RIGON, CHIARA
 Distribuzione geografica
Continente #
NA - Nord America 346
EU - Europa 205
AS - Asia 62
Continente sconosciuto - Info sul continente non disponibili 1
Totale 614
Nazione #
US - Stati Uniti d'America 346
IT - Italia 147
SG - Singapore 35
CN - Cina 25
FR - Francia 17
DE - Germania 15
FI - Finlandia 8
SE - Svezia 5
GB - Regno Unito 3
UA - Ucraina 3
NL - Olanda 2
RU - Federazione Russa 2
DK - Danimarca 1
EU - Europa 1
HU - Ungheria 1
IE - Irlanda 1
IL - Israele 1
IN - India 1
Totale 614
Città #
Houston 41
Fairfield 38
Chandler 37
Singapore 30
Ashburn 25
Seattle 21
Santa Clara 20
Naples 18
Woodbridge 15
Wilmington 14
Cambridge 13
Ann Arbor 12
Boardman 12
Jacksonville 11
Milan 8
Redmond 7
Bari 6
Beijing 6
Cagliari 6
Princeton 6
Quinto di Treviso 6
Helsinki 5
Ravenna 5
Giovinazzo 4
Medford 4
Padova 4
Paris 4
Rome 4
San Diego 4
Turin 4
Venice 4
Monreale 3
New York 3
Adelfia 2
Bologna 2
Canegrate 2
Capitol Heights 2
Cecina 2
Changsha 2
Cormano 2
Des Moines 2
Faggiano 2
Florence 2
Fregona 2
Fremont 2
Limbiate 2
Longarone 2
Los Angeles 2
Marano di Napoli 2
Napoli 2
Nardò 2
Noicattaro 2
Ogden 2
Parma 2
San Giovanni in Persiceto 2
Siena 2
Usmate Velate 2
Verona 2
Alpharetta 1
Anguillara 1
Atlanta 1
Battipaglia 1
Bayonne 1
Bergamo 1
Budapest 1
Camponogara 1
Carate Brianza 1
Cassino 1
Cava 1
Copenhagen 1
Dalian 1
Dongguan 1
Dublin 1
Edinburgh 1
Kirkland 1
Lappeenranta 1
London 1
Mira 1
Mumbai 1
Munich 1
Nanjing 1
Norwalk 1
Nuremberg 1
Nürnberg 1
Pavia 1
Piombino 1
Riese Pio X 1
Rieti 1
Rockville 1
Saint Petersburg 1
San Casciano in Val di Pesa 1
Sassari 1
Seriate 1
Shenyang 1
Stockholm 1
Tappahannock 1
Tel Aviv 1
Washington 1
Totale 490
Nome #
Caratterizzazione molecolare mediante array-CGH e origine parentale di anomalie cromosomiche strutturali in pazienti con ritardo mentale/psicomotorio/autismo e/o anomalie comportamentali 216
A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus 124
Association study of AMH and AMHRII polymorphisms with unexplained infertility. 104
Auditory Outcome after Cochlear Implantation in Children with DFNB7/11 Caused by Pathogenic Variants in TMC1 Gene 84
DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature 50
Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature 19
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome 17
From clinical to molecular diagnosis: relevance of diagnostic strategy in two cases of branchio-oto-renal syndrome - case report 12
Totale 626
Categoria #
all - tutte 3.059
article - articoli 2.305
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 5.364


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202021 0 0 0 0 0 0 4 5 5 3 3 1
2020/202166 3 1 1 5 3 1 19 6 8 5 5 9
2021/202261 6 3 3 0 2 7 6 3 7 9 6 9
2022/2023111 11 2 3 15 14 13 0 13 19 5 15 1
2023/2024156 5 6 16 15 8 17 19 17 8 7 17 21
2024/2025127 10 18 25 19 30 13 12 0 0 0 0 0
Totale 626