PAPPALARDO, XENA GIADA
 Distribuzione geografica
Continente #
EU - Europa 65
AF - Africa 33
NA - Nord America 31
Totale 129
Nazione #
FR - Francia 47
CI - Costa d'Avorio 33
US - Stati Uniti d'America 31
FI - Finlandia 8
IT - Italia 8
IE - Irlanda 1
NL - Olanda 1
Totale 129
Città #
Abidjan 33
Columbus 26
Lappeenranta 7
Avola 2
Catania 2
Paris 2
Prineville 2
Aci Catena 1
Dublin 1
Fort Worth 1
Helsinki 1
Milford 1
Oude Meer 1
Totale 80
Nome #
Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia, file 1dfba510-2a07-46a6-8311-4516c275adf4 14
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 12
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 12
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review, file 28692e45-c7b2-4815-b341-44c9b37af3fc 11
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development, file 32a206d7-e383-4133-838e-1ce2a06f66ec 11
A novel GABRB3 variant in Dravet syndrome: Case report and literature review, file d8192800-ffb8-40f2-abd1-34462e2af121 11
Novel malformations: Chiari type 1 and hydrocephalus in Zhu-Tokita-Takenouchi-Kim syndrome and novel SON variants, file f22b74dd-348f-4111-b51b-911b8b658e9e 11
VDAC Genes Expression and Regulation in Mammals, file dfe4d22e-e370-bb0a-e053-d805fe0a78d9 10
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?, file 9c07f115-198d-47cc-ac94-9fdd5e5eef3a 9
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability, file 1c50121c-0fa5-4f07-b21c-3cdd9af00459 8
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 8
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review, file 6aa2ddd4-f421-46f3-a23a-8f5e8711d342 6
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report, file 7bead13c-5f8b-43f0-b689-ae93df971afe 6
Totale 129
Categoria #
all - tutte 445
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 445


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/20235 0 0 0 0 0 0 1 2 0 0 0 2
2023/2024124 1 7 0 1 2 39 13 19 3 2 32 5
Totale 129