LERONE, MARGHERITA
 Distribuzione geografica
Continente #
EU - Europa 1.007
AS - Asia 187
NA - Nord America 142
Continente sconosciuto - Info sul continente non disponibili 36
SA - Sud America 22
AF - Africa 1
Totale 1.395
Nazione #
IT - Italia 986
US - Stati Uniti d'America 136
SG - Singapore 73
CN - Cina 44
BD - Bangladesh 27
VN - Vietnam 26
BR - Brasile 17
FR - Francia 6
HK - Hong Kong 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 1.359
Città #
Genoa 421
Genova 336
Vado Ligure 104
Rapallo 86
Ashburn 39
Singapore 39
San Jose 28
Beijing 8
Ho Chi Minh City 8
Turin 7
Hong Kong 6
Bordighera 5
Hanoi 5
Lauterbourg 5
Buffalo 4
New York 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
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
Goiás 1
Guatemala City 1
Guayaquil 1
Hebron 1
Helsinki 1
Houston 1
Iguaba Grande 1
Kajang 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
Quilmes 1
Recife 1
Riachão 1
Richmond 1
Rocca d'Evandro 1
Rome 1
Rotherham 1
Salinas 1
San José 1
San Justo 1
Totale 1.207
Nome #
Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability 216
Diagnostic Criteria of Pediatric Intestinal Myopathies 182
A spectrum of LMX1B mutations in Nail-Patella syndrome: New point mutations, deletion, and evidence of mosaicism in unaffected parents 174
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 156
Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs 144
P63 modulates the expression of the WDFY2 gene which is implicated in cancer regulation and limb development 124
null 96
Diagnostic and therapeutic approach to multiple endocrine neoplasia type 2B in pediatric patients 70
Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence) 64
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment 63
Dextrocardia in patients with Poland syndrome: Phenotypic characterization provides insight into the pathogenesis 60
Response to Klinger and Merlob re: Case description with review of the literature. Am J Med Genet Part A 149A:1597-1602, 2009 46
Totale 1.395
Categoria #
all - tutte 4.932
article - articoli 4.932
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.864


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/2026501 69 18 37 28 76 30 59 22 34 43 33 52
2026/202745 45 0 0 0 0 0 0 0 0 0 0 0
Totale 1.395