CNR Institutional Research Information System

SPADAFORA, PATRIZIA
 Distribuzione geografica
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Continente #
AS - Asia 4.573
NA - Nord America 1.971
EU - Europa 1.375
SA - Sud America 909
AF - Africa 77
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 1
Totale 8.918
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Nazione #
SG - Singapore 1.960
US - Stati Uniti d'America 1.873
CN - Cina 958
BR - Brasile 753
IT - Italia 593
HK - Hong Kong 467
VN - Vietnam 459
FR - Francia 305
JP - Giappone 220
NL - Olanda 166
KR - Corea 158
IN - India 78
DE - Germania 72
BD - Bangladesh 71
AR - Argentina 48
GB - Regno Unito 45
FI - Finlandia 43
ID - Indonesia 39
CA - Canada 32
MX - Messico 31
EC - Ecuador 30
CO - Colombia 26
IL - Israele 24
IE - Irlanda 23
ZA - Sudafrica 22
AT - Austria 20
ES - Italia 18
TR - Turchia 18
IQ - Iraq 17
SA - Arabia Saudita 16
RU - Federazione Russa 14
PK - Pakistan 13
PY - Paraguay 13
KE - Kenya 12
UZ - Uzbekistan 12
MA - Marocco 11
UA - Ucraina 11
VE - Venezuela 11
AU - Australia 10
CL - Cile 10
PL - Polonia 10
MY - Malesia 9
PE - Perù 9
SE - Svezia 9
TN - Tunisia 9
DZ - Algeria 7
TH - Thailandia 7
AZ - Azerbaigian 6
DO - Repubblica Dominicana 6
JO - Giordania 6
PH - Filippine 6
AE - Emirati Arabi Uniti 5
BO - Bolivia 5
EG - Egitto 5
GR - Grecia 5
JM - Giamaica 5
NO - Norvegia 5
CR - Costa Rica 4
CZ - Repubblica Ceca 4
HU - Ungheria 4
OM - Oman 4
BB - Barbados 3
BY - Bielorussia 3
HN - Honduras 3
NI - Nicaragua 3
RO - Romania 3
SK - Slovacchia (Repubblica Slovacca) 3
TT - Trinidad e Tobago 3
TW - Taiwan 3
UY - Uruguay 3
AL - Albania 2
EE - Estonia 2
ET - Etiopia 2
GE - Georgia 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LB - Libano 2
LT - Lituania 2
MD - Moldavia 2
NG - Nigeria 2
PA - Panama 2
PS - Palestinian Territory 2
PT - Portogallo 2
RS - Serbia 2
TZ - Tanzania 2
BE - Belgio 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BZ - Belize 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CY - Cipro 1
GF - Guiana Francese 1
GT - Guatemala 1
IR - Iran 1
KH - Cambogia 1
KW - Kuwait 1
LC - Santa Lucia 1
LU - Lussemburgo 1
Totale 8.904
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Città #
Singapore 1.179
Santa Clara 665
Hong Kong 459
Hefei 380
San Jose 249
Lauterbourg 211
Tokyo 195
Ho Chi Minh City 167
Beijing 156
Seoul 155
Ashburn 119
Hanoi 101
Dallas 100
Naples 77
New York 75
Los Angeles 72
São Paulo 70
Milan 48
Rome 48
Catania 34
Bari 33
Buffalo 29
Haiphong 23
Taranto 23
Curitiba 22
Dublin 22
Frankfurt am Main 22
Helsinki 22
Barcellona Pozzo di Gotto 20
Brasília 20
Minamishinagawa 20
Rio de Janeiro 19
Belo Horizonte 18
Amsterdam 15
Da Nang 15
Bengaluru 13
Nuremberg 13
Vienna 13
Biên Hòa 12
Guangzhou 12
Orem 12
Tashkent 12
Council Bluffs 11
Lappeenranta 11
London 11
Messina 11
Porto Alegre 11
Thái Bình 11
Boardman 10
Bologna 10
Brooklyn 10
Mumbai 10
Nairobi 10
Quito 10
Bắc Giang 9
Guarulhos 9
Jakarta 9
Johannesburg 9
Montreal 9
Quận Bình Thạnh 9
Atlanta 8
Fortaleza 8
Guayaquil 8
Ha Long 8
Phoenix 8
Salvador 8
Santo André 8
Shanghai 8
Surabaya 8
Turku 8
Asunción 7
Baghdad 7
Caltanissetta 7
Campinas 7
Chennai 7
Hải Dương 7
Madrid 7
Munich 7
New Delhi 7
Paris 7
Riyadh 7
Turin 7
Altamura 6
Anoia Superiore 6
Can Tho 6
Chicago 6
Delhi 6
Denver 6
Goiânia 6
Houston 6
Lấp Vò 6
Osasco 6
Phủ Lý 6
San Francisco 6
Stockholm 6
Toronto 6
Volta Redonda 6
Washington 6
Agadir 5
Amman 5
Totale 5.420
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Nome #
Tay Sachs in South Italy 148
Secondary metabolites of wild plants from Pollino National Park(CS), Gentiana lutea L. and Hypericum perforatum L. and their cytoprotective and anti-obesity activity 132
In vitro study of the cytoprotective effects of chitosan polymeric nanoparticles carrying active ingredients in response to exogenous stimuli of oxidative nature 129
The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future Directions 124
MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh 123
Exploring the FKRP Gene in Calabrian Patients with Duchenne/Becker-like Phenotype 106
Characterization of N-terminal acetylated Hb Raleigh by a MALDI-ISD approach 105
Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies 96
LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines 94
A new mutation detected by NGS in MT-ATP6 gene associated with MELAS and in silico 3D protein analysis 90
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 87
Targeted next-generation sequencing revealed a new mutation in GLRA1 gene in a family with Hereditary Hyperekplexia 86
A novel homozygous variant in DYSF gene is associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B 86
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 83
Identificato in un paziente del Sud Italia la variante Arg596Gly in omozigosi associata a Distrofia Muscolare dei Cingoli recessiva di tipo 8 82
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders 80
NOS2A AS CANDIDATE GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS: AN HAPLOTYPE STUDY BY USING A SUBSETS OF SNPs. 79
Ataxia with oculomotor apraxia in a family from southern italy : a clinical and genetic study 77
Sex and APOE genotype modulate neuropsychological profile and depression in temporal lobe epilepsy 77
Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype 75
A NEW CYS1678TYR MUTATION RESPONSIBLE OF LGMD2B IDENTIFIED IN A FAMILY FROM SOUTHERN ITALY 74
Potential cytoprotective effects of chitosan polymeric nanoparticles carrying active ingredients in response to external oxidative stimuli 73
Arg143Ser is the most frequent variant in Limb Girdle Muscular Dystrophy-R9 in southern Italy 73
HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT 72
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study. 71
EBV immortalized human lymphoblastoid cell lines as a source for iPSCs generation by nucleofection 71
IDENTITA' FEMMINILE E SCLEROSI MULTIPLA 68
Interruptions of the FXN GAA repeat tract delay the age at onset of Friedreich's ataxia in a location dependent manner. 67
Population genetics of VNTR markers (TPO and 3'APOB loci) in the Mediterranean area (Albania, Greece and Italy) 66
Mancanza di associazione tra la variante Ala29Val del gene NDUFV2 del complesso I mitocondriale e la malattia di Parkinson. 65
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype 63
Rare variants detected by Next Generation Sequencing in two siblings affected by late onset Parkinson's disease 63
Epigenetic Clocks and Their Prospective Application in the Complex Landscape of Aging and Alzheimer’s Disease 59
Polymorphisms of dopamine D2, D3 and D4 receptors genes and Parkinson's disease 58
Genomic analysis identifies a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease 58
No evidence for association of high and low activity alleles of COMT with Parkinson's disease. 57
Variants in CAV3, TRIM32 and PSN2 genes suggest an additive effect in the development of dilated cardiomyopathy in a family of south Italy 56
Characterization of Histone post-translational modifications using a Top-Down, label-free, LC- MALDI-TOF Mass Spectrometry approach. 56
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 55
An Italian child with myophosphorylase deficiency but with no detectable mutation in the exons of the PYGM gene 54
Familial essential tremor is not associated with SCA12 mutation in southern Italy. 53
Fast and accurate SNVs and CNVs screening in Parkinson's Disease patients using Next-Generation approach 52
Hemoglobin Raleigh in Southern Italy: a characterization with a pseudo MS3 approach of a post translational modified hemoglobin 51
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 50
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 48
CSF MALDI-TOF mass spectrometry protein profiling in Clinically Isolated Syndrome. 48
Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy. 48
Hypervariability of the human Thyroid Peroxidase gene in Italy 46
The Mitochondrial Dysfunction Hypothesis in Autism Spectrum Disorders: Current Status and Future Perspectives 46
Next-generation sequencing: identificazione di varianti geniche con effetto additivo nell'espressione del fenotipo patologico LGMD e cardiomiopatia dilatativa. 46
Two novel Nav1.1 mutations associated with Generalized Epilepsy with Febrile Seizures Plus 44
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
COGNITIVE DYSFUNCTION AND QUALITY OF LIFE IN MULTIPLE SCLEROSIS DISEASE 42
