IRIS
PETRUZZELLA, Vittoria
 Distribuzione geografica
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Continente #
NA - Nord America 4.959
EU - Europa 1.125
AS - Asia 351
SA - Sud America 6
Continente sconosciuto - Info sul continente non disponibili 3
AF - Africa 2
OC - Oceania 2
Totale 6.448
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Nazione #
US - Stati Uniti d'America 4.956
CN - Cina 317
IT - Italia 289
SE - Svezia 279
UA - Ucraina 158
DE - Germania 133
FI - Finlandia 118
GB - Regno Unito 72
BE - Belgio 20
IE - Irlanda 17
VN - Vietnam 16
FR - Francia 15
IN - India 8
RU - Federazione Russa 6
BR - Brasile 4
ES - Italia 4
BG - Bulgaria 3
CA - Canada 3
EU - Europa 3
HK - Hong Kong 3
NL - Olanda 3
GR - Grecia 2
IR - Iran 2
JP - Giappone 2
KR - Corea 2
AR - Argentina 1
AT - Austria 1
AU - Australia 1
CL - Cile 1
CZ - Repubblica Ceca 1
EG - Egitto 1
ID - Indonesia 1
LU - Lussemburgo 1
MA - Marocco 1
MD - Moldavia 1
MT - Malta 1
NZ - Nuova Zelanda 1
PL - Polonia 1
Totale 6.448
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Città #
Fairfield 665
Chandler 524
Woodbridge 515
Jacksonville 377
Houston 373
Ashburn 319
Cambridge 291
Seattle 268
Ann Arbor 255
Nyköping 219
Wilmington 202
Bari 108
Lawrence 104
Nanjing 103
Roxbury 101
Des Moines 70
New York 68
Beijing 60
Princeton 52
Boardman 51
San Diego 40
Foggia 39
Nanchang 38
Inglewood 35
Dearborn 31
Brooklyn 26
Helsinki 25
Hebei 21
Jiaxing 19
London 19
Shenyang 19
Brussels 18
Dong Ket 16
Dublin 16
Changsha 13
Conversano 12
Tianjin 12
Grafing 11
Washington 11
Monopoli 9
Norwalk 9
Mottola 8
Venezia 7
Giovinazzo 6
Paris 6
Leawood 5
Pescara 5
Pune 5
Augusta 4
Indiana 4
Kunming 4
Los Angeles 4
Ningbo 4
San Mateo 4
Bologna 3
Falls Church 3
Palermo 3
Sofia 3
Suffolk 3
Triggiano 3
Turin 3
Zhengzhou 3
Ardabil 2
Athens 2
Auburn Hills 2
Barletta 2
Bisceglie 2
Bova Marina 2
Chiswick 2
Florence 2
Frankfurt am Main 2
Gravina In Puglia 2
Hefei 2
Hounslow 2
Islington 2
Jinan 2
Johnson City 2
Madrid 2
Metairie 2
Milan 2
New Orleans 2
Padova 2
Redwood City 2
Shanghai 2
Stockholm 2
São Paulo 2
Tappahannock 2
Taranto 2
Tokyo 2
Vieste 2
Waanrode 2
Wuhan 2
Zaragoza 2
Acton 1
Adelaide 1
Bangalore 1
Bitritto 1
Brno 1
Cairo 1
Central 1
Totale 5.323
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Nome #
HmtDB, a genomic resource for mitochondrion-based human variability studies 133
NEW MORPHOLOGICAL APPROACHES TO THE STUDY OF MITOCHONDRIAL ENCEPHALOMYOPATHIES 124
Bilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: case study and effect of deep brain stimulation 123
High Mitochondrial DNA Copy Number is a Protective Factor From Vision Loss in Heteroplasmic Leber’s Hereditary Optic Neuropathy (LHON) 120
Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers 118
MOLECULAR ANALYSIS OF THE MUSCLE PATHOLOGY ASSOCIATED WITH MITOCHONDRIAL-DNA DELETIONS 107
Author Response: Increased mtDNA Copy Number Protects Against LHON 107
ACTN3/ACE GENOTYPES AND MITOCHONDRIAL GENOME IN PROFESSIONAL SOCCER PLAYERS’ PERFORMANCE 106
null 101
Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: the NDUFS4 gene 99
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 99
Dysfunction of mitochondrial respiratory chain complex I in neurological disorders: genetics and pathogenetic mechanisms 97
Respiratory chain complex I, a main regulatory target of the cAMP/PKA pathway is defective in different human diseases. 97
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy 96
IS A POINT MUTATION IN THE MITOCHONDRIAL ND2 GENE ASSOCIATED WITH ALZHEIMERS-DISEASE 94
Age-dependent structural variations in rat brain mitochondrial DNA 94
Mitochondrial DNA copy number differentiates the Leber's hereditary optic neuropathy affected individuals from the unaffected mutation carriers 93
