VERGANI, LODOVICA
 Distribuzione geografica
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Continente #
NA - Nord America 3.536
AS - Asia 1.639
EU - Europa 859
AF - Africa 389
SA - Sud America 317
OC - Oceania 36
Continente sconosciuto - Info sul continente non disponibili 13
AN - Antartide 1
Totale 6.790
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Nazione #
US - Stati Uniti d'America 3.332
SG - Singapore 624
CN - Cina 362
BR - Brasile 215
HK - Hong Kong 172
VN - Vietnam 135
SE - Svezia 102
DE - Germania 100
FI - Finlandia 93
IT - Italia 67
UA - Ucraina 63
GB - Regno Unito 46
FR - Francia 43
RU - Federazione Russa 34
PL - Polonia 32
NL - Olanda 31
MX - Messico 28
IN - India 27
BJ - Benin 26
AR - Argentina 20
CA - Canada 20
SA - Arabia Saudita 19
ZA - Sudafrica 19
IQ - Iraq 18
JP - Giappone 18
TR - Turchia 18
ML - Mali 16
AT - Austria 15
ES - Italia 15
PE - Perù 15
PA - Panama 14
UZ - Uzbekistan 14
DK - Danimarca 13
ID - Indonesia 13
IE - Irlanda 13
LC - Santa Lucia 13
MA - Marocco 13
RW - Ruanda 13
AL - Albania 12
AO - Angola 12
DZ - Algeria 12
EG - Egitto 12
GA - Gabon 12
KZ - Kazakistan 12
MZ - Mozambico 12
SN - Senegal 12
AD - Andorra 11
CO - Colombia 11
CR - Costa Rica 11
CV - Capo Verde 11
HR - Croazia 11
LB - Libano 11
MG - Madagascar 11
PS - Palestinian Territory 11
AE - Emirati Arabi Uniti 10
AU - Australia 10
CU - Cuba 10
ET - Etiopia 10
HN - Honduras 10
LA - Repubblica Popolare Democratica del Laos 10
ME - Montenegro 10
NI - Nicaragua 10
PK - Pakistan 10
SI - Slovenia 10
SY - Repubblica araba siriana 10
VE - Venezuela 10
ZM - Zambia 10
AM - Armenia 9
BA - Bosnia-Erzegovina 9
BS - Bahamas 9
BY - Bielorussia 9
CD - Congo 9
CH - Svizzera 9
CI - Costa d'Avorio 9
CM - Camerun 9
EC - Ecuador 9
GH - Ghana 9
GM - Gambi 9
GN - Guinea 9
GT - Guatemala 9
HU - Ungheria 9
IS - Islanda 9
JM - Giamaica 9
KE - Kenya 9
MN - Mongolia 9
MY - Malesia 9
PY - Paraguay 9
TN - Tunisia 9
UG - Uganda 9
UY - Uruguay 9
AZ - Azerbaigian 8
BE - Belgio 8
BO - Bolivia 8
BW - Botswana 8
BZ - Belize 8
CZ - Repubblica Ceca 8
EE - Estonia 8
GE - Georgia 8
GF - Guiana Francese 8
GR - Grecia 8
Totale 6.432
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Città #
Fairfield 400
Singapore 350
Ashburn 348
Chandler 284
Woodbridge 239
Jacksonville 218
Houston 197
Hong Kong 164
Ann Arbor 156
Wilmington 141
Cambridge 137
Seattle 127
Beijing 89
Boardman 83
Princeton 78
Santa Clara 75
Dong Ket 53
Roxbury 50
Des Moines 42
San Jose 39
Los Angeles 36
San Diego 36
Nanjing 35
Medford 34
New York 28
Cotonou 26
Helsinki 26
São Paulo 25
Ho Chi Minh City 23
Munich 22
Jinan 21
Bytom 20
Hanoi 20
Guangzhou 16
Turku 16
Bamako 14
Milan 14
Panama City 14
Castries 13
Kigali 13
The Dalles 13
Dakar 12
Hebei 12
Libreville 12
Andorra la Vella 11
Luanda 11
Nanchang 11
Tashkent 11
Tokyo 11
Antananarivo 10
Buffalo 10
Havana 10
London 10
Lusaka 10
Managua 10
Norwalk 10
Orem 10
Padova 10
Praia 10
San José 10
Shanghai 10
Tianjin 10
Abidjan 9
Addis Ababa 9
Brooklyn 9
Changsha 9
Chicago 9
Conakry 9
Denver 9
Dublin 9
Maputo 9
Minsk 9
Montreal 9
Nairobi 9
Nassau 9
Nuremberg 9
Shenyang 9
Vientiane 9
Accra 8
Bishkek 8
Dushanbe 8
Gaborone 8
Johannesburg 8
Kampala 8
Lima 8
Noumea 8
Rio de Janeiro 8
Tallinn 8
Tirana 8
Vienna 8
Yerevan 8
Baku 7
Bridgetown 7
Harare 7
Kingston 7
Melbourne 7
Montevideo 7
Phnom Penh 7
Port-au-Prince 7
Reykjavik 7
Totale 4.267
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Nome #
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients 261
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts 217
Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect. 195
Dominant optic atrophy caused by a novel OPA1 mutation: Disruption of the mitochondrial network with preserved bioenergetics. 192
Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants 185
MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases 184
Abnormal free radical homeostasis and oxphos activity in ALS muscle 181
The ALPINE–ALMA [C ii] Survey: Multiwavelength Ancillary Data and Basic Physical Measurements 180
Mitochondrial quality control: Cell-type-dependent responses to pathological mutant mitochondrial DNA. 178
Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells. 175
A pilot trial with clenbuterol in amyotrophic lateral sclerosis 173
null 171
Activities of mitochondrial complexes correlate with nNOS amount in muscle from ALS patients. 168
Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females. 167
Clinical and pathological findings in families with X-linked spinal and bulbar muscular atrophy (Kennedy's disease). 165
