CNR Institutional Research Information System

ANNESI, FERDINANDA
 Distribuzione geografica
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Continente #
AS - Asia 3.793
NA - Nord America 1.519
SA - Sud America 695
EU - Europa 671
AF - Africa 62
OC - Oceania 5
Totale 6.745
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Nazione #
SG - Singapore 1.656
US - Stati Uniti d'America 1.446
CN - Cina 825
BR - Brasile 581
HK - Hong Kong 390
VN - Vietnam 361
FR - Francia 275
JP - Giappone 164
KR - Corea 155
IT - Italia 134
IN - India 62
NL - Olanda 62
DE - Germania 44
GB - Regno Unito 42
AR - Argentina 33
CA - Canada 27
FI - Finlandia 26
ID - Indonesia 24
MX - Messico 23
BD - Bangladesh 22
EC - Ecuador 22
IL - Israele 22
CO - Colombia 21
ZA - Sudafrica 20
PK - Pakistan 16
TR - Turchia 16
ES - Italia 15
RU - Federazione Russa 12
UA - Ucraina 11
IQ - Iraq 10
PY - Paraguay 10
UZ - Uzbekistan 10
AT - Austria 9
EG - Egitto 9
VE - Venezuela 9
MA - Marocco 7
PE - Perù 7
PL - Polonia 7
SA - Arabia Saudita 7
TN - Tunisia 7
AE - Emirati Arabi Uniti 6
MY - Malesia 6
AZ - Azerbaigian 5
CL - Cile 5
DZ - Algeria 5
KE - Kenya 5
TT - Trinidad e Tobago 5
GE - Georgia 4
KZ - Kazakistan 4
LV - Lettonia 4
NI - Nicaragua 4
PS - Palestinian Territory 4
UY - Uruguay 4
HN - Honduras 3
LB - Libano 3
NP - Nepal 3
NZ - Nuova Zelanda 3
SE - Svezia 3
SN - Senegal 3
TH - Thailandia 3
AL - Albania 2
BG - Bulgaria 2
BO - Bolivia 2
BY - Bielorussia 2
CH - Svizzera 2
DO - Repubblica Dominicana 2
GR - Grecia 2
GT - Guatemala 2
IE - Irlanda 2
IR - Iran 2
KG - Kirghizistan 2
LK - Sri Lanka 2
PA - Panama 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
AU - Australia 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BW - Botswana 1
CR - Costa Rica 1
CY - Cipro 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
ET - Etiopia 1
GF - Guiana Francese 1
IS - Islanda 1
JM - Giamaica 1
JO - Giordania 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
LU - Lussemburgo 1
ME - Montenegro 1
MT - Malta 1
NC - Nuova Caledonia 1
NG - Nigeria 1
OM - Oman 1
PH - Filippine 1
PR - Porto Rico 1
Totale 6.736
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Città #
Singapore 956
Santa Clara 511
Hong Kong 385
Hefei 347
San Jose 254
Lauterbourg 197
Seoul 153
Beijing 144
Tokyo 143
Ho Chi Minh City 137
Ashburn 96
Hanoi 82
Los Angeles 60
Dallas 55
São Paulo 50
Buffalo 35
Rende 23
Rio de Janeiro 22
Helsinki 21
Minamishinagawa 18
Belo Horizonte 17
Frankfurt am Main 17
Haiphong 16
Bengaluru 15
Brasília 15
Da Nang 15
New York 15
Guangzhou 13
Naples 12
Curitiba 11
Orem 11
Biên Hòa 10
Brooklyn 9
Jakarta 9
Johannesburg 9
Mumbai 9
Quito 9
Shanghai 9
Tashkent 9
Chennai 8
Cosenza 8
Madrid 8
Manchester 8
Porto Alegre 8
Salvador 8
Taranto 8
Can Tho 7
Guarulhos 7
Milan 7
Montreal 7
Ribeirão Preto 7
Bogotá 6
Caltanissetta 6
Chicago 6
Council Bluffs 6
Goiânia 6
Houston 6
Joinville 6
London 6
Rome 6
Santo André 6
Ankara 5
Aparecida de Goiânia 5
Atlanta 5
Cairo 5
Campinas 5
Denver 5
Dhaka 5
Hortolândia 5
Hải Dương 5
Lahore 5
Lappeenranta 5
Manaus 5
Mauá 5
Nairobi 5
Phủ Lý 5
Recife 5
Sorocaba 5
Tunis 5
Turin 5
Warsaw 5
Asunción 4
Baghdad 4
Baku 4
Bình An 4
Bắc Giang 4
Bắc Ninh 4
Cerisano 4
Chengdu 4
Diadema 4
Feira de Santana 4
Fortaleza 4
Itaboraí 4
Managua 4
Maricá 4
Montevideo 4
Nuremberg 4
Phoenix 4
Port of Spain 4
Riga 4
Totale 4.246
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Nome #
Biocompatible and biomimetic keratin capped Au nanoparticles enable the inactivation of mesophilic bacteria via photo-thermal therapy 110
G-463A myeloperoxidase polymorphism and parkinson s disease 83
Ataxia with oculomotor apraxia in a family from southern italy : a clinical and genetic study 76
Clinic and genetic study in a family with a clinical picture of pantothenate kinase-associated neurodegeneration . 73
TARGETING CANCER CELLS WITH FLUORESCENTLY LABELED GNR S /DNA COMPLEXES 73
