DI FEO, MARIA FRANCESCA
 Distribuzione geografica
Continente #
NA - Nord America 112
AS - Asia 108
EU - Europa 69
Continente sconosciuto - Info sul continente non disponibili 9
SA - Sud America 4
AF - Africa 1
Totale 303
Nazione #
US - Stati Uniti d'America 105
IT - Italia 59
SG - Singapore 44
BD - Bangladesh 33
CN - Cina 12
VN - Vietnam 10
HK - Hong Kong 4
BR - Brasile 3
DE - Germania 3
GB - Regno Unito 3
CA - Canada 2
FI - Finlandia 2
JM - Giamaica 2
JP - Giappone 2
BH - Bahrain 1
BS - Bahamas 1
BZ - Belize 1
CO - Colombia 1
ES - Italia 1
GR - Grecia 1
SA - Arabia Saudita 1
TR - Turchia 1
VI - Stati Uniti Isole Vergini 1
ZA - Sudafrica 1
Totale 294
Città #
Genoa 32
San Jose 22
Singapore 21
Ashburn 11
New York 11
Hanoi 6
Rome 6
Council Bluffs 4
Hong Kong 4
Vado Ligure 4
Frankfurt am Main 3
Santa Clara 3
Bologna 2
Chicago 2
Dallas 2
Lake Forest 2
Los Angeles 2
Louisville 2
Lynchburg 2
Tokyo 2
Verona 2
Wilmington 2
Amarillo 1
Athens 1
Auburn 1
Bari 1
Bayonne 1
Beijing 1
Braidwood 1
Brescia 1
Buffalo 1
Cagliari 1
Cali 1
Cardiff 1
Cerquilho 1
Charlotte 1
Charlotte Amalie 1
Citrus Heights 1
City of London 1
Denver 1
Dhaka 1
Earlysville 1
Houston 1
Istanbul 1
Itaquaquecetuba 1
Jeddah 1
Jemison 1
Johannesburg 1
La Vergne 1
Lebanon 1
Lynwood 1
Madrid 1
Manama 1
Nassau 1
Orange Walk 1
Philadelphia 1
Phúc Thọ 1
Pozzuoli 1
San Francisco 1
Sarasota 1
Savannah 1
Seattle 1
Sobral 1
Sydney 1
Toronto 1
Victorville 1
Vimodrone 1
Waterbury 1
Yên Bái 1
Totale 194
Nome #
Expanding the phenotype of UPF3B-related disorder: Case reports and literature review 81
Congenital Nasal Bones Agenesis: Report of a Rare Malformation 45
Novel missense variants associated with GNE myopathy 41
Inferring disease course from differential exon usage in the wide titinopathy spectrum 28
Gene prioritisation for enhancing molecular diagnosis in rare skeletal muscle disease cohort 26
Counseling and prenatal diagnosis in facioscapulohumeral muscular dystrophy: A retrospective study on a 13‐year multidisciplinary approach 23
The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum 23
Salih Myopathy 18
Novel Mutations in Titin Exon 363 With Different Phenotypes Including a Founder Mutation in Eastern Europe 18
Totale 303
Categoria #
all - tutte 898
article - articoli 835
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 63
Totale 1.796


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2024/202523 0 0 0 0 0 7 3 5 3 1 2 2
2025/2026219 6 0 4 3 26 11 23 22 19 24 41 40
2026/202761 18 23 20 0 0 0 0 0 0 0 0 0
Totale 303