AGOLINI, EMANUELE
 Distribuzione geografica
Continente #
NA - Nord America 249
EU - Europa 193
AS - Asia 51
AF - Africa 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 496
Nazione #
US - Stati Uniti d'America 248
IT - Italia 122
SE - Svezia 35
SG - Singapore 24
IN - India 19
BG - Bulgaria 8
BE - Belgio 7
CN - Cina 5
FI - Finlandia 5
DE - Germania 3
NL - Olanda 3
RO - Romania 3
AT - Austria 2
RS - Serbia 2
TG - Togo 2
ES - Italia 1
EU - Europa 1
IE - Irlanda 1
MX - Messico 1
MY - Malesia 1
QA - Qatar 1
UA - Ucraina 1
VN - Vietnam 1
Totale 496
Città #
Rome 37
Fairfield 33
Chandler 31
Ashburn 20
Woodbridge 20
Houston 18
Singapore 15
Milan 14
Seattle 12
Wilmington 10
Sofia 8
Brussels 7
Princeton 7
Ann Arbor 6
Cagliari 6
Millbury 6
New York 6
San Paolo di Civitate 6
Genazzano 4
Lawrence 4
Plano 4
San Diego 4
Stockholm 4
Beijing 3
Cambridge 3
Guidonia 3
Belgrade 2
Bologna 2
Florence 2
Fremont 2
Lappeenranta 2
Lomé 2
Los Angeles 2
Norwalk 2
Pescara 2
Platania 2
Rieti 2
San Michele Al Tagliamento 2
Vienna 2
Viterbo 2
Andover 1
Boardman 1
Boston 1
Bremen 1
Bühl 1
Castrolibero 1
Colle Sannita 1
Doha 1
Dublin 1
Fiumicino 1
Fuzhou 1
Groningen 1
Hanoi 1
Helsinki 1
Hyderabad 1
Jinan 1
Mexico City 1
Mumbai 1
Redwood City 1
San Mateo 1
Santa Clara 1
Turin 1
Venezia 1
Totale 342
Nome #
p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas 93
Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 gene 84
Displasie ectodermiche causate da difetti genetici delle nectine 63
null 61
Low-grade gliomas in patients with Noonan syndrome: case-based review of the literature 50
null 33
null 27
Posterior fossa ependymoma in neurodevelopmental syndrome caused by a de novo germline pathogenic Polr2a variant 26
Safety and Efficacy of Mek Inhibitors in the Treatment of Plexiform Neurofibromas: A Retrospective Study 26
Identification of a robust DNA methylation signature for Fanconi anemia 23
Microcephalic osteodysplastic primordial dwarfism type II and pachygyria: Morphometric analysis in a 2-year-old girl 15
Targeted therapy for pediatric diffuse intrinsic pontine glioma: a single-center experience 11
Helsmoortel-Van der Aa Syndrome as emerging clinical diagnosis in intellectually disabled children with autistic traits and ocular involvement 11
Exploiting in silico structural analysis to introduce emerging genotype–phenotype correlations in DHCR24-related sterol biosynthesis disorder: a case study 10
Cancer predisposition syndromes and medulloblastoma in the molecular era 8
The Fight Just Born-Neonatal Cancer: Rare Occurrence with a Favorable Outcome but Challenging Management 8
Case report: A new pathogenic variant of LRBA deficiency with a complex phenotype and Rosai-Dorfman disease 2
Totale 551
Categoria #
all - tutte 1.780
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 1.780


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202038 0 2 1 1 6 3 6 8 4 4 3 0
2020/202173 1 1 3 8 15 2 3 3 11 12 11 3
2021/202291 5 3 6 6 16 3 0 11 20 3 6 12
2022/2023116 13 26 11 16 8 10 2 10 9 2 7 2
2023/2024104 2 10 2 6 12 16 7 12 0 9 19 9
2024/202531 11 20 0 0 0 0 0 0 0 0 0 0
Totale 551