CNR Institutional Research Information System

TARANTINO, PATRIZIA
 Distribuzione geografica
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Continente #
AS - Asia 2.489
NA - Nord America 976
SA - Sud America 455
EU - Europa 410
AF - Africa 33
OC - Oceania 3
Totale 4.366
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Nazione #
SG - Singapore 1.098
US - Stati Uniti d'America 928
CN - Cina 532
BR - Brasile 385
VN - Vietnam 256
HK - Hong Kong 236
FR - Francia 185
KR - Corea 109
JP - Giappone 103
IT - Italia 71
IN - India 39
NL - Olanda 35
DE - Germania 29
AR - Argentina 27
CA - Canada 19
BD - Bangladesh 17
GB - Regno Unito 17
ID - Indonesia 16
IL - Israele 16
FI - Finlandia 15
MX - Messico 15
EC - Ecuador 13
ES - Italia 12
CO - Colombia 11
PK - Pakistan 11
RU - Federazione Russa 9
IQ - Iraq 8
PY - Paraguay 8
ZA - Sudafrica 7
EG - Egitto 6
UZ - Uzbekistan 6
AZ - Azerbaigian 5
DZ - Algeria 5
TR - Turchia 5
UA - Ucraina 5
KZ - Kazakistan 4
MA - Marocco 4
PL - Polonia 4
SA - Arabia Saudita 4
TN - Tunisia 4
TT - Trinidad e Tobago 4
AE - Emirati Arabi Uniti 3
AT - Austria 3
CL - Cile 3
HN - Honduras 3
KE - Kenya 3
NP - Nepal 3
PE - Perù 3
AL - Albania 2
BY - Bielorussia 2
GE - Georgia 2
IE - Irlanda 2
IR - Iran 2
LT - Lituania 2
LV - Lettonia 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
OM - Oman 2
PA - Panama 2
QA - Qatar 2
RO - Romania 2
SE - Svezia 2
TH - Thailandia 2
UY - Uruguay 2
VE - Venezuela 2
BE - Belgio 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BS - Bahamas 1
CH - Svizzera 1
CY - Cipro 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GT - Guatemala 1
HR - Croazia 1
IS - Islanda 1
KH - Cambogia 1
LB - Libano 1
LK - Sri Lanka 1
ME - Montenegro 1
MY - Malesia 1
NC - Nuova Caledonia 1
NG - Nigeria 1
PH - Filippine 1
PS - Palestinian Territory 1
RS - Serbia 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TG - Togo 1
UG - Uganda 1
Totale 4.366
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Città #
Singapore 633
Santa Clara 339
Hefei 238
Hong Kong 230
San Jose 176
Lauterbourg 133
Seoul 108
Ho Chi Minh City 98
Beijing 97
Tokyo 87
Hanoi 58
Ashburn 52
Los Angeles 36
São Paulo 34
Dallas 25
Buffalo 19
Helsinki 14
Frankfurt am Main 13
Minamishinagawa 13
New York 12
Bengaluru 10
Curitiba 10
Rio de Janeiro 10
Biên Hòa 9
Orem 9
Belo Horizonte 8
Brooklyn 8
Naples 8
Brasília 7
Da Nang 7
Madrid 7
Ribeirão Preto 7
Rome 7
Caltanissetta 6
Cosenza 6
Haiphong 6
Hải Dương 6
Porto Alegre 6
Quito 6
Salvador 6
Tashkent 6
Campinas 5
Chennai 5
Goiânia 5
Guangzhou 5
Joinville 5
Mauá 5
Phủ Lý 5
Turin 5
Asunción 4
Baghdad 4
Baku 4
Bogotá 4
Buenos Aires 4
Bình An 4
Bắc Ninh 4
Chengdu 4
Feira de Santana 4
Hortolândia 4
Houston 4
Montreal 4
Mumbai 4
Phoenix 4
Shanghai 4
Thái Nguyên 4
Warsaw 4
Amsterdam 3
Atlanta 3
Aurora 3
Boardman 3
Boston 3
Bắc Giang 3
Can Tho 3
Caraguatatuba 3
Cerisano 3
Chicago 3
City of London 3
Dhaka 3
Diadema 3
Düsseldorf 3
Guarulhos 3
Itajaí 3
Jakarta 3
Johannesburg 3
Lahore 3
Manaus 3
Milan 3
Nairobi 3
New Delhi 3
Palhoça 3
Port of Spain 3
Praia Grande 3
Quận Bình Thạnh 3
Recife 3
Salt Lake City 3
San Francisco 3
Santo André 3
Tunis 3
Vĩnh Long 3
Vũng Tàu 3
Totale 2.780
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Nome #
Clinic and genetic study in a family with a clinical picture of pantothenate kinase-associated neurodegeneration . 73
Identification of a novel mutation homozygous mutation in the SIL1 gene in Marinesco-Sjögren syndrome (MSS). 71
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study. 71
Molecular studies of the PANK2 gene in patients with PKAN 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
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
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 55
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. 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
DESCRIPTION OF A FOUR-GENERATION FAMILY WITH AUTOSOMAL DOMINANT CEREBELLAR ATAXIA: CLINICAL AND GENETIC ANALYSIS 51
The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals. 50
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. 49
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
ROUTINE MRI MEASUREMENT OF THE BRAINSTEM STRUCTURES IN PATIENTS WITH SPINOCEREBELLAR ATAXIA TYPE 1 AND 2 ON: CORRELATION WITH CLINICAL AND GENETIC DATA 43
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
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy. 40
DENTATO-RUBRAL PALLIDOLUYSIAN ATROPHY: CLINICAL AND GENETIC ANALYSIS OF A SICILIAN PEDIGREE 40
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. 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
Spinocerebellar ataxia type 7: report of a new Italian family. 38
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
Fraxe intermediate alleles are associated with Parkinson's disease 35
Mutational Analysis of the DCX, LIS1, FLNA genes in patients with neuronal migration disorders from Southern Italy 34
Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, 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
