IRIS
PAPPALARDO, XENA GIADA
 Distribuzione geografica
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Continente #
NA - Nord America 340
EU - Europa 186
AS - Asia 161
AF - Africa 68
SA - Sud America 32
OC - Oceania 1
Totale 788
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Nazione #
US - Stati Uniti d'America 339
IT - Italia 126
SG - Singapore 106
CI - Costa d'Avorio 57
BR - Brasile 30
CN - Cina 28
IE - Irlanda 28
IN - India 19
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
CZ - Repubblica Ceca 1
EC - Ecuador 1
HK - Hong Kong 1
ID - Indonesia 1
JP - Giappone 1
MX - Messico 1
PL - Polonia 1
ZA - Sudafrica 1
Totale 788
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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
Kochi 19
Milan 12
Hefei 7
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
Belpasso 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
Olomouc 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
The Dalles 1
Tokyo 1
Tübingen 1
Vienna 1
Zhengzhou 1
Totale 653
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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 82
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 59
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 58
Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia 55
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 55
VDAC Genes Expression and Regulation in Mammals 54
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 48
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 47
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 44
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 41
Novel malformations: Chiari type 1 and hydrocephalus in Zhu-Tokita-Takenouchi-Kim syndrome and novel SON variants 40
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 38
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 30
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 29
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
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 24
Inferring gene regulatory networks of ALS from blood transcriptome profiles 19
NRXN1-related disorders, attempt to better define clinical assessment 12
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 11
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 7
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 3
Totale 818
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Categoria #
all - tutte 3.980
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 3.980
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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
2024/2025453 11 67 20 46 83 74 23 16 38 38 37 0
Totale 818