TRUNZO, ROBERTA
 Distribuzione geografica
Continente #
NA - Nord America 331
EU - Europa 278
AS - Asia 104
SA - Sud America 2
Totale 715
Nazione #
US - Stati Uniti d'America 327
CN - Cina 73
IE - Irlanda 71
IT - Italia 57
UA - Ucraina 48
SE - Svezia 32
AT - Austria 15
IN - India 14
GB - Regno Unito 13
FR - Francia 9
SG - Singapore 9
FI - Finlandia 8
PL - Polonia 8
DE - Germania 5
CR - Costa Rica 4
TR - Turchia 4
HK - Hong Kong 3
NL - Olanda 3
BA - Bosnia-Erzegovina 2
NO - Norvegia 2
PT - Portogallo 2
CL - Cile 1
GR - Grecia 1
PE - Perù 1
RO - Romania 1
RU - Federazione Russa 1
VN - Vietnam 1
Totale 715
Città #
Dublin 67
Chandler 46
Jacksonville 34
Wilmington 33
Nyköping 25
Dearborn 19
Vienna 15
Ashburn 14
Nanjing 14
Redwood City 14
Beijing 12
New York 12
Poznan 8
Milan 7
Nanchang 7
Princeton 7
Houston 6
Zhengzhou 6
San Mateo 5
Shanghai 5
Singapore 5
Ann Arbor 4
Bari 4
Cagliari 4
Fairfield 4
Hangzhou 4
Jinan 4
Kunming 4
San José 4
Shenyang 4
Tianjin 4
Woodbridge 4
Des Moines 3
Helsinki 3
Saint Paul 3
Bergen 2
Boardman 2
Catania 2
Changsha 2
Chapel Hill 2
Chicago 2
Este 2
Gaithersburg 2
Lanzhou 2
Los Angeles 2
Meitingen 2
Salt Lake City 2
Sandpoint 2
Seattle 2
Tuzla 2
Veniano 2
Absecon 1
Altamura 1
Anderson 1
Athens 1
Buffalo 1
Campbell 1
Changchun 1
Cutrofiano 1
Dallas 1
Dong Ket 1
Elkton 1
Falls Church 1
Ferentino 1
Foggia 1
Glenside 1
Hebei 1
Hilden 1
Jackson 1
Jiaxing 1
Leawood 1
Lima 1
Lisbon 1
London 1
Marco 1
Ningbo 1
Orange 1
Orbassano 1
Paris 1
Pinole 1
Pune 1
Redmond 1
Riesi 1
Rome 1
Rostock 1
Rotterdam 1
San Diego 1
Santiago 1
Stanford 1
Sudbury 1
Trieste 1
Turate 1
Turin 1
Vicenza 1
Wuhan 1
Ypsilanti 1
Totale 491
Nome #
Molecular analysis and genotype-phenotype correlation in patients affected by hyperphenylalaninemias in southern italy 305
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 89
In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU 89
Mutation analysis in hyperphenylalaninemia patients from South Italy. 73
Small Supernumerary Marker Chromosome Originating From Chromosome 10 Associated With an Apparently Normal Phenotype’ 71
The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype 56
Novel AKAP9 mutation and long QT syndrome in a patient with torsades des pointes 52
Totale 735
Categoria #
all - tutte 2.448
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 2.448


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020141 22 27 11 0 14 11 19 2 14 6 13 2
2020/2021100 10 0 9 9 19 5 10 4 15 10 4 5
2021/202256 7 1 0 0 0 1 4 3 11 11 5 13
2022/2023203 15 7 12 9 19 15 6 22 81 2 13 2
2023/202460 2 11 3 3 5 9 2 6 0 1 3 15
2024/20258 8 0 0 0 0 0 0 0 0 0 0 0
Totale 735