IRIS
PAPPALARDO, XENA GIADA
 Distribuzione geografica
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Continente #
NA - Nord America 1.524
EU - Europa 944
AS - Asia 856
SA - Sud America 160
AF - Africa 158
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 3.647
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Nazione #
US - Stati Uniti d'America 1.481
RU - Federazione Russa 422
SG - Singapore 391
IT - Italia 293
CN - Cina 213
BR - Brasile 129
CI - Costa d'Avorio 99
VN - Vietnam 86
KR - Corea 53
IE - Irlanda 41
FR - Francia 39
IN - India 35
NG - Nigeria 25
CA - Canada 24
DE - Germania 23
FI - Finlandia 23
GB - Regno Unito 23
SE - Svezia 16
NL - Olanda 14
HK - Hong Kong 12
ZA - Sudafrica 12
BD - Bangladesh 11
MX - Messico 11
UA - Ucraina 10
AR - Argentina 9
IQ - Iraq 9
JP - Giappone 9
EC - Ecuador 8
BJ - Benin 7
ES - Italia 7
PL - Polonia 7
SN - Senegal 7
PK - Pakistan 6
AT - Austria 5
ID - Indonesia 5
CH - Svizzera 4
JM - Giamaica 4
CO - Colombia 3
IR - Iran 3
KE - Kenya 3
LB - Libano 3
VE - Venezuela 3
AU - Australia 2
AZ - Azerbaigian 2
CL - Cile 2
CZ - Repubblica Ceca 2
DK - Danimarca 2
HU - Ungheria 2
IL - Israele 2
LT - Lituania 2
MA - Marocco 2
MY - Malesia 2
PT - Portogallo 2
SA - Arabia Saudita 2
TR - Turchia 2
UY - Uruguay 2
UZ - Uzbekistan 2
XK - ???statistics.table.value.countryCode.XK??? 2
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BE - Belgio 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EG - Egitto 1
GE - Georgia 1
GR - Grecia 1
HN - Honduras 1
JO - Giordania 1
KG - Kirghizistan 1
KW - Kuwait 1
LV - Lettonia 1
OM - Oman 1
PE - Perù 1
PS - Palestinian Territory 1
PW - Palau 1
PY - Paraguay 1
RO - Romania 1
SI - Slovenia 1
SO - Somalia 1
SR - Suriname 1
SY - Repubblica araba siriana 1
Totale 3.647
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Città #
Dallas 557
Singapore 262
Moscow 190
Santa Clara 151
San Jose 115
Abidjan 98
Catania 89
Hefei 78
Ashburn 71
Chandler 63
Los Angeles 60
Seoul 53
Chicago 52
Beijing 49
Dublin 41
Ho Chi Minh City 39
Lauterbourg 31
Boardman 29
Civitanova Marche 28
New York 28
Buffalo 23
Council Bluffs 21
Kochi 21
Lappeenranta 17
Milan 17
São Paulo 17
Lagos 15
Munich 13
Palermo 13
Hanoi 11
Cambridge 10
Johannesburg 10
Lawrence 10
Messina 10
Montreal 10
Rome 10
Abuja 9
Amsterdam 9
Andover 9
Hong Kong 9
Orem 9
Tokyo 9
Wilmington 8
Boston 7
Cotonou 7
Dakar 7
Seattle 7
Avola 6
Bari 6
Da Nang 6
Falls Church 6
London 6
Lucca 6
Phoenix 6
Stockholm 6
Warsaw 6
Baghdad 5
Brooklyn 5
Chennai 5
Des Moines 5
Guayaquil 5
Kyiv 5
Mumbai 5
Belo Horizonte 4
Denver 4
Manchester 4
Moscufo 4
Ottawa 4
Turku 4
Belpasso 3
Bernareggio 3
Biên Hòa 3
Bolzano 3
Bremen 3
Charlotte 3
Houston 3
Innsbruck 3
Jakarta 3
Kingston 3
Mexico City 3
Nairobi 3
Nanjing 3
Naples 3
Paris 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
Toronto 3
Annapolis 2
Augusta 2
Baku 2
Barra Mansa 2
Budapest 2
Cachoeiro de Itapemirim 2
Totale 2.602
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Nome #
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 445
Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse 150
Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia 148
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 147
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 144
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 137
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 133
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 133
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 128
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 127
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review 123
Novel malformations: Chiari type 1 and hydrocephalus in Zhu-Tokita-Takenouchi-Kim syndrome and novel SON variants 116
VDAC Genes Expression and Regulation in Mammals 116
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 116
Inferring gene regulatory networks of ALS from blood transcriptome profiles 109
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 109
Is the secret of vdac isoforms in their gene regulation? Characterization of human vdac genes expression profile, promoter activity, and transcriptional regulators 109
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. 109
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 103
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 101
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 95
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 94
PURA-Related Neurodevelopmental Disorders with Epilepsy Treated with Ketogenic Diet: A Case-Based Review 88
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability 87
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 77
NRXN1-related disorders, attempt to better define clinical assessment 72
Voltage-Dependent Anion Channels in Male Reproductive Cells: Players in Healthy Fertility? 64
A Novel 4q32.3 Deletion in a Child: Additional Signs and the Role of MARCH1 62
Primary Microcephaly with Novel Variant of MCPH1 Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's Thyroiditis 58
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review 44
Chromothriptic Translocation t(1;18): A Paradigm of Genomic Complexity in a Child with Normal Intellectual Development and Pyridoxine-Dependent Epilepsy 44
4q interstitial and terminal deletion: clinical features comparison in two unrelated children 40
Congenital Localized Hypopigmentation Disorders as a Clue of Severe Neurologic Involvement: An Update Review 33
The secret of VDAC isoforms is in their gene regulation? Characterization of human VDAC genes expression profile, promoter activity, and transcriptional regulators 29
WWOX-Related Epileptic Encephalopathy (WOREE Syndrome): Clinical Case Study and Literature Review 5
A Systematic Review of Cutaneous Hypopigmentation Disorder Associated with Neurologic Involvement 3
Totale 3.698
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Categoria #
all - tutte 10.673
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 10.673
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20218 0 0 0 0 0 0 0 0 0 0 0 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
2025/20262.538 103 170 648 139 317 485 178 57 148 136 105 52
Totale 3.698