IRIS
PAPPALARDO, XENA GIADA
 Distribuzione geografica
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Continente #
NA - Nord America 1.176
AS - Asia 514
EU - Europa 367
SA - Sud America 140
AF - Africa 130
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
Totale 2.331
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Nazione #
US - Stati Uniti d'America 1.160
IT - Italia 230
SG - Singapore 201
CN - Cina 180
BR - Brasile 117
CI - Costa d'Avorio 98
IE - Irlanda 40
VN - Vietnam 40
KR - Corea 35
IN - India 29
DE - Germania 20
FI - Finlandia 14
GB - Regno Unito 13
NL - Olanda 9
AR - Argentina 8
ZA - Sudafrica 8
BJ - Benin 7
EC - Ecuador 7
MX - Messico 7
RU - Federazione Russa 7
SN - Senegal 7
NG - Nigeria 6
AT - Austria 5
BD - Bangladesh 5
CA - Canada 5
ES - Italia 5
JP - Giappone 5
PL - Polonia 5
SE - Svezia 5
ID - Indonesia 4
UA - Ucraina 4
IR - Iran 3
AZ - Azerbaigian 2
CH - Svizzera 2
CO - Colombia 2
CZ - Repubblica Ceca 2
DK - Danimarca 2
HK - Hong Kong 2
IQ - Iraq 2
LT - Lituania 2
PK - Pakistan 2
XK - ???statistics.table.value.countryCode.XK??? 2
AU - Australia 1
BB - Barbados 1
BE - Belgio 1
BH - Bahrain 1
BO - Bolivia 1
CL - Cile 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
FR - Francia 1
HN - Honduras 1
KE - Kenya 1
LB - Libano 1
MA - Marocco 1
PE - Perù 1
PW - Palau 1
PY - Paraguay 1
SA - Arabia Saudita 1
SO - Somalia 1
UY - Uruguay 1
UZ - Uzbekistan 1
VE - Venezuela 1
Totale 2.331
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Città #
Dallas 555
Santa Clara 141
Singapore 125
Abidjan 98
Catania 78
Hefei 78
Chandler 63
Chicago 52
Beijing 40
Dublin 40
Ashburn 39
Los Angeles 39
Seoul 35
Boardman 29
Civitanova Marche 28
Kochi 21
Ho Chi Minh City 19
Munich 13
Milan 12
New York 12
São Paulo 12
Cambridge 10
Lawrence 10
Rome 10
Andover 9
Johannesburg 8
Lappeenranta 8
Palermo 8
Wilmington 8
Buffalo 7
Cotonou 7
Dakar 7
Messina 7
Abuja 6
Falls Church 6
Hanoi 6
Phoenix 6
Seattle 6
Amsterdam 5
Avola 5
Boston 5
Des Moines 5
Guayaquil 5
Stockholm 5
Tokyo 5
Belo Horizonte 4
Brooklyn 4
Chennai 4
Moscufo 4
Turku 4
Warsaw 4
Bari 3
Bernareggio 3
Bolzano 3
Bremen 3
Charlotte 3
Denver 3
Innsbruck 3
Lucca 3
Manchester 3
Nanjing 3
Naples 3
Ottawa 3
Rio de Janeiro 3
Salvador 3
San Filippo del Mela 3
San Giuliano Milanese 3
São Gonçalo 3
Tehran 3
Baghdad 2
Baku 2
Barra Mansa 2
Belpasso 2
Biên Hòa 2
Cachoeiro de Itapemirim 2
Cagliari 2
Caxias do Sul 2
Charleston 2
Copenhagen 2
Curitiba 2
Feira de Santana 2
Florence 2
Goiânia 2
Helsinki 2
Hong Kong 2
Jaciara 2
Jakarta 2
João Pessoa 2
Lago 2
London 2
Maringá 2
Moscow 2
Mumbai 2
Orem 2
Paduli 2
Paternò 2
Phủ Lý 2
Poplar 2
Porto Alegre 2
Pristina 2
Totale 1.833
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Nome #
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 397
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 106
Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse 105
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 100
Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia 96
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 94
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 92
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 91
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 87
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 82
VDAC Genes Expression and Regulation in Mammals 78
Novel malformations: Chiari type 1 and hydrocephalus in Zhu-Tokita-Takenouchi-Kim syndrome and novel SON variants 77
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 77
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 75
Is the secret of vdac isoforms in their gene regulation? Characterization of human vdac genes expression profile, promoter activity, and transcriptional regulators 75
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 73
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 73
Inferring gene regulatory networks of ALS from blood transcriptome profiles 64
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 62
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review 60
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 59
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. 54
NRXN1-related disorders, attempt to better define clinical assessment 53
PURA-Related Neurodevelopmental Disorders with Epilepsy Treated with Ketogenic Diet: A Case-Based Review 53
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 52
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability 44
Primary Microcephaly with Novel Variant of MCPH1 Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's Thyroiditis 44
Voltage-Dependent Anion Channels in Male Reproductive Cells: Players in Healthy Fertility? 31
A Novel 4q32.3 Deletion in a Boy: Additional Signs and the Role of MARCH1 13
4q interstitial and terminal deletion: clinical features comparison in two unrelated children 5
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review 3
The secret of VDAC isoforms is in their gene regulation? Characterization of human VDAC genes expression profile, promoter activity, and transcriptional regulators 2
Congenital Localized Hypopigmentation Disorders as a Clue of Severe Neurologic Involvement: An Update Review 2
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 1
Totale 2.380
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Categoria #
all - tutte 8.000
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 8.000
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202133 0 0 0 0 6 0 5 1 5 4 4 8
2021/202269 1 11 1 1 14 1 13 6 1 2 1 17
2022/2023185 11 15 5 18 14 29 4 25 43 2 3 16
2023/2024197 8 29 9 10 11 55 2 16 1 7 23 26
2024/2025660 12 81 24 53 101 81 35 18 42 47 102 64
2025/20261.220 103 170 648 139 160 0 0 0 0 0 0 0
Totale 2.380