CNR Institutional Research Information System

CITTADELLA, RITA
 Distribuzione geografica
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Continente #
AS - Asia 2.584
NA - Nord America 1.622
EU - Europa 835
SA - Sud America 593
AF - Africa 40
Continente sconosciuto - Info sul continente non disponibili 15
OC - Oceania 2
Totale 5.691
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Nazione #
US - Stati Uniti d'America 1.526
SG - Singapore 1.129
BR - Brasile 480
CN - Cina 469
IT - Italia 371
VN - Vietnam 297
HK - Hong Kong 269
FR - Francia 168
NL - Olanda 155
JP - Giappone 126
KR - Corea 65
BD - Bangladesh 39
IN - India 39
CA - Canada 35
AR - Argentina 33
ID - Indonesia 33
CO - Colombia 28
GB - Regno Unito 28
DE - Germania 26
EC - Ecuador 24
MX - Messico 18
MY - Malesia 16
TH - Thailandia 14
CR - Costa Rica 13
ES - Italia 11
VE - Venezuela 11
IL - Israele 10
MA - Marocco 10
PH - Filippine 10
ZA - Sudafrica 10
IQ - Iraq 9
TR - Turchia 9
JM - Giamaica 8
RU - Federazione Russa 8
SA - Arabia Saudita 8
FI - Finlandia 7
KE - Kenya 7
PY - Paraguay 7
SE - Svezia 7
UZ - Uzbekistan 7
CL - Cile 6
TN - Tunisia 6
AL - Albania 5
CH - Svizzera 5
HN - Honduras 5
PK - Pakistan 5
UA - Ucraina 5
AZ - Azerbaigian 4
HU - Ungheria 4
IE - Irlanda 4
PL - Polonia 4
AE - Emirati Arabi Uniti 3
AT - Austria 3
BB - Barbados 3
KG - Kirghizistan 3
KZ - Kazakistan 3
NI - Nicaragua 3
SK - Slovacchia (Repubblica Slovacca) 3
AU - Australia 2
CY - Cipro 2
CZ - Repubblica Ceca 2
DO - Repubblica Dominicana 2
HR - Croazia 2
LB - Libano 2
LT - Lituania 2
LV - Lettonia 2
NP - Nepal 2
RS - Serbia 2
SM - San Marino 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
AF - Afghanistan, Repubblica islamica di 1
BE - Belgio 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 1
CI - Costa d'Avorio 1
CU - Cuba 1
EE - Estonia 1
EG - Egitto 1
ET - Etiopia 1
GE - Georgia 1
GP - Guadalupe 1
GR - Grecia 1
IM - Isola di Man 1
IR - Iran 1
JO - Giordania 1
KH - Cambogia 1
KY - Cayman, isole 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
MG - Madagascar 1
MM - Myanmar 1
MT - Malta 1
MU - Mauritius 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
Totale 5.669
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Città #
Singapore 641
Santa Clara 480
Hong Kong 265
San Jose 152
Hefei 135
Lauterbourg 124
Ho Chi Minh City 121
Tokyo 113
Beijing 84
Ashburn 78
Seoul 63
Hanoi 57
Los Angeles 46
São Paulo 43
Dallas 34
Milan 28
Rome 21
New York 20
Jakarta 14
Naples 14
Buffalo 13
Porto Alegre 13
Turin 13
Bangkok 12
Bari 12
Bologna 12
Houston 12
Atlanta 11
Belo Horizonte 11
Quito 11
Rio de Janeiro 11
San José 11
Haiphong 10
Phoenix 10
Charlotte 9
Chicago 9
Council Bluffs 9
Frankfurt am Main 9
Guangzhou 9
Kuala Selangor 9
Minamishinagawa 9
Orem 9
Toronto 8
Anoia Superiore 7
Brooklyn 7
Chennai 7
Curitiba 7
Da Nang 7
Goiânia 7
Guayaquil 7
Helsinki 7
Hải Dương 7
Manaus 7
Philadelphia 7
Queens 7
Verona 7
Washington 7
Amsterdam 6
Biên Hòa 6
Brasília 6
Denver 6
Florence 6
Genoa 6
Kuala Lumpur 6
Las Vegas 6
Manila 6
Miami 6
Montreal 6
Nairobi 6
Sorocaba 6
Tashkent 6
Bắc Ninh 5
Campinas 5
Catania 5
Dhaka 5
Kingston 5
Lấp Vò 5
Newark 5
Santo André 5
Thái Bình 5
Volta Redonda 5
Baku 4
Bến Tre 4
Fort Lauderdale 4
Jeddah 4
Juiz de Fora 4
Ligornetto 4
Modena 4
Mumbai 4
Noicattaro 4
Nuremberg 4
Osasco 4
Padua 4
Paris 4
Phủ Lý 4
Salem 4
San Antonio 4
San Diego 4
Shanghai 4
Shenzhen 4
Totale 3.083
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Nome #
La sindrome di Mc Leod: un caso clinico 310
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 90
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders 87
Cst3: fattore di rischio genetico per la Malattia di Alzheimer sporadica? 85
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 82
Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy. 74
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man 69
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype 66
