CNR Institutional Research Information System

CITTADELLA, RITA
 Distribuzione geografica
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Continente #
AS - Asia 2.547
NA - Nord America 1.078
EU - Europa 689
SA - Sud America 547
AF - Africa 39
OC - Oceania 2
Totale 4.902
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Nazione #
SG - Singapore 1.132
US - Stati Uniti d'America 1.036
CN - Cina 471
BR - Brasile 470
VN - Vietnam 290
HK - Hong Kong 268
IT - Italia 244
FR - Francia 165
NL - Olanda 154
JP - Giappone 128
KR - Corea 65
IN - India 38
AR - Argentina 30
ID - Indonesia 30
DE - Germania 26
GB - Regno Unito 21
BD - Bangladesh 17
CA - Canada 14
MX - Messico 14
CO - Colombia 13
EC - Ecuador 13
MY - Malesia 13
TH - Thailandia 11
IL - Israele 10
MA - Marocco 10
ZA - Sudafrica 10
ES - Italia 9
IQ - Iraq 9
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
PK - Pakistan 5
TN - Tunisia 5
UA - Ucraina 5
VE - Venezuela 5
AL - Albania 4
AZ - Azerbaigian 4
HU - Ungheria 4
IE - Irlanda 4
AE - Emirati Arabi Uniti 3
AT - Austria 3
CR - Costa Rica 3
KG - Kirghizistan 3
KZ - Kazakistan 3
PL - Polonia 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
JM - Giamaica 2
LB - Libano 2
LT - Lituania 2
LV - Lettonia 2
NP - Nepal 2
RS - Serbia 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
TT - Trinidad e Tobago 1
TZ - Tanzania 1
YE - Yemen 1
Totale 4.902
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Città #
Singapore 641
Santa Clara 482
Hong Kong 264
Hefei 135
Lauterbourg 125
Ho Chi Minh City 119
Tokyo 115
San Jose 110
Beijing 84
Seoul 63
Ashburn 62
Hanoi 53
Los Angeles 45
São Paulo 42
Dallas 29
Milan 19
Rome 17
Jakarta 14
New York 13
Buffalo 12
Belo Horizonte 11
Porto Alegre 11
Rio de Janeiro 11
Turin 11
Bangkok 10
Guangzhou 10
Haiphong 10
Bologna 9
Frankfurt am Main 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
Naples 7
Amsterdam 6
Bari 6
Biên Hòa 6
Brasília 6
Curitiba 6
Nairobi 6
Phoenix 6
Sorocaba 6
Tashkent 6
Bắc Ninh 5
Campinas 5
Chicago 5
Florence 5
Lấp Vò 5
Manila 5
Quito 5
Santo André 5
Thái Bình 5
Volta Redonda 5
Baku 4
Brooklyn 4
Bến Tre 4
Catania 4
Guayaquil 4
Jeddah 4
Juiz de Fora 4
Kuala Lumpur 4
Ligornetto 4
Modena 4
Montreal 4
Mumbai 4
Nuremberg 4
Osasco 4
Padua 4
Phủ Lý 4
Shenzhen 4
Taranto 4
Tirana 4
Verona 4
Asunción 3
Atibaia 3
Atlanta 3
Baghdad 3
Bengaluru 3
Bishkek 3
Campos dos Goytacazes 3
Casablanca 3
Chengdu 3
Colombo 3
Delhi 3
Dhaka 3
Dublin 3
Fortaleza 3
Genoa 3
Glasgow 3
Guarulhos 3
Ha Long 3
Houston 3
Hà Tĩnh 3
Joinville 3
Totale 2.866
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Nome #
La sindrome di Mc Leod: un caso clinico 210
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 83
Cst3: fattore di rischio genetico per la Malattia di Alzheimer sporadica? 80
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders 79
Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy. 70
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 66
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. 59
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease. 57
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease 57
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man 56
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 55
Ruolo del gene Neuregulin 1 (NRG1) nella Sclerosi Multipla 53
Copy Number Variants in Alzheimer's Disease 53
McLeod syndrome in an Italian patient 53
Huntington's disease-like syndrome: a case report 53
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 50
Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency revealed by single strand conformation and sequence analysis 49
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 48
Role of the Neuregulin 1 gene (NRG1) in multiple sclerosis 48
Cognitive impairment and brain atrophy in patients with relapsing-remitting Multiple Sclerosis (RRMS): the role of brain derived neurotrophic factor (BDNF) gene. 46
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. 46
Peripheral mRNA expression of brain-derived neurotrophic factor Val66Met polymorphism in patients with relapsing-remitting multiple sclerosis 45
Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene. 43
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 43
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
Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). 40
Genetic association of α2-macroglobulin polymorphisms with AD in southern Italy 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. 38
