MEARINI, MARZIA
 Distribuzione geografica
Continente #
NA - Nord America 199
AS - Asia 136
EU - Europa 113
SA - Sud America 18
AF - Africa 3
Totale 469
Nazione #
US - Stati Uniti d'America 194
SG - Singapore 56
IE - Irlanda 30
IT - Italia 26
HK - Hong Kong 24
RU - Federazione Russa 23
CN - Cina 22
VN - Vietnam 17
BR - Brasile 15
FI - Finlandia 8
AT - Austria 6
PL - Polonia 6
CA - Canada 3
GB - Regno Unito 3
IN - India 3
KR - Corea 3
UA - Ucraina 3
AR - Argentina 2
DE - Germania 2
DK - Danimarca 2
JP - Giappone 2
SE - Svezia 2
ZA - Sudafrica 2
BD - Bangladesh 1
BE - Belgio 1
DZ - Algeria 1
ES - Italia 1
IQ - Iraq 1
JM - Giamaica 1
JO - Giordania 1
KG - Kirghizistan 1
KW - Kuwait 1
MX - Messico 1
NP - Nepal 1
PY - Paraguay 1
SA - Arabia Saudita 1
TR - Turchia 1
UZ - Uzbekistan 1
Totale 469
Città #
Chandler 36
Dublin 30
Singapore 30
Hong Kong 24
San Mateo 21
Ashburn 15
Dong Ket 14
Altamura 10
Beijing 9
Moscow 8
Santa Clara 8
Boardman 7
Medford 7
Princeton 7
Lawrence 6
Perugia 6
New York 5
Warsaw 4
Wilmington 4
Boston 3
Andover 2
Brooklyn 2
Dallas 2
Hanoi 2
Johannesburg 2
Los Angeles 2
Munich 2
Saint Petersburg 2
São Paulo 2
Tokyo 2
Abatiá 1
Ahmedabad 1
Amman 1
Ankara 1
Atlanta 1
Baghdad 1
Barreiros 1
Belo Horizonte 1
Berazategui 1
Bishkek 1
Brussels 1
Camaçari 1
Campinas 1
Charlotte 1
Chennai 1
Chicago 1
Cuiabá 1
Denver 1
Gimhae 1
Helsinki 1
Ho Chi Minh City 1
Houston 1
Huizhou 1
Ibirama 1
Ketchikan 1
Kingston 1
Kuwait City 1
Machado 1
Mar del Plata 1
Marília 1
Montreal 1
Noida 1
Norwalk 1
Paignton 1
Paranaguá 1
Poplar 1
Querétaro 1
Redmond 1
Ribeirão Preto 1
Riyadh 1
San Paolo di Civitate 1
Santa Rita 1
Secaucus 1
Seoul 1
Sorocaba 1
Stockholm 1
Toronto 1
Turek 1
Valinhos 1
Vienna 1
Winnipeg 1
Totale 325
Nome #
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 107
A clinico-genetical study in a large cohort of patients with spastic paraplegia type 4 (SPG4) 84
Spastic paraplegia type 4: a novel SPAST splice site donor mutation and expansion of the phenotype variability 82
Identification of ALS5/SPG11/KIAA1840 Mutations in Patients with Autosomal Recessive Form of Charcot-Marie-Tooth Disease Type 2 73
SPG11 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 65
Hereditary Spastic Paraplegia Type 4 (SPG4): A Clinico-Genetic Study in a Large Cohort of Patients with Spastic Paraplegia 62
miR128 up-regulation correlates with impaired Amyloid-β42 degradation in monocytes of patients with sporadic Alzheimer’s disease 61
Totale 534
Categoria #
all - tutte 2.734
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 2.734


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202114 0 0 0 0 0 0 0 0 0 0 0 14
2021/202254 0 15 1 0 4 0 0 16 0 1 6 11
2022/2023107 7 22 5 3 12 8 0 5 42 0 2 1
2023/202451 4 6 4 0 0 0 18 0 0 3 11 5
2024/202592 0 9 7 0 8 9 6 4 20 8 13 8
2025/2026115 14 10 2 37 47 5 0 0 0 0 0 0
Totale 534