CNR Institutional Research Information System

TARANTINO, PATRIZIA
 Distribuzione geografica
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Continente #
AS - Asia 2.528
NA - Nord America 1.140
SA - Sud America 468
EU - Europa 428
AF - Africa 33
Continente sconosciuto - Info sul continente non disponibili 19
OC - Oceania 3
Totale 4.619
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Nazione #
SG - Singapore 1.099
US - Stati Uniti d'America 1.068
CN - Cina 532
BR - Brasile 388
VN - Vietnam 259
HK - Hong Kong 238
FR - Francia 187
KR - Corea 109
JP - Giappone 103
IT - Italia 84
BD - Bangladesh 42
IN - India 39
NL - Olanda 35
DE - Germania 30
CA - Canada 29
AR - Argentina 28
EC - Ecuador 18
GB - Regno Unito 17
ID - Indonesia 17
IL - Israele 16
MX - Messico 16
FI - Finlandia 15
CO - Colombia 12
ES - Italia 12
PK - Pakistan 11
RU - Federazione Russa 9
IQ - Iraq 8
PY - Paraguay 8
ZA - Sudafrica 7
EG - Egitto 6
HN - Honduras 6
UZ - Uzbekistan 6
AZ - Azerbaigian 5
DZ - Algeria 5
SA - Arabia Saudita 5
TR - Turchia 5
UA - Ucraina 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
JM - Giamaica 4
KZ - Kazakistan 4
MA - Marocco 4
NI - Nicaragua 4
NP - Nepal 4
PL - Polonia 4
TN - Tunisia 4
TT - Trinidad e Tobago 4
AL - Albania 3
AT - Austria 3
CL - Cile 3
KE - Kenya 3
PA - Panama 3
PE - Perù 3
PH - Filippine 3
BY - Bielorussia 2
CZ - Repubblica Ceca 2
GE - Georgia 2
GT - Guatemala 2
IE - Irlanda 2
IR - Iran 2
LT - Lituania 2
LV - Lettonia 2
NZ - Nuova Zelanda 2
OM - Oman 2
QA - Qatar 2
RO - Romania 2
SE - Svezia 2
TH - Thailandia 2
UY - Uruguay 2
AM - Armenia 1
BE - Belgio 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BS - Bahamas 1
CH - Svizzera 1
CR - Costa Rica 1
CY - Cipro 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
HR - Croazia 1
IS - Islanda 1
KH - Cambogia 1
KY - Cayman, isole 1
LB - Libano 1
LK - Sri Lanka 1
ME - Montenegro 1
MN - Mongolia 1
MY - Malesia 1
NC - Nuova Caledonia 1
NG - Nigeria 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 4.600
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Città #
Singapore 634
Santa Clara 358
Hefei 238
Hong Kong 230
San Jose 176
Lauterbourg 133
Seoul 108
Ho Chi Minh City 99
Beijing 97
Tokyo 87
Ashburn 60
Hanoi 59
Los Angeles 38
São Paulo 35
Dallas 30
Buffalo 20
Helsinki 14
Frankfurt am Main 13
Minamishinagawa 13
New York 13
Bengaluru 10
Curitiba 10
Rio de Janeiro 10
Biên Hòa 9
Orem 9
Belo Horizonte 8
Brooklyn 8
Dhaka 8
Naples 8
Quito 8
Brasília 7
Da Nang 7
Madrid 7
Milan 7
Ribeirão Preto 7
Rome 7
Atlanta 6
Caltanissetta 6
Cosenza 6
Haiphong 6
Hải Dương 6
Porto Alegre 6
Salvador 6
Tashkent 6
Turin 6
Boardman 5
Boston 5
Campinas 5
Chennai 5
Goiânia 5
Guangzhou 5
Joinville 5
Mauá 5
Montreal 5
Phủ Lý 5
Asunción 4
Baghdad 4
Baku 4
Bari 4
Bogotá 4
Buenos Aires 4
Bình An 4
Bắc Ninh 4
Chengdu 4
Chicago 4
Feira de Santana 4
Guayaquil 4
Hortolândia 4
Houston 4
Mumbai 4
Phoenix 4
Shanghai 4
Thái Nguyên 4
Warsaw 4
Amsterdam 3
Aurora 3
Bologna 3
Bắc Giang 3
Can Tho 3
Caraguatatuba 3
Cerisano 3
Charlotte 3
City of London 3
Diadema 3
Düsseldorf 3
Guarulhos 3
Itajaí 3
Jakarta 3
Johannesburg 3
Lahore 3
Lakeland 3
Liverpool 3
Managua 3
Manaus 3
Nairobi 3
New Delhi 3
Palhoça 3
Pompano Beach 3
Port of Spain 3
Portland 3
Totale 2.843
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Nome #
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 76
Clinic and genetic study in a family with a clinical picture of pantothenate kinase-associated neurodegeneration . 74
Identification of a novel mutation homozygous mutation in the SIL1 gene in Marinesco-Sjögren syndrome (MSS). 73
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study. 73
Association study between the LINGO1 gene and Parkinson s disease in the Italian population 65
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease 63
