CNR Institutional Research Information System

CITTADELLA, RITA
 Distribuzione geografica
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Continente #
AS - Asia 2.550
NA - Nord America 1.217
EU - Europa 736
SA - Sud America 545
AF - Africa 39
OC - Oceania 2
Totale 5.089
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Nazione #
US - Stati Uniti d'America 1.152
SG - Singapore 1.125
BR - Brasile 468
CN - Cina 468
VN - Vietnam 289
IT - Italia 287
HK - Hong Kong 268
FR - Francia 165
NL - Olanda 155
JP - Giappone 126
KR - Corea 65
IN - India 38
BD - Bangladesh 33
AR - Argentina 30
ID - Indonesia 30
DE - Germania 26
CA - Canada 24
GB - Regno Unito 21
EC - Ecuador 14
MX - Messico 14
MY - Malesia 13
CO - Colombia 12
TH - Thailandia 11
IL - Israele 10
MA - Marocco 10
ZA - Sudafrica 10
ES - Italia 9
IQ - Iraq 9
CR - Costa Rica 8
RU - Federazione Russa 8
SA - Arabia Saudita 8
TR - Turchia 8
FI - Finlandia 7
KE - Kenya 7
PH - Filippine 7
PY - Paraguay 7
SE - Svezia 7
UZ - Uzbekistan 7
CH - Svizzera 5
CL - Cile 5
JM - Giamaica 5
PK - Pakistan 5
TN - Tunisia 5
UA - Ucraina 5
VE - Venezuela 5
AL - Albania 4
AZ - Azerbaigian 4
HN - Honduras 4
HU - Ungheria 4
IE - Irlanda 4
PL - Polonia 4
AE - Emirati Arabi Uniti 3
AT - Austria 3
KG - Kirghizistan 3
KZ - Kazakistan 3
SK - Slovacchia (Repubblica Slovacca) 3
AU - Australia 2
BB - Barbados 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
UY - Uruguay 2
AF - Afghanistan, Repubblica islamica di 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 1
CI - Costa d'Avorio 1
CU - Cuba 1
EG - Egitto 1
ET - Etiopia 1
GE - Georgia 1
GR - Grecia 1
IM - Isola di Man 1
IR - Iran 1
JO - Giordania 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
MG - Madagascar 1
MM - Myanmar 1
MT - Malta 1
MU - Mauritius 1
NI - Nicaragua 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
PT - Portogallo 1
SI - Slovenia 1
SN - Senegal 1
SV - El Salvador 1
TT - Trinidad e Tobago 1
Totale 5.087
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Città #
Singapore 637
Santa Clara 478
Hong Kong 264
Hefei 135
Lauterbourg 124
Ho Chi Minh City 118
Tokyo 113
San Jose 111
Beijing 84
Ashburn 70
Seoul 63
Hanoi 53
Los Angeles 45
São Paulo 42
Dallas 32
Milan 23
New York 18
Rome 18
Jakarta 14
Buffalo 13
Turin 12
Belo Horizonte 11
Bologna 11
Porto Alegre 11
Rio de Janeiro 11
Bangkok 10
Haiphong 10
Naples 10
Frankfurt am Main 9
Guangzhou 9
Kuala Selangor 9
Minamishinagawa 9
Orem 9
Anoia Superiore 7
Chennai 7
Da Nang 7
Goiânia 7
Helsinki 7
Hải Dương 7
Manaus 7
San José 7
Amsterdam 6
Bari 6
Biên Hòa 6
Brasília 6
Curitiba 6
Houston 6
Nairobi 6
Phoenix 6
Sorocaba 6
Tashkent 6
Toronto 6
Bắc Ninh 5
Campinas 5
Chicago 5
Florence 5
Genoa 5
Guayaquil 5
Lấp Vò 5
Manila 5
Montreal 5
Quito 5
Santo André 5
Thái Bình 5
Verona 5
Volta Redonda 5
Atlanta 4
Baku 4
Brooklyn 4
Bến Tre 4
Catania 4
Charlotte 4
Jeddah 4
Juiz de Fora 4
Kingston 4
Kuala Lumpur 4
Las Vegas 4
Ligornetto 4
Modena 4
Mumbai 4
Nuremberg 4
Osasco 4
Padua 4
Paris 4
Phủ Lý 4
Salem 4
Shanghai 4
Shenzhen 4
Taranto 4
Tirana 4
Washington 4
Asunción 3
Atibaia 3
Baghdad 3
Bengaluru 3
Bishkek 3
Campos dos Goytacazes 3
Casablanca 3
Chalmette 3
Chengdu 3
Totale 2.905
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Nome #
La sindrome di Mc Leod: un caso clinico 254
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders 85
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 84
Cst3: fattore di rischio genetico per la Malattia di Alzheimer sporadica? 82
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 73
Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy. 71
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man 65
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype 63
Apolipoprotein E genotype does not influence the progression of multiple sclerosis. 60
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease 59
McLeod syndrome in an Italian patient 59
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease. 58
Huntington's disease-like syndrome: a case report 58
Ruolo del gene Neuregulin 1 (NRG1) nella Sclerosi Multipla 56
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 55
Copy Number Variants in Alzheimer's Disease 55
Role of the Neuregulin 1 gene (NRG1) in multiple sclerosis 52
Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency revealed by single strand conformation and sequence analysis 52
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 51
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 50
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. 48
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 47
Peripheral mRNA expression of brain-derived neurotrophic factor Val66Met polymorphism in patients with relapsing-remitting multiple sclerosis 47
Cognitive impairment and brain atrophy in patients with relapsing-remitting Multiple Sclerosis (RRMS): the role of brain derived neurotrophic factor (BDNF) gene. 46
Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene. 44
Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). 44
DRD2 gene polymorphism and the risk of peak-dose dyskinesias in Parkinson's disease. 42
Molecular characterization of the APP gene in italian patients with familial Alzheimer disease. 41
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 40
D678N mutation in a patient with an early-onset Alzheimer's Disease 40
Genetic association of α2-macroglobulin polymorphisms with AD in southern Italy 40
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. 40
CASP-9 : a susceptibility locus for multiple sclerosis in Italy. 39
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 39
Neuropatia ottica ereditaria di Leber s e Sclerosi Multipla: Harding s syndrome. 39
