CNR Institutional Research Information System

TARANTINO, PATRIZIA
 Distribuzione geografica
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Continente #
AS - Asia 22
EU - Europa 17
NA - Nord America 6
Totale 45
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Nazione #
IT - Italia 15
KR - Corea 9
SG - Singapore 8
US - Stati Uniti d'America 6
CN - Cina 5
AT - Austria 1
GB - Regno Unito 1
Totale 45
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Città #
Seoul 9
Caltanissetta 6
Singapore 5
Boardman 3
Cerisano 3
Guangzhou 3
Cosenza 2
Forest City 2
London 1
Naples 1
Teverola 1
Vienna 1
Totale 37
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Nome #
Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease 17
Relationship between SCN1A mutations and SMEI 3
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. 2
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy. 2
Studio clinico-genetico in una famiglia con quadro clinico di neurodegenerazione associata alla Pantotenato Chinasi. 2
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 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
Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism" 2
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 1
Fraxe intermediate alleles are associated with Parkinson's disease 1
Relationship between SCN1A mutations and Severe Myoclonic Epilepsy in Infancy 1
Alpha-synuclein promoter haplotypes and dementia in Parkinson s disease . 1
A novel mutation in the sodium-channel gene SCN1A in a patient with severe myoclonic epilepsy (SMEI) 1
Alpha-synuclein promoter haplotypes and dementia in Parkinson s disease . 1
Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families 1
Association between DJ-1 gene polymorphism and Parkinson disease 1
ANALISI CLINICO-GENETICA IN UNA FAMIGLIA ITALIANA CON ATASSIA SPINOCEREBELLARE AUTOSOMICO-DOMINANTE 1
Alpha-synuclein in familial Parkinson s disease and Lewy Body Dementia 1
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. 1
Screening of genes causing Huntington disease like phenotype. 1
G-PROTEIN-COUPLED RECEPTOR KINASE 5 AND DEMENTIA IN PARKINSON S DISEASE 1
Relazione tra mutazioni nel gene SCN1A ed Epilessia Mioclonica Severa dell'Infanzia 1
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 1
Mutational analysis of the CHRNA4 and CHRNB2 genes in a family with autosomal dominant nocturnal frontal lobe epilepsy 1
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 1
A comprehensive mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 1
Association between DJ-1 gene polymorphism and PD 1
Early-onset Parkinson's disease associated with a new parkin mutation in an Italian patient 1
Totale 54
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Categoria #
all - tutte 1.667
article - articoli 604
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.271
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202426 0 0 0 0 0 0 0 0 2 0 14 10
2024/202528 27 1 0 0 0 0 0 0 0 0 0 0
Totale 54