SANCHINI, MARIABEATRICE
 Distribuzione geografica
Continente #
NA - Nord America 158
AS - Asia 153
EU - Europa 57
SA - Sud America 29
AF - Africa 3
Totale 400
Nazione #
US - Stati Uniti d'America 151
SG - Singapore 84
CN - Cina 24
BR - Brasile 22
HK - Hong Kong 17
IT - Italia 17
VN - Vietnam 14
RU - Federazione Russa 10
DE - Germania 8
ID - Indonesia 6
AR - Argentina 5
CA - Canada 4
AT - Austria 3
BD - Bangladesh 3
FI - Finlandia 3
GB - Regno Unito 3
UA - Ucraina 3
MX - Messico 2
PL - Polonia 2
SE - Svezia 2
TR - Turchia 2
AZ - Azerbaigian 1
CL - Cile 1
CR - Costa Rica 1
ET - Etiopia 1
FR - Francia 1
GR - Grecia 1
IQ - Iraq 1
LT - Lituania 1
NL - Olanda 1
NO - Norvegia 1
PY - Paraguay 1
QA - Qatar 1
RO - Romania 1
SN - Senegal 1
ZA - Sudafrica 1
Totale 400
Città #
Singapore 46
Ashburn 42
Santa Clara 18
Hong Kong 17
Beijing 14
New York 9
Ho Chi Minh City 6
Jakarta 6
Los Angeles 4
Shanghai 4
Dallas 3
Ottawa 3
São Paulo 3
Bologna 2
Boston 2
Campinas 2
Chandler 2
Chicago 2
Denver 2
Ferrara 2
Ha Long 2
Hefei 2
Houston 2
Inverigo 2
Lappeenranta 2
Mexico City 2
Milan 2
Munich 2
Phoenix 2
Pordenone 2
Princeton 2
Redondo Beach 2
Rio de Janeiro 2
San Lazzaro di Savena 2
Stockholm 2
Vistarino 2
Warsaw 2
Adana 1
Addis Ababa 1
Alajuela 1
Ankara 1
Asunción 1
Athens 1
Baku 1
Basra 1
Buenos Aires 1
Buffalo 1
Cambridge 1
Caxias do Sul 1
Charlotte 1
City of London 1
Corumbaíba 1
Decatur 1
Diadema 1
Diamantina 1
Doha 1
Dos de Mayo 1
Frankfurt am Main 1
Guernica 1
Haiphong 1
Hanoi 1
Helsinki 1
Jaboatão dos Guararapes 1
Jandira 1
Johannesburg 1
Juiz de Fora 1
Lages 1
Las Vegas 1
London 1
Luhansk 1
New Haven 1
Nha Trang 1
Nuremberg 1
Nārāyanganj 1
Olinda 1
Orlândia 1
Paso de los Libres 1
Penápolis 1
Ponta Grossa 1
Poplar 1
Puerto Varas 1
Rykene 1
Salvador 1
Thanh Hóa 1
Thái Bình 1
Toronto 1
Tupi Paulista 1
Turin 1
Vienna 1
Vitória 1
Zapala 1
Totale 277
Nome #
Left ventricular myocardial noncompaction with advanced atrioventricular conduction disorder and ventricular arrhythmias in a young patient: Role of MIB1 gene 109
THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder 84
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotype 82
Novel SCN5A Variant Shows Multiple Phenotypic Expression in the Same Family 74
Mother and daughter with Kenny-Caffey syndrome: the adult phenotype 67
Totale 416
Categoria #
all - tutte 2.822
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 2.822


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202211 0 0 0 0 0 0 3 1 0 0 2 5
2022/202317 2 0 0 0 0 1 4 2 3 2 3 0
2023/202428 0 3 2 0 1 7 3 0 1 2 1 8
2024/2025146 3 4 10 5 14 20 8 5 25 20 18 14
2025/2026214 41 23 29 43 74 4 0 0 0 0 0 0
Totale 416