IRIS Institutional Research Information System - OPENBS Open Archive UniBS

Giordano, Lucio
 Distribuzione geografica
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Continente #
NA - Nord America 343
EU - Europa 287
AS - Asia 105
Continente sconosciuto - Info sul continente non disponibili 1
Totale 736
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Nazione #
US - Stati Uniti d'America 338
DE - Germania 68
CN - Cina 67
NL - Olanda 47
UA - Ucraina 41
HK - Hong Kong 34
FR - Francia 29
IT - Italia 21
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
SG - Singapore 1
TR - Turchia 1
Totale 736
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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
Helsinki 15
Wilmington 15
Seattle 13
Dublin 11
Nanjing 11
Woodbridge 11
Brescia 8
Houston 8
Shanghai 7
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
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 494
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Nome #
Childhood Absence Epilepsy evolving to Eyelid Myoclonia with Absence Epilepsy 104
Epilessie idiopatiche dei primi tre anni di vita: revisione di una casisitica del CRE di Brescia 78
Utilizzo della zonisamide in pazienti pediatrici con epilessia parziale farmacoresistente: efficacia sulla frequenza critica e modificazioni EEG 78
Sindrome di Ohtahara familiare causata da una nuova mutazione del gene ARX 78
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome 73
Basal ganglia dysmorphism in patients with Aicardi syndrome 64
Generation of induced pluripotent stem cell (iPSC) lines from a Joubert syndrome patient with compound heterozygous mutations in C5orf42 gene 49
L'epilessia nella sindrome di Rett 48
Cognitive improvement after cochlear implantation in deaf children with associated disabilities 44
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) 36
null 18
A Case of Alpers-Huttenlocher Syndrome Due to a New POLG1 Mutation with Rapid Onset of Partial Status Epilepticus: Serial Neuroradiological and Neurophysiological Evaluation 15
WISC‐IV intellectual profiles in Italian children with self‐limited epilepsy with centrotemporal spikes 15
The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy 13
17p13.1 microdeletion: genetic and clinical findings in a new patient with epilepsy and comparison with literature 12
Non-epileptic myoclonic attacks in infancy: three cases 12
Repetitive and stereotyped behaviors in neurodevelopmental disorders: an observational analysis of four diagnostic groups 11
Setleis syndrome: genetic and clinical findings in a new case with epilepsy 8
Totale 756
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Categoria #
all - tutte 4.617
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 4.617
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201916 0 0 0 0 0 0 0 0 0 0 8 8
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
2023/2024151 13 9 15 12 12 37 8 3 39 1 2 0
Totale 756