FERRADINI, VALENTINA
 Distribuzione geografica
Continente #
NA - Nord America 2.088
EU - Europa 291
AS - Asia 167
SA - Sud America 2
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.550
Nazione #
US - Stati Uniti d'America 2.087
IT - Italia 103
SG - Singapore 74
KR - Corea 54
IE - Irlanda 44
CN - Cina 33
RU - Federazione Russa 28
DE - Germania 26
GB - Regno Unito 19
SE - Svezia 16
FR - Francia 15
UA - Ucraina 13
CZ - Repubblica Ceca 9
BE - Belgio 5
FI - Finlandia 4
NL - Olanda 3
BR - Brasile 2
JP - Giappone 2
PL - Polonia 2
PT - Portogallo 2
CA - Canada 1
CH - Svizzera 1
DK - Danimarca 1
EG - Egitto 1
EU - Europa 1
HK - Hong Kong 1
KG - Kirghizistan 1
TR - Turchia 1
VN - Vietnam 1
Totale 2.550
Città #
Wilmington 591
Houston 576
Woodbridge 285
Fairfield 113
Singapore 71
Chandler 70
Seattle 57
Ashburn 54
Ann Arbor 50
Rome 48
Cambridge 40
Dublin 34
Medford 24
Santa Clara 21
New York 18
Beijing 13
Menlo Park 12
Lawrence 11
San Diego 11
Dearborn 10
Brno 9
Milan 8
Munich 6
Brussels 5
Jacksonville 5
London 5
Moscow 5
Redwood City 5
Nanjing 4
Boardman 3
Hefei 3
Seoul 3
Turin 3
Bari 2
Casalecchio di Reno 2
Council Bluffs 2
Creede 2
Dego 2
Guangzhou 2
Helsinki 2
Maia 2
Palo Alto 2
Teresópolis 2
Acton 1
Al Mansurah 1
Amsterdam 1
Anzio 1
Augusta 1
Boston 1
Central District 1
Chengdu 1
Chongqing 1
Den Haag 1
Düsseldorf 1
Enfield 1
Geneva 1
Genoa 1
Genzano di Roma 1
Harbin 1
Hounslow 1
Jinan 1
Kraków 1
Krasnoyarsk 1
Kunming 1
L'isle-d'abeau 1
Marcianise 1
Mountain View 1
Nanning 1
New Bedfont 1
Orange 1
Prescot 1
Quzhou 1
Rubiana 1
Saint Petersburg 1
Salt Lake City 1
San Francisco 1
San Mateo 1
Scottsdale 1
Southwark 1
Strasbourg 1
Tokyo 1
Torino 1
Toronto 1
Velletri 1
Verona 1
Zhengzhou 1
Totale 2.236
Nome #
Targeted Next Generation Sequencing in patients with Myotonia Congenita 442
Genotype-phenotype correlation of F484L mutation in three Italian families with Thomsen myotonia 415
Novel X-linked inhibitor of apoptosis mutation in very early-onset inflammatory bowel disease child successfully treated with HLA-haploidentical hemapoietic stem cells transplant after removal of αβ+T and B cells 396
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 248
Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies. Front Immunol. 2019 Apr 11;10:316. doi: 10.3389/fimmu.2019.00316. eCollection 2019. Erratum in: Front Immunol. 2019 May 31;10:1184. 246
Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience 197
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 179
Corrigendum : Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies (Frontiers in Immunology (2019) 10 (316) DOI: 10.3389/fimmu.2019.00316) 136
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 128
Variants in mhy7 gene cause arrhythmogenic cardiomyopathy 68
Clinical features of LMNA-related cardiomyopathy in 18 patients and characterization of two novel variants 46
A likely pathogenic ACTG1 variant in a child showing partial phenotypic overlap with Baraitser-Winter syndrome 41
Genetic and epigenetic factors of Takotsubo syndrome: a systematic review 38
DSP-Related Cardiomyopathy as a Distinct Clinical Entity? Emerging Evidence from an Italian Cohort 18
Case Report: Crossing a rugged road in a primary immune regulatory disorder 14
Totale 2.612
Categoria #
all - tutte 7.028
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 7.028


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020591 0 0 0 0 48 61 97 81 84 97 61 62
2020/2021646 58 73 55 68 64 62 99 93 17 29 15 13
2021/2022186 5 12 9 7 22 8 17 22 24 6 17 37
2022/2023200 14 21 9 14 18 41 33 12 20 0 11 7
2023/202487 17 5 3 6 9 19 1 6 0 2 2 17
2024/2025183 22 71 39 20 31 0 0 0 0 0 0 0
Totale 2.612