PAGLIARDINI, Veronica
 Distribuzione geografica
Continente #
NA - Nord America 281
EU - Europa 133
AS - Asia 83
AF - Africa 4
Totale 501
Nazione #
US - Stati Uniti d'America 281
SG - Singapore 33
IT - Italia 32
AT - Austria 28
CN - Cina 28
IE - Irlanda 24
SE - Svezia 20
FR - Francia 12
FI - Finlandia 5
IN - India 5
VN - Vietnam 5
DE - Germania 4
ID - Indonesia 4
JP - Giappone 3
KR - Corea 2
NG - Nigeria 2
NO - Norvegia 2
PL - Polonia 2
CI - Costa d'Avorio 1
DK - Danimarca 1
ES - Italia 1
GB - Regno Unito 1
HK - Hong Kong 1
RO - Romania 1
SN - Senegal 1
TH - Thailandia 1
TR - Turchia 1
Totale 501
Città #
Chandler 34
Vienna 28
Singapore 24
Dublin 22
Beijing 17
Fairfield 17
Houston 16
Ashburn 15
Torino 14
Nyköping 12
Seattle 12
Woodbridge 10
Cambridge 9
Villeurbanne 9
Medford 7
Princeton 7
Wilmington 7
Dearborn 6
Ann Arbor 4
Jakarta 4
Pisa 4
Pune 4
Turin 4
Boston 3
Norwalk 3
Abuja 2
Dong Ket 2
Guiyang 2
Hangzhou 2
Hebei 2
Jacksonville 2
Santa Clara 2
Stavanger 2
Warsaw 2
Abidjan 1
Boardman 1
Bosco Chiesanuova 1
Bucharest 1
Central 1
Chiyoda-ku 1
Copenhagen 1
Dallas 1
Fremont 1
Gunzenhausen 1
Kocaeli 1
Kunming 1
Liverpool 1
Melito Di Napoli 1
Nonthaburi 1
Norristown 1
Oronoco 1
Phoenix 1
Redmond 1
Robbio 1
Rochester 1
Rubiana 1
San Diego 1
Shanghai 1
Takamatsu 1
Tokyo 1
Upper Marlboro 1
Vigo 1
Washington 1
Xian 1
Totale 340
Nome #
Metabolic progression to clinical phenotype in classic Fabry disease 129
Longitudinal monitoring of alpha-fetoprotein by dried blood spot for hepatoblastoma screening in beckwith-wiedemann syndrome 103
Newborn screening for galactosemia: a 30-year single center experience 59
Early higher dosage of alglucosidase alpha in classic Pompe disease 57
Functional assessment tools in children with Pompe disease: A pilot comparative study to identify suitable outcome measures for the standard of care 53
Studio epidemiologico della carenza iodica in Piemonte 50
Effect of alglucosidase alfa dosage on survival and walking ability in patients with classic infantile Pompe disease: a multicentre observational cohort study from the European Pompe Consortium 37
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy 18
Differential response to renal replacement therapy in neonatal-onset inborn errors of metabolism 11
Neonatal screening for biotinidase deficiency: A 30-year single center experience 9
The use of biomarkers, clinical assessments, and clinical history for a better approach to patients with complex diseases 2
Totale 528
Categoria #
all - tutte 1.967
article - articoli 0
book - libri 0
conference - conferenze 179
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.146


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202060 0 0 0 11 5 9 6 7 9 4 4 5
2020/202134 2 2 3 3 0 2 1 2 1 6 6 6
2021/202275 2 2 5 9 3 2 1 4 3 4 23 17
2022/2023136 9 3 4 9 15 28 8 15 29 4 6 6
2023/202462 8 15 1 4 1 12 0 5 0 2 3 11
2024/202540 2 27 8 3 0 0 0 0 0 0 0 0
Totale 528