CNR Institutional Research Information System

TARANTINO, PATRIZIA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 2.012
NA - Nord America 729
SA - Sud America 446
EU - Europa 201
AF - Africa 33
OC - Oceania 3
Totale 3.424
Salva come PNG Salva come JPEG
Nazione #
SG - Singapore 902
US - Stati Uniti d'America 689
CN - Cina 416
BR - Brasile 377
HK - Hong Kong 231
VN - Vietnam 199
KR - Corea 109
IT - Italia 48
NL - Olanda 34
IN - India 32
AR - Argentina 26
DE - Germania 23
FR - Francia 18
ID - Indonesia 16
IL - Israele 16
JP - Giappone 16
CA - Canada 15
FI - Finlandia 14
GB - Regno Unito 14
MX - Messico 14
EC - Ecuador 13
BD - Bangladesh 12
CO - Colombia 11
ES - Italia 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
TN - Tunisia 4
TT - Trinidad e Tobago 4
AT - Austria 3
CL - Cile 3
HN - Honduras 3
KE - Kenya 3
NP - Nepal 3
PE - Perù 3
PL - Polonia 3
SA - Arabia Saudita 3
AL - Albania 2
BY - Bielorussia 2
GE - Georgia 2
IE - Irlanda 2
IR - Iran 2
NZ - Nuova Zelanda 2
OM - Oman 2
PA - Panama 2
QA - Qatar 2
SE - Svezia 2
TH - Thailandia 2
UY - Uruguay 2
VE - Venezuela 2
AE - Emirati Arabi Uniti 1
BE - Belgio 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
CH - Svizzera 1
CY - Cipro 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
IS - Islanda 1
KH - Cambogia 1
LB - Libano 1
LK - Sri Lanka 1
LT - Lituania 1
LV - Lettonia 1
ME - Montenegro 1
MY - Malesia 1
NC - Nuova Caledonia 1
NG - Nigeria 1
NI - Nicaragua 1
PS - Palestinian Territory 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TG - Togo 1
UG - Uganda 1
Totale 3.424
Salva come PNG Salva come JPEG
Città #
Singapore 568
Santa Clara 338
Hefei 236
Hong Kong 230
Seoul 108
Beijing 96
Ho Chi Minh City 73
San Jose 60
Hanoi 44
São Paulo 32
Ashburn 25
Los Angeles 24
Dallas 23
Buffalo 16
Helsinki 13
Minamishinagawa 13
Bengaluru 10
Curitiba 10
Rio de Janeiro 10
Belo Horizonte 8
Biên Hòa 8
Frankfurt am Main 8
Madrid 7
Naples 7
Ribeirão Preto 7
Brasília 6
Caltanissetta 6
Cosenza 6
Porto Alegre 6
Quito 6
Salvador 6
Tashkent 6
Brooklyn 5
Campinas 5
Goiânia 5
Haiphong 5
Hải Dương 5
Joinville 5
Lauterbourg 5
Mauá 5
New York 5
Phủ Lý 5
Asunción 4
Baghdad 4
Baku 4
Bogotá 4
Buenos Aires 4
Bình An 4
Feira de Santana 4
Hortolândia 4
Houston 4
Rome 4
Turin 4
Atlanta 3
Boardman 3
Boston 3
Bắc Giang 3
Bắc Ninh 3
Can Tho 3
Caraguatatuba 3
Cerisano 3
Chennai 3
Da Nang 3
Dhaka 3
Diadema 3
Düsseldorf 3
Guangzhou 3
Guarulhos 3
Itajaí 3
Jakarta 3
Johannesburg 3
Lahore 3
Manaus 3
Montreal 3
Nairobi 3
New Delhi 3
Palhoça 3
Phoenix 3
Port of Spain 3
Praia Grande 3
Quận Bình Thạnh 3
Recife 3
Salt Lake City 3
Santo André 3
Thái Nguyên 3
Tunis 3
Vĩnh Long 3
Vũng Tàu 3
Warsaw 3
Alvorada 2
Amsterdam 2
Ankara 2
Barra Mansa 2
Bekasi 2
Bến Tre 2
Cabo Frio 2
Cachoeira do Sul 2
Cachoeirinha 2
Cairo 2
Campina Grande 2
Totale 2.240
Salva come PNG Salva come JPEG
Nome #
Clinic and genetic study in a family with a clinical picture of pantothenate kinase-associated neurodegeneration . 68
Identification of a novel mutation homozygous mutation in the SIL1 gene in Marinesco-Sjögren syndrome (MSS). 67
Molecular studies of the PANK2 gene in patients with PKAN 57
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study. 57
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 51
Analisi mutazionale del gene SCN2A in famiglie italiane con Convulsioni Neonatali-Infantili Familiari Benigne (BFINS). 50
DJ-1 is a Parkinson's disease susceptibility gene in southern Italy. 49
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. 48
Mutational Analysis of the CHRNA4 and CHRNB2 genes in a family with autosomal dominant nocturnal frontal lobe epilepsy 47
Association study between the LINGO1 gene and Parkinson s disease in the Italian population 47
G-protein-coupled receptor kinase 5 and dementia in Parkinson s disease 46
