IRIS
MARINO, SIMONA DOMENICA
 Distribuzione geografica
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Continente #
EU - Europa 48
AF - Africa 25
NA - Nord America 5
AS - Asia 2
Totale 80
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Nazione #
FR - Francia 40
CI - Costa d'Avorio 25
IT - Italia 5
US - Stati Uniti d'America 5
IE - Irlanda 2
VN - Vietnam 2
BE - Belgio 1
Totale 80
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Città #
Abidjan 25
Catania 3
Columbus 3
Avola 2
Dublin 2
Paris 2
Ashburn 1
Brussels 1
Dong Ket 1
Hanoi 1
Totale 41
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Nome #
A novel GABRB3 variant in Dravet syndrome: Case report and literature review, file d8192800-ffb8-40f2-abd1-34462e2af121 10
Hypoglossal nerve paralysis in a child after a dental procedure, file dfe4d22c-e62f-bb0a-e053-d805fe0a78d9 10
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures, file f725b218-3855-4917-87df-61f59c49d8b9 9
Graph theory in paediatric epilepsy: A systematic review, file 25fcb235-ab6e-4071-ab5a-cf6fbee6c10e 7
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome, file 4bf6623e-9354-49e9-91de-3a1d49db5eb6 7
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?, file 9c07f115-198d-47cc-ac94-9fdd5e5eef3a 6
Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy, file b9f808d4-7708-4104-a641-403dc055c43a 6
Impressive efficacy of the ketogenic diet in a KCNQ2 encephalopathy infant: a case report and exhaustive literature review, file 0f900b49-9f63-4dba-9c3a-4efc2c2598a9 5
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report, file 7bead13c-5f8b-43f0-b689-ae93df971afe 5
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability, file 1c50121c-0fa5-4f07-b21c-3cdd9af00459 4
Need for palliative care from birth to infancy in pediatric patients with neurological diseases, file 245291fa-da6e-40b8-86b1-ec42bff86b0b 4
West syndrome: a comprehensive review, file 2fee312d-5000-4323-a34c-f15b72db9ceb 4
Phacomatosis Pigmentokeratotica, file dfe4d229-8c2d-bb0a-e053-d805fe0a78d9 1
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi, file dfe4d229-dd67-bb0a-e053-d805fe0a78d9 1
E se non fossero solo incubi notturni?, file dfe4d229-dd6a-bb0a-e053-d805fe0a78d9 1
Totale 80
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Categoria #
all - tutte 307
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 307
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212 1 0 0 0 0 0 0 0 0 0 0 1
2021/20221 0 1 0 0 0 0 0 0 0 0 0 0
2022/20235 0 0 0 0 0 3 0 0 1 0 1 0
2023/202472 0 8 0 0 2 29 12 16 2 0 3 0
Totale 80