IRIS
ORLACCHIO, ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 10.888
AS - Asia 2.718
EU - Europa 2.199
SA - Sud America 362
AF - Africa 33
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 16.205
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Nazione #
US - Stati Uniti d'America 10.843
SG - Singapore 1.539
UA - Ucraina 417
CN - Cina 395
PL - Polonia 334
BR - Brasile 310
DE - Germania 293
HK - Hong Kong 269
RU - Federazione Russa 236
FR - Francia 229
IE - Irlanda 222
VN - Vietnam 171
IT - Italia 150
FI - Finlandia 99
KR - Corea 85
GB - Regno Unito 82
BD - Bangladesh 77
JP - Giappone 61
SE - Svezia 58
NL - Olanda 31
ID - Indonesia 25
AR - Argentina 23
BE - Belgio 21
IN - India 20
CA - Canada 17
TH - Thailandia 13
EC - Ecuador 12
MX - Messico 10
PK - Pakistan 9
AE - Emirati Arabi Uniti 8
EG - Egitto 7
ES - Italia 7
MY - Malesia 7
AT - Austria 6
IQ - Iraq 6
ZA - Sudafrica 6
MA - Marocco 5
PH - Filippine 5
TN - Tunisia 5
CL - Cile 4
CO - Colombia 4
JM - Giamaica 4
KE - Kenya 4
UZ - Uzbekistan 4
CH - Svizzera 3
CR - Costa Rica 3
JO - Giordania 3
KG - Kirghizistan 3
LB - Libano 3
VE - Venezuela 3
AL - Albania 2
AU - Australia 2
BG - Bulgaria 2
DZ - Algeria 2
EU - Europa 2
HN - Honduras 2
LA - Repubblica Popolare Democratica del Laos 2
PE - Perù 2
PS - Palestinian Territory 2
PT - Portogallo 2
PY - Paraguay 2
RO - Romania 2
SA - Arabia Saudita 2
SV - El Salvador 2
TR - Turchia 2
BB - Barbados 1
BO - Bolivia 1
CD - Congo 1
CI - Costa d'Avorio 1
CZ - Repubblica Ceca 1
DM - Dominica 1
DO - Repubblica Dominicana 1
FK - Isole Falkland (Malvinas) 1
GP - Guadalupe 1
HR - Croazia 1
IL - Israele 1
IR - Iran 1
KH - Cambogia 1
KW - Kuwait 1
LT - Lituania 1
MG - Madagascar 1
NC - Nuova Caledonia 1
NI - Nicaragua 1
NP - Nepal 1
PR - Porto Rico 1
SY - Repubblica araba siriana 1
TG - Togo 1
TT - Trinidad e Tobago 1
TW - Taiwan 1
Totale 16.205
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Città #
Woodbridge 2.526
Houston 1.805
Wilmington 1.412
Fairfield 796
Singapore 676
Ann Arbor 655
Jacksonville 403
Ashburn 382
Kraków 325
Cambridge 289
Seattle 288
San Jose 287
Hong Kong 267
Dublin 222
Chandler 202
Medford 174
Beijing 147
Santa Clara 110
The Dalles 110
Lawrence 83
Dearborn 66
New York 53
Tokyo 51
Lauterbourg 50
Menlo Park 49
Ho Chi Minh City 48
Buffalo 45
Hanoi 45
Los Angeles 45
San Diego 40
Moscow 35
Mülheim 33
Milan 28
London 25
São Paulo 24
Zhengzhou 22
University Park 21
Mountain View 20
Norwalk 20
Munich 19
Verona 19
Chicago 18
Jakarta 18
Falls Church 17
Rome 16
Waanrode 16
Council Bluffs 14
Dallas 14
Redondo Beach 14
Bangkok 13
Redwood City 13
Hefei 12
Detroit 11
Nanjing 11
Rio de Janeiro 11
Turku 9
Brasília 8
Helsinki 8
North Bergen 8
Warsaw 8
Dhaka 7
Frankfurt am Main 7
Miami 7
Atlanta 6
Boston 6
Brooklyn 6
Curitiba 6
Kunming 6
Phoenix 6
Saint Petersburg 6
Shanghai 6
Bologna 5
Brussels 5
Campinas 5
Columbus 5
Guangzhou 5
Haiphong 5
Indiana 5
Johannesburg 5
Manila 5
Mcallen 5
Nuremberg 5
Orem 5
Osasco 5
Porto Alegre 5
Stockholm 5
Toronto 5
Cairo 4
Catania 4
Chennai 4
Florianópolis 4
Fremont 4
Goiânia 4
Guayaquil 4
Hebei 4
Jinan 4
Kingston 4
Kuala Selangor 4
Lahore 4
Nairobi 4
Totale 12.357
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Nome #
Neuroacanthocytosis associated with a defect of the 4.1R membrane protein 521
Treatment of the symptoms of Huntington's disease: Preliminary results comparing aripiprazole and tetrabenazine 508
Spontaneous sleep modulates the firing pattern of Parkinsonian subthalamic nucleus 507
AD with subcortical white matter lesions and vascular dementia: CSF markers for differential diagnosis 494
Clinical and genetic study of a large SPG4 Italian family 494
Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy 451
Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4 445
Association analysis between Alzheimer's disease and the Nicastrin gene polymorphisms 424
Subthalamic stimulation activates internal pallidus: evidence from cGMP microdialysis in PD patients 423
CSF markers in Alzheimer disease patients are not related to the different degree of cognitive impairment 405
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis 393
Acanthocytosis as a predisposing factor non-ketotic hyperglycemia induced chorea-ballism 389
Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease 389
A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts 388
New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1 372
Therapy with drug product AZD-103 may ease Alzheimer’s disease 281
Exome sequencing identifies a novel intronic mutation in ENG that causes recurrence of pulmonary arteriovenous malformations 203
Vascular anomalies of the celiac trunk and implications in treatment of HCC with TACE. Description of a case and review of the literature 202
Late-onset spastic paraplegia: Aberrant SPG11 transcripts generated by a novel splice site donor mutation 198
Alpha2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease 193
Bridging Over the Troubled Heterogeneity of SPG-Related Pathologies: Mechanisms Unite What Genetics Divide 192
Neonatal SCA2 Presenting With Choreic Movements and Dystonia With Dystonic Jerks, Retinitis, Seizures, and Hypotonia 180
A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia 179
Up-regulation of glycohydrolases in Alzheimer's Disease fibroblasts correlates with Ras activation 177
The role of reticulons in neurodegenerative diseases 176
Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE 175