INHIBITION OF MITOCHONDRIAL FISSION FAVOURS MUTANT OVER WILD-TYPE MITOCHONDRIAL DNA 161
Human skeletal muscle atrophy in amyotrophic lateral sclerosis reveals a reduction in Akt and an increase in atrogin-1 152
Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues 150
Energy matters: Mitochondrial proteomics for biomedicine 149
Antioxidant defences and reactive oxygen species homeostasis in different human mitochondrial DNA-depleted cell lines. 136
Adult acid maltase deficiency: an open trial with albuterol and branched- chain aminoacids 135
Physiological responses in McArdle's patients during maximal aerobic exercise 135
Coordinated and reversible reduction of enzymes involved in terminal oxidative metabolism in skeletal muscle mitochondria from a riboflavin-responsive, multiple acyl-CoA dehydrogenase deficiency patient 133
Biased incorporation of ribonucleotides on the mitochondrial L-strand accounts for apparent strand-asymmetric DNA replication. 129
UV and Lyα luminosity functions of galaxies and star formation rate density at the end of HI reionization from the VIMOS UltraDeep Survey (VUDS) 127
Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues 119
Overexpression of microRNA-206 in the skeletalmuscle from myotonic dystrophy type 1 patients 117
Functional and molecular responses to stress conditions in heteroplasmic MELAS 3243 RD cybrids. 112
The mitochondrial fission protein hFis1 requires the endoplasmic reticulum gateway to induce apoptosis 112
"Polyspecific anti-mitochondrion antibodies detect up- and down-regulated proteins in in toto muscle homogenates from MELAS patients 111
Hereditary protein C deficiency associated with riboflavin-responsive lipid storage myopathy 111
Energy status and ROS production in three RHO0 cell lines with different nuclear background 110
Riboflavin therapy. Biochemical heterogeneity in two adult lipid storage myopathies. 110
Polyspecific anti-Mitochondrion Antibodies for Proteomics on in toto Tissue Homogenates 107
Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubes 101
Carnitine deficiency induced during hemodialysis and hyperlipidemia: Effect of replacement therapy 101
The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic distrophy type 1 patients. 98
Functional and molecular responses to stress conditions in heteroplasmic MELAS (3243) RD cybrids. 90
Characterisation of undifferentiated and differentiated RD-cybrids, harbouring 3243 MELAS mutation 88
Alteration of mechanisms responsible for the homeostasis of mitochondrial flavin cofactors are correlated with adult lipid storage myopathies 87
Altered mitochondrial morphology after in vitro muscle differentiation in MELAS (A3243G) RD cybrids 86
Immobilized pH gradients with electrodic plateaus (and other unusual procedures for 2DE) 85
MITOCHONDRIAL PROTEINS IN RIBOFLAVIN-RESPONSIVE MYOPATIES 84
Antioxidant capacity in cybrids harbouring the three mtDNA mutations primarly associated with Leber’s (LHON) 81
Clinical varieties of carnitine and carnitine palmitoyltransferase deficiency 80
Riboflovin responsive myopathy: correlation between mitochondrial oxidative phosphorilation enzymes and mitochondrial flavocoenzyme homeostasis. 77
Diagnosis and therapy of myophosphorylase deficiency: experience with a group of italian patients 75
Homeostasis of reactive oxygen species in mtDNA-depleted cell lines 74
ROS HOMEOSTASIS AND ENERGY STATUS IN mtDNA DEPLETION 74
ANTIOXIDANT CAPACITY IN CYBRIDS HARBORING THE THREE MTDNA RELATED TO COMPLEX I MUTATIONS SUBUNITS AND PRIMARILY ASSOCIATED WITH LEBER'S (LHON) 73
Muscle histopatology in patients with X-linked bulbar and spinal muscular atrophy (Kennedy's disease) and female carriers. 71
Childhood encephalomyopathy with cytochrome c oxidase deficiency, ataxia, muscle wasting, and mental impairment 69
Decreased fatty-acid beta-oxidation in riboflavin-responsive, multiple acylcoenzyme A dehydrogenase-deficient patients is associated with an increase in uncoupling protein-3 61
MODIFICAZIONI DELLE DIFESE ANTIOSSIDANTI IN CIBRIDI MELAS CON BACKGROUND NUCLEARE MUSCOLARE INDOTTE DAL DIFFERENZIAMENTO 51
Totale 6.814
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Categoria #
all - tutte 19.682
article - articoli 14.806
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 333
Totale 34.821
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021293 0 0 0 0 0 0 6 35 82 36 57 77
2021/2022633 7 66 85 60 67 46 11 58 34 4 49 146
2022/2023581 100 70 5 59 111 91 0 40 71 5 28 1
2023/2024248 7 46 29 16 23 41 14 8 8 8 26 22
2024/20251.072 2 71 48 52 146 33 32 99 77 38 192 282
2025/20262.336 189 338 554 547 447 186 75 0 0 0 0 0
Totale 6.814