IRIS
PETRUZZELLA, Vittoria
 Distribuzione geografica
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Continente #
NA - Nord America 6.040
AS - Asia 2.197
EU - Europa 1.666
SA - Sud America 502
AF - Africa 62
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 3
Totale 10.474
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Nazione #
US - Stati Uniti d'America 5.974
SG - Singapore 1.056
CN - Cina 542
BR - Brasile 436
IT - Italia 331
HK - Hong Kong 303
SE - Svezia 300
RU - Federazione Russa 237
DE - Germania 213
UA - Ucraina 162
FI - Finlandia 141
GB - Regno Unito 116
VN - Vietnam 108
IN - India 42
CA - Canada 34
AR - Argentina 30
BE - Belgio 28
FR - Francia 28
NL - Olanda 25
ID - Indonesia 23
JP - Giappone 20
CI - Costa d'Avorio 19
MX - Messico 19
BD - Bangladesh 18
IE - Irlanda 17
IQ - Iraq 17
PL - Polonia 15
ZA - Sudafrica 15
AT - Austria 14
ES - Italia 14
TR - Turchia 12
AE - Emirati Arabi Uniti 10
EC - Ecuador 10
CO - Colombia 7
LT - Lituania 7
MA - Marocco 7
VE - Venezuela 7
KE - Kenya 6
PK - Pakistan 6
CL - Cile 5
EG - Egitto 5
JO - Giordania 5
UZ - Uzbekistan 5
OM - Oman 4
BG - Bulgaria 3
EU - Europa 3
GR - Grecia 3
IL - Israele 3
IR - Iran 3
MD - Moldavia 3
MY - Malesia 3
NP - Nepal 3
PA - Panama 3
PY - Paraguay 3
SA - Arabia Saudita 3
TN - Tunisia 3
CR - Costa Rica 2
DZ - Algeria 2
GY - Guiana 2
HN - Honduras 2
JM - Giamaica 2
KR - Corea 2
KZ - Kazakistan 2
LU - Lussemburgo 2
NZ - Nuova Zelanda 2
PS - Palestinian Territory 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
TT - Trinidad e Tobago 2
AL - Albania 1
AO - Angola 1
AU - Australia 1
BH - Bahrain 1
BO - Bolivia 1
CZ - Repubblica Ceca 1
GA - Gabon 1
GF - Guiana Francese 1
HT - Haiti 1
KH - Cambogia 1
KW - Kuwait 1
MT - Malta 1
PR - Porto Rico 1
RO - Romania 1
RS - Serbia 1
SY - Repubblica araba siriana 1
TJ - Tagikistan 1
XK - ???statistics.table.value.countryCode.XK??? 1
YT - Mayotte 1
Totale 10.474
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Città #
Fairfield 676
Ashburn 559
Singapore 547
Woodbridge 519
Chandler 518
Houston 389
Jacksonville 377
Cambridge 303
Hong Kong 300
Seattle 278
Ann Arbor 268
Nyköping 222
Wilmington 206
Beijing 165
Bari 113
Lawrence 104
Nanjing 104
Roxbury 102
New York 96
Los Angeles 82
Dallas 81
Des Moines 70
Boardman 60
Princeton 53
Munich 46
Brooklyn 43
San Diego 41
Foggia 39
Nanchang 39
São Paulo 38
Dearborn 36
Inglewood 35
Buffalo 34
Helsinki 34
Ho Chi Minh City 33
Santa Clara 31
London 29
Chicago 25
Brussels 24
Hebei 22
Shenyang 22
Jiaxing 20
Abidjan 19
Hanoi 18
Rio de Janeiro 18
Jakarta 17
Denver 16
Dong Ket 16
Dublin 16
Nuremberg 16
Stockholm 16
Tokyo 16
Belo Horizonte 15
Phoenix 15
Montreal 14
Brasília 13
Changsha 13
Salt Lake City 13
Conversano 12
Council Bluffs 12
Moscow 12
Tianjin 12
Turku 12
Warsaw 12
Grafing 11
Nijmegen 11
Washington 11
Boston 10
The Dalles 10
Chennai 9
Frankfurt am Main 9
Johannesburg 9
Monopoli 9
Norwalk 9
Rome 9
San Francisco 9
Mexico City 8
Milan 8
Mottola 8
Pescara 8
Poplar 8
Toronto 8
Atlanta 7
Baghdad 7
Guangzhou 7
Shanghai 7
Sorocaba 7
Venezia 7
Amsterdam 6
Curitiba 6
Da Nang 6
Giovinazzo 6
Paris 6
San Jose 6
Amman 5
Elk Grove Village 5
Falkenstein 5
Haiphong 5
Leawood 5
Nairobi 5
Totale 7.378
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Nome #
Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers 185
Bilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: case study and effect of deep brain stimulation 175
ACTN3/ACE GENOTYPES AND MITOCHONDRIAL GENOME IN PROFESSIONAL SOCCER PLAYERS’ PERFORMANCE 175
High Mitochondrial DNA Copy Number is a Protective Factor From Vision Loss in Heteroplasmic Leber’s Hereditary Optic Neuropathy (LHON) 174
HmtDB, a genomic resource for mitochondrion-based human variability studies 169
Author Response: Increased mtDNA Copy Number Protects Against LHON 162
Interaction of COMT Val108/158Met genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 151
Mitochondrial DNA copy number differentiates the Leber's hereditary optic neuropathy affected individuals from the unaffected mutation carriers 146
A nonsense mutation in the NDUFS4 gene encoding the 18 kDa (AQDQ) subunit of complex I abolishes assembly and activity of the complex in a patient with Leigh-like syndrome 142
NEW MORPHOLOGICAL APPROACHES TO THE STUDY OF MITOCHONDRIAL ENCEPHALOMYOPATHIES 140
