanthomatosis: Evidence of Improvement after Chenodeoxycholic Acid Treatment. 199
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease. 198
A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids 198
Polyneuropathy in cerebrotendinous xanthomatosis and response to treatment with chenodeoxycholic acid. 196
SPG5 siblings with different phenotypes showing reduction of 27-hydroxycholesterol after simvastatin-ezetimibe treatment 161
From the liver to the brain: manganese matters : Focus on cirrhosis-related Parkinsonism. 159
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Enlarging brain xanthomas in a patient with cerebrotendinous xanthomatosis. 128
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Mitochondrial recessive ataxia syndrome: A neurological rarity not to be missed. 118
Ataxia with oculomotor apraxia type 2: not always an easy diagnosis 118
Erratum: Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1 (Scientific Reports (2016) 6 (38174) DOI: 10.1038/srep38174) 115
Evaluation of cholesterol metabolism in cerebrotendinous xanthomatosis 113
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Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review 108
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Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review (Journal of Neurology, (2022), 269, 1, (437-450), 10.1007/s00415-021-10792-3) 107
The safety and effectiveness of chenodeoxycholic acid treatment in patients withcerebrotendinous xanthomatosis:two retrospective cohort studies 107
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Familial Alzheimer’s disease associated with heterozygous NPC1 mutation 106
Primary familiall brain calcification caused by MYORG mutations in an Italian family 101
Oculomotor features in SCA27B patients 99
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Primary familial brain calcification with mild phenotype due to a new PDGFB mutation 87
Multiple sclerosis and chronic progressive external ophthalmoplegia associated with a large scale mitochondrial DNA single deletion 67
Treatment of SPG5 with cholesterol-lowering drugs 64
Primary familial brain calcification: update on molecular genetics 61
Neuromuscular excitability changes produced by sustained voluntary contraction and response to mexiletine in myotonia congenita 59
Syntactic complexity in Mild Cognitive Impairment due to Alzheimer’s disease (MCI-AD): long-distance dependencies and working memory in comprehension of relative clauses 23
Totale 12.856
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Categoria #
all - tutte 33.809
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 33.809
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021279 0 0 0 0 0 0 0 0 0 86 86 107
2021/2022699 33 89 39 41 47 26 49 17 48 85 76 149
2022/2023981 58 66 133 125 106 192 21 77 105 58 22 18
2023/2024677 36 21 58 30 17 192 246 15 3 13 4 42
2024/20251.479 17 73 136 60 227 102 64 66 130 42 153 409
2025/20263.739 283 532 910 434 703 114 316 117 139 191 0 0
Totale 12.856