IRIS
PETRUZZELLA, Vittoria
 Distribuzione geografica
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Continente #
NA - Nord America 7.886
AS - Asia 2.636
EU - Europa 2.415
SA - Sud America 662
Continente sconosciuto - Info sul continente non disponibili 239
AF - Africa 98
OC - Oceania 7
Totale 13.943
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Nazione #
US - Stati Uniti d'America 7.677
SG - Singapore 1.149
IT - Italia 846
CN - Cina 585
BR - Brasile 511
HK - Hong Kong 322
SE - Svezia 303
RU - Federazione Russa 250
DE - Germania 237
UA - Ucraina 168
FI - Finlandia 159
FR - Francia 139
VN - Vietnam 135
GB - Regno Unito 133
CA - Canada 84
IN - India 83
BD - Bangladesh 70
AR - Argentina 48
IQ - Iraq 36
NL - Olanda 36
TR - Turchia 35
MX - Messico 34
ID - Indonesia 33
BE - Belgio 28
CO - Colombia 27
JP - Giappone 26
PK - Pakistan 24
CI - Costa d'Avorio 21
VE - Venezuela 21
ES - Italia 20
ZA - Sudafrica 20
EC - Ecuador 19
IE - Irlanda 18
PL - Polonia 18
CL - Cile 17
IL - Israele 17
AT - Austria 16
TT - Trinidad e Tobago 14
AE - Emirati Arabi Uniti 13
SA - Arabia Saudita 13
CR - Costa Rica 12
LT - Lituania 12
GT - Guatemala 11
MA - Marocco 11
MY - Malesia 11
PR - Porto Rico 11
UZ - Uzbekistan 11
CW - ???statistics.table.value.countryCode.CW??? 10
EG - Egitto 9
JO - Giordania 9
KE - Kenya 9
SV - El Salvador 9
HN - Honduras 8
JM - Giamaica 8
NI - Nicaragua 8
PH - Filippine 8
KR - Corea 7
TN - Tunisia 7
GP - Guadalupe 6
GR - Grecia 6
KZ - Kazakistan 6
NP - Nepal 6
PY - Paraguay 6
AU - Australia 5
BO - Bolivia 5
OM - Oman 5
AZ - Azerbaigian 4
ET - Etiopia 4
MD - Moldavia 4
PE - Perù 4
SN - Senegal 4
AL - Albania 3
AO - Angola 3
BG - Bulgaria 3
DZ - Algeria 3
EU - Europa 3
IR - Iran 3
PA - Panama 3
PS - Palestinian Territory 3
QA - Qatar 3
SC - Seychelles 3
SY - Repubblica araba siriana 3
TH - Thailandia 3
BH - Bahrain 2
BY - Bielorussia 2
CZ - Repubblica Ceca 2
GY - Guiana 2
HU - Ungheria 2
KG - Kirghizistan 2
KW - Kuwait 2
LU - Lussemburgo 2
NZ - Nuova Zelanda 2
SK - Slovacchia (Repubblica Slovacca) 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 1
BN - Brunei Darussalam 1
CY - Cipro 1
DK - Danimarca 1
GA - Gabon 1
GF - Guiana Francese 1
Totale 13.705
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Città #
Ashburn 790
Fairfield 676
Singapore 599
San Jose 564
Chandler 519
Woodbridge 519
Houston 393
Jacksonville 378
Hong Kong 319
Cambridge 304
Seattle 280
Ann Arbor 268
Milan 243
Nyköping 222
Wilmington 209
Beijing 171
Council Bluffs 164
Bari 125
New York 119
Los Angeles 109
Dallas 107
Lauterbourg 107
Nanjing 105
Lawrence 104
Roxbury 102
Des Moines 71
Rome 69
Santa Clara 68
Boardman 64
Princeton 54
Helsinki 52
São Paulo 50
Brooklyn 47
Munich 46
Ho Chi Minh City 44
San Diego 42
Buffalo 41
Foggia 39
Nanchang 39
Columbus 37
Dearborn 36
Phoenix 36
Chicago 35
Inglewood 35
Figino 31
London 30
Brussels 24
Denver 24
Montreal 24
Rio de Janeiro 23
Frankfurt am Main 22
Hanoi 22
Hebei 22
Shenyang 22
Abidjan 21
Jiaxing 20
Orem 20
Tokyo 20
Jakarta 18
San Francisco 18
Stockholm 18
Dublin 17
Nuremberg 17
Belo Horizonte 16
Dong Ket 16
Washington 16
Atlanta 15
Baghdad 15
Mexico City 15
Toronto 15
Brasília 14
Changsha 14
Falkenstein 14
Moscow 13
Salt Lake City 13
Warsaw 13
Conversano 12
Tianjin 12
Turku 12
Bologna 11
Boston 11
Chennai 11
Florence 11
Grafing 11
Nijmegen 11
San José 11
The Dalles 11
Turin 11
Amsterdam 10
Johannesburg 10
Tashkent 10
Willemstad 10
Amman 9
Monopoli 9
Norwalk 9
Quito 9
Santiago 9
Da Nang 8
Elk Grove Village 8
Mottola 8
Totale 9.247
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Nome #
ACTN3/ACE GENOTYPES AND MITOCHONDRIAL GENOME IN PROFESSIONAL SOCCER PLAYERS’ PERFORMANCE 266
Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers 227
High Mitochondrial DNA Copy Number is a Protective Factor From Vision Loss in Heteroplasmic Leber’s Hereditary Optic Neuropathy (LHON) 224
Bilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: case study and effect of deep brain stimulation 204
HmtDB, a genomic resource for mitochondrion-based human variability studies 201
Author Response: Increased mtDNA Copy Number Protects Against LHON 190
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 182