Alteration of mitochondrial DNA and RNA level in human fibroblasts with impaired vitamin B12 coenzyme synthesis 92
The oxidative phosphorylation system in mammalian mitochondria 91
Cerebellar ataxia as atypical manifestation of the 3243A > G MELAS mutation 89
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 87
The regulation of PTC containing transcripts of the human NDUFS4 gene of complex I of respiratory chain and the impact of pathological mutations 86
A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H 86
Mitochondrial DNA metabolism in early development of zebrafish (Danio rerio). 84
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit 83
Fishing in the Cell Powerhouse: Zebrafish as A Tool for Exploration of Mitochondrial Defects Affecting the Nervous System 83
Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex I RID D-6064-2011 82
Decrease of D-loop frequency in heart and cerebral hemispheres mitochondrial DNA of aged rat 82
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 82
The cAMP cascade and mitochondrial oxidative phosphorylation. Physiopathological implications 80
Deep sequencing unearths NumtS under LHON-associated false heteroplasmic mitochondrial DNA variants 80
Bilateral progressive visual loss in an epileptic, mentally retarded boy 78
Author response: Do high mtDNA copy numbers truly prevent LHON manifestations? 78
Differential expression of ATPAF1 and ATPAF2 genes encoding F-1-ATPase assembly proteins in mouse tissues 76
Respiratory complex I in brian development and genetic disease 76
Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients. 75
Reduced synthesis of mtRNA in isolated mitochondria of senescent rat brain 75
ACETYL-L-CARNITINE INCREASES CYTOCHROME-OXIDASE SUBUNIT-I MESSENGER-RNA CONTENT IN HYPOTHYROID RAT-LIVER 74
null 72
Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex I 70
LIPID-COMPOSITION IN SYNAPTIC AND NONSYNAPTIC MITOCHONDRIA FROM RAT BRAINS AND EFFECT OF AGING 69
Late-onset Leber hereditary optic neuropathy mimicking Susac's syndrome 68
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 68
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 66
null 64
Survey of genes involved in mitochondrial biogenesis in early development of zebrafish as candidates for mitochondrial pathologies 63
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegia 62
cAMP-dependent phosphorylation and dephosphorylation of mitochondrial proteins. Molecular aspects and physiopathological implications 62
Faithful and highly efficient RNA synthesis in isolated mitochondria from rat liver 62
null 60
TRIM8 blunts the pro-proliferative action of ΔNp63α in a p53 wild-type background 60
Mitochondrial dysfunction as a mechanism of CNS injury. 58
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 57
Structure, Redox-Coupled Protonmotive activity, and Pathological Disorders of Respiratory Chain Complexes 56
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 56
CLINICAL AND MOLECULAR IMPLICATION IN A FAMILY WITH 3460 LEBER HEREDITARY OPTIC NEUROPATHY 56
The nuclear NDUFS4 gene of complex I (NADH-ubiquinone oxidoreductase): expression products and function 55
Pathogenetic mechanisms in hereditary dysfunctions of complex I of the respiratory chain in neurological diseases 55
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 53
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 53
Clinical and molecular characterization of a novel INCL mutation in an Italian patient 53
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 52
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGING 52
Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects 52
