VEGGIOTTI, PIERANGELO
 Distribuzione geografica
Continente #
EU - Europa 987
AS - Asia 126
NA - Nord America 75
SA - Sud America 21
AF - Africa 5
OC - Oceania 1
Totale 1.215
Nazione #
IT - Italia 966
US - Stati Uniti d'America 68
SG - Singapore 48
CN - Cina 32
VN - Vietnam 31
BR - Brasile 14
FR - Francia 7
DE - Germania 5
CA - Canada 4
GB - Regno Unito 4
AR - Argentina 3
IQ - Iraq 3
BD - Bangladesh 2
ID - Indonesia 2
IE - Irlanda 2
MX - Messico 2
ZA - Sudafrica 2
AU - Australia 1
CH - Svizzera 1
CL - Cile 1
CO - Colombia 1
DO - Repubblica Dominicana 1
EC - Ecuador 1
EG - Egitto 1
FI - Finlandia 1
HK - Hong Kong 1
JO - Giordania 1
KE - Kenya 1
MA - Marocco 1
NP - Nepal 1
OM - Oman 1
PE - Perù 1
PK - Pakistan 1
PL - Polonia 1
SA - Arabia Saudita 1
TR - Turchia 1
TW - Taiwan 1
Totale 1.215
Città #
Genoa 467
Genova 288
Rapallo 116
Vado Ligure 87
San Jose 26
Singapore 18
Ashburn 15
Council Bluffs 14
Ho Chi Minh City 14
Beijing 8
Lauterbourg 6
Frankfurt am Main 5
Hanoi 4
Bordighera 3
São Paulo 3
Da Nang 2
Dublin 2
Houston 2
Toronto 2
Turin 2
Agadir 1
Ajax 1
Almeirim Municipality 1
Amman 1
Ankara 1
Basra 1
Bắc Giang 1
Cairo 1
Cape Town 1
Carapicuíba 1
Cardiff 1
Chittagong 1
City of London 1
Corrientes 1
Daska Kalan 1
Des Moines 1
Erbil 1
Ha'il 1
Haiphong 1
Helsinki 1
Hong Kong 1
Huế 1
Ijuí 1
Jhāpā 1
Johannesburg 1
Jundiaí 1
Lima 1
Manchester 1
Mexico City 1
Milan 1
Montreal 1
Muscat 1
Nairobi 1
Nanning 1
Natal 1
New York 1
Palermo 1
Phủ Lý 1
Porto Alegre 1
Presidente Prudente 1
Quito 1
Rio Novo do Sul 1
Rio do Sul 1
Rosario 1
San Juan 1
San Luis Potosí City 1
Santiago 1
Saquarema 1
Shanghai 1
Simijaca 1
Surabaya 1
Sydney 1
Taboão da Serra 1
Tainan 1
Thái Nguyên 1
Việt Hưng 1
Warsaw 1
Zurich 1
Totale 1.142
Nome #
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 176
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′-phosphate supplementation 144
CHD2 variants are a risk factor for photosensitivity in epilepsy 135
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1 135
Generalized Epilepsy with Febrile Seizures Plus (GEFS+): Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations 127
Benign familial infantile convulsions: Mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity 120
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy 118
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications 106
Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity 87
Dravet syndrome: Early clinical manifestations and cognitive outcome in 37 Italian patients 85
Totale 1.233
Categoria #
all - tutte 4.857
article - articoli 4.857
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.714


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202120 0 0 0 0 0 0 0 0 0 14 2 4
2021/2022109 10 2 3 6 6 9 0 25 8 22 2 16
2022/2023133 8 8 2 13 18 20 14 10 15 5 16 4
2023/202484 4 10 0 11 8 22 3 9 2 1 4 10
2024/2025252 4 13 3 18 24 33 25 45 19 18 34 16
2025/2026461 60 18 107 31 68 25 64 22 31 35 0 0
Totale 1.233