Identification of a novel mutation homozygous mutation in the SIL1 gene in Marinesco-Sjögren syndrome (MSS). 71
ASSOCIATION STUDY BETWEEN THE LINGO1 GENE AND PARKINSON S DISEASE IN THE ITALIAN POPULATION 70
Micro- and Nano-Structured Bacteria Growth Media for Planar Bio-Photonics 69
Alpha synuclein in familial parkinson s disease and lewy body dementia. 67
Thermo-Plasmonic Killing of Escherichia coli TG1 Bacteria 63
Molecular studies of the PANK2 gene in patients with PKAN 62
Thermal liquid biopsy (TLB) of blood plasma as a potential tool to help in the early diagnosis of multiple sclerosis 62
Association study between the LINGO1 gene and Parkinson s disease in the Italian population 61
DJ-1 is a Parkinson's disease susceptibility gene in southern Italy. 60
ATR-FTIR spectroscopy of plasma supported by multivariate analysis discriminates multiple sclerosis disease 60
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease 59
Analisi mutazionale del gene SCN2A in famiglie italiane con Convulsioni Neonatali-Infantili Familiari Benigne (BFINS). 58
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 57
G-protein-coupled receptor kinase 5 and dementia in Parkinson s disease 56
Biological metasurfaces based on tailored Luria Bertani Agar growth medium formulations for photonic applications 56
Myocardial 123metaiodobenzylguadine uptake in genetic Parkinson's disease 55
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 55
Tailoring Resonant Energy Transfer Processes for Sustainable and Bio-Inspired Sensing 55
Mutational Analysis of the CHRNA4 and CHRNB2 genes in a family with autosomal dominant nocturnal frontal lobe epilepsy 52
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. 52
Envisioning quantum electrodynamic frameworks based on bio-photonic cavities 52
DESCRIPTION OF A FOUR-GENERATION FAMILY WITH AUTOSOMAL DOMINANT CEREBELLAR ATAXIA: CLINICAL AND GENETIC ANALYSIS 51
DJ-1 gene confers susceptibility to Parkinson s disease. 50
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. 49
Liquid crystalline DNA: A smart polymer with a variety of applications ranging from photonics to plasmonics 48
Templating gold nanorods with liquid crystalline DNA 46
Plasmonics Meets Biology through Optics 46
A comprehensive mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 46
G-protein-coupled receptor kinase 5 and dementia in Parkinsons disease. 44
Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism" 44
Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease 42
DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex. 42
Association study of NACP-REP1 polymorphism and Parkinson's disease 40
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. 39
Genome wide linkage of a large serbian family with GEFS+. 39
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 39
Linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy . 38
Biomedical application di "hot" gold nanorods/DNA complexes 38
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. 38
Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjogren Syndrome 37
Antimicrobial effects of chemically functionalized and/or photo-heated nanoparticles 37
A novel mutation in the sodium-channel gene SCN1A in a patient with severe myoclonic epilepsy (SMEI) 36
Association study between G-protein-coupled receptor kinase 5 gene and Parkinson s disease 36
Increased Risk for Alzheimer disease with the interaction of MPO and A2M Polymorphisms 36
Genetic study of SCN1A-related epilepsies in southern Italy. 35
Mutational Analysis of the DCX, LIS1, FLNA genes in patients with neuronal migration disorders from Southern Italy 34
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 33
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 33
No evidence for association of high and low activity alleles of COMT with Parkinson's disease. 33
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
