IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

CASTELLOTTI, BARBARA
 Distribuzione geografica
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Continente #
NA - Nord America 248
EU - Europa 243
AS - Asia 103
OC - Oceania 4
SA - Sud America 1
Totale 599
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Nazione #
US - Stati Uniti d'America 244
IT - Italia 84
GB - Regno Unito 78
CN - Cina 61
SG - Singapore 25
SE - Svezia 16
DK - Danimarca 15
DE - Germania 12
IE - Irlanda 10
FR - Francia 8
RU - Federazione Russa 6
HK - Hong Kong 5
AU - Australia 4
IN - India 4
NL - Olanda 4
CA - Canada 3
CH - Svizzera 3
ID - Indonesia 3
BE - Belgio 2
UA - Ucraina 2
BR - Brasile 1
ES - Italia 1
IR - Iran 1
JP - Giappone 1
KR - Corea 1
MX - Messico 1
PT - Portogallo 1
RO - Romania 1
TR - Turchia 1
TW - Taiwan 1
Totale 599
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Città #
Southend 72
Milan 60
Chandler 31
Ashburn 22
Fairfield 21
Houston 20
Ann Arbor 16
Singapore 16
Cambridge 15
Woodbridge 14
Wilmington 13
Dearborn 12
Dublin 10
Seattle 10
Beijing 8
Boardman 7
Nanjing 7
Princeton 6
Shenyang 5
Hong Kong 4
Jiaxing 4
Phoenix 4
Zhengzhou 4
Bengaluru 3
Frankfurt am Main 3
Jakarta 3
Jinan 3
Rotterdam 3
Shanghai 3
Battipaglia 2
Brussels 2
Changsha 2
Edinburgh 2
Fremont 2
Grafing 2
Guangzhou 2
Kent 2
Magenta 2
Melbourne 2
Moose Jaw 2
Nanchang 2
New York 2
Ningbo 2
Redwood City 2
Santa Clara 2
Turin 2
Udine 2
Xian 2
Ballabio 1
Baltimore 1
Chengdu 1
Cluj-napoca 1
Culiacán 1
Des Moines 1
Dongyang 1
Falkenstein 1
Göttingen 1
Hebei 1
Incheon 1
Istanbul 1
Kilburn 1
Lanzhou 1
Lichfield 1
Los Angeles 1
Ludlow 1
Maastricht 1
Monza 1
Mountain View 1
North Bergen 1
Perugia 1
Potsdam 1
Pune 1
Rho 1
Richmond 1
Roskilde 1
Roxbury 1
San Diego 1
Satteldorf 1
Silver Spring 1
Somerville 1
Sydney 1
São Paulo 1
Taipei 1
Taizhou 1
Takarazuka 1
Tehran 1
Tianjin 1
Valencia 1
Verona 1
Totale 478
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Nome #
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability 275
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability 225
HCN1 mutation spectrum : From neonatal epileptic encephalopathy to benign generalized epilepsy and beyond 78
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations 18
Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency 15
Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study 11
A novel de novo HCN2 loss‐of‐function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet 8
Totale 630
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Categoria #
all - tutte 2.068
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 2.068
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020147 0 0 7 21 10 23 16 7 29 22 4 8
2020/202195 8 9 6 9 5 7 8 12 12 9 8 2
2021/202248 4 7 2 1 2 5 7 1 2 4 3 10
2022/202385 7 9 9 6 11 9 6 8 14 0 3 3
2023/202489 6 7 7 6 19 6 1 8 2 10 11 6
2024/202540 7 30 3 0 0 0 0 0 0 0 0 0
Totale 630