DOCCINI, STEFANO
 Distribuzione geografica
Continente #
EU - Europa 367
NA - Nord America 201
AS - Asia 51
Continente sconosciuto - Info sul continente non disponibili 1
Totale 620
Nazione #
US - Stati Uniti d'America 200
PL - Polonia 192
IT - Italia 89
IE - Irlanda 25
CN - Cina 18
ES - Italia 16
HK - Hong Kong 14
RU - Federazione Russa 11
FI - Finlandia 9
VN - Vietnam 8
SE - Svezia 7
SG - Singapore 7
GB - Regno Unito 6
DE - Germania 5
CH - Svizzera 2
IN - India 2
RO - Romania 2
CA - Canada 1
EU - Europa 1
FR - Francia 1
GR - Grecia 1
JO - Giordania 1
TW - Taiwan 1
UA - Ucraina 1
Totale 620
Città #
Warsaw 192
Fairfield 30
Dublin 25
Ashburn 20
Cambridge 14
Chandler 14
Seattle 12
Houston 10
Princeton 10
Barcelona 8
Dong Ket 8
Hong Kong 8
Shanghai 8
Florence 7
Pontedera 7
Wilmington 7
Woodbridge 7
Beijing 6
Cagliari 6
Helsinki 6
Lawrence 6
Medford 6
Pisa 6
Andover 5
Campi Bisenzio 5
Milan 5
Altamura 4
Singapore 4
Livorno 3
Anzio 2
Bari 2
Bengaluru 2
Bern 2
Bethesda 2
Fiumicino 2
Frankfurt Am Main 2
Hamburg 2
Kilburn 2
Naples 2
Rome 2
Siena 2
Timisoara 2
Ann Arbor 1
Athens 1
Baltimore 1
Boston 1
Castelliri 1
Columbus 1
Dearborn 1
Deiva Marina 1
Dugenta 1
Falls Church 1
Guangzhou 1
Hillsboro 1
Lucca 1
Lurate Caccivio 1
Monsummano Terme 1
Moscow 1
Phoenix 1
San Diego 1
Scansano 1
Stevenage 1
Taipei 1
Toronto 1
Trumbull 1
Totale 498
Nome #
Functional omics approaches towards affected molecular pathways underlying various forms of Neuronal Ceroid Lipofuscinoses 221
The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells 148
Mitochondrial respiratory chain defects in skin fibroblasts from patients with Dravet syndrome 71
Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD 63
ANNUAL REPORT - IN VITRO STUDIES OF ENERGY DYSFUNCTION IN CLASSICAL-INFANTILE AND LATE-INFANTILE NEURONAL CEROID LIPOFUSCINOSIS 45
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction 33
Annual report - Proteomic analysis and molecular pathways in models of CLN5 disease 26
Additive effect of DNAJC30 and NDUFA9 mutations causing Leigh syndrome 23
Totale 630
Categoria #
all - tutte 1.741
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 1.741


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020113 0 12 5 8 15 11 10 15 13 11 10 3
2020/2021110 5 15 13 30 5 4 4 5 8 12 1 8
2021/202239 1 3 2 5 0 0 0 6 1 4 3 14
2022/2023109 21 10 2 6 5 20 12 5 12 4 8 4
2023/202470 5 5 15 1 5 0 6 23 0 1 3 6
2024/202531 14 17 0 0 0 0 0 0 0 0 0 0
Totale 630