Glucocerebrosidase gene mutations are associated with Parkinson s disease in a population from Souther Italy. 32
No evidence of association between Alpha 2 macroglobulin gene and Parkinson's disease in a case-control sample 32
Alpha-synuclein in familial Parkinson s disease and Lewy Body Dementia 32
Ceruloplasmin gene variations and Parkinson s disease: an association study in Southern Italian population. 32
Molecular analysis of the SCN1A gene in patients with Severe Myoclonic Epilepsy of Infancy 31
Fragile X premutation alleles in movement disorders. 31
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy. 31
Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2: an FP-CIT SPECT study. 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
MOLECULAR ANALYSIS OF THE SCN1A GENE IN SOUTHERN ITALIAN PATIENTS WITH SEVERE MYOCLONIC EPILEPSY OF INFANCY. 31
Association of tau polymorphism with Parkinson's disease 31
Huntington disease like 2 in Southern Italy: screening of JPH3 and other genes involved in huntington like phenotypes. 31
Association study of NACP-Rep1 polymorphism and Parkinson?s Disease 30
Studio clinico-genetico in una famiglia con quadro clinico di neurodegenerazione associata alla Pantotenato Chinasi. 30
A rapid non - isotopic method for sizing CTG repeat expansion in myotonic dystrophy 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
Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease. 30
GIGYF2 (TRNC15) MUTATION ANALYSIS IN PATIENTS WITH FAMILIAL PARKINSON DISEASE WITH AUTOSOMAL-DOMINANT TRANSMISSION 30
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy. 30
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 30
Correlazione Genotipo - fenotipo in alcune famiglie Italiane con Atassia Spinocerebellare tipo 2 (SCA2) 29
Association of the 5-HT6 receptor gene polymorphism C26TT with Parkinson's disease 29
The fragile X premutation presenting as postprandial hypotension. 29
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus. 29
Analisi di linkage in tre famiglie con Epilessia Frontale Notturna autosomica dominante. 29
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 29
Early-onset Parkinson's disease associated with a new parkin mutation in an Italian patient 29
Mutational analysis of EFHC1 gene in Italy families with Juvenile Myoclonic Epilepsy 28
Association study between HFE, TF, TFR1 genes and Parkinson disease. 28
CAG repeat lenght and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity 28
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy. 28
No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease in a case-control study 27
Gene-dosage influences the age at onset of SCA2 in a family from southern Italy 27
Mutational analysis of SCN2A gene in italian families with benign familial neonatal-infantile seizures (BFNIS) . 27
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 27
The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease 27
Description of a four-generation family with autosomal dominant cerebellar ataxia: clinical and genetic analysis. 26
CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocità. 26
Parkin, Pink1 and DJ-1 heterozygous mutations in southern italian patients with early-onset parkinsonism. 26
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus. 26
Isolated deletion of exon 8 of the survival motor neuron (SMN) gene in an adult case of spinal muscolar atrophy (SMA) 26
G-PROTEIN-COUPLED RECEPTOR KINASE 5 AND DEMENTIA IN PARKINSON S DISEASE 26
Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation. 26
Totale 4.140
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Categoria #
all - tutte 21.905
article - articoli 8.723
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 162
Totale 30.790
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202440 0 0 0 0 0 0 0 0 2 0 27 11
2024/20252.624 30 11 182 139 508 63 53 75 41 99 731 692
2025/20264.133 201 416 405 673 702 136 666 249 358 236 91 0
Totale 6.797