IRIS - Res&Arch Institutional Research Information System - Research & Archive

ORLACCHIO, Antonio
 Distribuzione geografica
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Continente #
NA - Nord America 6.581
AS - Asia 5.547
EU - Europa 4.520
Continente sconosciuto - Info sul continente non disponibili 1.622
SA - Sud America 1.302
AF - Africa 159
OC - Oceania 10
Totale 19.741
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Nazione #
US - Stati Uniti d'America 6.367
SG - Singapore 2.420
IE - Irlanda 1.121
RU - Federazione Russa 1.078
BR - Brasile 1.045
VN - Vietnam 893
HK - Hong Kong 715
CN - Cina 680
IT - Italia 568
FR - Francia 402
FI - Finlandia 337
DE - Germania 211
SE - Svezia 136
GB - Regno Unito 133
IN - India 127
UA - Ucraina 124
AT - Austria 109
CA - Canada 101
BD - Bangladesh 99
AR - Argentina 87
PL - Polonia 85
ID - Indonesia 77
KR - Corea 63
MX - Messico 60
IQ - Iraq 58
JP - Giappone 58
ZA - Sudafrica 56
TR - Turchia 49
NL - Olanda 46
EC - Ecuador 41
UZ - Uzbekistan 41
PK - Pakistan 37
EU - Europa 36
MY - Malesia 36
CO - Colombia 34
RO - Romania 32
SA - Arabia Saudita 30
TH - Thailandia 29
CH - Svizzera 28
PH - Filippine 28
VE - Venezuela 28
MA - Marocco 26
ES - Italia 25
CL - Cile 21
BE - Belgio 16
JO - Giordania 15
LB - Libano 15
PE - Perù 15
GR - Grecia 14
KE - Kenya 14
PY - Paraguay 14
EG - Egitto 13
CZ - Repubblica Ceca 12
AZ - Azerbaigian 11
JM - Giamaica 11
AU - Australia 10
LT - Lituania 9
NP - Nepal 9
OM - Oman 9
TN - Tunisia 9
KZ - Kazakistan 8
PA - Panama 8
UY - Uruguay 8
AE - Emirati Arabi Uniti 7
BO - Bolivia 7
DZ - Algeria 7
NI - Nicaragua 7
DK - Danimarca 6
ET - Etiopia 6
IL - Israele 6
KW - Kuwait 6
SN - Senegal 6
AL - Albania 5
KG - Kirghizistan 5
SK - Slovacchia (Repubblica Slovacca) 5
TT - Trinidad e Tobago 5
CI - Costa d'Avorio 4
CR - Costa Rica 4
GH - Ghana 4
HN - Honduras 4
SY - Repubblica araba siriana 4
DO - Repubblica Dominicana 3
GT - Guatemala 3
MD - Moldavia 3
PT - Portogallo 3
QA - Qatar 3
BG - Bulgaria 2
BY - Bielorussia 2
GA - Gabon 2
GD - Grenada 2
HR - Croazia 2
LV - Lettonia 2
MU - Mauritius 2
PS - Palestinian Territory 2
SC - Seychelles 2
SV - El Salvador 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AO - Angola 1
BF - Burkina Faso 1
Totale 18.134
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Città #
Singapore 1.566
Dublin 1.113
San Jose 812
Hong Kong 705
San Mateo 675
Dong Ket 520
Chandler 503
Ashburn 459
Moscow 385
Santa Clara 358
Boardman 308
Medford 291
Princeton 291
Lauterbourg 270
Altamura 193
Wilmington 180
Redmond 169
Lawrence 155
Ho Chi Minh City 144
Beijing 136
Los Angeles 125
Perugia 118
New York 100
Ann Arbor 96
Saint Petersburg 91
São Paulo 83
Munich 81
Hanoi 76
The Dalles 72
Vienna 67
Seoul 57
Helsinki 56
Norwalk 51
Tokyo 47
Jakarta 44
Montreal 37
Nuremberg 35
Warsaw 35
Andover 34
Brooklyn 34
Rio de Janeiro 34
San Paolo di Civitate 32
Orem 31
Rome 30
Boston 28
Johannesburg 28
Stockholm 28
Timisoara 28
Bangkok 27
Chennai 27
Houston 27
Kraków 27
Chicago 26
Dallas 26
Baghdad 25
Shanghai 25
Denver 24
Amsterdam 23
Belo Horizonte 22
Frankfurt am Main 22
Guangzhou 22
Phoenix 22
Piscataway 22
Atlanta 21
Milan 21
Haiphong 20
Kuala Selangor 19
Mumbai 19
Turku 19
Jacksonville 18
Den Haag 17
London 17
Tashkent 17
Brussels 16
Amman 15
Campinas 15
Curitiba 15
Manila 15
Mexico City 15
Poplar 15
Quito 15
Dhaka 14
Lahore 14
Manchester 14
Ottawa 14
Porto Alegre 14
Redwood City 14
Brasília 13
Charlotte 13
Council Bluffs 13
Salvador 13
Cape Town 12
Falkenstein 12
Guarulhos 12
Tianjin 12
Baku 11
Changsha 11
Goiânia 11
Istanbul 11
Medellín 11
Totale 11.726
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Nome #
Beneficial effect of Crocus sativus stigma extract in amyloid-beta degradation by monocytes from sporadic Alzheimer's disease patients 162
Alpha2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease 156
COX inhibitors and bone: A safer impact on osteoblasts by NO-releasing NSAIDs 136
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 130
Clinical and genetic study of an Italian family with complicated hereditary spastic paraplegia and Alzheimer's disease 130
1H-MRS in patients with multiple sclerosis undergoing treatment with interferon beta-1a: results of a preliminary study 125
CSF biomarkers, impairment of cerebral hemodynamics and degree of cognitive decline: An overview in different dementia subtypes 125
Beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I 123
Trans-crocetin improves amyloid-β degradation in monocytes from Alzheimer's Disease patients 123
Lesser motor disability in adulthood: A ten-year follow-up of a dyskinetic patient with ADCY5 mutation 120
