SALSANO, ETTORE
 Distribuzione geografica
Continente #
EU - Europa 304
NA - Nord America 282
AS - Asia 105
SA - Sud America 6
OC - Oceania 2
AF - Africa 1
Totale 700
Nazione #
US - Stati Uniti d'America 273
GB - Regno Unito 120
CN - Cina 57
DE - Germania 43
SE - Svezia 43
IT - Italia 35
IN - India 18
IE - Irlanda 11
UA - Ucraina 11
CA - Canada 9
KR - Corea 9
TR - Turchia 8
FI - Finlandia 7
NL - Olanda 7
EU - Europa 6
FR - Francia 6
HK - Hong Kong 6
SG - Singapore 5
BE - Belgio 4
CO - Colombia 4
DK - Danimarca 4
PT - Portogallo 3
CH - Svizzera 2
GR - Grecia 2
JP - Giappone 2
RO - Romania 2
AR - Argentina 1
AU - Australia 1
EE - Estonia 1
ES - Italia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PL - Polonia 1
RU - Federazione Russa 1
ZA - Sudafrica 1
Totale 706
Città #
Southend 110
Chandler 45
Seattle 26
Fairfield 25
Ashburn 17
Milan 17
Beijing 16
Woodbridge 13
Princeton 12
Wilmington 12
Dublin 11
Ann Arbor 10
Houston 10
Toronto 9
Phoenix 7
Redmond 7
Shanghai 7
Bengaluru 6
Boardman 6
Frankfurt am Main 6
Hong Kong 6
Jacksonville 6
Nanjing 6
Somerville 6
Cambridge 5
Jinan 5
Bogotá 4
Dearborn 4
Des Moines 4
Philadelphia 4
Waanrode 4
Andover 3
Lisbon 3
Medford 3
Nanchang 3
Redwood City 3
Sakarya 3
Singapore 3
Athens 2
Berlin 2
Bitonto 2
Columbus 2
Dallas 2
Frankfurt 2
Grafing 2
Hebei 2
Hefei 2
Margão 2
Mountain View 2
New York 2
San Diego 2
Serra 2
Tokyo 2
Brisbane 1
Brugherio 1
Campo Ligure 1
Catania 1
Changchun 1
Changsha 1
Charleston 1
Cologne 1
Hangzhou 1
Helsinki 1
Kilburn 1
Kunming 1
Lanzhou 1
Lima 1
London 1
Madrid 1
Novokuznetsk 1
Nuremberg 1
Nürnberg 1
Palermo 1
Pretoria 1
Santo Stefano Roero 1
Shenyang 1
Tallinn 1
Tappahannock 1
Tianjin 1
Washington 1
Whangarei 1
Zhengzhou 1
Zurich 1
Totale 507
Nome #
Human adipose-derived mesenchymal stem cells as a new model of spinal and bulbar muscular atrophy 196
Molecular epidemiology and clinical features of a large Italian cohort of 291 dystrophinopathic patients. 128
Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features 116
One gene, two clinical profiles:novel GBE1 mutations in GSD type IV and Adult Polyglucosan Body Disease. 111
Phenotypic heterogeneity of GBE1 mutations: congenital glycogen storage disease type IV and adult polyglucosan body disease. 94
Adult polyglucosan body disease in a patient originally diagnosed with Fabry's disease 82
Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency 12
RARS1-related hypomyelinating leukodystrophy : Expanding the spectrum 11
Identification of a new candidate gene in the insurgence of leukodystrophies 4
null 3
null 3
Totale 760
Categoria #
all - tutte 1.766
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 1.766


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201926 0 0 0 0 0 0 0 0 0 14 7 5
2019/202081 11 2 2 5 3 5 14 3 20 12 4 0
2020/2021118 6 39 11 0 8 4 5 6 10 8 18 3
2021/202275 2 2 1 1 7 0 5 3 14 14 5 21
2022/2023114 16 15 10 11 9 22 0 10 18 1 2 0
2023/202491 3 7 11 6 25 7 1 8 11 12 0 0
Totale 760