IRIS
ORLACCHIO, ANTONIO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 10.695
AS - Asia 2.644
EU - Europa 2.160
SA - Sud America 361
AF - Africa 33
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 15.898
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 10.664
SG - Singapore 1.535
UA - Ucraina 417
CN - Cina 385
PL - Polonia 334
BR - Brasile 309
DE - Germania 293
HK - Hong Kong 267
RU - Federazione Russa 235
FR - Francia 229
IE - Irlanda 222
VN - Vietnam 170
IT - Italia 113
FI - Finlandia 99
KR - Corea 85
GB - Regno Unito 82
JP - Giappone 61
SE - Svezia 58
NL - Olanda 31
ID - Indonesia 25
AR - Argentina 23
BD - Bangladesh 22
BE - Belgio 21
IN - India 20
TH - Thailandia 13
CA - Canada 12
EC - Ecuador 12
MX - Messico 10
PK - Pakistan 9
AE - Emirati Arabi Uniti 7
EG - Egitto 7
ES - Italia 7
AT - Austria 6
IQ - Iraq 6
MY - Malesia 6
ZA - Sudafrica 6
MA - Marocco 5
PH - Filippine 5
TN - Tunisia 5
CL - Cile 4
CO - Colombia 4
KE - Kenya 4
UZ - Uzbekistan 4
CH - Svizzera 3
JO - Giordania 3
KG - Kirghizistan 3
LB - Libano 3
VE - Venezuela 3
AL - Albania 2
AU - Australia 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
TR - Turchia 2
BB - Barbados 1
BG - Bulgaria 1
BO - Bolivia 1
CD - Congo 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
CZ - Repubblica Ceca 1
DM - Dominica 1
DO - Repubblica Dominicana 1
FK - Isole Falkland (Malvinas) 1
HR - Croazia 1
IL - Israele 1
IR - Iran 1
JM - Giamaica 1
KH - Cambogia 1
KW - Kuwait 1
LT - Lituania 1
MG - Madagascar 1
NC - Nuova Caledonia 1
NP - Nepal 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
TG - Togo 1
TT - Trinidad e Tobago 1
TW - Taiwan 1
Totale 15.898
Salva come PNG Salva come JPEG
Città #
Woodbridge 2.526
Houston 1.804
Wilmington 1.411
Fairfield 796
Singapore 676
Ann Arbor 655
Jacksonville 403
Ashburn 374
Kraków 325
Cambridge 289
Seattle 287
Hong Kong 266
Dublin 222
San Jose 213
Chandler 202
Medford 174
Beijing 147
The Dalles 110
Santa Clara 108
Lawrence 83
Dearborn 66
Tokyo 51
Lauterbourg 50
Menlo Park 49
Ho Chi Minh City 48
Hanoi 44
Los Angeles 40
New York 40
San Diego 40
Buffalo 38
Moscow 34
Mülheim 33
London 25
Milan 24
São Paulo 24
Zhengzhou 22
University Park 21
Mountain View 20
Norwalk 20
Munich 19
Verona 19
Jakarta 18
Chicago 17
Falls Church 17
Waanrode 16
Rome 15
Redondo Beach 14
Bangkok 13
Redwood City 13
Council Bluffs 12
Hefei 12
Dallas 11
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
Atlanta 6
Boston 6
Brooklyn 6
Curitiba 6
Miami 6
Phoenix 6
Saint Petersburg 6
Shanghai 6
Brussels 5
Campinas 5
Columbus 5
Guangzhou 5
Haiphong 5
Indiana 5
Johannesburg 5
Kunming 5
Manila 5
Mcallen 5
Nuremberg 5
Orem 5
Osasco 5
Porto Alegre 5
Stockholm 5
Cairo 4
Chennai 4
Florianópolis 4
Fremont 4
Goiânia 4
Guayaquil 4
Hebei 4
Jinan 4
Kuala Selangor 4
Lahore 4
Nairobi 4
Palo Alto 4
San Francisco 4
Santo André 4
Toronto 4
Totale 12.227
Salva come PNG Salva come JPEG
Nome #
Neuroacanthocytosis associated with a defect of the 4.1R membrane protein 518
Treatment of the symptoms of Huntington's disease: Preliminary results comparing aripiprazole and tetrabenazine 506
Spontaneous sleep modulates the firing pattern of Parkinsonian subthalamic nucleus 503
AD with subcortical white matter lesions and vascular dementia: CSF markers for differential diagnosis 492
Clinical and genetic study of a large SPG4 Italian family 491
Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy 447
Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4 443
Association analysis between Alzheimer's disease and the Nicastrin gene polymorphisms 423
Subthalamic stimulation activates internal pallidus: evidence from cGMP microdialysis in PD patients 422
CSF markers in Alzheimer disease patients are not related to the different degree of cognitive impairment 399
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis 390
Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease 387
Acanthocytosis as a predisposing factor non-ketotic hyperglycemia induced chorea-ballism 386
A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts 383
New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1 368
Therapy with drug product AZD-103 may ease Alzheimer’s disease 280
Exome sequencing identifies a novel intronic mutation in ENG that causes recurrence of pulmonary arteriovenous malformations 200
Vascular anomalies of the celiac trunk and implications in treatment of HCC with TACE. Description of a case and review of the literature 199
Late-onset spastic paraplegia: Aberrant SPG11 transcripts generated by a novel splice site donor mutation 194
Bridging Over the Troubled Heterogeneity of SPG-Related Pathologies: Mechanisms Unite What Genetics Divide 190
Alpha2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease 189
Neonatal SCA2 Presenting With Choreic Movements and Dystonia With Dystonic Jerks, Retinitis, Seizures, and Hypotonia 179
A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia 175
Up-regulation of glycohydrolases in Alzheimer's Disease fibroblasts correlates with Ras activation 173
Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE 173
The role of reticulons in neurodegenerative diseases 163
1H-MRS in patients with multiple sclerosis undergoing treatment with interferon beta-1a: results of a preliminary study 161
Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees 158
Stem cells: an overview of the current status of therapies for central and peripheral nervous system diseases 156
A new CSF1R mutation presenting with an extensive white matter lesion mimicking primary progressive multiple sclerosis 155
miR128 up-regulation correlates with impaired amyloid β(1-42) degradation in monocytes from patients with sporadic Alzheimer's disease 153
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity 152
Increasing and persistent DWI changes in a patient with hereditary diffuse leukoencephalopathy with spheroids 152
Application of long-range polymerase chain reaction in the diagnosis of X-linked dystonia-parkinsonism 152
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12 145
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity 145
Late-onset CMT2 associated with a novel missense mutation in the cytoplasmic domain of the MPZ gene 144
Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation 143
Oromandibular dystonia associated with SCA36 142
Spastic paraplegia in Romania: high prevalence of SPG4 mutations 141
Patented therapeutic RNAi strategies for neurodegenerative diseases of the CNS. 141
Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease 141
Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms 141
Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia 140
RNA interference as a tool for Alzheimer's disease therapy 137
Effects of Vitamin C on Fibroblasts from Sporadic Alzheimer’s Disease Patients 134
Research actuality in the genetics of stroke 134
Characterization of human Enah gene. 134
PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier 133
Caspase 3 activation and PARP cleavage in lymphocytes from newborn babies of diabetic mothers with unbalanced glycaemic control 130
Platelets release their lysosomal content in vivo in humans upon activation 130
MicroRNA Implications across Neurodevelopment and Neuropathology 129
Beta-N-acetylhexosaminidase in peripheral blood lymphocytes and monocytes in the different forms and stages of multiple sclerosis 129
Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis 129
Nitric oxide depletion alters hematopoietic stem cell commitment toward immunogenic dendritic cells 129
Lysosomal β-galactosidase and β-hexosaminidase activities correlate with clinical stages of dementia associated with Alzheimer's disease and type 2 diabetes mellitus 128
Compositions and methods for treatment of Parkinson's disease: a patent evaluation of WO2011/102847A1 128
Platelet glycohydrolase activities: characterization and release 127
Expression of cathepsins S and D signals a distinctive biochemical trait in CD34+ hematopoietic stem cells of relapsing-remitting multiple sclerosis patients 126
Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis 126
Cytokine secretion and nitric oxide production by mononuclear cells of patients with multiple sclerosis 126
Clinical and genetic study of a large Italian family linked to SPG12 locus 125
Identification of maternal uniparental isodisomy of chromosome 10 in a patient with mitochondrial DNA depletion syndrome 124
Stem cells and neurological diseases 122
Cathepsin D expression is decreased in Alzheimer's disease fibroblasts 122
Development of a New Tool for 3D Modeling for Regenerative Medicine 122
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease 122
Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease 120
beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I 119
Constitutive expression of beta-N-acetylhexosaminidase in a microglial cell line: transcriptional modulation by lipopolysaccharide and serum factors 116
The apolipoprotein E2 isoform is associated with accelerated onset of coronary artery disease in systemic lupus erythematosus 114
Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene 113
Hexosaminidase in Trichinella spiralis is a single protein with alpha- and beta-subunits catalytic activities 111
Activity levels of a beta1,6 N-acetylglucosaminyltransferase in lymphomonocytes from multiple sclerosis patients 109
Non-replication of association between MAPT-SNCA synergistical interaction and susceptibility to Parkinson’s Disease in a southern European population 107
Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis 106
Purification and properties of human urinary beta-D-mannosidase 101
On the identification of two beta-D-mannosidase forms in human kidney and urine 100
Polymorphisms in the MAPT gene and risk of Parkinson disease in a Greek population: A case-control study. 95
Hereditary spastic paraplegia: clinical genetic study of 15 families 93
Promoter characterization and structure of the gene encoding mouse lysosomal alpha-d-mannosidase 88
Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease 87
Elevated beta-N-acetylhexosaminidase activity in focal dystonia fibroblasts 83
Totale 15.943
Salva come PNG Salva come JPEG
Categoria #
all - tutte 49.710
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 49.710
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021254 0 0 0 0 0 0 0 0 0 57 172 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
2025/20261.949 138 115 298 152 161 107 264 313 219 182 0 0
Totale 15.943