IRIS
MARCIANO, ELIO
 Distribuzione geografica
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Continente #
EU - Europa 3.330
AS - Asia 3.176
NA - Nord America 3.122
SA - Sud America 517
AF - Africa 96
OC - Oceania 6
AN - Antartide 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 10.249
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Nazione #
US - Stati Uniti d'America 2.980
SG - Singapore 1.868
RU - Federazione Russa 1.425
CN - Cina 636
IT - Italia 604
BR - Brasile 437
DE - Germania 282
HK - Hong Kong 276
VN - Vietnam 221
UA - Ucraina 202
NL - Olanda 163
FI - Finlandia 149
CH - Svizzera 148
CA - Canada 87
GB - Regno Unito 84
IE - Irlanda 71
FR - Francia 47
SE - Svezia 43
IN - India 39
CI - Costa d'Avorio 36
MX - Messico 35
AR - Argentina 34
ZA - Sudafrica 28
PL - Polonia 26
BD - Bangladesh 21
ES - Italia 19
BE - Belgio 18
ID - Indonesia 18
IQ - Iraq 16
PY - Paraguay 13
EC - Ecuador 12
TR - Turchia 12
LT - Lituania 11
JP - Giappone 10
PK - Pakistan 10
RO - Romania 9
AT - Austria 7
CL - Cile 7
IR - Iran 7
AU - Australia 6
BG - Bulgaria 6
UZ - Uzbekistan 6
CO - Colombia 5
EG - Egitto 5
KE - Kenya 5
TN - Tunisia 5
KR - Corea 4
SA - Arabia Saudita 4
VE - Venezuela 4
BB - Barbados 3
IL - Israele 3
LB - Libano 3
MA - Marocco 3
NP - Nepal 3
UY - Uruguay 3
AD - Andorra 2
AE - Emirati Arabi Uniti 2
BA - Bosnia-Erzegovina 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GP - Guadalupe 2
JM - Giamaica 2
JO - Giordania 2
LC - Santa Lucia 2
MW - Malawi 2
PH - Filippine 2
TH - Thailandia 2
AM - Armenia 1
AQ - Antartide 1
BH - Bahrain 1
BJ - Benin 1
BO - Bolivia 1
BS - Bahamas 1
BW - Botswana 1
BY - Bielorussia 1
BZ - Belize 1
CD - Congo 1
CG - Congo 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
GD - Grenada 1
GR - Grecia 1
GY - Guiana 1
HN - Honduras 1
HU - Ungheria 1
IM - Isola di Man 1
KH - Cambogia 1
KW - Kuwait 1
KZ - Kazakistan 1
LV - Lettonia 1
MD - Moldavia 1
ME - Montenegro 1
MR - Mauritania 1
MU - Mauritius 1
MY - Malesia 1
NE - Niger 1
NG - Nigeria 1
OM - Oman 1
PA - Panama 1
Totale 10.237
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Città #
Singapore 823
Chandler 443
Moscow 356
Hong Kong 274
Beijing 213
Ashburn 210
Jacksonville 177
Santa Clara 170
Amsterdam 133
Millbury 123
Dallas 111
Princeton 107
Los Angeles 92
Munich 87
Nanjing 83
Cagliari 78
Ho Chi Minh City 78
Zurich 72
Naples 67
Boston 60
Napoli 60
Ottawa 51
Buffalo 48
Hanoi 48
The Dalles 45
Wilmington 43
New York 40
São Paulo 35
Redondo Beach 33
Giubiasco 32
Hefei 31
Turku 31
Nanchang 28
Des Moines 26
Dietikon 26
Milan 23
Shenyang 23
Menlo Park 21
Seattle 20
Rio de Janeiro 19
Dong Ket 18
Kronberg 18
Falkenstein 17
Mexico City 17
Rome 17
San Jose 17
Norwalk 16
Boardman 15
Helsinki 15
London 15
Toronto 15
Brooklyn 14
Houston 14
Frankfurt am Main 13
Hebei 13
Dearborn 12
Denver 12
Lawrence 12
Orem 12
Phoenix 12
Chicago 11
Warsaw 11
Chennai 10
Poplar 10
Pune 10
Salerno 10
Tokyo 10
Atlanta 9
Changsha 9
Jiaxing 9
Salvador 9
Tianjin 9
Timisoara 9
Trieste 9
Biên Hòa 8
Brasília 8
Falls Church 8
Guangzhou 8
Montreal 8
Nürnberg 8
Redwood City 8
Stockholm 8
Ankara 7
Baghdad 7
Bologna 7
Caxias do Sul 7
Johannesburg 7
Kunming 7
Leawood 7
Porto Alegre 7
San Francisco 7
Sanremo 7
Secaucus 7
Turin 7
Dublin 6
Nijmegen 6
Nuremberg 6
Perugia 6
Shanghai 6
São Bernardo do Campo 6
Totale 5.053
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Nome #
Lo Screening Neonatale Dei Disturbi Permanenti Dell'udito 195
A new database of healthy and pathological voices☆ Ugo Cesari a, Giuseppe De Pietro b, Elio Marciano c, Ciro Niri d, Giovanna Sannino,b, Laura Verde e a Department of Otorhinolaryngology, University Hospital (Policlinico) Federico II of Naples, Via S.Pansini, 5 Naples, Italy b Institute of High Performance Computing and Networking (ICAR-CNR), Via Pietro Castellino, 111, Naples, Italy c Area of Audiology, Department of Neurosciences, Reproductive and Odontostomatological Sciences, University of Naples Federico II, Via S.Pansini, 5, Naples, Italy d Independent Doctor Surgeon Specialized in Audiology and Phoniatrics, Naples, Italy e Department of Engineering, University of Naples Parthenope, Centro Direzionale di Napoli, Isola C4, Naples, Italy 171
Espressione genica differenziale in cellule endoteliali progenitrici (EPC) da soggetti normali e da pazienti affetti da Sindrome di Down 157