Dentatorubral pallidoluysian atrophy: clinical and genetic analysis of a Sicilian pedigree 33
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences. 33
Analisi mutazionale del gene parkina in pazienti affetti da malattia a insorgenza giovanile: identificazione di nuove varianti. 32
Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families 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
MOLECULAR ANALYSIS OF THE SCN1A GENE IN SOUTHERN ITALIAN PATIENTS WITH SEVERE MYOCLONIC EPILEPSY OF INFANCY. 31
Early-onset SCA17 with 43 TBP repeats: expanding the phenotype? 31
Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia. 31
Studio clinico-genetico in una famiglia con quadro clinico di neurodegenerazione associata alla Pantotenato Chinasi. 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
The fragile X premutation presenting as postprandial hypotension. 29
Analisi di linkage in tre famiglie con Epilessia Frontale Notturna autosomica dominante. 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
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
Description of a four-generation family with autosomal dominant cerebellar ataxia: clinical and genetic analysis. 26
Parkin, Pink1 and DJ-1 heterozygous mutations in southern italian patients with early-onset parkinsonism. 26
G-PROTEIN-COUPLED RECEPTOR KINASE 5 AND DEMENTIA IN PARKINSON S DISEASE 26
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease 26
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy. 25
Parkin mutations in patients with early onset parkinsonism . 25
Pink1 mutations and the risk of Parkinson s disease in family members of Southern Italy 25
Studio di linkage in tre famiglie calabresi con epilessia frontale notturna autosomica dominante 25
Association between DJ-1 gene polymorphism and PD 25
IDENTIFICATION OF A NOVEL HOMOZYGOUS MUTATION IN THE SIL1 GENE IN MARINESCO-SJOGREN SYNDROME 24
Screening for PINK1 mutations in patients with early-and late-onset Parkinson s disease 24
ANALISI MUTAZIONALE DEI GENI RESPONSABILI DELLA MALATTIA DI PARKINSON AD ESORDIO PRECOCE IN UNA POPOLAZIONE DEL SUD ITALIA 24
Screening mutazionale del DJ-1 in pazienti con malattia di Parkinson ad esordio precoce. 24
Relationship between SCN1A mutations and SMEI 24
A common founder for the Lrrk2 Gly2019Ser mutation in Italian PD patients . 24
Gene dosage influences the age at onset of SCA2 in a family from southern Italy 24
ASSOCIATION STUDY BETWEEN HFE, TF , TFR1 GENES AND PARKINSON S DISEASE 24
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 24
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 24
The Tau haplotype contributes to susceptibility to Parkinson s disease in a Souther Italy population. 23
Screening for PINK1 mutations in patients with early- and late-onset Parkinson disease 23
Linkage analysis in a family with autosomal dominant nocturnal frontal lobe epilepsy in european human genetics conference 23
Clinic and genetic study in a family with a clinical picture of pantothenase kinase-associated neurodegeneration . 23
Mutational analysis of SCN2A gene in Italian families with Benign Neonatal-Infantile Seizures (BFNIS) . 23
Un polimorfismo del gene TAU incrementa il rischio del Parkinson idiopatico 23
Dysbindin C-A-T haplotype is associated with thicker medial orbitofrontal cortex in healthy population 23
Relationship between SCN1A mutations and Severe Myoclonic Epilepsy in Infancy 22
GIGYF2 (TRNC15) mutation analysis in patients with familial Parkinson s disease with autosomal-dominant transmission. 22
Frequenza della mutazione Gly2019Ser del gene LRRK2 in pazienti italiani affetti da malattia di Parkinson. 22
Genetic analysis of three Serbian families with GEFS+ 22
Association between DJ-1 gene polymorphism and Parkinson disease 22
Mitochondrial DNA haplogroups and the risk of Parkinson disease in a cohort of patients from South Italy 22
Relazione tra mutazioni nel gene SCN1A ed Epilessia Mioclonica Severa dell'Infanzia 22
MUTATIONAL DETECTION OF EARLY ONSET PARKINSON DISEASE GENES IN PATIENTS FROM SOUTHERN ITALY 22
Origine da un fondatore comune della mutazione g6055a (gly2019ser) nel gene LRRK2 in pazienti affetti da malattia di Parkinson provenienti dall Italia Meridionale. 22
DJ-1 gene in late-onset recessive Parkinsons disease. 21
ANALISI CLINICO-GENETICA IN UNA FAMIGLIA ITALIANA CON ATASSIA SPINOCEREBELLARE AUTOSOMICO-DOMINANTE 21
I geni SIL1 e SARA2 mutati responsabili della Sindrome di Marinesco-Sjögren e della malattia di ritenzione dei chilomicroni in una famiglia proveniente dal Sud Italia. 21
Ataxia with oculomotor apraxia in a family from southern Italy 21
Molecular studies of the PANK2 gene in patients with PKAN 21
Totale 3.384
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Categoria #
all - tutte 14.638
article - articoli 5.114
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 19.752
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202424 0 0 0 0 0 0 0 0 2 0 12 10
2024/20251.732 27 7 129 96 319 35 41 34 45 55 479 465
2025/20262.629 130 257 255 421 478 79 434 155 196 157 67 0
Totale 4.385