AGOLINI, EMANUELE
 Distribuzione geografica
Continente #
NA - Nord America 265
EU - Europa 213
AS - Asia 75
AF - Africa 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 556
Nazione #
US - Stati Uniti d'America 262
IT - Italia 130
SG - Singapore 40
SE - Svezia 35
IN - India 19
DE - Germania 13
BG - Bulgaria 8
BE - Belgio 7
CN - Cina 7
FI - Finlandia 6
ID - Indonesia 6
NL - Olanda 3
RO - Romania 3
AT - Austria 2
CA - Canada 2
RS - Serbia 2
TG - Togo 2
ES - Italia 1
EU - Europa 1
GB - Regno Unito 1
IE - Irlanda 1
MX - Messico 1
MY - Malesia 1
QA - Qatar 1
UA - Ucraina 1
VN - Vietnam 1
Totale 556
Città #
Rome 41
Fairfield 33
Chandler 31
Singapore 29
Ashburn 22
Woodbridge 20
Houston 18
Milan 15
Seattle 12
Santa Clara 11
Wilmington 10
Munich 8
Sofia 8
Brussels 7
Princeton 7
Ann Arbor 6
Cagliari 6
Jakarta 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
Lappeenranta 3
Belgrade 2
Boardman 2
Bologna 2
Florence 2
Frankfurt am Main 2
Fremont 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
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
Marino 1
Mexico City 1
Mumbai 1
Ottawa 1
Redwood City 1
Romola 1
San Mateo 1
Toronto 1
Turin 1
Venezia 1
Xi'an 1
Totale 396
Nome #
p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas 97
Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 gene 87
Displasie ectodermiche causate da difetti genetici delle nectine 64
null 61
Low-grade gliomas in patients with Noonan syndrome: case-based review of the literature 55
Identification of a robust DNA methylation signature for Fanconi anemia 33
null 33
Safety and Efficacy of Mek Inhibitors in the Treatment of Plexiform Neurofibromas: A Retrospective Study 30
Posterior fossa ependymoma in neurodevelopmental syndrome caused by a de novo germline pathogenic Polr2a variant 29
null 27
Microcephalic osteodysplastic primordial dwarfism type II and pachygyria: Morphometric analysis in a 2-year-old girl 18
Exploiting in silico structural analysis to introduce emerging genotype–phenotype correlations in DHCR24-related sterol biosynthesis disorder: a case study 16
Cancer predisposition syndromes and medulloblastoma in the molecular era 15
Targeted therapy for pediatric diffuse intrinsic pontine glioma: a single-center experience 13
Helsmoortel-Van der Aa Syndrome as emerging clinical diagnosis in intellectually disabled children with autistic traits and ocular involvement 13
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 7
SHH medulloblastoma and very early onset of bowel polyps in a child with PTEN hamartoma tumor syndrome 6
The coexistence of a BRCA2 germline and a DICER1 somatic variant in two first-degree cousins suggests their potential synergic effect 3
Case report: A safeguard in the sea of variants of uncertain significance: a case study on child with high risk neuroblastoma and acute myeloid leukemia 1
A second case report of medulloblastoma in a patient carrying biallelic pathogenic MUTYH germline variants 1
Totale 617
Categoria #
all - tutte 2.154
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 2.154


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202034 0 0 0 0 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
2024/202597 11 20 15 19 32 0 0 0 0 0 0 0
Totale 617