miR128 up-regulation correlates with impaired amyloid β(1-42) degradation in monocytes from patients with sporadic Alzheimer's disease 171
1H-MRS in patients with multiple sclerosis undergoing treatment with interferon beta-1a: results of a preliminary study 164
A new CSF1R mutation presenting with an extensive white matter lesion mimicking primary progressive multiple sclerosis 161
Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees 161
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity 160
Stem cells: an overview of the current status of therapies for central and peripheral nervous system diseases 158
Increasing and persistent DWI changes in a patient with hereditary diffuse leukoencephalopathy with spheroids 158
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity 156
Application of long-range polymerase chain reaction in the diagnosis of X-linked dystonia-parkinsonism 153
Platelet glycohydrolase activities: characterization and release 152
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12 151
Cytokine secretion and nitric oxide production by mononuclear cells of patients with multiple sclerosis 150
Spastic paraplegia in Romania: high prevalence of SPG4 mutations 147
Late-onset CMT2 associated with a novel missense mutation in the cytoplasmic domain of the MPZ gene 146
Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease 145
Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms 145
Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation 144
Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia 143
Oromandibular dystonia associated with SCA36 143
Patented therapeutic RNAi strategies for neurodegenerative diseases of the CNS. 142
RNA interference as a tool for Alzheimer's disease therapy 140
Effects of Vitamin C on Fibroblasts from Sporadic Alzheimer’s Disease Patients 138
Research actuality in the genetics of stroke 135
Characterization of human Enah gene. 135
PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier 134
Caspase 3 activation and PARP cleavage in lymphocytes from newborn babies of diabetic mothers with unbalanced glycaemic control 133
Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis 132
Platelets release their lysosomal content in vivo in humans upon activation 132
MicroRNA Implications across Neurodevelopment and Neuropathology 131
Lysosomal β-galactosidase and β-hexosaminidase activities correlate with clinical stages of dementia associated with Alzheimer's disease and type 2 diabetes mellitus 131
Nitric oxide depletion alters hematopoietic stem cell commitment toward immunogenic dendritic cells 131
Beta-N-acetylhexosaminidase in peripheral blood lymphocytes and monocytes in the different forms and stages of multiple sclerosis 130
Compositions and methods for treatment of Parkinson's disease: a patent evaluation of WO2011/102847A1 129
Expression of cathepsins S and D signals a distinctive biochemical trait in CD34+ hematopoietic stem cells of relapsing-remitting multiple sclerosis patients 127
Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis 127
Identification of maternal uniparental isodisomy of chromosome 10 in a patient with mitochondrial DNA depletion syndrome 126
Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease 126
Clinical and genetic study of a large Italian family linked to SPG12 locus 126
Development of a New Tool for 3D Modeling for Regenerative Medicine 124
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease 124
Stem cells and neurological diseases 123
Cathepsin D expression is decreased in Alzheimer's disease fibroblasts 123
beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I 122
Constitutive expression of beta-N-acetylhexosaminidase in a microglial cell line: transcriptional modulation by lipopolysaccharide and serum factors 120
The apolipoprotein E2 isoform is associated with accelerated onset of coronary artery disease in systemic lupus erythematosus 115
Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene 115
Activity levels of a beta1,6 N-acetylglucosaminyltransferase in lymphomonocytes from multiple sclerosis patients 113
Hexosaminidase in Trichinella spiralis is a single protein with alpha- and beta-subunits catalytic activities 113
Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis 111
Non-replication of association between MAPT-SNCA synergistical interaction and susceptibility to Parkinson’s Disease in a southern European population 108
Purification and properties of human urinary beta-D-mannosidase 105
On the identification of two beta-D-mannosidase forms in human kidney and urine 102
Hereditary spastic paraplegia: clinical genetic study of 15 families 97
Polymorphisms in the MAPT gene and risk of Parkinson disease in a Greek population: A case-control study. 97
Promoter characterization and structure of the gene encoding mouse lysosomal alpha-d-mannosidase 91
Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease 89
Elevated beta-N-acetylhexosaminidase activity in focal dystonia fibroblasts 86
Totale 16.250
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Categoria #
all - tutte 52.193
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 52.193
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202125 0 0 0 0 0 0 0 0 0 0 0 25
2021/2022735 18 120 20 23 39 60 43 30 44 45 47 246
2022/2023686 102 55 8 53 55 204 65 21 52 0 52 19
2023/2024152 19 7 9 5 18 34 5 3 5 1 1 45
2024/20252.123 31 480 200 90 23 56 158 47 164 143 426 305
2025/20262.256 138 115 298 152 161 107 264 313 219 205 96 188
Totale 16.250