CNR Institutional Research Information System

CITTADELLA, RITA
 Distribuzione geografica
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Continente #
AS - Asia 1.922
NA - Nord America 857
SA - Sud America 537
EU - Europa 386
AF - Africa 35
Totale 3.737
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Nazione #
SG - Singapore 900
US - Stati Uniti d'America 825
BR - Brasile 467
CN - Cina 285
HK - Hong Kong 254
VN - Vietnam 236
IT - Italia 145
NL - Olanda 139
KR - Corea 65
IN - India 35
AR - Argentina 27
ID - Indonesia 23
GB - Regno Unito 19
FR - Francia 16
BD - Bangladesh 15
DE - Germania 15
JP - Giappone 14
MX - Messico 13
CO - Colombia 12
EC - Ecuador 12
IL - Israele 10
MA - Marocco 10
MY - Malesia 10
ZA - Sudafrica 10
CA - Canada 8
IQ - Iraq 8
RU - Federazione Russa 8
SA - Arabia Saudita 8
TH - Thailandia 8
FI - Finlandia 7
KE - Kenya 7
PY - Paraguay 7
TR - Turchia 7
ES - Italia 6
PH - Filippine 6
UZ - Uzbekistan 6
CL - Cile 5
PK - Pakistan 5
SE - Svezia 5
AL - Albania 4
AZ - Azerbaigian 4
TN - Tunisia 4
UA - Ucraina 4
HU - Ungheria 3
IE - Irlanda 3
KG - Kirghizistan 3
KZ - Kazakistan 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
AT - Austria 2
BB - Barbados 2
DO - Repubblica Dominicana 2
LB - Libano 2
LT - Lituania 2
PL - Polonia 2
RS - Serbia 2
UY - Uruguay 2
AF - Afghanistan, Repubblica islamica di 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 1
CR - Costa Rica 1
CU - Cuba 1
CY - Cipro 1
EG - Egitto 1
GE - Georgia 1
IM - Isola di Man 1
IR - Iran 1
JM - Giamaica 1
JO - Giordania 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LV - Lettonia 1
MM - Myanmar 1
MU - Mauritius 1
NI - Nicaragua 1
NP - Nepal 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TT - Trinidad e Tobago 1
TZ - Tanzania 1
YE - Yemen 1
Totale 3.737
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Città #
Singapore 558
Santa Clara 482
Hong Kong 252
Hefei 135
Ho Chi Minh City 100
Beijing 82
Seoul 63
Hanoi 42
São Paulo 42
Los Angeles 31
Ashburn 29
Dallas 29
San Jose 25
Milan 14
Belo Horizonte 11
Porto Alegre 11
Rio de Janeiro 11
Buffalo 10
Minamishinagawa 9
Jakarta 8
Anoia Superiore 7
Bangkok 7
Bologna 7
Da Nang 7
Goiânia 7
Haiphong 7
Helsinki 7
Manaus 7
Bari 6
Brasília 6
Curitiba 6
Frankfurt am Main 6
Kuala Selangor 6
Nairobi 6
Phoenix 6
Sorocaba 6
Turin 6
Biên Hòa 5
Bắc Ninh 5
Campinas 5
Chennai 5
Hải Dương 5
Lấp Vò 5
Manila 5
New York 5
Quito 5
Rome 5
Santo André 5
Tashkent 5
Volta Redonda 5
Baku 4
Brooklyn 4
Chicago 4
Florence 4
Jeddah 4
Juiz de Fora 4
Kuala Lumpur 4
Modena 4
Mumbai 4
Naples 4
Osasco 4
Taranto 4
Thái Bình 4
Tirana 4
Amsterdam 3
Asunción 3
Atibaia 3
Baghdad 3
Bengaluru 3
Bishkek 3
Campos dos Goytacazes 3
Casablanca 3
Catania 3
Colombo 3
Delhi 3
Dhaka 3
Glasgow 3
Guarulhos 3
Guayaquil 3
Ha Long 3
Hà Tĩnh 3
Lahore 3
London 3
Mogi Guaçu 3
Montes Claros 3
Novo Hamburgo 3
Orem 3
Orlando 3
Quilmes 3
Quận Hai 3
Quận Năm 3
Rabat 3
Rio Verde 3
Rio das Ostras 3
Salvador 3
Stockholm 3
São Bernardo do Campo 3
São Gonçalo 3
São Leopoldo 3
Trento 3
Totale 2.283
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Nome #
La sindrome di Mc Leod: un caso clinico 116
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders 70
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 68
Cst3: fattore di rischio genetico per la Malattia di Alzheimer sporadica? 66
Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy. 61
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease. 54
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype 52
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 51
Apolipoprotein E genotype does not influence the progression of multiple sclerosis. 49
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 46
Ruolo del gene Neuregulin 1 (NRG1) nella Sclerosi Multipla 46
Copy Number Variants in Alzheimer's Disease 44
McLeod syndrome in an Italian patient 44
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 43
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man 43
Huntington's disease-like syndrome: a case report 42
Cognitive impairment and brain atrophy in patients with relapsing-remitting Multiple Sclerosis (RRMS): the role of brain derived neurotrophic factor (BDNF) gene. 41
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 40
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. 40
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease 40
Peripheral mRNA expression of brain-derived neurotrophic factor Val66Met polymorphism in patients with relapsing-remitting multiple sclerosis 38
Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene. 36
Role of the Neuregulin 1 gene (NRG1) in multiple sclerosis 36
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 36
Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency revealed by single strand conformation and sequence analysis 36
Genetic association of α2-macroglobulin polymorphisms with AD in southern Italy 35
DRD2 gene polymorphism and the risk of peak-dose dyskinesias in Parkinson's disease. 34
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 33
Apo-1/Fas gene polymorphisms and multiple sclerosis in Southern Italy. 32
CASP-9 : a susceptibility locus for multiple sclerosis in Italy. 32
Molecular characterization of the APP gene in italian patients with familial Alzheimer disease. 32
D678N mutation in a patient with an early-onset Alzheimer's Disease 32
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 31
Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). 31
Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in Calabria 30
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. 30
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 29
