ZANETTI, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 963
EU - Europa 171
AS - Asia 90
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
SA - Sud America 1
Totale 1.227
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Nazione #
US - Stati Uniti d'America 962
CN - Cina 48
IT - Italia 44
SE - Svezia 40
SG - Singapore 37
DE - Germania 22
FI - Finlandia 18
UA - Ucraina 13
FR - Francia 11
GB - Regno Unito 11
IN - India 5
AT - Austria 3
ES - Italia 3
IE - Irlanda 2
RU - Federazione Russa 2
AU - Australia 1
BR - Brasile 1
EU - Europa 1
PA - Panama 1
PT - Portogallo 1
SI - Slovenia 1
Totale 1.227
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Città #
Fairfield 155
Houston 138
Chandler 84
Woodbridge 68
Ashburn 65
Ann Arbor 60
Cambridge 59
Seattle 58
Wilmington 47
Jacksonville 38
Singapore 24
Beijing 16
Princeton 15
San Diego 13
Medford 11
Padova 11
Boardman 10
Des Moines 10
Helsinki 10
New York 10
Nanjing 8
Cagliari 6
Milan 5
Rome 4
Santa Clara 4
Auburn Hills 3
Munich 3
Changsha 2
Dublin 2
Fremont 2
Girona 2
Kharkiv 2
Legnano 2
Mumbai 2
Neustadt am Ruebenberge 2
Paris 2
Pune 2
Shenyang 2
Stockholm 2
Vicenza 2
Vienna 2
Chongqing 1
Crato 1
Dallas 1
Frankfurt am Main 1
Gunzenhausen 1
Haikou 1
Hefei 1
Huzhou 1
Jinhua 1
Kilburn 1
Leawood 1
Los Angeles 1
Montesilvano Marina 1
Nanchang 1
Panama City 1
Phoenix 1
Redwood City 1
Rockville 1
San Francisco 1
San Jose 1
Sant'elena 1
Shanghai 1
Sydney 1
Teaneck 1
Tianjin 1
Vasto 1
Totale 989
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Nome #
Circadian transcriptome analysis in human fibroblasts from Hunter syndrome and impact of iduronate-2-sulfatase treatment 151
QueryOR: a comprehensive web platform for genetic variant analysis and prioritization 139
RNA-seq Transcriptome Profiling Of Primary Hunter Cells Following Treatment With Recombinant IDS As A First Step For Identification Of ERT Efficacy Markers 134
Gene therapy of Hunter syndrome: Evaluation of the efficiency of muscle electro genetransfer for the production and release of recombinant iduronate-2-sulfatase (IDS) 121
Segregation analysis in a family at risk for the Maroteaux-Lamy syndrome conclusively reveals c.1151G > A (p.S384N) as to be a polymorphism 120
A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus 116
Brain RNA-seq profiling of the mucopolysaccharidosis type II mouse model 107
Clinical efficacy of Enzyme Replacement Therapy in paediatric Hunter patients, an independent study of 3.5 years 79
Caratterizzazione molecolare delle variazioni di sequenza del gene hIDS in pazienti affetti da sindrome di Hunter 79
Gene therapy approaches for lysosomal storage disorders, a good model for the treatment of mendelian diseases. 67
Molecular diagnosis of patients affected by mucopolysaccharidosis: a multicenter study 44
Setup and Validation of a Targeted Next-Generation Sequencing Approach for the Diagnosis of Lysosomal Storage Disorders 39
Mucopolysaccharidosis type II: One hundred years of research, diagnosis, and treatment 29
Glycosaminoglycan signatures in body fluids of mucopolysaccharidosis type II mouse model under long-term enzyme replacement therapy 18
Totale 1.243
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Categoria #
all - tutte 4.999
article - articoli 4.633
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.632
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020188 0 0 2 19 23 19 21 28 23 28 18 7
2020/2021210 13 7 3 17 9 24 5 18 23 64 18 9
2021/2022219 11 13 28 7 30 23 8 17 16 15 21 30
2022/2023187 30 12 3 26 27 30 1 14 26 6 10 2
2023/2024111 3 17 13 11 6 18 8 8 1 3 14 9
2024/202553 5 26 22 0 0 0 0 0 0 0 0 0
Totale 1.243