Mitochondrial DNA copy number differentiates the Leber's hereditary optic neuropathy affected individuals from the unaffected mutation carriers 178
Alteration of mitochondrial DNA and RNA level in human fibroblasts with impaired vitamin B12 coenzyme synthesis 175
Author response: Do high mtDNA copy numbers truly prevent LHON manifestations? 172
Interaction of COMT Val108/158Met genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 170
A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H 170
The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10 169
NEW MORPHOLOGICAL APPROACHES TO THE STUDY OF MITOCHONDRIAL ENCEPHALOMYOPATHIES 169
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 166
Age-dependent structural variations in rat brain mitochondrial DNA 165
Deep sequencing unearths NumtS under LHON-associated false heteroplasmic mitochondrial DNA variants 164
Fishing in the Cell Powerhouse: Zebrafish as A Tool for Exploration of Mitochondrial Defects Affecting the Nervous System 163
The oxidative phosphorylation system in mammalian mitochondria 161
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit 161
MOLECULAR ANALYSIS OF THE MUSCLE PATHOLOGY ASSOCIATED WITH MITOCHONDRIAL-DNA DELETIONS 152
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 150
Dysfunction of mitochondrial respiratory chain complex I in neurological disorders: genetics and pathogenetic mechanisms 150
ACETYL-L-CARNITINE INCREASES CYTOCHROME-OXIDASE SUBUNIT-I MESSENGER-RNA CONTENT IN HYPOTHYROID RAT-LIVER 149
Mitochondrial DNA metabolism in early development of zebrafish (Danio rerio). 147
Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: the NDUFS4 gene 145
TRIM8 blunts the pro-proliferative action of ΔNp63α in a p53 wild-type background 144
Bilateral progressive visual loss in an epileptic, mentally retarded boy 142
Respiratory chain complex I, a main regulatory target of the cAMP/PKA pathway is defective in different human diseases. 142
The cAMP cascade and mitochondrial oxidative phosphorylation. Physiopathological implications 136
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 136
IS A POINT MUTATION IN THE MITOCHONDRIAL ND2 GENE ASSOCIATED WITH ALZHEIMERS-DISEASE 134
The regulation of PTC containing transcripts of the human NDUFS4 gene of complex I of respiratory chain and the impact of pathological mutations 134
ALTERAZIONI STRUTTURALI DEL DNA MITOCONDRIALE IN TESSUTI DI RATTO VECCHIO 133
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy 133
Decrease of D-loop frequency in heart and cerebral hemispheres mitochondrial DNA of aged rat 132
Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects 132
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegia 129
A novel insertion mutation (A(169i)) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient 129
Differential expression of ATPAF1 and ATPAF2 genes encoding F-1-ATPase assembly proteins in mouse tissues 127
Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients. 127
Reduced synthesis of mtRNA in isolated mitochondria of senescent rat brain 126
Survey of genes involved in mitochondrial biogenesis in early development of zebrafish as candidates for mitochondrial pathologies 124
Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex I RID D-6064-2011 124
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 122
Cerebellar ataxia as atypical manifestation of the 3243A > G MELAS mutation 121
Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblasts 120
A novel mutation in the LRSAM1 gene in a family with early onset autosomal dominant Charcot-Marie-Tooth type 2P 118
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 117
Late-onset Leber hereditary optic neuropathy mimicking Susac's syndrome 117
cAMP-dependent phosphorylation and dephosphorylation of mitochondrial proteins. Molecular aspects and physiopathological implications 117
CMT2A harboring mitofusin 2 mutation with optic nerve atrophy and normal visual acuity 117
A Gel-Based Proteomic Analysis Reveals Synovial α-Enolase and Fibrinogen β-Chain Dysregulation in Knee Osteoarthritis: A Controlled Trial 116
Respiratory complex I in brian development and genetic disease 116
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction 115
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 110
