Bruno, Carmelina
 Distribuzione geografica
Continente #
NA - Nord America 128
AS - Asia 103
EU - Europa 67
SA - Sud America 11
AF - Africa 2
Totale 311
Nazione #
US - Stati Uniti d'America 122
SG - Singapore 45
CN - Cina 22
DE - Germania 16
FR - Francia 11
SE - Svezia 10
VN - Vietnam 10
GB - Regno Unito 8
BR - Brasile 7
IT - Italia 7
IN - India 5
TR - Turchia 5
CA - Canada 3
ID - Indonesia 3
JP - Giappone 3
RU - Federazione Russa 3
AT - Austria 2
BD - Bangladesh 2
CO - Colombia 2
FI - Finlandia 2
HK - Hong Kong 2
IE - Irlanda 2
NL - Olanda 2
UZ - Uzbekistan 2
CR - Costa Rica 1
EC - Ecuador 1
ES - Italia 1
ET - Etiopia 1
IQ - Iraq 1
IR - Iran 1
JM - Giamaica 1
JO - Giordania 1
KR - Corea 1
MX - Messico 1
NO - Norvegia 1
PL - Polonia 1
PY - Paraguay 1
UA - Ucraina 1
ZA - Sudafrica 1
Totale 311
Città #
Singapore 23
Chandler 15
San Jose 12
Ashburn 9
Houston 7
New York 6
Angri 5
Beijing 5
Ho Chi Minh City 5
Izmir 5
Jacksonville 5
San Mateo 5
Dearborn 4
Hefei 3
Lancaster 3
Lauterbourg 3
Los Angeles 3
Marseille 3
Moscow 3
Munich 3
Nanjing 3
Paris 3
Tokyo 3
Wilmington 3
Amsterdam 2
Boston 2
Buffalo 2
Cambridge 2
Dublin 2
Fairfield 2
Frankfurt am Main 2
Hong Kong 2
Ninh Bình 2
Ottawa 2
Redwood City 2
Santa Clara 2
Seattle 2
Tashkent 2
Woodbridge 2
Addis Ababa 1
Ahmedabad 1
Albany 1
Amman 1
Ann Arbor 1
Araranguá 1
Bexley 1
Bogotá 1
Brasília 1
Bremen 1
Brooklyn 1
Bến Tre 1
Camboriú 1
Changsha 1
Dallas 1
Denpasar 1
Denver 1
Depok 1
Dhaka 1
Düsseldorf 1
Edinburgh 1
Erbil 1
Heredia 1
Honolulu 1
Ibarra 1
Jakarta 1
Jinan 1
Johannesburg 1
Kent 1
Lawrence 1
Leawood 1
Limpio 1
London 1
Medellín 1
Mexico City 1
Milan 1
Mountain View 1
Nanchang 1
New Delhi 1
North Bergen 1
Nuremberg 1
Oslo 1
Princeton 1
Salvador 1
Santo Antônio do Descoberto 1
Santo Estêvão 1
Seoul 1
Shenyang 1
São Paulo 1
Thái Bình 1
Tianjin 1
Toronto 1
Turku 1
University Park 1
Vĩnh Tường 1
Yellow Springs 1
Totale 225
Nome #
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy 148
Copy Number Variants Account for a Tiny Fraction of Undiagnosed Myopathic Patients. 117
Novel GNE mutations in Italian families with autosomal recessive hereditary inclusion-body myopathy 49
Totale 314
Categoria #
all - tutte 1.313
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 1.313


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211 0 0 0 0 0 0 0 0 0 0 1 0
2021/202221 1 0 0 1 1 6 2 7 0 0 1 2
2022/202340 3 5 3 5 3 5 3 2 8 1 1 1
2023/202420 1 4 0 1 1 4 0 0 0 0 7 2
2024/202545 1 1 1 4 4 3 3 0 5 5 9 9
2025/2026127 24 1 5 15 33 5 24 11 6 3 0 0
Totale 314