D678N mutation in a patient with an early-onset Alzheimer's Disease 38
Neuropatia ottica ereditaria di Leber s e Sclerosi Multipla: Harding s syndrome. 38
Apo-1/Fas gene polymorphisms and multiple sclerosis in Southern Italy. 37
Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in Calabria 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
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. 35
Brain-derived Neurotrophic Factor Val66Met polimorphism and the cortical response to spatial working memory. 34
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION 33
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
Analisi demografica, endogamica e polimorfismo genetico del locus PGM1 nella minoranza etnica albanese della provincia di Cosenza 32
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 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
Screening for MELAS mutations in Italian patients having stroke-like episodes. 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
CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis. 31
Alzheimer s Disease and the Cystatin C gene polymorphism: an association study. 31
Two SNPs in the Fas gene on chromosome 10 are not associated with Sporadic Alzheimer s Disease in southern Italy. 31
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 30
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2. 30
Leber s hereditary optic neuropathy and Multiple Sclerosis: Harding's syndrome. 30
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy. 30
Alzheimer's Disease and the Cystatin C gene polymorphism: an association study 30
Is M129V of the Prion protein gene ( PRNP) associated with mild temporal lobe epilepsy? 30
A novel mutation in FKRP gene in Italian patient with LGMD. 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
Presenilin Enhancer-2 Gene mutations and Familial Alzheimer s Disease 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
Cognitive performances and brain volumes in patients with relapsing-remitting multiple sclerosis: investigating the role of BDNF Val66Met polymorphism. 28
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 screening of the CAPN3 in LGMD patients from Southern Italy. 28
Laboratory diagnosis of G6PD deficiency in association with beta thalassemia trait 28
A novel mutation (Thr116IIe) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease 28
Valutazione dell'attività G6PD asica eritrocitaria mediante pH-metria differenziale 28
APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers 28
CASP-9 exon 1 polymorphism in patients with Multiple Sclerosis. 28
Trauma cranico e genotipo APO-E: causa o rischio di malatia di Alzheimer? 28
AK, ADA and 6-PGD polymorphisms in Cosenza province (Calabria, Italy) 27
LRP1- LRPAP1 polymorphisms and risk of sporadic Alzheimer s disease. 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
Gaba(b) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy 26
Mutational analysis of the mitochondrial tRNAleu gene In Italian patients with stroke-like episodes of undetermined origin. 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
Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis. 26
Caspase-9 gene C93T polymorphism and Multiple Sclerosis patients from Southern Italy 26
A new human mtDNA polymorphism: MTND6: 14562 (C-->T). 25
Gkucose-6-phosphate dehydrogenase (G6PD) deficiency in southern Italy: a study on the population of the Cosenza province 25
pH-metria differenziale e test citochimico di Betke nella diagnostica di laboratorio del deficit di G6PD: validità dei metodi e loro correlazioni 25
The association of single nucleotide E-selectin gene polymorphism with Multiple Sclerosis . 25
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis. 25
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy. 24
Molecular characterization of the Presenilin-2 gene in Italian patients with familial Alzheimer Disease. 24
VLA-4 and Multiple Sclerosis in Italian population. 24
Totale 3.863
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Categoria #
all - tutte 15.623
article - articoli 8.445
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 24.068
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202418 0 0 0 0 0 0 0 0 3 0 14 1
2024/20251.964 5 11 141 86 491 24 28 73 29 146 467 463
2025/20262.935 102 252 275 444 515 136 486 225 270 174 56 0
Totale 4.917