ZEULI, ROBERTA
 Distribuzione geografica
Continente #
EU - Europa 216
AS - Asia 187
NA - Nord America 76
SA - Sud America 27
AF - Africa 3
Totale 509
Nazione #
RU - Federazione Russa 130
US - Stati Uniti d'America 72
SG - Singapore 62
CN - Cina 46
IT - Italia 41
HK - Hong Kong 26
BR - Brasile 21
KR - Corea 16
DE - Germania 13
IE - Irlanda 11
VN - Vietnam 11
IN - India 9
JP - Giappone 7
AT - Austria 5
FR - Francia 3
TR - Turchia 3
AR - Argentina 2
CA - Canada 2
EC - Ecuador 2
ES - Italia 2
GB - Regno Unito 2
ID - Indonesia 2
PA - Panama 2
SA - Arabia Saudita 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
BE - Belgio 1
BJ - Benin 1
CO - Colombia 1
CZ - Repubblica Ceca 1
FI - Finlandia 1
IQ - Iraq 1
LT - Lituania 1
MA - Marocco 1
NL - Olanda 1
PE - Perù 1
PL - Polonia 1
RO - Romania 1
TN - Tunisia 1
UA - Ucraina 1
UZ - Uzbekistan 1
Totale 509
Città #
Moscow 50
Singapore 28
Hong Kong 26
Santa Clara 20
Hefei 19
Seoul 16
Dublin 11
Munich 10
Bengaluru 7
Ashburn 5
Caprecano 4
Dallas 4
Milan 4
Naples 4
Beijing 3
Boardman 3
Castelfranco Emilia 3
Castellammare di Stabia 3
Ercolano 3
Ho Chi Minh City 3
Los Angeles 3
Nuremberg 3
Aversa 2
Biên Hòa 2
Hanoi 2
Istanbul 2
New York 2
Porto Alegre 2
Vienna 2
Wuhan 2
'Asir Region 1
Ankara 1
Barra do Piraí 1
Berazategui 1
Bologna 1
Boston 1
Boydton 1
Brno 1
Brooklyn 1
Brussels 1
Campinas 1
Cedar Knolls 1
Cianorte 1
Cotonou 1
Denver 1
Dubai 1
Duque de Caxias 1
Fortaleza 1
Gaspar 1
Ha Long 1
Hưng Yên 1
Igarassu 1
Joinville 1
Lappeenranta 1
Lima 1
London 1
Maceió 1
Machado 1
Manchester 1
Medellín 1
Medina 1
Mt. Dora 1
Mumbai 1
Nashville 1
Olinda 1
Osasco 1
Ottawa 1
Paraipaba 1
Paulista 1
Phủ Lý 1
Rabat 1
Ramos Mejía 1
Rio de Janeiro 1
Roanoke 1
Rome 1
Roubaix 1
Salt Lake City 1
Santa Elena 1
São Paulo 1
Tashkent 1
Thanh Hóa 1
The Dalles 1
Tianjin 1
Tirana 1
Toronto 1
Tunis 1
Turmalina 1
Vera 1
Warsaw 1
Winder 1
Totale 308
Nome #
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy 107
A Novel Variant in TUBB4B Causes Progressive Cone‐Rod Dystrophy and Early Onset Sensorineural Hearing Loss 80
A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A 74
Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients 71
Joint contractures is a recurrent clinical feature of individuals with neurodevelopmental disorder due to FOXP1 likely gene disruptive variants 67
Variants in the AGBL5 gene are responsible for autosomal recessive Retinitis pigmentosa with hearing loss 61
Digital health and Clinical Patient Management System (CPMS) platform utility for data sharing of neuromuscular patients: the Italian EURO-NMD experience 61
Totale 521
Categoria #
all - tutte 1.875
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 1.875


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/202319 0 0 0 0 0 8 0 1 9 0 1 0
2023/202425 1 2 1 1 7 2 0 0 0 0 4 7
2024/2025167 8 9 0 3 23 14 20 29 17 10 9 25
2025/2026310 39 52 36 25 68 90 0 0 0 0 0 0
Totale 521