FORTUNATO, Fernanda
 Distribuzione geografica
Continente #
NA - Nord America 450
EU - Europa 142
AS - Asia 139
AF - Africa 2
OC - Oceania 1
Totale 734
Nazione #
US - Stati Uniti d'America 441
SG - Singapore 70
IT - Italia 63
CN - Cina 51
DE - Germania 26
GB - Regno Unito 20
FI - Finlandia 12
ID - Indonesia 11
CA - Canada 9
CZ - Repubblica Ceca 4
SE - Svezia 4
BE - Belgio 3
SI - Slovenia 3
UA - Ucraina 3
DZ - Algeria 2
LT - Lituania 2
TR - Turchia 2
VN - Vietnam 2
BD - Bangladesh 1
IN - India 1
JO - Giordania 1
LV - Lettonia 1
NL - Olanda 1
NZ - Nuova Zelanda 1
Totale 734
Città #
Chandler 66
Singapore 55
Fairfield 54
Santa Clara 54
Ashburn 37
Ferrara 30
Beijing 19
Seattle 15
Shanghai 15
Cambridge 14
Woodbridge 14
Houston 12
New York 12
Jakarta 11
Helsinki 10
Bremen 9
Munich 9
Princeton 9
Wilmington 9
San Diego 8
Los Angeles 7
Milan 6
Toronto 6
Falls Church 5
London 5
Rome 5
Ann Arbor 4
Boardman 4
Bologna 3
Brno 3
Frankfurt am Main 3
Jacksonville 3
Brussels 2
Dearborn 2
Dong Ket 2
Duck Lake 2
Falkenstein 2
Guangzhou 2
Hounslow 2
Nanjing 2
Shenyang 2
Addison 1
Amman 1
Amsterdam 1
Anyang 1
Auckland 1
Chengdu 1
Chicago 1
Cingoli 1
Espoo 1
Ferrara di Monte Baldo 1
Hyderabad 1
Izmir 1
Kilburn 1
Lacco Ameno 1
Lappeenranta 1
Leawood 1
Lowell 1
Newark 1
Norwalk 1
Orange 1
Ottawa 1
Padova 1
Prague 1
Redwood City 1
Riga 1
San Mateo 1
Shenzhen 1
Washington 1
Totale 562
Nome #
A CMT2 family carrying the P7R mutation in the N- terminal region of the HSPB1 gene 87
DMD gene molecular genetic characterization in Eastern Europe and non European countries 84
Report of a novel ATP7A mutation causing distal motor neuropathy 83
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries 77
Response to raltegravir-based salvage therapy in HIV-infected patients with hepatitis C virus or hepatitis B virus coinfection 75
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 60
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy 59
ISS-NIA ITALIAN COHORT: NEW ANTI-HIV INHIBITORS IN PATIENTS EXPERIENCED TO IP, NRTI, NNRTI 38
Three-years follow up of raltegravir and/or maraviroc-based regimens in patients experienced to PI, NRTI, NNRTI. Update from the ISS-NIA cohort 36
Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project 30
AFG3L2 Biallelic Mutation: Clinical Heterogeneity in Two Italian Patients 27
TeleNEwCARe: An Italian case-control telegenetics study in patients with Hereditary NEuromuscular and CARdiac diseases 25
The DMD gene and therapeutic approaches to restore dystrophin 19
Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe 19
DMD deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosis 18
mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies 18
Digital health and Clinical Patient Management System (CPMS) platform utility for data sharing of neuromuscular patients: the Italian EURO-NMD experience 16
Totale 771
Categoria #
all - tutte 6.755
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 6.755


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202074 0 0 0 0 0 8 12 8 19 14 9 4
2020/2021102 1 9 0 12 1 12 7 18 7 8 18 9
2021/202293 1 13 0 2 8 6 1 0 12 11 4 35
2022/2023131 12 22 4 13 24 11 5 11 23 1 3 2
2023/2024126 7 11 5 1 11 22 4 10 15 4 3 33
2024/2025221 20 13 37 24 67 60 0 0 0 0 0 0
Totale 771