Top level professional soccer players: association between gene polymorphisms and myDNA copy number as potential factors in modulating exercise-related phenotypes 51
Complementation tests and sequence analysis of seven genes controlling the formation of cytochrome c oxidase in Leigh disease 50
Complex I and the cAMP cascade in human physiopathology 50
The NADH: Ubiquinone oxidoreductase (complex 1) of the mammalian respiratory chain and the cAMP cascade 50
A novel insertion mutation (A(169i)) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient 50
ALTERAZIONI STRUTTURALI DEL DNA MITOCONDRIALE IN TESSUTI DI RATTO VECCHIO 48
Disorders of nuclear-mitochondrial intergenomic signalling 47
The NDUFS4 nuclear gene of complex I encodes a subunit essential for the assembly and cAMP-dependent regulation of the activity of the complex 44
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 43
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGED RAT TISSUES 42
MITOCHONDRIAL DNA TRANSCRIPTION IN AGING RAT 42
GRM3 genotype and olanzapine treatment: Differential effects on prefrontal cortical function during working memory in patients with schizophrenia 40
Mitochondrial ND5 geme nucleotide variants in a patient with ptical atrophy and renal involvement 38
The cAMP cascade regulates mitochondrial respiration in mammalian cells. The role of complex I 38
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 38
The effect of GRM3 genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 37
MITOCHONDRIAL DISEASE MIMIKING POLYMYOSITIS: A CASE REPORT 36
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 36
null 35
NMD of mutated and alternatively spliced transcripts in human complex I deficiency 34
REDUCED TRANSCRIPTION OF MITOCHONDRIAL DNA IN THE SENESCENT RAT. TISSUE DEPENDENCE AND EFFECT OF ACETYL-L-CARNITINE 34
Mitochondrial DNA transcription and translation in aged rat: effect of acetyl-L-carnitine 34
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 32
null 32
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 32
REDUCED SYNTHESIS OF MESSENGER TRANSFER-RNA IN ISOLATED-MITOCHONDRIA OF SENESCENT RAT-BRAIN 32
DNA MITOCONDRIALE E INVECCHIAMENTO 31
Deficit complesso V mitocondriale e fenotipo epilettico. Descrizione di un caso clinico 31
MECCANISMO D'AZIONE DELL'ACETIL-L-CARNITINA SULL'ESPRESSIONE DEL DNA MITOCONDRIALE IN CERVELLO DI RATTO INVECCHIATO 29
Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNA 28
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction 27
Deep sequencing unearths Nuclear mitochondrial sequences under Leber's hereditary optic neuropathy-associated false heteroplasmic mitochondrial DNA variants 26
THE NDUFS4 NUCLEAR GENE OF COMPLEX I ENCODED A SUBUNIT ESSENTIAL FOR THE ASSEMBLY AND CAMP-DEPENDENT REGULATION OF THE ACTIVITY OF THE COMPLEX 26
CMT2A harboring mitofusin 2 mutation with optic nerve atrophy and normal visual acuity 24
RUOLO DEL SISTEMA GENETICO MITOCONDRIALE E DELLE MEMBRANE MITOCONDRIALI NEI PROCESSI DI INVECCHIAMENTO DELLA CELLULA 23
Identification of a novel mutation of the CNL1 gene leading to infantile neuronal ceroid lipofuscinosis in an Italian patient 22
Totale 6.393
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Categoria #
all - tutte 25.682
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 25.682
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019459 0 0 0 0 0 0 0 0 0 90 184 185
2019/20201.776 293 94 52 124 212 116 197 162 229 87 158 52
2020/20211.052 89 89 98 76 116 45 58 59 104 177 60 81
2021/2022763 35 132 4 22 40 45 49 38 55 36 129 178
2022/20231.292 183 98 86 160 153 175 10 142 224 10 26 25
2023/2024401 41 96 32 32 51 106 16 17 4 6 0 0
Totale 6.622