CNR Institutional Research Information System

ANNESI, FERDINANDA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 557
AS - Asia 310
EU - Europa 75
Totale 942
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 557
SG - Singapore 279
IT - Italia 43
FI - Finlandia 20
CN - Cina 14
KR - Corea 14
ES - Italia 7
DE - Germania 3
HK - Hong Kong 2
AT - Austria 1
GB - Regno Unito 1
IN - India 1
Totale 942
Salva come PNG Salva come JPEG
Città #
Santa Clara 502
Singapore 192
Helsinki 20
Seoul 14
Guangzhou 8
Taranto 8
Madrid 7
Caltanissetta 6
Cosenza 6
Cerisano 4
Naples 4
Boardman 3
Falkenstein 3
Catanzaro 2
Forest City 2
Hong Kong 2
Milan 2
Phoenix 2
London 1
Rome 1
Teverola 1
Vienna 1
Totale 791
Salva come PNG Salva come JPEG
Nome #
Biocompatible and biomimetic keratin capped Au nanoparticles enable the inactivation of mesophilic bacteria via photo-thermal therapy 21
Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease 21
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease 15
DJ-1 is a Parkinson's disease susceptibility gene in southern Italy. 11
ASSOCIATION STUDY BETWEEN THE LINGO1 GENE AND PARKINSON S DISEASE IN THE ITALIAN POPULATION 10
A novel mutation in the sodium-channel gene SCN1A in a patient with severe myoclonic epilepsy (SMEI) 10
Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism" 10
Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2: an FP-CIT SPECT study. 9
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. 9
Association of tau polymorphism with Parkinson's disease 9
Liquid crystalline DNA: A smart polymer with a variety of applications ranging from photonics to plasmonics 9
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 9
DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex. 9
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 9
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. 8
Micro- and Nano-Structured Bacteria Growth Media for Planar Bio-Photonics 8
Association study of NACP-REP1 polymorphism and Parkinson's disease 8
Biomedical application di "hot" gold nanorods/DNA complexes 8
No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease in a case-control study 8
Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease. 8
Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjogren Syndrome 8
Huntington disease like 2 in Southern Italy: screening of JPH3 and other genes involved in huntington like phenotypes. 8
A comprehensive mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 8
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. 8
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 8
Early-onset Parkinson's disease associated with a new parkin mutation in an Italian patient 8
Templating gold nanorods with liquid crystalline DNA 7
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 7
Studio clinico-genetico in una famiglia con quadro clinico di neurodegenerazione associata alla Pantotenato Chinasi. 7
Association of the 5-HT6 receptor gene polymorphism C26TT with Parkinson's disease 7
No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease ina case-control sample. 7
TARGETING CANCER CELLS WITH FLUORESCENTLY LABELED GNR S /DNA COMPLEXES 7
Individual susceptibility of dopaminergic responsiveness in "De Novo" patients with Parkinson's Disease 7
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 7
Association study between the LINGO1 gene and Parkinson s disease in the Italian population 7
Analisi Genetica e Clinica in 5 famiglie con espansione nucleotidica CAG del gene SCA1 7
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 7
Vitamin E deficiency due to chylomicron retention disease im Marinesco-Sjogren syndrome 7
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease 7
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. 7
Identification of a novel mutation homozygous mutation in the SIL1 gene in Marinesco-Sjögren syndrome (MSS). 6
Ataxia with oculomotor apraxia in a family from southern italy : a clinical and genetic study 6
Thermo-Plasmonic Killing of Escherichia coli TG1 Bacteria 6
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy. 6
Association study of NACP-Rep1 polymorphism and Parkinson?s Disease 6
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 6
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy. 6
A rapid non - isotopic method for sizing CTG repeat expansion in myotonic dystrophy 6
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. 6
Oxidative stress in patients with myotonic dystrophy. 6
The fragile X premutation presenting as postprandial hypotension. 6
