PAPPALARDO, XENA GIADA
 Distribuzione geografica
Continente #
NA - Nord America 136
EU - Europa 108
AF - Africa 68
AS - Asia 33
OC - Oceania 1
Totale 346
Nazione #
US - Stati Uniti d'America 136
IT - Italia 63
CI - Costa d'Avorio 58
IE - Irlanda 28
SG - Singapore 17
CN - Cina 16
NG - Nigeria 6
DE - Germania 4
RU - Federazione Russa 4
SN - Senegal 4
FI - Finlandia 3
GB - Regno Unito 2
UA - Ucraina 2
AU - Australia 1
NL - Olanda 1
PL - Polonia 1
Totale 346
Città #
Abidjan 58
Chandler 45
Dublin 28
Catania 26
Singapore 10
Boardman 8
Abuja 6
Cambridge 6
Falls Church 6
Lawrence 6
Wilmington 6
Andover 5
Avola 5
Ashburn 4
Dakar 4
Seattle 4
Des Moines 3
Lappeenranta 3
Lucca 3
Milan 3
Rome 3
Cagliari 2
Paduli 2
Tremestieri Etneo 2
Amsterdam 1
Bremen 1
Camden 1
Giarre 1
Lago 1
Mainz 1
Melbourne 1
Messina 1
Moscow 1
Munich 1
Naso 1
Pavia 1
Redwood City 1
Rozzano 1
Tübingen 1
Totale 263
Nome #
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 56
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 38
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 33
Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia 31
VDAC Genes Expression and Regulation in Mammals 31
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 31
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 29
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 24
Novel malformations: Chiari type 1 and hydrocephalus in Zhu-Tokita-Takenouchi-Kim syndrome and novel SON variants 21
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 14
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 14
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 10
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 8
Approccio di biologia dei sistemi per analizzare la regolazione trascrizionale in stato normale e patologico. Reti basate su ARACNe per dedurre la firma dell'espressione nella sclerosi laterale amiotrofica e l'analisi trascrizionale dell'espressione dei geni VDAC. 8
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 8
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 7
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review 4
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability 4
Totale 371
Categoria #
all - tutte 1.701
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 1.701


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201 0 0 0 0 0 0 0 1 0 0 0 0
2020/202112 0 0 0 0 1 0 1 1 2 0 0 7
2021/202241 0 5 1 1 8 1 7 4 1 2 1 10
2022/2023132 6 12 1 13 13 19 4 15 31 2 1 15
2023/2024185 6 24 15 10 10 51 2 16 1 6 23 21
Totale 371