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease. 64
Apolipoprotein E genotype does not influence the progression of multiple sclerosis. 63
Copy Number Variants in Alzheimer's Disease 62
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease 62
Role of the Neuregulin 1 gene (NRG1) in multiple sclerosis 61
McLeod syndrome in an Italian patient 61
Huntington's disease-like syndrome: a case report 61
Ruolo del gene Neuregulin 1 (NRG1) nella Sclerosi Multipla 60
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 58
Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency revealed by single strand conformation and sequence analysis 58
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 55
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 55
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. 53
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 52
Peripheral mRNA expression of brain-derived neurotrophic factor Val66Met polymorphism in patients with relapsing-remitting multiple sclerosis 51
Cognitive impairment and brain atrophy in patients with relapsing-remitting Multiple Sclerosis (RRMS): the role of brain derived neurotrophic factor (BDNF) gene. 49
Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene. 49
DRD2 gene polymorphism and the risk of peak-dose dyskinesias in Parkinson's disease. 49
Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). 47
D678N mutation in a patient with an early-onset Alzheimer's Disease 45
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. 45
Increased Risk for Alzheimer disease with the interaction of MPO and A2M Polymorphisms 44
Molecular characterization of the APP gene in italian patients with familial Alzheimer disease. 43
Apo-1/Fas gene polymorphisms and multiple sclerosis in Southern Italy. 42
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 42
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 42
Neuropatia ottica ereditaria di Leber s e Sclerosi Multipla: Harding s syndrome. 42
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 42
Genetic association of α2-macroglobulin polymorphisms with AD in southern Italy 42
CASP-9 : a susceptibility locus for multiple sclerosis in Italy. 41
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION 41
APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers 41
APP gene mutation (D678N) in a patient with an Early-Onset Alzheimer's Disease 41
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report 41
Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in Calabria 40
Brain-derived Neurotrophic Factor Val66Met polimorphism and the cortical response to spatial working memory. 40
Two SNPs in the Fas gene on chromosome 10 are not associated with Italian Sporadic Alzheimer s Disease. 39
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. 39
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 38
A Novel Lys 130 Gln Mutation of the TAU gene. 38
Screening for MELAS mutations in Italian patients having stroke-like episodes. 38
CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis. 38
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2. 37
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 36
Leber s hereditary optic neuropathy and Multiple Sclerosis: Harding's syndrome. 36
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy. 36
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy. 35
Sulla validità di alcuni metodi di screening di massa per il deficit di G6PD: considerazioni alla luce di una indagine eseguita su 42000 soggetti in provincia di Cosenza 35
Analisi demografica, endogamica e polimorfismo genetico del locus PGM1 nella minoranza etnica albanese della provincia di Cosenza 35
Analisi mutazionale del gene OPA1 in una famiglia affetta da atrofia ottica autosomica dominante. 35
Trauma cranico e genotipo APO-E: causa o rischio di malatia di Alzheimer? 35
Two SNPs in the Fas gene on chromosome 10 are not associated with Sporadic Alzheimer s Disease in southern Italy. 35
Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease. 35
Mutational screening of the CAPN3 in LGMD patients from Southern Italy. 34
A novel mutation (Thr116IIe) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease 34
Presenilin Enhancer-2 Gene mutations and Familial Alzheimer s Disease 34
Dati preliminare sulla struttura genetica nella provincia di Cosenza 33
A novel mutation in FKRP gene in Italian patient with LGMD. 33
Leber s hereditary optic neuropathy associated with multiple sclerosis like picture in a man. 33
Alzheimer s Disease and the Cystatin C gene polymorphism: an association study. 33
NOTCH3 gene mutations and mtDNA variations 33
A new intronic deletion of presenilin 1 gene in a patient with early onset Alzheimer Disease 33
Is M129V of the Prion protein gene ( PRNP) associated with mild temporal lobe epilepsy? 33
The frequency of Limb Girdle Muscular Dystrophy 1C in southern Italy 33
The association of the regulatory region of the PS-2 gene with Alzheimer s disease. 32
AK, ADA and 6-PGD polymorphisms in Cosenza province (Calabria, Italy) 32
Gaba(b) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy 32
Mutational analysis of the mitochondrial tRNAleu gene In Italian patients with stroke-like episodes of undetermined origin. 32
LRP1- LRPAP1 polymorphisms and risk of sporadic Alzheimer s disease. 32
Glucose 6 phpsphate dehydrogenase deficiency and endogamic study in the albanian ethnic minority of Cosenza province 32
Aspetti epidemiologici del deficit di G6PD in provincia di Cosenza. Dati preliminari 32
Elam-1 genotyping in Italian population with Multiple Sclerosis : molecular characterization of A561C variation. 31
VLA-4 and Multiple Sclerosis in Italian population. 31
Valutazione dell'attività G6PD asica eritrocitaria mediante pH-metria differenziale 31
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis. 31
Caspase-9 gene C93T polymorphism and Multiple Sclerosis patients from Southern Italy 31
Cognitive performances and brain volumes in patients with relapsing-remitting multiple sclerosis: investigating the role of BDNF Val66Met polymorphism. 30
Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis. 30
N-methyl-D-aspartate receptor subunit NR1 gene (GRIN1) and temporal lobe epilepsy: no evidence of association analysis for genetic variant in promoter region of the gene. 30
Laboratory diagnosis of G6PD deficiency in association with beta thalassemia trait 30
Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis. 30
Gene symbol: PSEN2. Disease: Alzheimer disease. 29
A new human mtDNA polymorphism: MTND6: 14562 (C-->T). 29
Two snps in the Fas gene on chromosome 10 are not associated with sporadic Alzheimer s disease. 29
pH-metria differenziale e test citochimico di Betke nella diagnostica di laboratorio del deficit di G6PD: validità dei metodi e loro correlazioni 29
The association of single nucleotide E-selectin gene polymorphism with Multiple Sclerosis . 29
CASP-9 exon 1 polymorphism in patients with Multiple Sclerosis. 29
Variations in two lipid metabolizing genes and susceptibility to sporadic Alzheimer s disease. 29
Identificazione di marcatori nel gene della presenilina-2 predittivi di malattia di alzheimer familiare. 29
Gkucose-6-phosphate dehydrogenase (G6PD) deficiency in southern Italy: a study on the population of the Cosenza province 28
Determinazione potenziometrica della piruvato chinasi eritrocitaria 28
The frequency of limb girdle muscular dystrophy 1c in southern Italy 28
Totale 4.478
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Categoria #
all - tutte 19.698
article - articoli 10.619
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 30.317
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202417 0 0 0 0 0 0 0 0 3 0 13 1
2024/20251.954 5 11 141 85 486 24 28 73 29 145 465 462
2025/20263.006 102 252 273 439 514 134 482 224 267 173 96 50
2026/2027714 167 184 363 0 0 0 0 0 0 0 0 0
Totale 5.691