APP gene mutation (D678N) in a patient with an Early-Onset Alzheimer's Disease 29
Analisi demografica, endogamica e polimorfismo genetico del locus PGM1 nella minoranza etnica albanese della provincia di Cosenza 27
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report 27
The association of the regulatory region of the PS-2 gene with Alzheimer s disease. 26
Leber s hereditary optic neuropathy associated with multiple sclerosis like picture in a man. 26
Glucose 6 phpsphate dehydrogenase deficiency and endogamic study in the albanian ethnic minority of Cosenza province 26
Brain-derived Neurotrophic Factor Val66Met polimorphism and the cortical response to spatial working memory. 26
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2. 25
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 25
Leber s hereditary optic neuropathy and Multiple Sclerosis: Harding's syndrome. 25
Increased Risk for Alzheimer disease with the interaction of MPO and A2M Polymorphisms 25
Presenilin Enhancer-2 Gene mutations and Familial Alzheimer s Disease 25
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION 24
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 24
A Novel Lys 130 Gln Mutation of the TAU gene. 24
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy. 24
Valutazione dell'attività G6PD asica eritrocitaria mediante pH-metria differenziale 24
CASP-9 exon 1 polymorphism in patients with Multiple Sclerosis. 24
CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis. 24
Two SNPs in the Fas gene on chromosome 10 are not associated with Italian Sporadic Alzheimer s Disease. 23
Dati preliminare sulla struttura genetica nella provincia di Cosenza 23
Aspetti epidemiologici del deficit di G6PD in provincia di Cosenza. Dati preliminari 23
Identification of Pen-2 gene mutations in Italian patients with Familial Alzheimer s Disease 23
A new intronic deletion of presenilin 1 gene in a patient with early onset Alzheimer Disease 23
Two SNPs in the Fas gene on chromosome 10 are not associated with Sporadic Alzheimer s Disease in southern Italy. 23
AK, ADA and 6-PGD polymorphisms in Cosenza province (Calabria, Italy) 22
Mutational analysis of the mitochondrial tRNAleu gene In Italian patients with stroke-like episodes of undetermined origin. 22
Screening for MELAS mutations in Italian patients having stroke-like episodes. 22
Neuropatia ottica ereditaria di Leber s e Sclerosi Multipla: Harding s syndrome. 22
Alzheimer s Disease and the Cystatin C gene polymorphism: an association study. 22
Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease. 22
Gene symbol: PSEN2. Disease: Alzheimer disease. 21
Cognitive performances and brain volumes in patients with relapsing-remitting multiple sclerosis: investigating the role of BDNF Val66Met polymorphism. 21
A novel mutation in FKRP gene in Italian patient with LGMD. 21
A novel mutation (Thr116IIe) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease 21
APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers 21
Analisi mutazionale del gene OPA1 in una famiglia affetta da atrofia ottica autosomica dominante. 21
Variations in two lipid metabolizing genes and susceptibility to sporadic Alzheimer s disease. 21
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 21
Identificazione di marcatori nel gene della presenilina-2 predittivi di malattia di alzheimer familiare. 21
Identificazione di una nuova mutazione nel gene OPA1 in una famiglia affetta da atrofia ottica e sordità. 21
Alzheimer's Disease and the Cystatin C gene polymorphism: an association study 21
Is M129V of the Prion protein gene ( PRNP) associated with mild temporal lobe epilepsy? 21
Two snps in the Fas gene on chromosome 10 are not associated with sporadic Alzheimer s disease. 20
Mutational screening of the CAPN3 in LGMD patients from Southern Italy. 20
Laboratory diagnosis of G6PD deficiency in association with beta thalassemia trait 20
Molecular characterization of the Presenilin-2 gene in Italian patients with familial Alzheimer Disease. 20
LRP1- LRPAP1 polymorphisms and risk of sporadic Alzheimer s disease. 20
NOTCH3 mutations and mtDNA variations 20
Dopamine D-2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD 20
The frequency of Limb Girdle Muscular Dystrophy 1C in southern Italy 20
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. 20
Gaba(b) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy 19
Gkucose-6-phosphate dehydrogenase (G6PD) deficiency in southern Italy: a study on the population of the Cosenza province 19
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. 19
A social-demographic, isonymyc and genetic investigation on an isolated Calabrian village 19
The association of single nucleotide E-selectin gene polymorphism with Multiple Sclerosis . 19
Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis. 19
The frequency of limb girdle muscular dystrophy 1c in southern Italy 19
Caspase-9 gene C93T polymorphism and Multiple Sclerosis patients from Southern Italy 19
Elam-1 genotyping in Italian population with Multiple Sclerosis : molecular characterization of A561C variation. 18
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy. 18
pH-metria differenziale e test citochimico di Betke nella diagnostica di laboratorio del deficit di G6PD: validità dei metodi e loro correlazioni 18
Totale 3.007
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Categoria #
all - tutte 12.920
article - articoli 7.012
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 19.932
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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
2025/20261.770 102 252 275 444 515 136 46 0 0 0 0 0
Totale 3.752