IRIS Institutional Research Information System - OPENBS Open Archive UniBS

VALENTE, ENZA MARIA
 Distribuzione geografica
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Continente #
AS - Asia 99
NA - Nord America 93
EU - Europa 80
Totale 272
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Nazione #
US - Stati Uniti d'America 89
SG - Singapore 42
HK - Hong Kong 32
IT - Italia 29
CN - Cina 15
RU - Federazione Russa 15
FI - Finlandia 10
TR - Turchia 8
UA - Ucraina 8
DE - Germania 6
CA - Canada 4
GB - Regno Unito 3
AT - Austria 1
CZ - Repubblica Ceca 1
FR - Francia 1
IE - Irlanda 1
IL - Israele 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
LV - Lettonia 1
NL - Olanda 1
PL - Polonia 1
RO - Romania 1
Totale 272
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Città #
Singapore 34
Hong Kong 32
Helsinki 9
Chandler 8
Fairfield 8
Istanbul 8
Brescia 7
Wilmington 6
Ashburn 5
Beijing 5
Jacksonville 5
Moscow 5
Milan 4
Romola 4
Shanghai 4
Des Moines 3
Los Angeles 3
Munich 3
Spring Valley 3
Vancouver 3
Cambridge 2
Frankfurt am Main 2
New York 2
Princeton 2
Seattle 2
Trieste 2
Ann Arbor 1
Brno 1
Changsha 1
Dublin 1
Florence 1
Holon 1
Jiaxing 1
Kunming 1
Lappeenranta 1
Levate 1
Nanchang 1
Orange 1
Ottawa 1
Riga 1
Sommacampagna 1
Vienna 1
Vientiane 1
Woodbridge 1
Zhengzhou 1
Totale 190
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Nome #
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome 90
Expanding the spectrum of clinical severity of AICA-ribosiduria: Report of two siblings with mild phenotype caused by a novel pathogenic variant in ATIC gene 33
ACOX1 gain‐of‐function variation in a 10‐years‐old patient responsive to immunomodulating therapy 26
Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro 24
Benign Hereditary Chorea as a Manifestation of HPCA Mutation 22
Establishment of three Joubert syndrome-derived induced pluripotent stem cell (iPSC) lines harbouring compound heterozygous mutations in CC2D2A gene 22
Prenatal findings in oral-facial-digital syndrome type VI: Report of three cases and literature review 21
Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case report 20
Family History in Parkinson's Disease: A National Cross-Sectional Study 13
Novel molecular, structural and clinical findings in an Italian cohort of congenital cataract 11
Totale 282
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Categoria #
all - tutte 2.341
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 2.341
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20208 0 0 0 0 0 0 0 0 3 2 2 1
2020/202119 1 1 2 1 1 2 0 3 1 4 1 2
2021/202212 0 8 0 0 0 0 1 0 0 0 1 2
2022/202326 1 0 1 2 0 5 8 3 4 0 2 0
2023/202454 3 2 1 6 1 5 2 0 8 0 15 11
2024/2025152 5 10 7 31 19 16 28 17 19 0 0 0
Totale 282