IRIS
PAPPALARDO, XENA GIADA
 Distribuzione geografica
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Continente #
NA - Nord America 1.168
AS - Asia 495
EU - Europa 367
SA - Sud America 137
AF - Africa 127
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
Totale 2.298
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Nazione #
US - Stati Uniti d'America 1.152
IT - Italia 230
SG - Singapore 200
CN - Cina 180
BR - Brasile 116
CI - Costa d'Avorio 98
IE - Irlanda 40
KR - Corea 35
IN - India 29
VN - Vietnam 24
DE - Germania 20
FI - Finlandia 14
GB - Regno Unito 13
NL - Olanda 9
BJ - Benin 7
EC - Ecuador 7
MX - Messico 7
RU - Federazione Russa 7
SN - Senegal 7
ZA - Sudafrica 7
AR - Argentina 6
NG - Nigeria 6
AT - Austria 5
BD - Bangladesh 5
CA - Canada 5
ES - Italia 5
JP - Giappone 5
PL - Polonia 5
SE - Svezia 5
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
ID - Indonesia 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
FR - Francia 1
HN - Honduras 1
KE - Kenya 1
LB - Libano 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 2.298
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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 36
Seoul 35
Boardman 29
Civitanova Marche 28
Kochi 21
Ho Chi Minh City 13
Munich 13
Milan 12
New York 12
São Paulo 12
Cambridge 10
Lawrence 10
Rome 10
Andover 9
Lappeenranta 8
Palermo 8
Wilmington 8
Cotonou 7
Dakar 7
Johannesburg 7
Messina 7
Abuja 6
Falls Church 6
Phoenix 6
Seattle 6
Amsterdam 5
Avola 5
Boston 5
Buffalo 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
Hanoi 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
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
João Pessoa 2
Lago 2
London 2
Maringá 2
Moscow 2
Mumbai 2
Orem 2
Paduli 2
Paternò 2
Poplar 2
Porto Alegre 2
Pristina 2
Querétaro 2
Ribeirão Preto 2
Secaucus 2
Totale 1.818
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Nome #
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 396
Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse 104
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 104
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 98
Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia 94
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 93
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 91
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 90
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 77
Novel malformations: Chiari type 1 and hydrocephalus in Zhu-Tokita-Takenouchi-Kim syndrome and novel SON variants 76
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 75
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 74
Is the secret of vdac isoforms in their gene regulation? Characterization of human vdac genes expression profile, promoter activity, and transcriptional regulators 73
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 73
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 71
Inferring gene regulatory networks of ALS from blood transcriptome profiles 61
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 61
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review 59
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 58
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 51
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? 30
A Novel 4q32.3 Deletion in a Boy: Additional Signs and the Role of MARCH1 12
4q interstitial and terminal deletion: clinical features comparison in two unrelated children 3
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review 2
The secret of VDAC isoforms is in their gene regulation? Characterization of human VDAC genes expression profile, promoter activity, and transcriptional regulators 2
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 1
Congenital Localized Hypopigmentation Disorders as a Clue of Severe Neurologic Involvement: An Update Review 1
Totale 2.347
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Categoria #
all - tutte 7.926
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 7.926
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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
2025/20261.187 103 170 648 139 127 0 0 0 0 0 0 0
Totale 2.347