TALARICO, MARIAGRAZIA
 Distribuzione geografica
Continente #
NA - Nord America 164
EU - Europa 107
AS - Asia 101
SA - Sud America 30
AF - Africa 1
Totale 403
Nazione #
US - Stati Uniti d'America 162
SG - Singapore 54
IT - Italia 52
BR - Brasile 26
DE - Germania 24
CN - Cina 20
VN - Vietnam 15
FI - Finlandia 12
AT - Austria 8
HK - Hong Kong 4
AL - Albania 2
AR - Argentina 2
GB - Regno Unito 2
ID - Indonesia 2
IN - India 2
MX - Messico 2
PL - Polonia 2
AE - Emirati Arabi Uniti 1
CZ - Repubblica Ceca 1
EE - Estonia 1
ES - Italia 1
FR - Francia 1
IL - Israele 1
IQ - Iraq 1
MA - Marocco 1
NL - Olanda 1
PE - Perù 1
TR - Turchia 1
VE - Venezuela 1
Totale 403
Città #
Dallas 45
Singapore 38
Santa Clara 29
Munich 18
Hefei 13
Ashburn 12
Turku 11
Ho Chi Minh City 8
Naples 8
Secaucus 6
Los Angeles 5
Hong Kong 4
Pasadena 4
Rome 4
Vallefiorita 4
Buffalo 3
Catania 3
Columbus 3
Hanoi 3
New York 3
Rimini 3
San Francisco 3
Aversa 2
Boardman 2
Bovisio-Masciago 2
Brasília 2
Denver 2
Elk Grove Village 2
Mendicino 2
Mexico City 2
Palermo 2
Pisa 2
San Nicola Manfredi 2
San Vito dei Normanni 2
São Paulo 2
Tirana 2
Vicopisano 2
Warsaw 2
Afragola 1
Almont 1
Amsterdam 1
Arame 1
Atlanta 1
Barro Alto 1
Basra 1
Biên Hòa 1
Boa Vista 1
Bom Jesus 1
Boston 1
Brooklyn 1
Camaçari 1
Campinas 1
Can Tho 1
Caracas 1
Chennai 1
Chicago 1
Corumbaíba 1
Curitiba 1
Denpasar 1
Dubai 1
Duque de Caxias 1
Formiga 1
Getúlio Vargas 1
Goiânia 1
Ha Long 1
Hanover 1
Helsinki 1
Jakarta 1
Jequié 1
Jundiaí 1
Lamezia Terme 1
Lima 1
Lissone 1
London 1
Los Polvorines 1
Macaé 1
Maceió 1
Mazara del Vallo 1
Miami 1
Mumbai 1
Olomouc 1
Pescara 1
Piripiri 1
Pizzo 1
Posadas 1
Poços de Caldas 1
Rio de Janeiro 1
Rottenburg 1
Serra San Bruno 1
Sete Lagoas 1
Silver Spring 1
Tangier 1
Tel Aviv 1
The Dalles 1
Tubarão 1
Vienna 1
Vitória 1
Totale 321
Nome #
Idiopathic generalized epilepsy in a family with SCN4A-related myotonia 47
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 46
Distinct microRNA signatures define sporadic PSP-RS and PD in patient-derived midbrain organoids 39
A novel phenotype in an Italian family with a rare progranulin mutation 39
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 38
ANXA1 mutation analysis in Italian patients with early onset PD 34
Modeling Sporadic Progressive Supranuclear Palsy in 3D Midbrain Organoids: Recapitulating Disease Features for In Vitro Diagnosis and Drug Discovery 33
Neuronally-Derived Extracellular Vesicles Transforming Growth Factor Beta-1 Levels in Progressive Supranuclear Palsy 29
Neuronally Derived Extracellular Vesicles’ Oligomeric and p129-α-Synuclein Levels for Differentiation of Parkinson’s Disease from Essential Tremor 24
Two Novel Variants in the CHRNA2 and SCN2A Genes in Italian Patients with Febrile Seizures 22
Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson’s disease from Southern Italy 20
Transcriptomic and electrophysiological alterations underlying phenotypic variability in SCN1A-associated febrile seizures 18
Genome-wide association meta-analyses of drug-resistant epilepsy 17
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in Italy 11
Novel KCNQ2 Variants Related to a Variable Phenotypic Spectrum Ranging from Epilepsy with Auditory Features to Severe Developmental and Epileptic Encephalopathies 7
Totale 424
Categoria #
all - tutte 2.299
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 2.299


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/20237 0 0 0 0 1 0 0 1 2 1 0 2
2023/202415 3 1 0 5 2 1 0 0 0 0 0 3
2024/2025207 2 1 1 28 7 17 9 22 15 8 22 75
2025/2026195 45 71 79 0 0 0 0 0 0 0 0 0
Totale 424