Molecular studies of the PANK2 gene in patients with PKAN 62
DJ-1 is a Parkinson's disease susceptibility gene in southern Italy. 61
Analisi mutazionale del gene SCN2A in famiglie italiane con Convulsioni Neonatali-Infantili Familiari Benigne (BFINS). 58
G-protein-coupled receptor kinase 5 and dementia in Parkinson s disease 58
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 56
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. 56
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. 56
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. 55
The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals. 54
DESCRIPTION OF A FOUR-GENERATION FAMILY WITH AUTOSOMAL DOMINANT CEREBELLAR ATAXIA: CLINICAL AND GENETIC ANALYSIS 53
Mutational Analysis of the CHRNA4 and CHRNB2 genes in a family with autosomal dominant nocturnal frontal lobe epilepsy 53
A comprehensive mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 50
Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism" 47
G-protein-coupled receptor kinase 5 and dementia in Parkinsons disease. 44
ROUTINE MRI MEASUREMENT OF THE BRAINSTEM STRUCTURES IN PATIENTS WITH SPINOCEREBELLAR ATAXIA TYPE 1 AND 2 ON: CORRELATION WITH CLINICAL AND GENETIC DATA 44
Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease 44
DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex. 44
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 43
Spinocerebellar ataxia type 7: report of a new Italian family. 43
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy. 42
DENTATO-RUBRAL PALLIDOLUYSIAN ATROPHY: CLINICAL AND GENETIC ANALYSIS OF A SICILIAN PEDIGREE 42
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. 41
Linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy . 39
Association study between G-protein-coupled receptor kinase 5 gene and Parkinson s disease 39
Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy. 38
A novel mutation in the sodium-channel gene SCN1A in a patient with severe myoclonic epilepsy (SMEI) 37
Early-onset SCA17 with 43 TBP repeats: expanding the phenotype? 36
Fraxe intermediate alleles are associated with Parkinson's disease 35
Fragile X premutation alleles in movement disorders. 35
Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families 35
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences. 35
Mutational Analysis of the DCX, LIS1, FLNA genes in patients with neuronal migration disorders from Southern Italy 34
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 34
Dentatorubral pallidoluysian atrophy: clinical and genetic analysis of a Sicilian pedigree 34
Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia. 34
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 33
Alpha-synuclein in familial Parkinson s disease and Lewy Body Dementia 33
Early-onset Parkinson's disease associated with a new parkin mutation in an Italian patient 33
Analisi mutazionale del gene parkina in pazienti affetti da malattia a insorgenza giovanile: identificazione di nuove varianti. 32
MOLECULAR ANALYSIS OF THE SCN1A GENE IN SOUTHERN ITALIAN PATIENTS WITH SEVERE MYOCLONIC EPILEPSY OF INFANCY. 32
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease 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
The fragile X premutation presenting as postprandial hypotension. 31
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 31
Studio clinico-genetico in una famiglia con quadro clinico di neurodegenerazione associata alla Pantotenato Chinasi. 30
Mutational analysis of EFHC1 gene in Italy families with Juvenile Myoclonic Epilepsy 30
Association study between HFE, TF, TFR1 genes and Parkinson disease. 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
Gene-dosage influences the age at onset of SCA2 in a family from southern Italy 30
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy. 30
