IRIS
PAPPALARDO, XENA GIADA
 Distribuzione geografica
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Continente #
NA - Nord America 339
EU - Europa 182
AS - Asia 135
AF - Africa 68
SA - Sud America 32
OC - Oceania 1
Totale 757
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Nazione #
US - Stati Uniti d'America 338
IT - Italia 123
SG - Singapore 106
CI - Costa d'Avorio 57
BR - Brasile 30
IE - Irlanda 28
CN - Cina 21
DE - Germania 9
FI - Finlandia 7
NG - Nigeria 6
RU - Federazione Russa 6
SN - Senegal 4
UA - Ucraina 3
AZ - Azerbaigian 2
GB - Regno Unito 2
IQ - Iraq 2
NL - Olanda 2
AR - Argentina 1
AT - Austria 1
AU - Australia 1
BH - Bahrain 1
EC - Ecuador 1
HK - Hong Kong 1
ID - Indonesia 1
JP - Giappone 1
MX - Messico 1
PL - Polonia 1
ZA - Sudafrica 1
Totale 757
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Città #
Santa Clara 120
Singapore 69
Abidjan 57
Chandler 45
Chicago 42
Catania 34
Dublin 28
Boardman 25
Civitanova Marche 24
Milan 10
Messina 7
Rome 7
Abuja 6
Cambridge 6
Falls Church 6
Lawrence 6
Wilmington 6
Andover 5
Ashburn 5
Avola 5
Lappeenranta 5
Munich 5
Seattle 5
São Paulo 5
Dakar 4
Moscufo 4
Bernareggio 3
Des Moines 3
Lucca 3
Baghdad 2
Baku 2
Cagliari 2
Helsinki 2
Los Angeles 2
Maringá 2
Moscow 2
Paduli 2
Ribeirão Preto 2
Sona 2
Tremestieri Etneo 2
Amsterdam 1
Aversa 1
Bari 1
Bauru 1
Belo Horizonte 1
Botuporã 1
Bremen 1
Camden 1
Caxias do Sul 1
Dalian 1
Giarre 1
Goiânia 1
Gravatá 1
Guayaquil 1
Hong Kong 1
Ibitinga 1
Ibiúna 1
Jaciara 1
Johannesburg 1
Lago 1
Maceió 1
Madalena 1
Mainz 1
Manama 1
Medan 1
Melbourne 1
Mexico City 1
Mirante 1
Monte Carmelo 1
Naso 1
Nueve de Julio 1
Nuremberg 1
Palermo 1
Pavia 1
Phoenix 1
Ponte Nova 1
Presidente Olegário 1
Redwood City 1
Rio Quente 1
Rozzano 1
Samara 1
Santana do Matos 1
Senhor do Bonfim 1
Sertãozinho 1
Suzano 1
São José 1
Tokyo 1
Tübingen 1
Vienna 1
Zhengzhou 1
Totale 622
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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 79
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 57
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 56
VDAC Genes Expression and Regulation in Mammals 54
Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia 53
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 53
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 47
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 46
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 43
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 40
Novel malformations: Chiari type 1 and hydrocephalus in Zhu-Tokita-Takenouchi-Kim syndrome and novel SON variants 38
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 36
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. 29
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 29
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 28
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability 25
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review 23
Inferring gene regulatory networks of ALS from blood transcriptome profiles 18
NRXN1-related disorders, attempt to better define clinical assessment 10
Severe Unilateral Microtia with Aural Atresia, Hair White Patch, Stereotypes in a Young Boy with De novo 16p13.11 Deletion: Reasons for a New Genotype–Phenotype Correlation 9
Voltage-Dependent Anion Channels in Male Reproductive Cells: Players in Healthy Fertility? 8
PURA-Related Neurodevelopmental Disorders with Epilepsy Treated with Ketogenic Diet: A Case-Based Review 5
Totale 786
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Categoria #
all - tutte 3.873
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 3.873
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2023/2024179 6 24 9 10 10 49 2 16 1 6 22 24
2024/2025421 11 67 20 46 83 74 23 16 38 38 5 0
Totale 786