CNR Institutional Research Information System

NICOLETTI, GIUSEPPE
 Distribuzione geografica
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Continente #
AS - Asia 40
NA - Nord America 6
EU - Europa 4
Totale 50
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Nazione #
CN - Cina 22
SG - Singapore 11
KR - Corea 7
US - Stati Uniti d'America 6
IT - Italia 4
Totale 50
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Città #
Guangzhou 8
Singapore 8
Seoul 7
Boardman 4
Caltanissetta 2
Totale 29
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Nome #
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. 2
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy. 2
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 2
A Fully Automated, Atlas-Based Approach for Superior Cerebellar Peduncle Evaluation in Progressive Supranuclear Palsy Phenotypes. 2
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. 2
A common founder for the Lrrk2 Gly2019Ser mutation in Italian PD patients . 2
Analisi Genetica e Clinica in 5 famiglie con espansione nucleotidica CAG del gene SCA1 2
Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism" 2
Refining initial diagnosis of Parkinson's disease after follow-up: A 4-year prospective clinical and magnetic resonance imaging study. 2
Cardiac MIBG scintigraphy in Primary Progressive Freezing Gait 2
Fraxe intermediate alleles are associated with Parkinson's disease 1
Association of the 5-HT6 receptor gene polymorphism C26TT with Parkinson's disease 1
G-463A myeloperoxidase polymorphism and parkinson s disease 1
Acute levodopa and ropinirolo tests in Parkinson s disease 1
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. 1
Color vision inpatients with Parkinson disease. Usefulness of three pseudoisochromatic tests 1
A new MR imaging index for differentiation of progressive supranuclear palsy-parkinsonism from Parkinson's disease. 1
Apparent diffusion coefficient measurements of the Middle Cerebellar Peduncle differentiates MSA from PD and PSP 1
Alpha-synuclein promoter haplotypes and dementia in Parkinson s disease . 1
Alpha-synuclein promoter haplotypes and dementia in Parkinson s disease . 1
Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern Italy 1
Refining initial diagnosis of Parkinson's disease after follow-up: A 4-year prospective clinical and magnetic resonance imaging study 1
Association of 5-HT6 receptor gene polymorphism C267T with Parkinson's disease 1
Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesia in PD 1
Cerebellar atrophy in Essential tremor using automated segmentation method. 1
5-HT6 receptor gene polymorphism and Parkinson's disease. 1
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 1
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 1
Alpha-synuclein in familial Parkinson s disease and Lewy Body Dementia 1
Dopaminergic modulation of cognitive interference after pharmacological washout in Parkinson's disease 1
Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern Italy 1
Administration of levodopa modulates the neural and behavioural response associated with cognitive interference in PD patients 1
Voxel-based morphometry to detect effect of APOE on brain gray matter changes in Parkinson's Disease. 1
The FRAGAMP study: environmental and genetic factors in Parkinson's disease, methods and clinical features. 1
Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia 1
Dopaminergic modulation of cognitive interference after pharmacological washout in parkinson's disease 1
Alzheimer s Disease and the Cystatin C gene polymorphism: an association study. 1
Alzheimer's Disease and the Cystatin C gene polymorphism: an association study 1
A comprehensive mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 1
MPO and A2M polymorphisms interact to increase the risk for Alzheimer?s disease 1
Totale 50
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Categoria #
all - tutte 1.871
article - articoli 1.268
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 3.139
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202437 0 0 0 0 0 0 0 0 2 0 29 6
2024/202513 13 0 0 0 0 0 0 0 0 0 0 0
Totale 50