Alteration of mitochondrial DNA and RNA level in human fibroblasts with impaired vitamin B12 coenzyme synthesis 139
Leber's hereditary optic neuropathy, intellectual disability and epilepsy presenting with variable penetrance associated to the m.3460G>A mutation and a heteroplasmic expansion of the microsatellite in MTRNR1 gene - case report 138
A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H 137
Age-dependent structural variations in rat brain mitochondrial DNA 136
The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10 135
Author response: Do high mtDNA copy numbers truly prevent LHON manifestations? 134
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit 134
Deep sequencing unearths NumtS under LHON-associated false heteroplasmic mitochondrial DNA variants 132
MOLECULAR ANALYSIS OF THE MUSCLE PATHOLOGY ASSOCIATED WITH MITOCHONDRIAL-DNA DELETIONS 130
Dysfunction of mitochondrial respiratory chain complex I in neurological disorders: genetics and pathogenetic mechanisms 129
The oxidative phosphorylation system in mammalian mitochondria 129
Fishing in the Cell Powerhouse: Zebrafish as A Tool for Exploration of Mitochondrial Defects Affecting the Nervous System 125
ACETYL-L-CARNITINE INCREASES CYTOCHROME-OXIDASE SUBUNIT-I MESSENGER-RNA CONTENT IN HYPOTHYROID RAT-LIVER 124
Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: the NDUFS4 gene 120
Respiratory chain complex I, a main regulatory target of the cAMP/PKA pathway is defective in different human diseases. 119
Bilateral progressive visual loss in an epileptic, mentally retarded boy 117
Mitochondrial DNA metabolism in early development of zebrafish (Danio rerio). 117
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy 116
IS A POINT MUTATION IN THE MITOCHONDRIAL ND2 GENE ASSOCIATED WITH ALZHEIMERS-DISEASE 115
The regulation of PTC containing transcripts of the human NDUFS4 gene of complex I of respiratory chain and the impact of pathological mutations 115
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 111
TRIM8 blunts the pro-proliferative action of ΔNp63α in a p53 wild-type background 110
Decrease of D-loop frequency in heart and cerebral hemispheres mitochondrial DNA of aged rat 108
The cAMP cascade and mitochondrial oxidative phosphorylation. Physiopathological implications 107
Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex I RID D-6064-2011 106
Cerebellar ataxia as atypical manifestation of the 3243A > G MELAS mutation 106
ALTERAZIONI STRUTTURALI DEL DNA MITOCONDRIALE IN TESSUTI DI RATTO VECCHIO 105
In vivo effect of acetyl-L-carnitine on succinate oxidation, adenine nucleotide pool and lipid composition of synaptic and non-synaptic mitochondria from cerebral hemispheres of senescent rats 105
Differential expression of ATPAF1 and ATPAF2 genes encoding F-1-ATPase assembly proteins in mouse tissues 102
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 101
null 101
A novel insertion mutation (A(169i)) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient 100
Reduced synthesis of mtRNA in isolated mitochondria of senescent rat brain 100
Respiratory complex I in brian development and genetic disease 98
Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects 98
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegia 97
cAMP-dependent phosphorylation and dephosphorylation of mitochondrial proteins. Molecular aspects and physiopathological implications 96
Late-onset Leber hereditary optic neuropathy mimicking Susac's syndrome 94
Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients. 93
Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex I 91
Survey of genes involved in mitochondrial biogenesis in early development of zebrafish as candidates for mitochondrial pathologies 89
The nuclear NDUFS4 gene of complex I (NADH-ubiquinone oxidoreductase): expression products and function 86
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 85
LIPID-COMPOSITION IN SYNAPTIC AND NONSYNAPTIC MITOCHONDRIA FROM RAT BRAINS AND EFFECT OF AGING 85
Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain 83
Mitochondrial dysfunction as a mechanism of CNS injury. 83
Faithful and highly efficient RNA synthesis in isolated mitochondria from rat liver 83
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 82
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 81
