SANTA PAOLA, SANDRO
 Distribuzione geografica
Continente #
NA - Nord America 148
AS - Asia 125
EU - Europa 96
SA - Sud America 18
AF - Africa 8
Totale 395
Nazione #
US - Stati Uniti d'America 144
SG - Singapore 54
IT - Italia 46
CN - Cina 31
RU - Federazione Russa 29
VN - Vietnam 14
KR - Corea 11
BD - Bangladesh 10
BR - Brasile 10
FR - Francia 6
AR - Argentina 4
IE - Irlanda 4
GB - Regno Unito 3
NG - Nigeria 3
NL - Olanda 3
BJ - Benin 2
CA - Canada 2
FI - Finlandia 2
ID - Indonesia 2
IQ - Iraq 2
PL - Polonia 2
BW - Botswana 1
CI - Costa d'Avorio 1
CL - Cile 1
CR - Costa Rica 1
JM - Giamaica 1
MY - Malesia 1
PY - Paraguay 1
SE - Svezia 1
UY - Uruguay 1
VE - Venezuela 1
ZA - Sudafrica 1
Totale 395
Città #
Dallas 73
Singapore 29
Catania 18
Moscow 16
Hefei 14
San Jose 14
Santa Clara 14
Seoul 11
Ashburn 10
Ho Chi Minh City 6
New York 5
Rome 5
Civitanova Marche 4
Dublin 4
Lauterbourg 4
Amsterdam 3
Da Nang 3
Hanoi 3
Troina 3
Beijing 2
Buffalo 2
Cotonou 2
La Plata 2
Lappeenranta 2
London 2
Los Angeles 2
Palermo 2
São Paulo 2
Thái Bình 2
Verona 2
Warsaw 2
Abidjan 1
Abuja 1
Arlington 1
Asunción 1
Avellaneda 1
Baghdad 1
Bellizzi 1
Boardman 1
Campos dos Goytacazes 1
Caracas 1
Castelo 1
Chicago 1
Conceição das Alagoas 1
Council Bluffs 1
Denver 1
Dhaka 1
Duque de Caxias 1
Gaborone 1
Itapevi 1
Itaúna 1
Jacksonville 1
Johannesburg 1
Kuala Lumpur 1
Lagos 1
Luling 1
Manchester 1
Minneapolis 1
Mojokerto 1
Montevideo 1
Naples 1
Orem 1
Pittsburgh 1
Port Arthur 1
Port Harcourt 1
Ragusa 1
San José 1
San Juan Bautista 1
Santiago 1
Secaucus 1
Sidoarjo 1
Stockholm 1
Sulaymaniyah 1
Tampa 1
Teixeira de Freitas 1
Toronto 1
Vancouver 1
Varjota 1
Waco 1
Wake Forest 1
Totale 312
Nome #
The 9 bp Deletion between the Mitochondrial COII and Lysine tRNA Genes in a Caucasian Population with Cognitive Disorders: An Observational Study 121
Expansion of the Genotypic and Phenotypic Spectrum of TCTN3-Related Joubert Syndrome 100
Mitochondrial DNA involvement in patients with autism spectrum disorders and intellectual disability 91
Focus on Clinical and Genetic Aspects of PKAN Through the Description of New Patients 76
Maternal uniparental isodisomy in a patient with autosomal recessive spastic paraplegia type 20 13
Totale 401
Categoria #
all - tutte 901
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 901


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/202317 0 0 0 0 0 9 0 1 4 0 1 2
2023/20248 1 0 4 0 0 1 0 0 0 1 1 0
2024/202560 1 2 1 12 10 8 1 5 5 4 5 6
2025/2026316 7 38 68 16 51 42 19 16 9 14 21 15
Totale 401