IRIS
PAPPALARDO, XENA GIADA
 Distribuzione geografica
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Continente #
NA - Nord America 1.306
EU - Europa 802
AS - Asia 660
SA - Sud America 145
AF - Africa 132
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
Totale 3.049
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Nazione #
US - Stati Uniti d'America 1.284
RU - Federazione Russa 422
SG - Singapore 327
IT - Italia 243
CN - Cina 184
BR - Brasile 120
CI - Costa d'Avorio 98
VN - Vietnam 44
IE - Irlanda 40
KR - Corea 35
IN - India 30
DE - Germania 20
GB - Regno Unito 17
FI - Finlandia 14
CA - Canada 10
NL - Olanda 9
ZA - Sudafrica 9
AR - Argentina 8
JP - Giappone 8
MX - Messico 8
BJ - Benin 7
EC - Ecuador 7
SN - Senegal 7
HK - Hong Kong 6
NG - Nigeria 6
PL - Polonia 6
SE - Svezia 6
AT - Austria 5
BD - Bangladesh 5
ES - Italia 5
ID - Indonesia 4
UA - Ucraina 4
IR - Iran 3
PK - Pakistan 3
AZ - Azerbaigian 2
CH - Svizzera 2
CL - Cile 2
CO - Colombia 2
CZ - Repubblica Ceca 2
DK - Danimarca 2
FR - Francia 2
IQ - Iraq 2
KE - Kenya 2
LT - Lituania 2
UZ - Uzbekistan 2
XK - ???statistics.table.value.countryCode.XK??? 2
AU - Australia 1
BB - Barbados 1
BE - Belgio 1
BH - Bahrain 1
BO - Bolivia 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
HN - Honduras 1
KG - Kirghizistan 1
LB - Libano 1
MA - Marocco 1
PE - Perù 1
PW - Palau 1
PY - Paraguay 1
SA - Arabia Saudita 1
SO - Somalia 1
SR - Suriname 1
TR - Turchia 1
UY - Uruguay 1
VE - Venezuela 1
Totale 3.049
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Città #
Dallas 555
Singapore 214
Moscow 190
Santa Clara 144
Abidjan 98
Catania 80
Hefei 78
Chandler 63
Ashburn 54
Chicago 52
Los Angeles 51
San Jose 49
Beijing 41
Dublin 40
Seoul 35
Boardman 29
Civitanova Marche 28
Ho Chi Minh City 21
Kochi 21
New York 19
Buffalo 18
São Paulo 14
Munich 13
Milan 12
Palermo 11
Cambridge 10
Lawrence 10
Rome 10
Andover 9
Johannesburg 9
Hanoi 8
Lappeenranta 8
Messina 8
Tokyo 8
Wilmington 8
Boston 7
Cotonou 7
Dakar 7
Seattle 7
Abuja 6
Falls Church 6
Hong Kong 6
Lucca 6
Phoenix 6
Stockholm 6
Amsterdam 5
Avola 5
Bari 5
Brooklyn 5
Des Moines 5
Guayaquil 5
London 5
Montreal 5
Orem 5
Warsaw 5
Belo Horizonte 4
Chennai 4
Denver 4
Moscufo 4
Turku 4
Bernareggio 3
Bolzano 3
Bremen 3
Charlotte 3
Houston 3
Innsbruck 3
Manchester 3
Mumbai 3
Nanjing 3
Naples 3
Ottawa 3
Poplar 3
Querétaro 3
Rio de Janeiro 3
Salvador 3
San Filippo del Mela 3
San Giuliano Milanese 3
Secaucus 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
Jaciara 2
Jakarta 2
João Pessoa 2
Lago 2
Maringá 2
Totale 2.252
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Nome #
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 427
Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse 133
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 133
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 129
Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia 126
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 119
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 116
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 116
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 113
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 106
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 101
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 97
Novel malformations: Chiari type 1 and hydrocephalus in Zhu-Tokita-Takenouchi-Kim syndrome and novel SON variants 96
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 95
VDAC Genes Expression and Regulation in Mammals 93
Is the secret of vdac isoforms in their gene regulation? Characterization of human vdac genes expression profile, promoter activity, and transcriptional regulators 92
Inferring gene regulatory networks of ALS from blood transcriptome profiles 89
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review 88
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 87
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 84
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 83
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. 77
PURA-Related Neurodevelopmental Disorders with Epilepsy Treated with Ketogenic Diet: A Case-Based Review 69
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability 66
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 64
NRXN1-related disorders, attempt to better define clinical assessment 62
Primary Microcephaly with Novel Variant of MCPH1 Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's Thyroiditis 51
Voltage-Dependent Anion Channels in Male Reproductive Cells: Players in Healthy Fertility? 50
A Novel 4q32.3 Deletion in a Child: Additional Signs and the Role of MARCH1 41
4q interstitial and terminal deletion: clinical features comparison in two unrelated children 26
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review 23
Congenital Localized Hypopigmentation Disorders as a Clue of Severe Neurologic Involvement: An Update Review 22
The secret of VDAC isoforms is in their gene regulation? Characterization of human VDAC genes expression profile, promoter activity, and transcriptional regulators 16
Chromothriptic Translocation t(1;18): A Paradigm of Genomic Complexity in a Child with Normal Intellectual Development and Pyridoxine-Dependent Epilepsy 8
Totale 3.098
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Categoria #
all - tutte 9.160
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 9.160
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202127 0 0 0 0 0 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
2025/20261.938 103 170 648 139 317 485 76 0 0 0 0 0
Totale 3.098