A Gel-Based Proteomic Analysis Reveals Synovial α-Enolase and Fibrinogen β-Chain Dysregulation in Knee Osteoarthritis: A Controlled Trial 80
Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblasts 80
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGING 79
The NADH: Ubiquinone oxidoreductase (complex 1) of the mammalian respiratory chain and the cAMP cascade 79
Pathogenetic mechanisms in hereditary dysfunctions of complex I of the respiratory chain in neurological diseases 79
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction 77
CLINICAL AND MOLECULAR IMPLICATION IN A FAMILY WITH 3460 LEBER HEREDITARY OPTIC NEUROPATHY 76
Autophagy and proliferation are dysregulated in Charcot-Marie-Tooth disease type 2A cells harboring MFN2 (mitofusin 2) mutation 75
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 75
Clinical and molecular characterization of a novel INCL mutation in an Italian patient 75
Structure, Redox-Coupled Protonmotive activity, and Pathological Disorders of Respiratory Chain Complexes 74
Complementation tests and sequence analysis of seven genes controlling the formation of cytochrome c oxidase in Leigh disease 74
EXTREMELY HIGH-LEVELS OF MUTANT MTDNAS CO-LOCALIZE WITH CYTOCHROME-C OXIDASE-NEGATIVE RAGGED-RED FIBERS IN PATIENTS HARBORING A POINT MUTATION AT NT-3243 74
CMT2A harboring mitofusin 2 mutation with optic nerve atrophy and normal visual acuity 74
null 72
Complex I and the cAMP cascade in human physiopathology 71
Deep sequencing unearths Nuclear mitochondrial sequences under Leber's hereditary optic neuropathy-associated false heteroplasmic mitochondrial DNA variants 70
Additive effects of genetic variation in dopamine regulating genes on working memory cortical activity in human brain 69
Generation and characterization of CSSi016-A (9938) human pluripotent stem cell line carrying two biallelic variants in MTMR5/SBF1 gene resulting in a case of severe CMT4B3 68
The NDUFS4 nuclear gene of complex I encodes a subunit essential for the assembly and cAMP-dependent regulation of the activity of the complex 68
Top level professional soccer players: association between gene polymorphisms and myDNA copy number as potential factors in modulating exercise-related phenotypes 68
Disorders of nuclear-mitochondrial intergenomic signalling 66
MITOCHONDRIAL DNA TRANSCRIPTION IN AGING RAT 66
The cAMP cascade regulates mitochondrial respiration in mammalian cells. The role of complex I 64
null 64
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 64
A novel mutation in the LRSAM1 gene in a family with early onset autosomal dominant Charcot-Marie-Tooth type 2P 63
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 62
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGED RAT TISSUES 62
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 62
GRM3 genotype and olanzapine treatment: Differential effects on prefrontal cortical function during working memory in patients with schizophrenia 60
MITOCHONDRIAL DISEASE MIMIKING POLYMYOSITIS: A CASE REPORT 60
null 60
NMD of mutated and alternatively spliced transcripts in human complex I deficiency 58
Pathological mutations of the human NDUFS4 gene of the 18-kDa (AQDQ) subunit of complex I affect the expression of the protein and the assembly and function of the complex 58
Deficit complesso V mitocondriale e fenotipo epilettico. Descrizione di un caso clinico 57
The effect of GRM3 genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 57
MECCANISMO D'AZIONE DELL'ACETIL-L-CARNITINA SULL'ESPRESSIONE DEL DNA MITOCONDRIALE IN CERVELLO DI RATTO INVECCHIATO 57
REDUCED SYNTHESIS OF MESSENGER TRANSFER-RNA IN ISOLATED-MITOCHONDRIA OF SENESCENT RAT-BRAIN 57
OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts 56
Tackling dysfunction of mitochondrial bioenergetics in the brain 55
Totale 9.711
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Categoria #
all - tutte 46.800
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 46.800
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021590 0 0 0 0 0 45 59 61 105 178 61 81
2021/2022773 36 132 4 22 43 46 49 39 56 37 130 179
2022/20231.284 184 99 87 159 151 176 9 137 222 10 25 25
2023/2024459 42 94 31 31 50 106 16 18 4 22 13 32
2024/20251.851 35 19 148 60 38 135 132 171 80 86 323 624
2025/20262.082 633 162 241 389 443 214 0 0 0 0 0 0
Totale 10.695