IRIS
AULETTA, GENNARO
 Distribuzione geografica
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Continente #
NA - Nord America 849
EU - Europa 456
AS - Asia 95
AF - Africa 18
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
SA - Sud America 1
Totale 1.421
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Nazione #
US - Stati Uniti d'America 833
IT - Italia 176
UA - Ucraina 68
CN - Cina 60
NL - Olanda 59
DE - Germania 39
FI - Finlandia 31
SE - Svezia 30
VN - Vietnam 25
CI - Costa d'Avorio 18
CA - Canada 16
IE - Irlanda 16
GB - Regno Unito 12
RO - Romania 9
PL - Polonia 8
IN - India 5
BE - Belgio 4
SG - Singapore 3
FR - Francia 2
AU - Australia 1
CL - Cile 1
ES - Italia 1
EU - Europa 1
HK - Hong Kong 1
IL - Israele 1
LV - Lettonia 1
Totale 1.421
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Città #
Chandler 222
Jacksonville 65
Amsterdam 53
Ashburn 52
Millbury 41
Princeton 35
Napoli 34
Dong Ket 24
Boston 23
Des Moines 22
Nanjing 18
Naples 17
Ottawa 14
Lawrence 13
Milan 13
Kronberg 12
Wilmington 11
Beijing 9
Timisoara 9
Dearborn 7
Hebei 7
Sanremo 7
Nanchang 6
Shenyang 6
Jiaxing 5
Norwalk 5
Padova 4
Pune 4
Waanrode 4
Barano D'ischia 3
Boardman 3
Bologna 3
Fairfield 3
Falls Church 3
Mirano 3
Salerno 3
Washington 3
Woodbridge 3
Aachen 2
Ann Arbor 2
Castel Morrone 2
Changsha 2
Frankfurt am Main 2
Gerace 2
Guangzhou 2
Marano Di Napoli 2
Marigliano 2
Medicina 2
Oegstgeest 2
Saludecio 2
Spin 2
Tianjin 2
Torre Del Greco 2
Abbiategrasso 1
Alvignano 1
Bacoli 1
Baotou 1
Bari 1
Birmingham 1
Casalnuovo di Napoli 1
Esslingen am Neckar 1
Falconara Marittima 1
Formia 1
Genova 1
Houston 1
Indiana 1
Kunming 1
Lanzhou 1
Las Vegas 1
Los Angeles 1
Mainz 1
Orange 1
Ramat HaSharon 1
Redwood City 1
Riano 1
Riga 1
Rome 1
Santiago 1
Seattle 1
Singapore 1
Stockholm 1
Sydney 1
Torre Annunziata 1
Villacidro 1
Yellow Springs 1
Totale 831
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Nome #
”Sviluppo comunicativo linguistico nel bambino ipoacusico” 68
Otosclerosi:analisi di associazione cromosomica e identificazione di geni candidati 61
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss 48
Analisi di associazione cromosomica in famiglie con ricorrenza di otosclerosi 46
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11). 44
Performance and characteristics of the Newborn Hearing Screening Program in Campania region (Italy) between 2013 and 2019 42
Middle ear involvement in children with chronic rheumatoid juvenile arthritis 41
Middle ear involvement in children with chronic rheumatoid juvenile arthritis 41
Methodological approach to select patients with genetic ipoacusia and otosclerosis: identification and characterization of putative involved genes 39
PARALLEL EVALUATION OF ACOUSTICAL SENSORY AIDS PERFORMANCE . 39
Parallel evaluation of acoustical sensory aids performance 39
New evidence for the correlation of the p.G130V mutation in the GJB2 gene and syndromic hearing loss with palmoplantar keratoderma 39
A peculiar case of hearing loss followed years later by tinnitus and vertigo. 39
PARALLEL EVALUATION OF ACOUSTICAL SENSORY AIDS PERFORMANCE . 38
Integrated Bimodal Fitting for Unilateral CI Users with Residual Contralateral Hearing 37
Middle ear involvement in children with chronic rheumatoid juvenile arthritis 34
Ipoacusie Di Tipo Genetico: Identificazione Di Geni-Malattia 34
Audio-Vestibular Alterations During the Phases of the Menstrual Cycle in Patients with Cochlear Implant 34
Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss 32
Audiometric evaluation of carriers of the connexin 26 mutation 35delG 31
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss 31
Feasibility and effectiveness of a population-based newborn hearing screening in an economically deprived region of Italy 30
Functional dissection of auditory cortex with magnetic resonance imaging 29
Targeted Audiological Surveillance Program in Campania, Italy 29
Parkinsonism may be part of the symptom complex of DOOR syndrome. 29
Screening uditivo neonatale: implementazione del processo ed esperienza della Regione Campania 28
Middle ear involvement in children with chronic rheumatoid juvenile arthritis. 27
Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme 27
Middle ear involvement in children with chronic rheumatoid juvenile arthritis 27
Multicentre evaluation of the Naída Ci Q70 sound processor: Feedback from cochlear implant users and professionals 27
Screening del gene connessina 26 e connessina 30 (DELB6-D1351830) in soggetti della regione Campania affetti da ipoacusia non sindromica 25
Current research trends in clinical audiology 25
Nuove metodica per la valutazione della riproduzione del suono in protesi acustiche 24
Bimodal strategy for excellent audiological rehabilitation in a subject with a novel nonsense mutation of the SLC26A4 gene: A case report 24
Le sordità diseguali 23
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11). 22
Newborn hearing screening in the Campania region (Italy): early language and perceptual outcomes of infants with permanent hearing los 22
Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families 21
Neonatal Hearing Screening: Campania Experience 20
Il recupero quantitativo mediante protesi nelle ipoacusie percettive. Contributo casistico e prospettive medico-legali 20
Sensorineural Hearing Loss in a Patient Affected by Congenital Cytomegalovirus Infection: Is It Useful to Identify Comorbid Pathologies? 20
Le sordità diseguali: il caso rosolia congenita 19
Survey of Cochlear Implant User Satisfaction with the Neptune™ Waterproof Sound Processor 19
X-Linked Sensorineural Hearing Loss: A Literature Review 18
Vestibular findings in patients with schwannoma of the 8th cranial nerve: a survey of nine cases and review of the literature 18
Very good performance with bimodal stimulation in a like-hybrid modality in a patient with profound bilateral sensorineural hearing loss with low-frequencies preservation. 17
Il recupero quantitativo mediante protesi nelle ipoacusie percettive. Contributo casistico e prospettive medico-legali 16
Hearing impairment: new frontiers of regenerative medicine 14
Enlarged vestibular aqueduct and Mondini Malformation: audiological, clinical, radiologic and genetic features 13
The Absence of Permanent Sensorineural Hearing Loss in a Cohort of Children with SARS-CoV-2 Infection and the Importance of Performing the Audiological “Work-Up" 12
Totale 1.502
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Categoria #
all - tutte 5.469
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 5.469
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20194 0 0 0 0 0 0 0 0 0 0 2 2
2019/2020137 48 1 14 0 17 3 9 6 6 2 12 19
2020/2021231 13 14 14 14 16 23 18 25 27 24 19 24
2021/2022257 4 0 15 9 0 4 4 5 21 21 65 109
2022/2023494 53 56 22 28 53 56 15 44 75 57 23 12
2023/2024225 22 41 22 23 25 31 15 35 3 8 0 0
Totale 1.502