DI NAPOLI, CLAUDIA
 Distribuzione geografica
Continente #
AS - Asia 55
EU - Europa 55
NA - Nord America 41
SA - Sud America 22
AF - Africa 1
Totale 174
Nazione #
US - Stati Uniti d'America 40
SG - Singapore 26
HK - Hong Kong 21
BR - Brasile 19
IT - Italia 19
FR - Francia 9
DE - Germania 7
IE - Irlanda 6
GB - Regno Unito 5
AT - Austria 2
FI - Finlandia 2
IN - India 2
IR - Iran 2
TR - Turchia 2
AM - Armenia 1
AR - Argentina 1
BO - Bolivia 1
LK - Sri Lanka 1
LV - Lettonia 1
MX - Messico 1
NL - Olanda 1
NO - Norvegia 1
PE - Perù 1
RU - Federazione Russa 1
SE - Svezia 1
ZA - Sudafrica 1
Totale 174
Città #
Hong Kong 21
Singapore 13
Catania 10
Santa Clara 8
Dallas 7
Dublin 6
The Dalles 6
Frankfurt am Main 4
Düsseldorf 3
Rome 3
Helsinki 2
Los Angeles 2
Milan 2
Agira 1
Agudos 1
Aparecida de Goiânia 1
Ashburn 1
Bexley 1
Bonate Sopra 1
Bradenton 1
Brasília 1
Brescia 1
Buenos Aires 1
Cajamarca 1
Campina Grande 1
Chatham 1
Colombo 1
Contagem 1
Cuiabá 1
Delhi 1
Duque de Caxias 1
Ecatepec 1
Eskişehir 1
Feira de Santana 1
Istanbul 1
La Paz 1
Laguna 1
Lauterbourg 1
Lytham St Annes 1
Maricá 1
Marilândia 1
Middle Island 1
Minneapolis 1
New Haven 1
New York 1
Oslo 1
Pelotas 1
Praia Grande 1
Raipur 1
Riga 1
Rio de Janeiro 1
Roubaix 1
Sant'Antimo 1
Santa Rosa 1
Sarasota 1
Sinop 1
Socorro 1
Stockholm 1
Stockton-on-Tees 1
São Paulo 1
São Vicente 1
Vienna 1
Yerevan 1
Totale 137
Nome #
Anomalies of the Mesenchyme (Meninges and Skull)-Defects of Neural Tube Closure: Cephalocele and Other Calvarial and Skull Base Defects; Intracranial Lipomas; Arachnoid Cysts; Nonsyndromic and Syndromic Craniosynostoses 25
Schizencephaly: Etiopathogenesis, Classification, Therapeutic, and Rehabilitative Approach 24
Lissencephaly, Pachygyrias, Band Heterotopias, RELN Pathway, and ARX Mutations (Incomplete Neuron Migration) 23
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 22
Clinical Features, Genetic Landscape and Management of Behçet's Syndrome: A Comprehensive Review 22
CTNND1‐Related Disorder: New Insight on Prenatal Phenotype 20
At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation 18
Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes 17
Genetic screening of tuberous sclerosis complex in Sicily with a focus on neurological manifestations 11
Sleep Disorders in Pediatric Patients Affected by Neurofibromatosis Type 1: Reports of a Questionnaire and an Apple Watch Sleep Assessment 7
Genetic Screening of Tuberous Sclerosis Complex in Sicily with a Focus on Neurological Manifestations 3
Totale 192
Categoria #
all - tutte 1.208
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 1.208


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2024/2025162 0 0 0 10 25 26 15 4 12 22 28 20
2025/202630 30 0 0 0 0 0 0 0 0 0 0 0
Totale 192