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease 45
DESCRIPTION OF A FOUR-GENERATION FAMILY WITH AUTOSOMAL DOMINANT CEREBELLAR ATAXIA: CLINICAL AND GENETIC ANALYSIS 44
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. 44
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 43
The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals. 41
G-protein-coupled receptor kinase 5 and dementia in Parkinsons disease. 40
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. 40
DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex. 39
A comprehensive mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 38
Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease 37
ROUTINE MRI MEASUREMENT OF THE BRAINSTEM STRUCTURES IN PATIENTS WITH SPINOCEREBELLAR ATAXIA TYPE 1 AND 2 ON: CORRELATION WITH CLINICAL AND GENETIC DATA 36
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy. 36
Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism" 35
DENTATO-RUBRAL PALLIDOLUYSIAN ATROPHY: CLINICAL AND GENETIC ANALYSIS OF A SICILIAN PEDIGREE 35
Linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy . 34
Spinocerebellar ataxia type 7: report of a new Italian family. 34
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. 33
A novel mutation in the sodium-channel gene SCN1A in a patient with severe myoclonic epilepsy (SMEI) 33
Mutational Analysis of the DCX, LIS1, FLNA genes in patients with neuronal migration disorders from Southern Italy 31
Association study between G-protein-coupled receptor kinase 5 gene and Parkinson s disease 31
Dentatorubral pallidoluysian atrophy: clinical and genetic analysis of a Sicilian pedigree 31
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 30
Fraxe intermediate alleles are associated with Parkinson's disease 29
Early-onset SCA17 with 43 TBP repeats: expanding the phenotype? 29
Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy. 29
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences. 28
Molecular analysis of the SCN1A gene in patients with Severe Myoclonic Epilepsy of Infancy 27
Studio clinico-genetico in una famiglia con quadro clinico di neurodegenerazione associata alla Pantotenato Chinasi. 27
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 27
Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families 26
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 25
Analisi mutazionale del gene parkina in pazienti affetti da malattia a insorgenza giovanile: identificazione di nuove varianti. 25
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy. 25
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 25
Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia. 25
Ceruloplasmin gene variations and Parkinson s disease: an association study in Southern Italian population. 25
Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease. 24
The fragile X premutation presenting as postprandial hypotension. 23
Alpha-synuclein in familial Parkinson s disease and Lewy Body Dementia 23
GIGYF2 (TRNC15) MUTATION ANALYSIS IN PATIENTS WITH FAMILIAL PARKINSON DISEASE WITH AUTOSOMAL-DOMINANT TRANSMISSION 23
Mutational analysis of EFHC1 gene in Italy families with Juvenile Myoclonic Epilepsy 22
Screening for PINK1 mutations in patients with early-and late-onset Parkinson s disease 22
Analisi di linkage in tre famiglie con Epilessia Frontale Notturna autosomica dominante. 22
Mutational analysis of SCN2A gene in italian families with benign familial neonatal-infantile seizures (BFNIS) . 22
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy. 21
Parkin, Pink1 and DJ-1 heterozygous mutations in southern italian patients with early-onset parkinsonism. 21
MOLECULAR ANALYSIS OF THE SCN1A GENE IN SOUTHERN ITALIAN PATIENTS WITH SEVERE MYOCLONIC EPILEPSY OF INFANCY. 21
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease 21