Caspase 3 activation and PARP cleavage in lymphocytes from newborn babies of diabetic mothers with unbalanced glycaemic control 118
Activity levels of a beta1,6 N-acetylglucosaminyltransferase in lymphomonocytes from multiple sclerosis patients 115
Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability 115
miR128 up-regulation correlates with impaired amyloid β(1-42) degradation in monocytes from patients with sporadic Alzheimer's disease 115
Effects of vitamin C on fibroblasts from sporadic Alzheimer's disease patients 114
Acid glycohydrolase activities in lymphomonocyte plasma- membranes of patients with multiple sclerosis 114
Clinico-genetic study of two Japanese pedigrees with hereditary spastic paraparesis and Alzheimer’s disease 114
HSP-SPG5A/CYP7B1: unusual clinical and genetic characteristics in an Indian family 107
Recurrent de novo missense variant E210K in UBTF causes juvenile dystonia-parkinsonism 106
A novel AIFM1 missense mutation in a Japanese patient with ataxic sensory neuronopathy and hearing impairment 104
SPG11-related parkinsonism: Clinical profile, molecular imaging and l-dopa response 103
a-D-Mannosidases in patients with familial Alzheimer’s disease 102
Phenotype variability and allelic heterogeneity in KMT2B-Associated disease 102
Prevalence of Cardiovascular Diseases in South Asians: Scrutinizing Traditional Risk Factors and Newly Recognized Risk Factors Sarcopenia and Osteopenia/Osteoporosis 101
Cathepsin D expression is decreased in Alzheimer's disease fibroblasts 101
Transmission Jeopardy of Adenomatosis Polyposis Coli and Methylenetetrahydrofolate Reductase in Colorectal Cancer 101
Nano- from nature to nurture: A comprehensive review on facets, trends, perspectives and sustainability of nanotechnology in the food sector 101
A clinico-genetical study in a large cohort of patients with spastic paraplegia type 4 (SPG4) 100
Crocus sativus L. stigma extract improves amyloid-β degradation mediated by Cathepsin B in monocytes from Alzheimer’s Disease patients 100
Hereditary spastic paraplegia and Alzheimer’s disease: clinical and genetic study of a Brazilian family 100
Lysosomal proteases cathepsin D, B, and L are down-regulated in fibroblasts from Alzheimer’s disease patients 99
Clinical and genetic features of a large cohort of Italian SPG4 patients from the D.A.I.S.Y. collaborative network 99
New pathological findings in an international cohort of hereditary spastic paraplegia 4 patients. 98
Clinical and genetic research in a large Ukrainian family with autosomal recessive hereditary spastic paraplegia 96
Association analysis between Alzheimer's disease and the Nicastrin gene polymorphisms 95
Spastic paraplegia type 4: a novel SPAST splice site donor mutation and expansion of the phenotype variability 94
Identification of ALS5/SPG11/KIAA1840 Mutations in Patients with Autosomal Recessive Form of Charcot-Marie-Tooth Disease Type 2 93
ALS phenotypes with mutations in SPG11 93
Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE 93
Haploinsufficiency of KMT2B causes myoclonus-dystonia with impaired psychomotor ability 92
The Puzzle of Hereditary Spastic Paraplegia: From Epidemiology to Treatment 90
A new SPG4/SPAST mutation in an Italian family with hereditary spastic paraplegia and Alzheimer's disease 90
Hereditary Spastic Paraplegia: An Update 90
Expression of cathepsins S and D signals a distinctive biochemical trait in CD34(+) hematopoietic stem cells of relapsing-remitting multiple sclerosis patients 88
A homozygous loss-of-function mutation in DNAJA3 causes hereditary motor and sensory neuropathy with spastic paraplegia (HMSN type V) 88
A new CSF1R mutation presenting with an extensive white matter lesion mimicking primary progressive multiple sclerosis 88
Ras differentially regulates lysosomal enzymes expression 88
Acanthocytosis as a predisposing factor for non-ketotic hyperglycaemia induced chorea-ballism 88
Differential regulation of lysosomal enzymes in fibroblasts from Alzheimer’s disease patients 87
Cathepsin D expression and processing in fibroblasts from Alzheimer’s disease patients 87
Cytokine secretion and nitric oxide production by mononuclear cells of patients with multiple sclerosis 87
Spastic paraplegia type 4: a novel SPAST splice site donor mutation and expansion of the phenotype variability 87
Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis 86
Cathepsin D expression and regulation in fibroblasts from Alzheimer’s disease patients 86
A homozygous loss-of-function mutation in DNAJA3 causes hereditary motor and sensory neuropathy with spastic paraplegia (HMSN type V) 86
