LERONE, MARGHERITA
 Distribuzione geografica
Continente #
EU - Europa 1.011
AS - Asia 190
NA - Nord America 164
Continente sconosciuto - Info sul continente non disponibili 36
SA - Sud America 22
AF - Africa 1
Totale 1.424
Nazione #
IT - Italia 990
US - Stati Uniti d'America 158
SG - Singapore 73
CN - Cina 45
BD - Bangladesh 27
VN - Vietnam 27
BR - Brasile 17
HK - Hong Kong 7
FR - Francia 6
GB - Regno Unito 4
AR - Argentina 3
CA - Canada 3
IQ - Iraq 3
PL - Polonia 3
RU - Federazione Russa 3
DE - Germania 2
ID - Indonesia 2
BW - Botswana 1
CR - Costa Rica 1
DK - Danimarca 1
EC - Ecuador 1
FI - Finlandia 1
GT - Guatemala 1
IL - Israele 1
IN - India 1
JM - Giamaica 1
JP - Giappone 1
MY - Malesia 1
PK - Pakistan 1
PS - Palestinian Territory 1
PT - Portogallo 1
UY - Uruguay 1
Totale 1.388
Città #
Genoa 421
Genova 336
Vado Ligure 104
Rapallo 86
Ashburn 44
Singapore 39
San Jose 37
Ho Chi Minh City 9
Beijing 8
Hong Kong 7
Turin 7
Bordighera 5
Hanoi 5
Lauterbourg 5
New York 5
Buffalo 4
Haiphong 3
London 3
Palermo 3
Albany 2
Atlanta 2
Biên Hòa 2
Frankfurt am Main 2
Los Angeles 2
Naples 2
Orem 2
Pasadena 2
Pinole 2
São Paulo 2
Verona 2
Warsaw 2
Ahmedabad 1
Alexandria 1
Amilly 1
Baltimore 1
Banfield 1
Belo Horizonte 1
Bettendorf 1
Blumenau 1
Boca Raton 1
Boituva 1
Boston 1
Brooklyn 1
Burnsville 1
Bắc Ninh 1
Cambiano 1
Caxias do Sul 1
Chesapeake 1
Chicago 1
Copenhagen 1
Council Bluffs 1
DeFuniak Springs 1
Detroit 1
Dodge City 1
Erbil 1
Florence 1
Fort Smith 1
Franca 1
Freeport 1
Gaborone 1
Galatina 1
Goiás 1
Guatemala City 1
Guayaquil 1
Hebron 1
Helsinki 1
Houston 1
Iguaba Grande 1
Kajang 1
Kansas City 1
Kazan' 1
Kingman 1
Lahore 1
Las Vegas 1
Lisbon 1
Malang 1
Mandeville 1
Miami 1
Milan 1
Mobile 1
Montevideo 1
Montreal 1
Mosul 1
Newark 1
Ninh Bình 1
North Charleston 1
Oswego 1
Padua 1
Peruíbe 1
Pescara 1
Phoenix 1
Portland 1
Providence 1
Queens 1
Quilmes 1
Recife 1
Riachão 1
Richmond 1
Rocca d'Evandro 1
Rome 1
Totale 1.224
Nome #
Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability 219
Diagnostic Criteria of Pediatric Intestinal Myopathies 187
A spectrum of LMX1B mutations in Nail-Patella syndrome: New point mutations, deletion, and evidence of mosaicism in unaffected parents 176
Case Report: Whole Exome Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Autism Spectrum Disorder, Intellectual Disability, Hyperactivity, Sleep and Gastrointestinal Disturbances 157
Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs 147
P63 modulates the expression of the WDFY2 gene which is implicated in cancer regulation and limb development 128
null 96
Diagnostic and therapeutic approach to multiple endocrine neoplasia type 2B in pediatric patients 71
Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence) 68
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment 65
Dextrocardia in patients with Poland syndrome: Phenotypic characterization provides insight into the pathogenesis 62
Response to Klinger and Merlob re: Case description with review of the literature. Am J Med Genet Part A 149A:1597-1602, 2009 48
Totale 1.424
Categoria #
all - tutte 5.162
article - articoli 5.162
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 10.324


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202276 0 0 4 9 3 9 4 19 5 11 2 10
2022/2023115 11 10 2 6 14 10 5 9 21 1 21 5
2023/202494 4 6 1 8 5 13 8 11 6 6 4 22
2024/2025278 13 16 6 13 36 28 21 56 7 11 38 33
2025/2026501 69 18 37 28 76 30 59 22 34 43 33 52
2026/202774 45 19 10 0 0 0 0 0 0 0 0 0
Totale 1.424