Effetto del sesso su fattori di rischio clinico-genetici associati allo sviluppo delle discinesie di picco indotte dalla levodopa nella malattia di Parkinson. 6
Association of 5-HT6 receptor gene polymorphism C267T with Parkinson's disease 6
Relationship between SCN1A mutations and SMEI 6
Spinal muscolar atropy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene . 6
A common founder for the Lrrk2 Gly2019Ser mutation in Italian PD patients . 6
Plasmonics Meets Biology through Optics 6
Increased Risk for Alzheimer disease with the interaction of MPO and A2M Polymorphisms 6
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 6
ATR-FTIR spectroscopy of plasma supported by multivariate analysis discriminates multiple sclerosis disease 6
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 6
A novel exon 1 mutation in a patient with atypical Lafora?s progressive myoclonus epilepsy presenting as childhood-onset cognitive deficit. 6
Clinic and genetic study in a family with a clinical picture of pantothenate kinase-associated neurodegeneration . 5
Molecular studies of the PANK2 gene in patients with PKAN 5
Alpha synuclein in familial parkinson s disease and lewy body dementia. 5
Mutational Analysis of the CHRNA4 and CHRNB2 genes in a family with autosomal dominant nocturnal frontal lobe epilepsy 5
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 5
Linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy . 5
An adult case of spinal muscolar atrophy (SMA) with isolated deletion of exon 8 of survival motor neuron (SMN) gene 5
Parkin, Pink1 and DJ-1 heterozygous mutations in southern italian patients with early-onset parkinsonism. 5
Association study between G-protein-coupled receptor kinase 5 gene and Parkinson s disease 5
No evidence for association of high and low activity alleles of COMT with Parkinson's disease. 5
Association between DJ-1 gene polymorphism and Parkinson disease 5
Parkin mutations in patients with early onset parkinsonism . 5
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit. 5
5-HT6 receptor gene polymorphism and Parkinson's disease. 5
No evidence of association between Alpha 2 macroglobulin gene and Parkinson's disease in a case-control sample 5
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus. 5
Alpha-synuclein in familial Parkinson s disease and Lewy Body Dementia 5
Biological metasurfaces based on tailored Luria Bertani Agar growth medium formulations for photonic applications 5
Antimicrobial effects of chemically functionalized and/or photo-heated nanoparticles 5
Gene dosage influences the age at onset of SCA2 in a family from southern Italy 5
Clinic and genetic study in a family with a clinical picture of pantothenase kinase-associated neurodegeneration . 5
Parkin mutations in patients with early-onset parkinsonism . 5
Analisi di linkage in tre famiglie con Epilessia Frontale Notturna autosomica dominante. 5
Linkage study in three Italian families with autosomal dominant nocturnal frontal lobe epilepsy . 5
Envisioning quantum electrodynamic frameworks based on bio-photonic cavities 5
Mutational analysis of SCN2A gene in italian families with benign familial neonatal-infantile seizures (BFNIS) . 5
Tailoring Resonant Energy Transfer Processes for Sustainable and Bio-Inspired Sensing 5
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy. 5
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 5
Association between DJ-1 gene polymorphism and PD 5
G-protein-coupled receptor kinase 5 and dementia in Parkinsons disease. 4
G-protein-coupled receptor kinase 5 and dementia in Parkinson s disease 4
Mutational Analysis of the DCX, LIS1, FLNA genes in patients with neuronal migration disorders from Southern Italy 4
Molecular analysis of the SCN1A gene in patients with Severe Myoclonic Epilepsy of Infancy 4
Analisi mutazionale del gene parkina in pazienti affetti da malattia a insorgenza giovanile: identificazione di nuove varianti. 4
IDENTIFICATION OF A NOVEL HOMOZYGOUS MUTATION IN THE SIL1 GENE IN MARINESCO-SJOGREN SYNDROME 4
Fragile X premutation alleles in movement disorders. 4
Mutational analysis of EFHC1 gene in Italy families with Juvenile Myoclonic Epilepsy 4
Totale 669
Salva come PNG Salva come JPEG
Categoria #
all - tutte 5.371
article - articoli 2.043
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 38
Totale 7.452
Salva come PNG Salva come JPEG


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
2024/2025935 30 10 182 137 502 63 11 0 0 0 0 0
Totale 975