Autophagy and proliferation are dysregulated in Charcot-Marie-Tooth disease type 2A cells harboring MFN2 (mitofusin 2) mutation 109
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 109
Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex I 109
The nuclear NDUFS4 gene of complex I (NADH-ubiquinone oxidoreductase): expression products and function 106
Pathogenetic mechanisms in hereditary dysfunctions of complex I of the respiratory chain in neurological diseases 106
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 105
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGING 105
Mitochondrial ND5 geme nucleotide variants in a patient with ptical atrophy and renal involvement 104
Complementation tests and sequence analysis of seven genes controlling the formation of cytochrome c oxidase in Leigh disease 104
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 103
LIPID-COMPOSITION IN SYNAPTIC AND NONSYNAPTIC MITOCHONDRIA FROM RAT BRAINS AND EFFECT OF AGING 103
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 102
The NADH: Ubiquinone oxidoreductase (complex 1) of the mammalian respiratory chain and the cAMP cascade 101
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Structure, Redox-Coupled Protonmotive activity, and Pathological Disorders of Respiratory Chain Complexes 100
CLINICAL AND MOLECULAR IMPLICATION IN A FAMILY WITH 3460 LEBER HEREDITARY OPTIC NEUROPATHY 99
The cAMP cascade regulates mitochondrial respiration in mammalian cells. The role of complex I 98
Faithful and highly efficient RNA synthesis in isolated mitochondria from rat liver 97
Mitochondrial dysfunction as a mechanism of CNS injury. 96
MITOCHONDRIAL DNA TRANSCRIPTION IN AGING RAT 96
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 95
Additive effects of genetic variation in dopamine regulating genes on working memory cortical activity in human brain 95
Disorders of nuclear-mitochondrial intergenomic signalling 94
Deep sequencing unearths Nuclear mitochondrial sequences under Leber's hereditary optic neuropathy-associated false heteroplasmic mitochondrial DNA variants 93
OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts 92
Complex I and the cAMP cascade in human physiopathology 92
Tackling dysfunction of mitochondrial bioenergetics in the brain 92
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 89
Clinical and molecular characterization of a novel INCL mutation in an Italian patient 89
The NDUFS4 nuclear gene of complex I encodes a subunit essential for the assembly and cAMP-dependent regulation of the activity of the complex 88
Deficit complesso V mitocondriale e fenotipo epilettico. Descrizione di un caso clinico 87
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 86
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 82
DNA MITOCONDRIALE E INVECCHIAMENTO 80
The effect of GRM3 genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 80
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGED RAT TISSUES 80
GRM3 genotype and olanzapine treatment: Differential effects on prefrontal cortical function during working memory in patients with schizophrenia 78
MECCANISMO D'AZIONE DELL'ACETIL-L-CARNITINA SULL'ESPRESSIONE DEL DNA MITOCONDRIALE IN CERVELLO DI RATTO INVECCHIATO 78
MITOCHONDRIAL DISEASE MIMIKING POLYMYOSITIS: A CASE REPORT 77
Top level professional soccer players: association between gene polymorphisms and myDNA copy number as potential factors in modulating exercise-related phenotypes 77
Mitochondrial DNA transcription and translation in aged rat: effect of acetyl-L-carnitine 77
NMD of mutated and alternatively spliced transcripts in human complex I deficiency 76
Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNA 76
Torin1 restores proliferation rate in Charcot-Marie-Tooth disease type 2A cells harbouring MFN2 (mitofusin 2) mutation 75
Totale 12.441
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Categoria #
all - tutte 58.123
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 58.123
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022579 0 0 0 0 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
2025/20264.088 633 162 241 389 443 258 432 120 430 424 119 437
2026/20271.242 107 195 364 507 69 0 0 0 0 0 0 0
Totale 13.943