IRIS
ROMANIELLO, ROMINA
 Distribuzione geografica
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Continente #
NA - Nord America 283
EU - Europa 145
AS - Asia 34
OC - Oceania 1
Totale 463
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Nazione #
US - Stati Uniti d'America 282
IE - Irlanda 109
CN - Cina 21
DE - Germania 13
IN - India 13
FI - Finlandia 11
IT - Italia 6
SE - Svezia 4
AU - Australia 1
BE - Belgio 1
CA - Canada 1
HU - Ungheria 1
Totale 463
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Città #
Chandler 112
Dublin 109
Ashburn 22
Shanghai 19
Lawrence 14
Princeton 14
Wilmington 14
Pune 13
Medford 12
Helsinki 11
New York 10
Cremona 5
Ann Arbor 2
Beijing 2
Berlin 2
Falls Church 2
Norwalk 2
Brisbane 1
Brussels 1
Budapest 1
Maniago 1
Santa Clara 1
Toronto 1
Washington 1
Totale 372
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Nome #
CASK related disorder: Epilepsy and developmental outcome 44
Feasibility of a home-based computerized cognitive training for pediatric patients with congenital or acquired brain damage: An explorative study 40
A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype 37
Tubulin genes and malformations of cortical development 36
Aberrant supracallosal longitudinal bundle: MR features, pathogenesis and associated clinical phenotype 35
The phenotypic spectrum of WWOX -related disorders: 20 additional cases of WOREE syndrome and review of the literature 35
Challenges and resources in adult life with Joubert syndrome: issues from an international classification of functioning (ICF) perspective 35
Virtual Reality Social Prediction Improvement and Rehabilitation Intensive Training (VR-SPIRIT) for paediatric patients with congenital cerebellar diseases: Study protocol of a randomised controlled trial 34
Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: Results of a multicentric study 34
Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients with Agenesis of the Corpus Callosum 33
Characterizingwhite matter tract organization in polymicrogyria and lissencephaly: A multifiber diffusion mri modeling and tractography study 30
Learning to live without the cerebellum 30
Mutations in α- and β-tubulin encoding genes: implications in brain malformations 28
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders 27
Totale 478
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Categoria #
all - tutte 2.235
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 2.235
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202120 0 0 0 0 0 4 7 2 6 0 0 1
2021/202261 0 0 1 0 4 4 1 8 4 1 6 32
2022/2023296 35 28 2 27 17 27 0 15 134 1 7 3
2023/2024101 10 18 2 5 6 39 21 0 0 0 0 0
Totale 478