TIRANTI, VALERIA SONIA
 Distribuzione geografica
Continente #
NA - Nord America 315
EU - Europa 201
AS - Asia 74
AF - Africa 9
Totale 599
Nazione #
US - Stati Uniti d'America 315
IT - Italia 67
GB - Regno Unito 38
SE - Svezia 28
DE - Germania 22
SG - Singapore 22
IE - Irlanda 14
VN - Vietnam 13
CN - Cina 12
IN - India 12
HK - Hong Kong 6
RU - Federazione Russa 6
BE - Belgio 5
CI - Costa d'Avorio 5
FR - Francia 5
EE - Estonia 3
FI - Finlandia 3
NL - Olanda 3
TW - Taiwan 3
CZ - Repubblica Ceca 2
JO - Giordania 2
KR - Corea 2
PK - Pakistan 2
UA - Ucraina 2
ZA - Sudafrica 2
AT - Austria 1
CH - Svizzera 1
PL - Polonia 1
SC - Seychelles 1
TG - Togo 1
Totale 599
Città #
Chandler 51
Southend 37
Bologna 33
Ashburn 27
Fairfield 24
Woodbridge 21
Houston 19
Singapore 19
Ann Arbor 18
Cambridge 15
Dublin 14
Princeton 12
Seattle 12
Wilmington 9
Redmond 7
Santa Clara 7
Hong Kong 6
Turin 6
Abidjan 5
Berlin 5
Boydton 5
Brussels 5
Naples 4
San Diego 4
Westminster 4
Boardman 3
Frederick 3
Fremont 3
Milan 3
Nanchang 3
Padova 3
Parma 3
Philadelphia 3
Taipei 3
Amman 2
Beijing 2
Des Moines 2
Falls Church 2
Helsinki 2
Jinan 2
Olomouc 2
Rome 2
Saint Petersburg 2
Sejong 2
Amsterdam 1
Bern 1
Castelfranco Emilia 1
Dearborn 1
Doylestown 1
Florence 1
Forlì 1
Frankfurt am Main 1
Groningen 1
Hebei 1
Hounslow 1
Hyderabad 1
Islamabad 1
Kunming 1
Lappeenranta 1
Lodz 1
Lomé 1
Los Angeles 1
Mahé 1
Mardan 1
Moscow 1
Mülheim 1
Nijmegen 1
Olalla 1
Rho 1
Shenyang 1
Tianjin 1
Verdellino 1
Verona 1
Vienna 1
Totale 446
Nome #
Coenzyme A corrects pathological defects in human neurons of PANK2-associated neurodegeneration 112
Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts 106
Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patients 101
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 96
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs 70
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy 52
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy 45
Reduced mitochondrial Ca 2+ transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenase 44
Totale 626
Categoria #
all - tutte 1.987
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 1.987


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020104 0 3 0 4 17 12 16 20 16 8 4 4
2020/202156 10 6 1 1 1 0 2 2 8 1 4 20
2021/202294 3 2 2 3 7 9 3 17 2 9 18 19
2022/2023177 10 20 4 22 23 24 5 11 33 3 12 10
2023/202486 0 12 5 6 6 7 5 10 13 5 9 8
2024/202567 35 32 0 0 0 0 0 0 0 0 0 0
Totale 626