BAFUNNO, VALERIA
 Distribuzione geografica
Continente #
EU - Europa 219
NA - Nord America 192
AS - Asia 143
SA - Sud America 31
AF - Africa 1
OC - Oceania 1
Totale 587
Nazione #
US - Stati Uniti d'America 191
CN - Cina 60
IE - Irlanda 58
SG - Singapore 48
SE - Svezia 44
UA - Ucraina 37
IT - Italia 28
BR - Brasile 19
RU - Federazione Russa 17
TR - Turchia 13
DE - Germania 10
GB - Regno Unito 9
AR - Argentina 7
FR - Francia 7
IN - India 7
VN - Vietnam 7
HK - Hong Kong 6
NL - Olanda 4
FI - Finlandia 3
CO - Colombia 2
EC - Ecuador 2
RO - Romania 2
BH - Bahrain 1
ID - Indonesia 1
MX - Messico 1
NZ - Nuova Zelanda 1
PY - Paraguay 1
ZA - Sudafrica 1
Totale 587
Città #
Dublin 58
Nyköping 28
Chandler 25
Jacksonville 25
Singapore 24
Dearborn 19
Wilmington 18
Ashburn 16
Nanjing 14
Beijing 11
New York 11
Foggia 10
Santa Clara 7
Hong Kong 6
Nanchang 6
Princeton 6
Dallas 5
Ann Arbor 4
Buenos Aires 3
Hanoi 3
Hebei 3
Moscow 3
Munich 3
San Mateo 3
Shenyang 3
Tianjin 3
Boardman 2
Changchun 2
Jiaxing 2
Kunming 2
London 2
Los Angeles 2
São Paulo 2
Amsterdam 1
Apóstoles 1
Araucária 1
Auckland 1
Blumenau 1
Bogotá 1
Bologna 1
Bom Princípio 1
Brusque 1
Bắc Giang 1
Changsha 1
Chicago 1
Conselheiro Lafaiete 1
Correntes 1
Delhi 1
Duluth 1
Fortaleza 1
Guangzhou 1
Haiphong 1
Hangzhou 1
Hanover 1
Helena 1
Ho Chi Minh City 1
Isidro Casanova 1
Itanhém 1
Jakarta 1
Jaraguá do Sul 1
Jinan 1
Johannesburg 1
La Puntilla 1
La Rioja 1
Manama 1
Maricá 1
Medellín 1
Mexico City 1
Milan 1
Navegantes 1
Nuremberg 1
Oak Ridge 1
Piracicaba 1
Praia Grande 1
Quito 1
Rodeo de la Cruz 1
San Francisco 1
Serrana 1
Shenzhen 1
Sikeston 1
Simi Valley 1
Stevenage 1
Strasbourg 1
São José dos Pinhais 1
São Vicente 1
Taizhou 1
Tampa 1
Thái Nguyên 1
Ubatuba 1
Zhengzhou 1
Totale 388
Nome #
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema. 138
Characterization of patients with angioedema without wheals: the importance of F12 gene screening 116
A novel congenital dysprothrombinemia leading to defective prothrombin maturation 106
Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations 105
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 97
Impaired control of the contact system in hereditary angioedema with normal C1-inhibitor 64
Totale 626
Categoria #
all - tutte 3.612
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 3.612


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202151 0 0 0 0 0 0 6 4 31 10 0 0
2021/202251 3 0 0 0 4 1 2 4 9 11 3 14
2022/2023135 15 8 9 4 6 11 0 13 64 0 3 2
2023/202434 3 3 3 1 2 13 2 0 0 0 0 7
2024/202570 3 1 1 2 1 13 2 2 25 2 9 9
2025/202695 18 18 27 24 8 0 0 0 0 0 0 0
Totale 626