NOVELLI, MARIA
 Distribuzione geografica
Continente #
EU - Europa 131
NA - Nord America 87
AS - Asia 68
AF - Africa 2
Totale 288
Nazione #
IT - Italia 98
US - Stati Uniti d'America 87
SG - Singapore 45
ID - Indonesia 9
FI - Finlandia 8
CN - Cina 6
DE - Germania 5
IN - India 5
RU - Federazione Russa 5
NL - Olanda 4
FR - Francia 3
GB - Regno Unito 2
IE - Irlanda 2
NG - Nigeria 2
AT - Austria 1
AZ - Azerbaigian 1
BG - Bulgaria 1
IL - Israele 1
JP - Giappone 1
LT - Lituania 1
SE - Svezia 1
Totale 288
Città #
Rome 48
Singapore 36
Santa Clara 19
Jakarta 9
Helsinki 7
Milan 7
Boardman 6
Ashburn 4
New York 4
Ann Arbor 3
Chandler 3
Moscow 3
Naples 3
Pozzuolo del Friuli 3
Verona 3
Boston 2
Chicago 2
Dublin 2
Evanston 2
Hyderabad 2
Lagos 2
Los Angeles 2
Marino 2
Perugia 2
Romainville 2
Rotterdam 2
San Paolo di Civitate 2
Seattle 2
Vigodarzere 2
Wilmington 2
Baku 1
Bremen 1
Chongqing 1
Dallas 1
Fairfield 1
Falkenstein 1
Ficarazzi 1
Fort Worth 1
Houston 1
Lappeenranta 1
Lawrence 1
London 1
Macerata 1
Millbury 1
Nuremberg 1
Osaka 1
Princeton 1
Prineville 1
Pune 1
Reggio Emilia 1
San Diego 1
Shenzhen 1
Shijiazhuang 1
Sofia 1
Springfield 1
Tel Aviv 1
Torre del Greco 1
Turin 1
Vasto 1
Woodbridge 1
Totale 218
Nome #
New pathogenic variants in COQ4 cause ataxia and neurodevelopmental disorder without detectable CoQ10 deficiency in muscle or skin fibroblasts 49
Early neurodevelopmental outcomes in children with asymptomatic congenital CMV infection 40
Neurodevelopmental outcome of a child with UPD(16)mat: A case report 40
Comorbidities and Disease Duration in Tourette Syndrome: Impact on Cognition and Quality of Life of Children 34
GNAO1 Haploinsufficiency: The Milder End of the GNAO1 Phenotypic Spectrum 31
One-year neurodevelopmental outcome in children with asymptomatic congenital CMV infection 30
Diagnostic and Therapeutic Challenges of Comorbid ASD, ADHD and Psychosis: A Case Report 29
Array-comparative genomic hybridization analysis in a cohort of 130 children with Autism Spectrum Disorders: A single Center Italian Study 27
GNAO1-related movement disorder: An update on phenomenology, clinical course, and response to treatments 21
Motor, epileptic, and developmental phenotypes in genetic disorders affecting G protein coupled receptors-cAMP signaling 19
Autosomal Recessive Guanosine Triphosphate Cyclohydrolase I Deficiency: Redefining the Phenotypic Spectrum and Outcomes 9
Totale 329
Categoria #
all - tutte 1.670
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 1.670


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202113 0 0 0 0 0 0 0 0 0 5 2 6
2021/202212 0 0 0 0 1 3 0 2 0 1 3 2
2022/202339 1 3 0 2 1 2 12 1 8 2 4 3
2023/2024100 2 3 3 4 2 9 4 6 18 6 11 32
2024/2025165 7 44 25 35 29 25 0 0 0 0 0 0
Totale 329