Apo-1/Fas gene polymorphisms and multiple sclerosis in Southern Italy. 37
Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in Calabria 37
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION 37
APP gene mutation (D678N) in a patient with an Early-Onset Alzheimer's Disease 37
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report 37
Two SNPs in the Fas gene on chromosome 10 are not associated with Italian Sporadic Alzheimer s Disease. 36
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. 36
Increased Risk for Alzheimer disease with the interaction of MPO and A2M Polymorphisms 36
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 35
Screening for MELAS mutations in Italian patients having stroke-like episodes. 34
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 34
Brain-derived Neurotrophic Factor Val66Met polimorphism and the cortical response to spatial working memory. 34
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 33
Leber s hereditary optic neuropathy and Multiple Sclerosis: Harding's syndrome. 33
APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers 33
CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis. 33
Two SNPs in the Fas gene on chromosome 10 are not associated with Sporadic Alzheimer s Disease in southern Italy. 33
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 32
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy. 32
Analisi demografica, endogamica e polimorfismo genetico del locus PGM1 nella minoranza etnica albanese della provincia di Cosenza 32
Trauma cranico e genotipo APO-E: causa o rischio di malatia di Alzheimer? 32
NOTCH3 gene mutations and mtDNA variations 32
Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease. 32
The association of the regulatory region of the PS-2 gene with Alzheimer s disease. 31
Leber s hereditary optic neuropathy associated with multiple sclerosis like picture in a man. 31
Aspetti epidemiologici del deficit di G6PD in provincia di Cosenza. Dati preliminari 31
Presenilin Enhancer-2 Gene mutations and Familial Alzheimer s Disease 31
Alzheimer s Disease and the Cystatin C gene polymorphism: an association study. 31
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2. 30
Is M129V of the Prion protein gene ( PRNP) associated with mild temporal lobe epilepsy? 30
Cognitive performances and brain volumes in patients with relapsing-remitting multiple sclerosis: investigating the role of BDNF Val66Met polymorphism. 29
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy. 29
A novel mutation in FKRP gene in Italian patient with LGMD. 29
Laboratory diagnosis of G6PD deficiency in association with beta thalassemia trait 29
A novel mutation (Thr116IIe) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease 29
LRP1- LRPAP1 polymorphisms and risk of sporadic Alzheimer s disease. 29
Glucose 6 phpsphate dehydrogenase deficiency and endogamic study in the albanian ethnic minority of Cosenza province 29
Analisi mutazionale del gene OPA1 in una famiglia affetta da atrofia ottica autosomica dominante. 29
A new intronic deletion of presenilin 1 gene in a patient with early onset Alzheimer Disease 29
The frequency of Limb Girdle Muscular Dystrophy 1C in southern Italy 29
Dati preliminare sulla struttura genetica nella provincia di Cosenza 28
Elam-1 genotyping in Italian population with Multiple Sclerosis : molecular characterization of A561C variation. 28
A Novel Lys 130 Gln Mutation of the TAU gene. 28
Mutational analysis of the mitochondrial tRNAleu gene In Italian patients with stroke-like episodes of undetermined origin. 28
Mutational screening of the CAPN3 in LGMD patients from Southern Italy. 28
Valutazione dell'attività G6PD asica eritrocitaria mediante pH-metria differenziale 28
CASP-9 exon 1 polymorphism in patients with Multiple Sclerosis. 28
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis. 28
Caspase-9 gene C93T polymorphism and Multiple Sclerosis patients from Southern Italy 28
A new human mtDNA polymorphism: MTND6: 14562 (C-->T). 27
AK, ADA and 6-PGD polymorphisms in Cosenza province (Calabria, Italy) 27
Gaba(b) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy 27
pH-metria differenziale e test citochimico di Betke nella diagnostica di laboratorio del deficit di G6PD: validità dei metodi e loro correlazioni 27
Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis. 27
Variations in two lipid metabolizing genes and susceptibility to sporadic Alzheimer s disease. 27
Identificazione di marcatori nel gene della presenilina-2 predittivi di malattia di alzheimer familiare. 27
Identification of Pen-2 gene mutations in Italian patients with Familial Alzheimer s Disease 27
Identificazione di una nuova mutazione nel gene OPA1 in una famiglia affetta da atrofia ottica e sordità. 27
Gene symbol: PSEN2. Disease: Alzheimer disease. 26
Two snps in the Fas gene on chromosome 10 are not associated with sporadic Alzheimer s disease. 26
Gkucose-6-phosphate dehydrogenase (G6PD) deficiency in southern Italy: a study on the population of the Cosenza province 26
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. 26
Determinazione potenziometrica della piruvato chinasi eritrocitaria 26
VLA-4 and Multiple Sclerosis in Italian population. 26
The association of single nucleotide E-selectin gene polymorphism with Multiple Sclerosis . 25
Totale 4.046
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Categoria #
all - tutte 17.331
article - articoli 9.341
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 26.672
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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
2026/2027127 127 0 0 0 0 0 0 0 0 0 0 0
Totale 5.104