Early-onset Parkinson's disease associated with a new parkin mutation in an Italian patient 21
Fragile X premutation alleles in movement disorders. 20
Linkage analysis in a family with autosomal dominant nocturnal frontal lobe epilepsy in european human genetics conference 20
ASSOCIATION STUDY BETWEEN HFE, TF , TFR1 GENES AND PARKINSON S DISEASE 20
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 20
Association between DJ-1 gene polymorphism and PD 20
Description of a four-generation family with autosomal dominant cerebellar ataxia: clinical and genetic analysis. 19
Parkin mutations in patients with early onset parkinsonism . 19
Relationship between SCN1A mutations and SMEI 19
Gene-dosage influences the age at onset of SCA2 in a family from southern Italy 19
Dysbindin C-A-T haplotype is associated with thicker medial orbitofrontal cortex in healthy population 19
Association study between HFE, TF, TFR1 genes and Parkinson disease. 18
The Tau haplotype contributes to susceptibility to Parkinson s disease in a Souther Italy population. 18
G-PROTEIN-COUPLED RECEPTOR KINASE 5 AND DEMENTIA IN PARKINSON S DISEASE 18
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 18
Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy. 17
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. 17
Screening for PINK1 mutations in patients with early- and late-onset Parkinson disease 17
Screening mutazionale del DJ-1 in pazienti con malattia di Parkinson ad esordio precoce. 17
GIGYF2 (TRNC15) mutation analysis in patients with familial Parkinson s disease with autosomal-dominant transmission. 17
Association between DJ-1 gene polymorphism and Parkinson disease 17
SIL1 and SARA2 mutations in a family with Marinesco-S¼ogren and Chylomicron Retention Diseases . 17
Pink1 mutations and the risk of Parkinson s disease in family members of Southern Italy 17
Gene dosage influences the age at onset of SCA2 in a family from southern Italy 17
Clinic and genetic study in a family with a clinical picture of pantothenase kinase-associated neurodegeneration . 17
Screening for DJ-1 mutations in early onset Parkinson s disease. 17
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 17
Origine da un fondatore comune della mutazione g6055a (gly2019ser) nel gene LRRK2 in pazienti affetti da malattia di Parkinson provenienti dall Italia Meridionale. 17
Association study between HFE, TF, TFR genes and Parkinson s disease. 17
IDENTIFICATION OF A NOVEL HOMOZYGOUS MUTATION IN THE SIL1 GENE IN MARINESCO-SJOGREN SYNDROME 16
ANALISI MUTAZIONALE DEI GENI RESPONSABILI DELLA MALATTIA DI PARKINSON AD ESORDIO PRECOCE IN UNA POPOLAZIONE DEL SUD ITALIA 16
Frequenza della mutazione Gly2019Ser del gene LRRK2 in pazienti italiani affetti da malattia di Parkinson. 16
A common founder for the Lrrk2 Gly2019Ser mutation in Italian PD patients . 16
DJ-1 gene in late-onset recessive Parkinsons disease 16
Ataxia with oculomotor apraxia in a family from southern Italy 16
Mutational analysis of SCN2A gene in Italian families with Benign Neonatal-Infantile Seizures (BFNIS) . 16
Un polimorfismo del gene TAU incrementa il rischio del Parkinson idiopatico 16
Aplotipi del promotore dell Alfa-sinucleina e Demenza nella malattia di Parkinson. 16
Relationship between SCN1A mutations and Severe Myoclonic Epilepsy in Infancy 15
SEC24Agene analysis in Marinesco-Sjogren Sindrome 15
Met 158 variant of the COMT genotype is associated with thicker cortex in adult brain 15
Totale 2.749
Salva come PNG Salva come JPEG
Categoria #
all - tutte 12.077
article - articoli 4.320
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 16.397
Salva come PNG Salva come JPEG


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
2025/20261.687 130 257 255 421 478 79 67 0 0 0 0 0
Totale 3.443