DRD2 gene polymorphism and the risk of peak-dose dyskinesias in Parkinson's disease. 42
Gly269Ser mutation in compound heterozygosity with Leu127Arg is associated with adult onset of Tay-Sachs: a case report from south Italy 41
Molecular characterization of the APP gene in italian patients with familial Alzheimer disease. 41
Mutation analysis of the GRIN2B gene in Alzheimer's disease 41
Vitamin E deficiency as a result of Chylomicron Retention Disease in autosomal recessive Marinesco-Sjogren syndrome. 40
ADULT ONSET TAY-SACHS ASSOCIATED WITH -HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY 40
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 40
Association study of NACP-REP1 polymorphism and Parkinson's disease 40
Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). 40
Proteomic profiling in multiple sclerosis clinical courses reveals potential biomarkers of neurodegeneration 40
Linkage Disequilibrium Studies in the Thyroid Peroxidase and Apolipoprotein B Genes 39
Haplotype analysis of the Thyroid Peroxidase gene in families affected by congenital Thyroid Disease 39
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 39
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
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. 38
FKRP expression in Lymphoblastoid cell lines:a human cellular model to study the impact of the mutations on the protein functionality 37
Normal immunofluorescence pattern of skin basement membranes in a family with porencephaly due to COL4A1 G749S mutation 37
Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjogren Syndrome 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
A novel mutation in the sodium-channel gene SCN1A in a patient with severe myoclonic epilepsy (SMEI) 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
TRIM32 as susceptibility gene for pathological cardiac hypertrophy 36
Fraxe intermediate alleles are associated with Parkinson's disease 35
PERIPHERAL MRNA EXPRESSION OF BRAIN-DERIVED NEUROTROPHIC FACTOR VAL66MET POLYMORPHISM IN PATIENTS WITH RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS). 35
G56S and ARG143SER mutations in CAV3 and FKRP gene respectively contribute to the expression of phenotypic characteristics of an LGMD patient of southern Italy 34
Analisi Genetica e Clinica in 5 famiglie con espansione nucleotidica CAG del gene SCA1 33
Analisi mutazionale del gene parkina in pazienti affetti da malattia a insorgenza giovanile: identificazione di nuove varianti. 32
No evidence of association between Alpha 2 macroglobulin gene and Parkinson's disease in a case-control sample 32
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 32
Analisi molecolare del promotore del gene PSEN-2 nella Malattia di Alzheimer: uno studio di associazione nella popolazione calabrese 32
The association of the regulatory region of the PS-2 gene with Alzheimer s disease. 31
A rapid non-isotopic method for sizing CTG repeat expansion in myiotonic dystrophy. 31
Association of 5-HT6 receptor gene polymorphism C267T with Parkinson's disease 31
Screening for MELAS mutations in Italian patients having stroke-like episodes. 31
Association of tau polymorphism with Parkinson's disease 31
5-HT6 receptor gene polymorphism and Parkinson's disease 30
Association study of NACP-Rep1 polymorphism and Parkinson?s Disease 30
A rapid non - isotopic method for sizing CTG repeat expansion in myotonic dystrophy 30
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 30
Effetto del sesso su fattori di rischio clinico-genetici associati allo sviluppo delle discinesie di picco indotte dalla levodopa nella malattia di Parkinson. 30
Polimorfismi del gene del recettore serotoninergico 5-HT2A e malattia di Parkinson. 30
Leber s hereditary optic neuropathy and Multiple Sclerosis: Harding's syndrome. 30
A rare case of multiple sclerosis and McArdle disease 30
Totale 5.523
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Categoria #
all - tutte 28.540
article - articoli 14.582
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 83
Totale 43.205
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202495 0 0 0 0 0 0 0 0 61 0 31 3
2024/20253.441 93 31 292 167 726 120 66 92 99 188 841 726
2025/20265.511 254 550 566 857 956 206 802 329 451 325 160 55
Totale 9.047