VALENTE, ENZA MARIA
 Distribuzione geografica
Continente #
NA - Nord America 585
EU - Europa 237
AS - Asia 136
SA - Sud America 17
AF - Africa 2
Totale 977
Nazione #
US - Stati Uniti d'America 575
IT - Italia 138
SG - Singapore 65
CN - Cina 28
SE - Svezia 26
FI - Finlandia 25
IN - India 20
BR - Brasile 15
ID - Indonesia 12
DE - Germania 10
CA - Canada 7
GB - Regno Unito 7
BG - Bulgaria 6
IE - Irlanda 6
TR - Turchia 6
CH - Svizzera 5
NL - Olanda 5
MX - Messico 3
UA - Ucraina 3
CY - Cipro 2
AR - Argentina 1
BD - Bangladesh 1
CL - Cile 1
DK - Danimarca 1
EE - Estonia 1
FR - Francia 1
IQ - Iraq 1
IR - Iran 1
LU - Lussemburgo 1
PL - Polonia 1
RU - Federazione Russa 1
TG - Togo 1
ZA - Sudafrica 1
Totale 977
Città #
Fairfield 99
Ashburn 49
Singapore 47
Santa Clara 44
Chandler 38
Woodbridge 37
Rome 35
Seattle 33
Wilmington 32
Houston 29
Cambridge 26
Princeton 15
Beijing 13
New York 13
Jakarta 12
Helsinki 11
Lappeenranta 11
Ann Arbor 10
San Paolo di Civitate 10
Lawrence 9
San Diego 9
Millbury 7
Dublin 6
Istanbul 6
Lambeth 6
Plano 6
Sofia 6
Turin 6
Milan 5
Naples 5
Bremen 4
Formello 4
Toronto 4
Torre del Greco 4
Andover 3
Bern 3
Boston 3
Dearborn 3
Maddaloni 3
Vicopisano 3
Bari 2
Boardman 2
Carmignano di Brenta 2
Crespiatica 2
Lecce 2
Manduria 2
Mannheim 2
Mexico City 2
Norwalk 2
Ottawa 2
Paphos 2
Pescara 2
Ragusa 2
Redwood City 2
Scandiano 2
Acton 1
Baghdad 1
Baotou 1
Bauru 1
Belleville 1
Betim 1
Brindisi 1
Buffalo 1
Cagliari 1
Canguaretama 1
Carol Stream 1
Civitavecchia 1
Contagem 1
Copenhagen 1
Cuneo 1
Falkenstein 1
Federal 1
Frankfurt am Main 1
Fremont 1
Grafing 1
Hangzhou 1
Hefei 1
Holland 1
Jaboatão dos Guararapes 1
Japeri 1
Johannesburg 1
Kiev 1
Kish 1
Le Grand-Saconnex 1
Lomé 1
Los Angeles 1
Luis Eduardo Magalhães 1
Maceió 1
Mentana 1
Moscow 1
Mumbai 1
Nanjing 1
Nanning 1
Phoenix 1
Pignola 1
Pune 1
Pétange 1
Quanzhou 1
Sacramento 1
Shenyang 1
Totale 744
Nome #
Production and characterization of human induced pluripotent stem cells (iPSC) CSSi007-A (4383) from Joubert Syndrome 99
Genetic paradoxes in an italian family with PARK2 multiexon duplication 95
Progressive Supranuclear Palsy-Like Phenotype in a GBA E326K Mutation Carrier 93
Protracted late infantile ceroid lipofuscinosis due to TPP1 mutations. clinical, molecular and biochemical characterization in three sibs 93
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies 85
Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects 81
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders 81
Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism 55
Parkinson disease genetics. A “continuum” from mendelian to multifactorial inheritance 55
Diagnostic and therapeutic recommendations in adult dystonia: a joint document by the Italian Society of Neurology, the Italian Academy for the Study of Parkinson's Disease and Movement Disorders, and the Italian Network on Botulinum Toxin 50
Successful subthalamic stimulation, but levodopa-induced dystonia, in a genetic Parkinson's disease 49
Get Your Molar Tooth Right: Joubert Syndrome Misdiagnosis Unmasked by Whole-Exome Sequencing 40
Next generation molecular diagnosis of hereditary spastic paraplegias: an italian cross-sectional study 38
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease 23
Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers 22
Embracing Monogenic Parkinson's Disease. The MJFF Global Genetic PD Cohort 22
Pathogenic cryptic variants detectable through exome data reanalysis significantly increase the diagnostic yield in Joubert syndrome 18
Genome-wide Association and Meta-analysis of Age-at-Onset in Parkinson Disease. Evidence From COURAGE-PD Consortium 18
Dairy Intake and Parkinson's Disease. A Mendelian Randomization Study 17
The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited 13
Dystonia as Presenting Feature of Compound Heterozygous PMPCA Gene Variants 9
Totale 1.056
Categoria #
all - tutte 4.016
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.016


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020168 0 0 0 0 0 21 34 32 27 33 11 10
2020/202171 7 17 8 7 5 1 0 3 12 7 4 0
2021/2022137 4 7 16 2 12 9 5 13 7 6 32 24
2022/2023204 30 24 7 23 20 14 12 15 37 7 6 9
2023/2024161 7 25 12 12 10 35 5 8 3 21 16 7
2024/2025192 10 22 22 38 64 36 0 0 0 0 0 0
Totale 1.056