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings 147
”Sviluppo comunicativo linguistico nel bambino ipoacusico” 139
NeonaTal Assisted TelerehAbilitation (T.A.T.A. Web App) for Hearing-Impaired Children: A Family-Centered Care Model for Early Intervention in Congenital Hearing Loss 132
Dialogic reading in the rehabilitation of Children with Hearing Loss and the “Born to Read” Project: A pilot study 131
Otosclerosi:analisi di associazione cromosomica e identificazione di geni candidati 128
Hearing impairment: new frontiers of regenerative medicine 125
Paraoxonase and superoxide dismutase gene polymorphisms and noise-induced hearing loss. 123
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss 123
Integrated Bimodal Fitting for Unilateral CI Users with Residual Contralateral Hearing 123
Genetica della funzione uditiva normale e patologica 117
Middle ear involvement in children with chronic rheumatoid juvenile arthritis 116
The Natural History of Hearing Disorders in Asymptomatic Congenital Cytomegalovirus Infection 116
Down-regulation of otospiralin mRNA in response to acoustic stress in guinea pig 113
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss 112
Parallel evaluation of acoustical sensory aids performance 111
Neuro-otological features of benign paroxysmal vertigo and benign paroxysmal positioning vertigo in children: a follow-up study 109
Enlarging the spectrum of cluster headache: Extracranial autonomic involvement revealed by voice analysis 107
Effect over time of allopurinol on noise-induced hearing loss in guinea pigs. 106
Analisi di associazione cromosomica in famiglie con ricorrenza di otosclerosi 106
Age-related hearing loss in four Italian genetic isolates: An epidemiological study 106
Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme 106
Methodological approach to select patients with genetic ipoacusia and otosclerosis: identification and characterization of putative involved genes 105
PARALLEL EVALUATION OF ACOUSTICAL SENSORY AIDS PERFORMANCE . 105
New evidence for the correlation of the p.G130V mutation in the GJB2 gene and syndromic hearing loss with palmoplantar keratoderma 105
Quality of life determinants and hearing function in an elderly population: Osservatorio Geriatrico Campano Study Group. 104
Novel USH1G homozygous variant underlying USH2-like phenotype of Usher syndrome 104
R75Q dominant mutation in GJB2 gene silenced by the in Cis recessive mutation c.35delG 104
Allargare lo spettro della cefalea a grappolo: l'analisi vocale può rivelare un coinvolgimento autonomico extracranico? 103
Quality of life determinants and hearing function in an elderly population 102
PARALLEL EVALUATION OF ACOUSTICAL SENSORY AIDS PERFORMANCE . 102
Exclusion of TNFRS11B as a candidate gene for otosclerosis in Campania population 102
Screening uditivo neonatale: implementazione del processo ed esperienza della Regione Campania 102
Current research trends in clinical audiology 102
LOCALISATION AND CHARACTERISATION OF AUDITORY PERCEPTION THROUGH FUNCTIONAL MAGNETICA RESONANCE IMAGING 101
Analisi spettroacustica del parlato di bambini ipoacusici: implicazioni fonetiche e riabilitative 101
Spatio-temporal pattern of vestibular information processing after brief caloric stimulation 101
Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss 100
Forme ereditarie di ipoacusie neurosensoriali isolate e sindromiche nel bambino 100
Ipoacusie Di Tipo Genetico: Identificazione Di Geni-Malattia 99
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 99
Audio-Vestibular Alterations During the Phases of the Menstrual Cycle in Patients with Cochlear Implant 98
Targeted Audiological Surveillance Program in Campania, Italy 98
Objective pulsatile tinnitus: Case report. 97
Voice Disorder Detection via an m-Health System: Design and Results of a Clinical Study to Evaluate Vox4Health 97
Functional characterization of a novel Cx26 (T55N) mutation associated to non-syndromic hearing loss. 92
Middle ear involvement in children with chronic rheumatoid juvenile arthritis. 92
Acoustic discomfort in non-industrial indoor environments 90
Psychiatric comorbidity in a population of outpatients affected by tinnitus 89
Vestibular Pathways Involvement in Children With Migraine: A Neuro-Otological Study 89
Effetto protettivo dell’ allopurinolo nel danno uditivo da rumore in relazione a piu’ fattori 88
