IRIS
PAPPALARDO, XENA GIADA
 Distribuzione geografica
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Continente #
NA - Nord America 1.223
EU - Europa 795
AS - Asia 636
SA - Sud America 141
AF - Africa 131
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
Totale 2.930
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Nazione #
US - Stati Uniti d'America 1.205
RU - Federazione Russa 421
SG - Singapore 313
IT - Italia 239
CN - Cina 181
BR - Brasile 118
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
NL - Olanda 9
AR - Argentina 8
MX - Messico 8
ZA - Sudafrica 8
BJ - Benin 7
EC - Ecuador 7
SN - Senegal 7
CA - Canada 6
NG - Nigeria 6
PL - Polonia 6
AT - Austria 5
BD - Bangladesh 5
ES - Italia 5
JP - Giappone 5
SE - Svezia 5
ID - Indonesia 4
UA - Ucraina 4
IR - Iran 3
PK - Pakistan 3
AZ - Azerbaigian 2
CH - Svizzera 2
CO - Colombia 2
CZ - Repubblica Ceca 2
DK - Danimarca 2
HK - Hong Kong 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
CL - Cile 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
FR - Francia 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
TR - Turchia 1
UY - Uruguay 1
VE - Venezuela 1
Totale 2.930
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Città #
Dallas 555
Singapore 205
Moscow 190
Santa Clara 141
Abidjan 98
Catania 80
Hefei 78
Chandler 63
Chicago 52
Ashburn 48
Los Angeles 46
Beijing 40
Dublin 40
Seoul 35
Boardman 29
Civitanova Marche 28
Ho Chi Minh City 21
Kochi 21
Buffalo 18
New York 15
Munich 13
São Paulo 13
Milan 12
Palermo 11
Cambridge 10
Lawrence 10
Rome 10
Andover 9
Hanoi 8
Johannesburg 8
Lappeenranta 8
Wilmington 8
Boston 7
Cotonou 7
Dakar 7
Messina 7
Seattle 7
Abuja 6
Falls Church 6
Phoenix 6
Amsterdam 5
Avola 5
Bari 5
Brooklyn 5
Des Moines 5
Guayaquil 5
London 5
Stockholm 5
Tokyo 5
Warsaw 5
Belo Horizonte 4
Chennai 4
Moscufo 4
Turku 4
Bernareggio 3
Bolzano 3
Bremen 3
Charlotte 3
Denver 3
Innsbruck 3
Lucca 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
Hong Kong 2
Houston 2
Jaciara 2
Jakarta 2
João Pessoa 2
Lago 2
Maringá 2
Nairobi 2
Orem 2
Paduli 2
Totale 2.155
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Nome #
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 421
Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse 130
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 130
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 124
Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia 120
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 115
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 113
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 112
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 109
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 102
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 97
Novel malformations: Chiari type 1 and hydrocephalus in Zhu-Tokita-Takenouchi-Kim syndrome and novel SON variants 93
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 93
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 92
Is the secret of vdac isoforms in their gene regulation? Characterization of human vdac genes expression profile, promoter activity, and transcriptional regulators 91
VDAC Genes Expression and Regulation in Mammals 89
Inferring gene regulatory networks of ALS from blood transcriptome profiles 85
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review 82
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 82
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 81
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 79
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. 75
PURA-Related Neurodevelopmental Disorders with Epilepsy Treated with Ketogenic Diet: A Case-Based Review 67
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability 62
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 61
NRXN1-related disorders, attempt to better define clinical assessment 58
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? 45
A Novel 4q32.3 Deletion in a Child: Additional Signs and the Role of MARCH1 40
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review 22
4q interstitial and terminal deletion: clinical features comparison in two unrelated children 22
Congenital Localized Hypopigmentation Disorders as a Clue of Severe Neurologic Involvement: An Update Review 21
The secret of VDAC isoforms is in their gene regulation? Characterization of human VDAC genes expression profile, promoter activity, and transcriptional regulators 14
Chromothriptic Translocation t(1;18): A Paradigm of Genomic Complexity in a Child with Normal Intellectual Development and Pyridoxine-Dependent Epilepsy 1
Totale 2.979
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Categoria #
all - tutte 8.949
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 8.949
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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
2025/20261.819 103 170 648 139 317 442 0 0 0 0 0 0
Totale 2.979