IRIS
ORLACCHIO, ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 11.912
AS - Asia 2.759
EU - Europa 2.239
SA - Sud America 378
Continente sconosciuto - Info sul continente non disponibili 47
AF - Africa 34
OC - Oceania 3
Totale 17.372
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Nazione #
US - Stati Uniti d'America 11.810
SG - Singapore 1.542
UA - Ucraina 417
CN - Cina 403
PL - Polonia 334
BR - Brasile 318
DE - Germania 294
HK - Hong Kong 270
RU - Federazione Russa 236
FR - Francia 229
IE - Irlanda 222
IT - Italia 181
VN - Vietnam 171
FI - Finlandia 99
BD - Bangladesh 96
GB - Regno Unito 87
KR - Corea 85
JP - Giappone 62
SE - Svezia 60
CA - Canada 34
NL - Olanda 31
ID - Indonesia 26
AR - Argentina 24
BE - Belgio 21
IN - India 20
CR - Costa Rica 16
TH - Thailandia 14
JM - Giamaica 13
EC - Ecuador 12
CO - Colombia 10
MX - Messico 10
MY - Malesia 10
PK - Pakistan 9
AE - Emirati Arabi Uniti 8
ES - Italia 8
EG - Egitto 7
HN - Honduras 7
PH - Filippine 7
AT - Austria 6
IQ - Iraq 6
ZA - Sudafrica 6
MA - Marocco 5
TN - Tunisia 5
CL - Cile 4
KE - Kenya 4
PR - Porto Rico 4
UZ - Uzbekistan 4
CH - Svizzera 3
JO - Giordania 3
KG - Kirghizistan 3
LB - Libano 3
NI - Nicaragua 3
PY - Paraguay 3
SA - Arabia Saudita 3
SV - El Salvador 3
TT - Trinidad e Tobago 3
VE - Venezuela 3
AL - Albania 2
AU - Australia 2
BG - Bulgaria 2
DM - Dominica 2
DZ - Algeria 2
EU - Europa 2
GT - Guatemala 2
LA - Repubblica Popolare Democratica del Laos 2
PE - Perù 2
PS - Palestinian Territory 2
PT - Portogallo 2
RO - Romania 2
TR - Turchia 2
BB - Barbados 1
BO - Bolivia 1
BS - Bahamas 1
CD - Congo 1
CI - Costa d'Avorio 1
CZ - Repubblica Ceca 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
KZ - Kazakistan 1
LT - Lituania 1
MG - Madagascar 1
NC - Nuova Caledonia 1
NG - Nigeria 1
NP - Nepal 1
SY - Repubblica araba siriana 1
TG - Togo 1
TW - Taiwan 1
VC - Saint Vincent e Grenadine 1
Totale 17.327
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Città #
Woodbridge 2.526
Houston 1.806
Wilmington 1.414
Fairfield 796
Singapore 677
Ann Arbor 655
Ashburn 603
Jacksonville 404
San Jose 370
Kraków 325
Cambridge 289
Seattle 289
Hong Kong 268
Dublin 222
Chandler 203
Medford 174
Beijing 150
Santa Clara 117
The Dalles 110
Council Bluffs 85
Lawrence 83
Dearborn 66
Los Angeles 56
New York 55
Tokyo 52
Lauterbourg 50
Menlo Park 49
Buffalo 48
Ho Chi Minh City 48
Hanoi 45
San Diego 41
Moscow 35
Milan 33
Mülheim 33
São Paulo 29
London 25
Chicago 23
Rome 22
Zhengzhou 22
Denver 21
University Park 21
Mountain View 20
Norwalk 20
Munich 19
Verona 19
Jakarta 18
Dallas 17
Falls Church 17
North Bergen 16
Waanrode 16
Bangkok 14
Redondo Beach 14
San José 14
Detroit 13
Redwood City 13
Atlanta 12
Hefei 12
Nanjing 11
Rio de Janeiro 11
Steuben 11
Toronto 11
Turku 9
Brasília 8
Brooklyn 8
Helsinki 8
Miami 8
Warsaw 8
Boston 7
Dhaka 7
Frankfurt am Main 7
Kingston 7
New Orleans 7
Philadelphia 7
Phoenix 7
Catania 6
Curitiba 6
Kunming 6
Saint Petersburg 6
Shanghai 6
The Bronx 6
Bologna 5
Brussels 5
Campinas 5
Columbus 5
Guangzhou 5
Haiphong 5
Indiana 5
Johannesburg 5
Manila 5
Mcallen 5
Naples 5
Nuremberg 5
Orem 5
Osasco 5
Porto Alegre 5
Stockholm 5
Cairo 4
Charlotte 4
Chennai 4
Florianópolis 4
Totale 12.868
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Nome #
Neuroacanthocytosis associated with a defect of the 4.1R membrane protein 530
Treatment of the symptoms of Huntington's disease: Preliminary results comparing aripiprazole and tetrabenazine 528
Spontaneous sleep modulates the firing pattern of Parkinsonian subthalamic nucleus 518
AD with subcortical white matter lesions and vascular dementia: CSF markers for differential diagnosis 515
Clinical and genetic study of a large SPG4 Italian family 507
Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy 476
Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4 464
Subthalamic stimulation activates internal pallidus: evidence from cGMP microdialysis in PD patients 440
Association analysis between Alzheimer's disease and the Nicastrin gene polymorphisms 435
CSF markers in Alzheimer disease patients are not related to the different degree of cognitive impairment 422
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis 410
A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts 409
Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease 402
Acanthocytosis as a predisposing factor non-ketotic hyperglycemia induced chorea-ballism 401
New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1 385
Therapy with drug product AZD-103 may ease Alzheimer’s disease 308
Exome sequencing identifies a novel intronic mutation in ENG that causes recurrence of pulmonary arteriovenous malformations 219
Late-onset spastic paraplegia: Aberrant SPG11 transcripts generated by a novel splice site donor mutation 209
Vascular anomalies of the celiac trunk and implications in treatment of HCC with TACE. Description of a case and review of the literature 207
Alpha2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease 204
Bridging Over the Troubled Heterogeneity of SPG-Related Pathologies: Mechanisms Unite What Genetics Divide 200
A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia 192
The role of reticulons in neurodegenerative diseases 190
Up-regulation of glycohydrolases in Alzheimer's Disease fibroblasts correlates with Ras activation 189
Neonatal SCA2 Presenting With Choreic Movements and Dystonia With Dystonic Jerks, Retinitis, Seizures, and Hypotonia 185
Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE 185
1H-MRS in patients with multiple sclerosis undergoing treatment with interferon beta-1a: results of a preliminary study 182
miR128 up-regulation correlates with impaired amyloid β(1-42) degradation in monocytes from patients with sporadic Alzheimer's disease 178
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity 178
Stem cells: an overview of the current status of therapies for central and peripheral nervous system diseases 174
A new CSF1R mutation presenting with an extensive white matter lesion mimicking primary progressive multiple sclerosis 172
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity 171
Increasing and persistent DWI changes in a patient with hereditary diffuse leukoencephalopathy with spheroids 171
Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees 170
Spastic paraplegia in Romania: high prevalence of SPG4 mutations 167
Application of long-range polymerase chain reaction in the diagnosis of X-linked dystonia-parkinsonism 166
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12 163
Platelet glycohydrolase activities: characterization and release 163
Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease 161
Cytokine secretion and nitric oxide production by mononuclear cells of patients with multiple sclerosis 161
Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms 158
RNA interference as a tool for Alzheimer's disease therapy 157
Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation 156
Late-onset CMT2 associated with a novel missense mutation in the cytoplasmic domain of the MPZ gene 155
Patented therapeutic RNAi strategies for neurodegenerative diseases of the CNS. 154
Effects of Vitamin C on Fibroblasts from Sporadic Alzheimer’s Disease Patients 152
Oromandibular dystonia associated with SCA36 152
Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia 150
Characterization of human Enah gene. 150
Research actuality in the genetics of stroke 148
PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier 147
Lysosomal β-galactosidase and β-hexosaminidase activities correlate with clinical stages of dementia associated with Alzheimer's disease and type 2 diabetes mellitus 146
Beta-N-acetylhexosaminidase in peripheral blood lymphocytes and monocytes in the different forms and stages of multiple sclerosis 146
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease 146
Platelets release their lysosomal content in vivo in humans upon activation 146
Caspase 3 activation and PARP cleavage in lymphocytes from newborn babies of diabetic mothers with unbalanced glycaemic control 145
Nitric oxide depletion alters hematopoietic stem cell commitment toward immunogenic dendritic cells 143
Stem cells and neurological diseases 140
MicroRNA Implications across Neurodevelopment and Neuropathology 140
Constitutive expression of beta-N-acetylhexosaminidase in a microglial cell line: transcriptional modulation by lipopolysaccharide and serum factors 140
Cathepsin D expression is decreased in Alzheimer's disease fibroblasts 139
Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis 138
Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis 137
beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I 136
Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis 135
Compositions and methods for treatment of Parkinson's disease: a patent evaluation of WO2011/102847A1 134
Development of a New Tool for 3D Modeling for Regenerative Medicine 134
Identification of maternal uniparental isodisomy of chromosome 10 in a patient with mitochondrial DNA depletion syndrome 134
Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease 134
The apolipoprotein E2 isoform is associated with accelerated onset of coronary artery disease in systemic lupus erythematosus 133
Expression of cathepsins S and D signals a distinctive biochemical trait in CD34+ hematopoietic stem cells of relapsing-remitting multiple sclerosis patients 133
Clinical and genetic study of a large Italian family linked to SPG12 locus 132
Hexosaminidase in Trichinella spiralis is a single protein with alpha- and beta-subunits catalytic activities 131
On the identification of two beta-D-mannosidase forms in human kidney and urine 129
Polymorphisms in the MAPT gene and risk of Parkinson disease in a Greek population: A case-control study. 127
Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene 124
Non-replication of association between MAPT-SNCA synergistical interaction and susceptibility to Parkinson’s Disease in a southern European population 122
Activity levels of a beta1,6 N-acetylglucosaminyltransferase in lymphomonocytes from multiple sclerosis patients 122
Purification and properties of human urinary beta-D-mannosidase 117
Hereditary spastic paraplegia: clinical genetic study of 15 families 108
Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease 103
Promoter characterization and structure of the gene encoding mouse lysosomal alpha-d-mannosidase 99
Elevated beta-N-acetylhexosaminidase activity in focal dystonia fibroblasts 93
Totale 17.372
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Categoria #
all - tutte 56.348
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 56.348
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022577 0 0 0 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
2025/20262.257 138 115 298 152 161 107 264 313 219 205 96 189
2026/20271.121 135 142 512 332 0 0 0 0 0 0 0 0
Totale 17.372