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy. 29
Analisi di linkage in tre famiglie con Epilessia Frontale Notturna autosomica dominante. 29
Mutational analysis of SCN2A gene in italian families with benign familial neonatal-infantile seizures (BFNIS) . 29
Studio di linkage in tre famiglie calabresi con epilessia frontale notturna autosomica dominante 28
IDENTIFICATION OF A NOVEL HOMOZYGOUS MUTATION IN THE SIL1 GENE IN MARINESCO-SJOGREN SYNDROME 27
Parkin, Pink1 and DJ-1 heterozygous mutations in southern italian patients with early-onset parkinsonism. 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
A common founder for the Lrrk2 Gly2019Ser mutation in Italian PD patients . 26
Mutational analysis of SCN2A gene in Italian families with Benign Neonatal-Infantile Seizures (BFNIS) . 26
G-PROTEIN-COUPLED RECEPTOR KINASE 5 AND DEMENTIA IN PARKINSON S DISEASE 26
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 26
Screening mutazionale del DJ-1 in pazienti con malattia di Parkinson ad esordio precoce. 25
Parkin mutations in patients with early onset parkinsonism . 25
Relationship between SCN1A mutations and SMEI 25
Pink1 mutations and the risk of Parkinson s disease in family members of Southern Italy 25
Linkage analysis in a family with autosomal dominant nocturnal frontal lobe epilepsy in european human genetics conference 25
Gene dosage influences the age at onset of SCA2 in a family from southern Italy 25
Association between DJ-1 gene polymorphism and PD 25
The Tau haplotype contributes to susceptibility to Parkinson s disease in a Souther Italy population. 24
Screening for PINK1 mutations in patients with early-and late-onset Parkinson s disease 24
Screening for PINK1 mutations in patients with early- and late-onset Parkinson disease 24
ANALISI MUTAZIONALE DEI GENI RESPONSABILI DELLA MALATTIA DI PARKINSON AD ESORDIO PRECOCE IN UNA POPOLAZIONE DEL SUD ITALIA 24
Met 158 variant of the COMT genotype is associated with thicker cortex in adult brain 24
Association between DJ-1 gene polymorphism and Parkinson disease 24
Clinic and genetic study in a family with a clinical picture of pantothenase kinase-associated neurodegeneration . 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
Relationship between SCN1A mutations and Severe Myoclonic Epilepsy in Infancy 23
Frequenza della mutazione Gly2019Ser del gene LRRK2 in pazienti italiani affetti da malattia di Parkinson. 23
Ataxia with oculomotor apraxia in a family from southern Italy 23
Mitochondrial DNA haplogroups and the risk of Parkinson disease in a cohort of patients from South Italy 23
Un polimorfismo del gene TAU incrementa il rischio del Parkinson idiopatico 23
Molecular studies of the PANK2 gene in patients with PKAN 23
Dysbindin C-A-T haplotype is associated with thicker medial orbitofrontal cortex in healthy population 23
MUTATIONAL DETECTION OF EARLY ONSET PARKINSON DISEASE GENES IN PATIENTS FROM SOUTHERN ITALY 23
Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy. 22
DJ-1 gene in late-onset recessive Parkinsons disease. 22
GIGYF2 (TRNC15) mutation analysis in patients with familial Parkinson s disease with autosomal-dominant transmission. 22
Genetic analysis of three Serbian families with GEFS+ 22
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. 22
Relazione tra mutazioni nel gene SCN1A ed Epilessia Mioclonica Severa dell'Infanzia 22
Totale 3.558
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Categoria #
all - tutte 17.056
article - articoli 5.993
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 23.049
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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
2025/20262.673 130 257 255 421 478 79 434 155 196 157 69 42
2026/2027190 141 49 0 0 0 0 0 0 0 0 0 0
Totale 4.619