TIRANTI, VALERIA SONIA
 Distribuzione geografica
Continente #
NA - Nord America 346
EU - Europa 234
AS - Asia 117
AF - Africa 10
Totale 707
Nazione #
US - Stati Uniti d'America 346
IT - Italia 87
SG - Singapore 44
GB - Regno Unito 38
CN - Cina 28
SE - Svezia 28
DE - Germania 24
IE - Irlanda 14
IN - India 14
RU - Federazione Russa 13
VN - Vietnam 13
BE - Belgio 6
CI - Costa d'Avorio 6
HK - Hong Kong 6
FR - Francia 5
FI - Finlandia 4
NL - Olanda 4
TW - Taiwan 4
CZ - Repubblica Ceca 3
EE - Estonia 3
JO - Giordania 2
KR - Corea 2
PK - Pakistan 2
UA - Ucraina 2
ZA - Sudafrica 2
AT - Austria 1
CH - Svizzera 1
ID - Indonesia 1
PL - Polonia 1
SC - Seychelles 1
TG - Togo 1
TR - Turchia 1
Totale 707
Città #
Chandler 51
Southend 37
Bologna 36
Singapore 36
Ashburn 28
Santa Clara 27
Fairfield 24
Woodbridge 21
Houston 19
Ann Arbor 18
Cambridge 15
Dublin 14
Princeton 12
Seattle 12
Boardman 11
Wilmington 9
Redmond 7
Turin 7
Abidjan 6
Brussels 6
Hong Kong 6
Berlin 5
Boydton 5
Rome 5
Milan 4
Naples 4
San Diego 4
Taipei 4
Westminster 4
Frederick 3
Fremont 3
Nanchang 3
Padova 3
Parma 3
Philadelphia 3
San Giorgio di Piano 3
Amman 2
Beijing 2
Des Moines 2
Falls Church 2
Florence 2
Gurugram 2
Helsinki 2
Jinan 2
Modena 2
Nuremberg 2
Olomouc 2
Saint Petersburg 2
Sejong 2
Shanghai 2
Amsterdam 1
Ankara 1
Anyang 1
Bern 1
Castelfranco Emilia 1
Dearborn 1
Doylestown 1
Forlì 1
Frankfurt am Main 1
Groningen 1
Hebei 1
Hounslow 1
Hwang Chow 1
Hyderabad 1
Islamabad 1
Jakarta 1
Kunming 1
Lappeenranta 1
Lodz 1
Lomé 1
Los Angeles 1
Mahé 1
Mardan 1
Moscow 1
Mülheim 1
Nijmegen 1
Olalla 1
Prague 1
Qingdao 1
Rho 1
Shenyang 1
Tianjin 1
Verdellino 1
Verona 1
Vienna 1
Wuhan 1
Wuxi 1
Yubileyny 1
Totale 524
Nome #
Coenzyme A corrects pathological defects in human neurons of PANK2-associated neurodegeneration 122
Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts 114
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 112
Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patients 110
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy 94
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs 79
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy 55
Reduced mitochondrial Ca 2+ transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenase 53
Totale 739
Categoria #
all - tutte 2.443
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 2.443


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202052 0 0 0 0 0 0 0 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
2024/2025180 35 32 14 25 35 19 18 2 0 0 0 0
Totale 739