LERONE, MARGHERITA
 Distribuzione geografica
Continente #
EU - Europa 989
AS - Asia 177
NA - Nord America 111
SA - Sud America 21
AF - Africa 1
Totale 1.299
Nazione #
IT - Italia 973
US - Stati Uniti d'America 107
SG - Singapore 73
CN - Cina 43
VN - Vietnam 26
BD - Bangladesh 18
BR - Brasile 16
HK - Hong Kong 6
FR - Francia 5
AR - Argentina 3
GB - Regno Unito 3
IQ - Iraq 3
RU - Federazione Russa 3
CA - Canada 2
ID - Indonesia 2
BW - Botswana 1
CR - Costa Rica 1
DE - Germania 1
DK - Danimarca 1
EC - Ecuador 1
FI - Finlandia 1
IL - Israele 1
IN - India 1
JM - Giamaica 1
JP - Giappone 1
MY - Malesia 1
PK - Pakistan 1
PL - Polonia 1
PS - Palestinian Territory 1
PT - Portogallo 1
UY - Uruguay 1
Totale 1.299
Città #
Genoa 421
Genova 336
Vado Ligure 104
Rapallo 86
Singapore 39
Ashburn 36
San Jose 28
Beijing 8
Ho Chi Minh City 8
Hong Kong 6
Turin 6
Bordighera 5
Hanoi 5
Lauterbourg 5
New York 4
Haiphong 3
London 3
Palermo 3
Atlanta 2
Biên Hòa 2
Buffalo 2
Los Angeles 2
Orem 2
São Paulo 2
Ahmedabad 1
Baltimore 1
Banfield 1
Belo Horizonte 1
Blumenau 1
Boca Raton 1
Boituva 1
Boston 1
Bắc Ninh 1
Cambiano 1
Caxias do Sul 1
Chicago 1
Copenhagen 1
Council Bluffs 1
Dodge City 1
Erbil 1
Florence 1
Fort Smith 1
Franca 1
Frankfurt am Main 1
Freeport 1
Gaborone 1
Goiás 1
Guayaquil 1
Hebron 1
Helsinki 1
Iguaba Grande 1
Kajang 1
Kazan' 1
Kingman 1
Lahore 1
Lisbon 1
Malang 1
Mandeville 1
Miami 1
Milan 1
Montevideo 1
Montreal 1
Mosul 1
Ninh Bình 1
Padua 1
Pasadena 1
Peruíbe 1
Portland 1
Providence 1
Quilmes 1
Recife 1
Riachão 1
Richmond 1
Rome 1
Salinas 1
San José 1
San Justo 1
Saratov 1
Smolensk 1
Sumaré 1
Tel Aviv 1
Teresina 1
Thái Bình 1
Tijucas 1
Tokyo 1
Toronto 1
Três Marias 1
Venice 1
Verona 1
Vinh 1
Warsaw 1
Watertown 1
Xiamen 1
Totale 1.187
Nome #
Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability 205
Diagnostic Criteria of Pediatric Intestinal Myopathies 176
A spectrum of LMX1B mutations in Nail-Patella syndrome: New point mutations, deletion, and evidence of mosaicism in unaffected parents 168
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 151
Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs 143
P63 modulates the expression of the WDFY2 gene which is implicated in cancer regulation and limb development 121
null 96
Diagnostic and therapeutic approach to multiple endocrine neoplasia type 2B in pediatric patients 64
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment 60
Dextrocardia in patients with Poland syndrome: Phenotypic characterization provides insight into the pathogenesis 55
Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence) 53
Response to Klinger and Merlob re: Case description with review of the literature. Am J Med Genet Part A 149A:1597-1602, 2009 43
Totale 1.335
Categoria #
all - tutte 4.715
article - articoli 4.715
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.430


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202113 0 0 0 0 0 0 0 0 0 0 0 13
2021/202281 4 1 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
2025/2026486 69 18 37 28 76 30 59 22 34 43 33 37
Totale 1.335