Neuronal inclusion formation and axonal degeneration in mutant TFG transgenic mice 86
Hereditary spastic paraplegia type 4 (SPG4): an international multicenter clinical and genetic study. 85
Constitutive expression of beta-N-acetylhexosaminidase in a microglial cell line: transcriptional modulation by lipopolysaccharide and serum factors 85
Clinical and genetic study of a Japanese family with complicated hereditary spastic paraplegia and Alzheimer's disease 85
Clinical and molecular profile of a Japanese cohort of patients with dyskinesia 85
A novel compound heterozygous TH mutation in a Japanese case of dopa-responsive dystonia with mild clinical course 84
Active secretion of lysosomal glycohydrolases by activated human platelets “in vivo” studies on lysosomal release and molecular mechanisms regulating their secretion 83
Elevated beta-N-acetylhexosaminidase activity in focal dystonia fibroblasts 83
Association study of the 5-HT6 receptor gene in Alzheimer’s disease 82
Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability 82
a-D-Mannosidases in fibroblasts from patients with Alzheimer’s disease 81
AD with subcortical white matter lesions and vascular dementia: CSF markers for differential diagnosis 81
An α-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease 81
Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene 80
Epidemiological, clinical, and genetic study in a large cohort of patients with spastic paraplegia 80
Up-regulation of glycohydrolases in Alzheimer's Disease fibroblasts correlates with Ras activation 80
Spastic paraplegia type 31: A novel REEP1 splice site donor variant and expansion of the phenotype variability 80
Hereditary Spastic Paraplegia Type 4 (SPG4): A Clinico-Genetic Study in a Large Cohort of Patients with Spastic Paraplegia 79
A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia 79
Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis 79
Characterization of human Enah gene 79
A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts 79
Hereditary spastic paraplegia: Genetic heterogeneity and common pathways 78
Search for new genes causing dementia: targets for novel diagnostics and therapeutics 78
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network 78
A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability 77
Regulation of lysosomal enzymes expression in fibroblasts from Alzheimer’s disease patients 77
Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4 77
SPG11 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 77
Apolipoprotein E 3/2 genotype is associated with early onset cognitive dysfunction in SLE 75
Restoration of arylsulphatase A activity in murine metachromatic leukodistrophy oligodendrocytes by retroviral vector-mediated gene transfer 75
Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease 74
A clinico-genetic study in a large cohort of patients with hereditary spastic paraplegia type 4 (SPG4) 74
Expression and processing of cathepsin D in fibroblasts of patients with Alzheimer’s disease 74
Cathepsin D, B and L are down-regulated in fibroblasts from Alzheimer’s disease patients 74
Impairment of lysosomal system in neurodegenerative diseases 74
Cloning of human MENA gene 74
Choreoathetosis, dystonia, and myoclonus in 3 siblings with autosomal recessive spinocerebellar ataxia type 16 73
Absence of association between APOA1 polymorphism and Alzheimer’s disease 73
Cohort profile of the Japan Dystonia Consortium: Genetic diagnosis and characteristics of movement disorders in Japan 73
miR128 up-regulation correlates with impaired Amyloid-β42 degradation in monocytes of patients with sporadic Alzheimer’s disease 73
Cathepsin B and L are down-regulated in fibroblasts from Alzheimer’s disease patients 72
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: A novel mutation in the SPG11 gene and further evidence for genetic heterogeneity 72
Influence of Ras up-regulation on lysosomal enzymes expression 72
Hereditary spastic paraplegia and Alzheimer's disease: hypothesis of a founder effect of a SPG4/SPAST mutation 72
Totale 9.245
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Categoria #
all - tutte 103.772
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 103.772
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.149 0 406 171 20 167 18 59 662 25 53 267 301
2022/20232.592 300 489 34 70 158 128 1 89 1.238 9 54 22
2023/2024993 45 88 49 23 3 12 251 27 21 52 219 203
2024/20253.651 21 329 73 61 338 273 165 205 940 251 715 280
2025/20267.085 506 371 435 1.150 883 640 1.098 354 865 512 208 63
2026/2027199 79 120 0 0 0 0 0 0 0 0 0 0
Totale 19.741