IRIS Institutional Research Information System - OPENBS Open Archive UniBS

Giordano, Lucio
 Distribuzione geografica
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Continente #
NA - Nord America 345
EU - Europa 291
AS - Asia 129
Continente sconosciuto - Info sul continente non disponibili 1
Totale 766
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Nazione #
US - Stati Uniti d'America 340
CN - Cina 71
DE - Germania 68
NL - Olanda 47
UA - Ucraina 41
HK - Hong Kong 35
FR - Francia 29
IT - Italia 25
SG - Singapore 20
GB - Regno Unito 19
FI - Finlandia 18
RU - Federazione Russa 15
SE - Svezia 13
IE - Irlanda 11
CA - Canada 5
BE - Belgio 3
IN - India 2
AL - Albania 1
AT - Austria 1
EU - Europa 1
TR - Turchia 1
Totale 766
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Città #
Chandler 46
Groningen 44
Fairfield 39
Hong Kong 34
Ashburn 33
Jacksonville 32
New York 22
Princeton 20
Cambridge 19
Beijing 18
Singapore 16
Helsinki 15
Wilmington 15
Seattle 13
Dublin 11
Nanjing 11
Shanghai 11
Woodbridge 11
Brescia 8
Houston 8
Ann Arbor 6
Changsha 4
Des Moines 4
Hebei 4
Jiaxing 4
Tianjin 4
Brussels 3
Lappeenranta 3
London 3
North York 3
Nürnberg 3
Rhoon 3
Shenyang 3
Trieste 3
Barnwell 2
Bologna 2
Genoa 2
Lanzhou 2
Nanchang 2
Padova 2
Portland 2
Pune 2
Redwood City 2
Rome 2
San Diego 2
Zhengzhou 2
Borås 1
Erie 1
Frankfurt am Main 1
Guangzhou 1
Kunming 1
Leawood 1
Milan 1
Norwalk 1
Orange 1
Palo Del Colle 1
San Francisco 1
San Mateo 1
Southwark 1
Taiyuan 1
Tirana 1
Toronto 1
Vienna 1
Washington 1
Totale 518
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Nome #
Childhood Absence Epilepsy evolving to Eyelid Myoclonia with Absence Epilepsy 107
Epilessie idiopatiche dei primi tre anni di vita: revisione di una casisitica del CRE di Brescia 79
Utilizzo della zonisamide in pazienti pediatrici con epilessia parziale farmacoresistente: efficacia sulla frequenza critica e modificazioni EEG 79
Sindrome di Ohtahara familiare causata da una nuova mutazione del gene ARX 79
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome 75
Basal ganglia dysmorphism in patients with Aicardi syndrome 66
Generation of induced pluripotent stem cell (iPSC) lines from a Joubert syndrome patient with compound heterozygous mutations in C5orf42 gene 50
L'epilessia nella sindrome di Rett 49
Cognitive improvement after cochlear implantation in deaf children with associated disabilities 45
Corrigendum to “Prognostic indicators in clinically node-negative malignant primary salivary tumours of the parotid: A multicentre experience”. [Oral Oncol. 123 (2021) 105577](S1368837521006849)(10.1016/j.oraloncology.2021.105577) 37
A Case of Alpers-Huttenlocher Syndrome Due to a New POLG1 Mutation with Rapid Onset of Partial Status Epilepticus: Serial Neuroradiological and Neurophysiological Evaluation 19
null 18
WISC‐IV intellectual profiles in Italian children with self‐limited epilepsy with centrotemporal spikes 16
17p13.1 microdeletion: genetic and clinical findings in a new patient with epilepsy and comparison with literature 14
The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy 14
Repetitive and stereotyped behaviors in neurodevelopmental disorders: an observational analysis of four diagnostic groups 13
Non-epileptic myoclonic attacks in infancy: three cases 13
Setleis syndrome: genetic and clinical findings in a new case with epilepsy 9
Frequency of SCN2A-related disorder in the regional epilepsy centre of brescia between 2002 and 2021 4
A PUS7 gene pathogenic variant causing self‐injurious behavior, sleep disturbances, and developmental delay: A case report 2
Totale 788
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Categoria #
all - tutte 5.099
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 5.099
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020151 27 8 8 7 6 15 15 14 16 21 7 7
2020/2021127 1 10 4 17 9 15 15 11 11 16 12 6
2021/202293 4 13 3 16 0 6 2 3 5 7 9 25
2022/2023146 21 5 15 13 17 37 5 11 14 0 7 1
2023/2024177 13 9 15 12 12 37 8 3 39 1 6 22
2024/20256 6 0 0 0 0 0 0 0 0 0 0 0
Totale 788