IRIS
ORLACCHIO, ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 10.183
EU - Europa 1.859
AS - Asia 742
SA - Sud America 6
AF - Africa 5
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
Totale 12.799
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Nazione #
US - Stati Uniti d'America 10.178
SG - Singapore 423
UA - Ucraina 414
PL - Polonia 348
DE - Germania 260
IE - Irlanda 225
CN - Cina 204
FR - Francia 179
IT - Italia 99
FI - Finlandia 86
KR - Corea 84
GB - Regno Unito 74
RU - Federazione Russa 58
SE - Svezia 53
NL - Olanda 29
BE - Belgio 21
JP - Giappone 14
CA - Canada 4
EG - Egitto 4
IN - India 4
CL - Cile 3
ES - Italia 3
KG - Kirghizistan 3
AL - Albania 2
AU - Australia 2
CH - Svizzera 2
EU - Europa 2
PT - Portogallo 2
RO - Romania 2
UZ - Uzbekistan 2
VN - Vietnam 2
AE - Emirati Arabi Uniti 1
AR - Argentina 1
AT - Austria 1
BD - Bangladesh 1
BG - Bulgaria 1
BR - Brasile 1
DM - Dominica 1
FK - Isole Falkland (Malvinas) 1
IQ - Iraq 1
IR - Iran 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
TN - Tunisia 1
Totale 12.799
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Città #
Woodbridge 2.627
Houston 1.846
Wilmington 1.454
Fairfield 797
Ann Arbor 659
Jacksonville 407
Singapore 390
Kraków 348
Ashburn 334
Cambridge 292
Seattle 285
Dublin 225
Chandler 203
Medford 176
Beijing 114
Santa Clara 99
Lawrence 84
Dearborn 66
Menlo Park 50
San Diego 41
Mülheim 33
New York 33
Moscow 24
Milan 23
London 22
University Park 21
Zhengzhou 21
Mountain View 20
Norwalk 20
Verona 19
Falls Church 17
Waanrode 16
Hefei 13
Redwood City 13
Rome 13
Nanjing 11
Chicago 10
Detroit 9
Saint Petersburg 6
Brussels 5
Indiana 5
Kunming 5
Mcallen 5
Fremont 4
Guangzhou 4
Hebei 4
Jinan 4
Palo Alto 4
Shanghai 4
Tokyo 4
Bologna 3
Helsinki 3
Islington 3
Prescot 3
Toronto 3
Xian 3
Ypsilanti 3
Cairo 2
Casarsa della Delizia 2
Chiswick 2
Defiance 2
Groningen 2
Kilburn 2
Leawood 2
Newry 2
Nuremberg 2
Odessa 2
Prato 2
San Francisco 2
Shenyang 2
Tiranë 2
Turin 2
Antwerp 1
Bangalore 1
Baotou 1
Basra 1
Brisbane 1
Cagliari 1
Ceres 1
Chengdu 1
Columbus 1
Cupertino 1
Dong Ket 1
Dubai 1
Federal 1
Genova 1
Hangzhou 1
Hanoi 1
Hounslow 1
Jinhua 1
Kannur 1
Kumar 1
Lausanne 1
Los Angeles 1
Madrid 1
Miami 1
Nürnberg 1
Perm 1
Perugia 1
Phnom Penh 1
Totale 10.968
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Nome #
Treatment of the symptoms of Huntington's disease: Preliminary results comparing aripiprazole and tetrabenazine 472
Spontaneous sleep modulates the firing pattern of Parkinsonian subthalamic nucleus 440
AD with subcortical white matter lesions and vascular dementia: CSF markers for differential diagnosis 432
Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy 402
Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4 402
Association analysis between Alzheimer's disease and the Nicastrin gene polymorphisms 379
Subthalamic stimulation activates internal pallidus: evidence from cGMP microdialysis in PD patients 376
CSF markers in Alzheimer disease patients are not related to the different degree of cognitive impairment 352
New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1 348
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis 346
Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease 345
Acanthocytosis as a predisposing factor non-ketotic hyperglycemia induced chorea-ballism 336
Neuroacanthocytosis associated with a defect of the 4.1R membrane protein 326
A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts 322
Clinical and genetic study of a large SPG4 Italian family 299
Hereditary spastic paraplegia:A novel mutation and expansion of the phenotype variability in SPG10 273
Late-onset spastic paraplegia: Aberrant SPG11 transcripts generated by a novel splice site donor mutation 163
Neonatal SCA2 Presenting With Choreic Movements and Dystonia With Dystonic Jerks, Retinitis, Seizures, and Hypotonia 157
Exome sequencing identifies a novel intronic mutation in ENG that causes recurrence of pulmonary arteriovenous malformations 153
Bridging Over the Troubled Heterogeneity of SPG-Related Pathologies: Mechanisms Unite What Genetics Divide 148
Vascular anomalies of the celiac trunk and implications in treatment of HCC with TACE. Description of a case and review of the literature 143
Up-regulation of glycohydrolases in Alzheimer's Disease fibroblasts correlates with Ras activation 139
The role of reticulons in neurodegenerative diseases 138
Stem cells: an overview of the current status of therapies for central and peripheral nervous system diseases 130
1H-MRS in patients with multiple sclerosis undergoing treatment with interferon beta-1a: results of a preliminary study 126
Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE 126
Increasing and persistent DWI changes in a patient with hereditary diffuse leukoencephalopathy with spheroids 125
A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia 122
A new CSF1R mutation presenting with an extensive white matter lesion mimicking primary progressive multiple sclerosis 119
Late-onset CMT2 associated with a novel missense mutation in the cytoplasmic domain of the MPZ gene 118
Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees 118
Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation 117
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity 117
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity 115
Effects of Vitamin C on Fibroblasts from Sporadic Alzheimer’s Disease Patients 114
Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia 113
Patented therapeutic RNAi strategies for neurodegenerative diseases of the CNS. 111
Research actuality in the genetics of stroke 111
Characterization of human Enah gene. 111
Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease 111
RNA interference as a tool for Alzheimer's disease therapy 110
PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier 109
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12 108
Application of long-range polymerase chain reaction in the diagnosis of X-linked dystonia-parkinsonism 107
Expression of cathepsins S and D signals a distinctive biochemical trait in CD34+ hematopoietic stem cells of relapsing-remitting multiple sclerosis patients 107
Platelets release their lysosomal content in vivo in humans upon activation 105
Caspase 3 activation and PARP cleavage in lymphocytes from newborn babies of diabetic mothers with unbalanced glycaemic control 104
MicroRNA Implications across Neurodevelopment and Neuropathology 103
miR128 up-regulation correlates with impaired amyloid β(1-42) degradation in monocytes from patients with sporadic Alzheimer's disease 103
Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms 103
Spastic paraplegia in Romania: high prevalence of SPG4 mutations 102
Lysosomal β-galactosidase and β-hexosaminidase activities correlate with clinical stages of dementia associated with Alzheimer's disease and type 2 diabetes mellitus 101
Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis 101
Alpha2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease 101
Identification of maternal uniparental isodisomy of chromosome 10 in a patient with mitochondrial DNA depletion syndrome 100
Oromandibular dystonia associated with SCA36 100
Nitric oxide depletion alters hematopoietic stem cell commitment toward immunogenic dendritic cells 99
Development of a New Tool for 3D Modeling for Regenerative Medicine 98
Compositions and methods for treatment of Parkinson's disease: a patent evaluation of WO2011/102847A1 97
Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease 97
Cytokine secretion and nitric oxide production by mononuclear cells of patients with multiple sclerosis 97
Clinical and genetic study of a large Italian family linked to SPG12 locus 97
Platelet glycohydrolase activities: characterization and release 96
Therapy with drug product AZD-103 may ease Alzheimer’s disease 95
Stem cells and neurological diseases 94
Cathepsin D expression is decreased in Alzheimer's disease fibroblasts 94
The apolipoprotein E2 isoform is associated with accelerated onset of coronary artery disease in systemic lupus erythematosus 93
Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene 90
Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis 85
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease 83
Beta-N-acetylhexosaminidase in peripheral blood lymphocytes and monocytes in the different forms and stages of multiple sclerosis 79
beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I 78
Hexosaminidase in Trichinella spiralis is a single protein with alpha- and beta-subunits catalytic activities 78
Purification and properties of human urinary beta-D-mannosidase 75
Non-replication of association between MAPT-SNCA synergistical interaction and susceptibility to Parkinson’s Disease in a southern European population 74
Constitutive expression of beta-N-acetylhexosaminidase in a microglial cell line: transcriptional modulation by lipopolysaccharide and serum factors 70
Activity levels of a beta1,6 N-acetylglucosaminyltransferase in lymphomonocytes from multiple sclerosis patients 69
Elevated beta-N-acetylhexosaminidase activity in focal dystonia fibroblasts 68
On the identification of two beta-D-mannosidase forms in human kidney and urine 68
Polymorphisms in the MAPT gene and risk of Parkinson disease in a Greek population: A case-control study. 66
Hereditary spastic paraplegia: clinical genetic study of 15 families 65
Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis 64
Promoter characterization and structure of the gene encoding mouse lysosomal alpha-d-mannosidase 63
Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease 59
Totale 12.850
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Categoria #
all - tutte 35.223
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 35.223
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.570 0 0 227 366 244 357 240 335 277 236 104 184
2020/20211.401 106 191 112 166 92 92 159 116 110 57 175 25
2021/2022744 18 120 21 23 40 60 43 30 46 48 47 248
2022/2023693 104 56 9 53 55 206 66 21 52 0 52 19
2023/2024158 20 8 9 5 20 36 5 3 5 1 1 45
2024/2025712 32 484 196 0 0 0 0 0 0 0 0 0
Totale 12.850