Nuove metodica per la valutazione della riproduzione del suono in protesi acustiche 87
Audiometric evaluation of carriers of the connexin 26 mutation 35delG 87
Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families 87
Componente del del Consiglio Direttivo del Centro di Ateneo per l'Inclusione Attiva e Parrecipata degli Studenti SINAPSI 87
Correlazione genetica nei DSA 86
Effect over time of allopurinol on noise-induced hearing loss in guinea pigs. 86
Genetica della funzione uditiva normale e patologica 86
fMRI of the auditory system: understanding the neural basis of auditory gestalt. 85
Il recupero quantitativo mediante protesi nelle ipoacusie percettive. Contributo casistico e prospettive medico-legali 85
Postural restrictions in labyrintholithiasis 84
Analysis of otospiralin down-regulation and acoustic damage to organ of Corti in guinea pig. 84
Patologia testa-collo organi di senso 84
Middle ear involvement in children with chronic rheumatoid juvenile arthritis 83
Indagini genetiche sulle ipoacusie non sindromiche 82
La crescita di loudness nei soggetti portatori di impianto cocleare: sperimentazione e simulazione 81
GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss. 80
Trigeminal stimulation elicits a peripheral vestibular imbalance in migraine patients. 79
Genetics Aspects in Non-Syndromic Forms of Sensorineural Hearing Loss 79
Nuovi fattori di rischio ?La sorveglianza audiologica nel territorio (che strumenti fornire al pediatra?) e i centri di II livello.Aggiornamenti in Audiologia Infantile 78
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11). 77
Cervico-oculo-Acoustic syndrome in a male with consanguineous parents. 77
DSA, funzionamento, abilitazione, strategie. La gestione del disturbo dalla scuola primaria alla secondaria di secondo grado 77
Newborn hearing screening in the Campania region (Italy): early language and perceptual outcomes of infants with permanent hearing los 77
Vestibular impairment and adaptive postural imbalance in parkinsonian patients with lateral trunk flexion 76
THE PERCEPTION OF THE CLOSURE LENGTH CONTINUUM ITALIAN 75
The development of language in babies and the role of the family 75
Action processing: neural basis and clinical implications 73
Very good performance with bimodal stimulation in a like-hybrid modality in a patient with profound bilateral sensorineural hearing loss with low-frequencies preservation. 73
Feasibility and effectiveness of a population-based newborn hearing screening in an economically deprived region of Italy 73
null 73
Vertigo in paeditric migraine 71
Il recupero quantitativo mediante protesi nelle ipoacusie percettive. Contributo casistico e prospettive medico-legali 71
Action processing: neural basis and clinical implications 69
Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variants 69
Functional dissection of auditory cortex with magnetic resonance imaging 69
Analisi comparativa delle più diffuse tabelle utilizzate per la determinazione dell'invalidità correlata al danno uditivo 68
Psychiatric co-morbidity in a population of outpatients affected by tinnitus 67
CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A 67
Patologia testa-collo organi di senso 64
Hearing impairment in congenital hypothyroidism. 64
Abnormal thalamic function in patients with vestibular migraine 63
Vibrazioni Meccaniche Nei Luoghi Di Lavoro 62
Midle ear involvement in children with chronic rheumatoid juvenile arthritis 61
Independent component model of the default-mode brain function: combining individual-level and population-level analyses in resting-state fMRI 57
Indagine conoscitiva sugli attuali orientamenti valutativi, clinici e medico-legali, in tema di ipoacusie professionali 57
GJB2 gene mutations in syndromic skin diseases with sensorineural hearing loss 57
Postural restrictions in labirintholithiasis 56
Totale 9.398
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Categoria #
all - tutte 34.372
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 34.372
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021208 0 0 0 0 0 0 44 24 49 27 43 21
2021/2022608 6 3 17 21 5 10 5 23 62 49 141 266
2022/2023987 133 105 36 60 129 93 20 93 133 127 40 18
2023/2024680 36 75 39 43 30 65 22 175 42 14 88 51
2024/20253.253 162 239 10 19 121 162 330 237 266 289 1.131 287
2025/20263.465 653 457 563 470 1.109 199 14 0 0 0 0 0
Totale 10.427