MAGNOLO, Antonia Lucia
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 951
EU - Europa 351
AS - Asia 69
Continente sconosciuto - Info sul continente non disponibili 6
Totale 1.377
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 948
GB - Regno Unito 152
SE - Svezia 56
DE - Germania 45
CN - Cina 42
UA - Ucraina 26
FR - Francia 18
IT - Italia 17
FI - Finlandia 14
TR - Turchia 11
HK - Hong Kong 10
BG - Bulgaria 9
BE - Belgio 7
EU - Europa 5
SG - Singapore 4
CA - Canada 2
NL - Olanda 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BA - Bosnia-Erzegovina 1
BZ - Belize 1
IE - Irlanda 1
IN - India 1
JP - Giappone 1
PL - Polonia 1
RO - Romania 1
RU - Federazione Russa 1
Totale 1.377
Salva come PNG Salva come JPEG
Città #
Fairfield 149
Southend 129
Woodbridge 107
Ashburn 89
Houston 71
Seattle 63
Jacksonville 60
Wilmington 59
Ann Arbor 57
Cambridge 53
Chandler 52
Dearborn 47
Nyköping 32
Modena 12
Falls Church 11
Grafing 11
Beijing 10
Eugene 10
Hong Kong 10
Princeton 10
Bremen 9
Sofia 9
Izmir 7
San Diego 6
Shanghai 6
Brussels 5
Helsinki 5
Los Angeles 5
New York 4
Des Moines 3
Hefei 3
London 3
Washington 3
Hounslow 2
Islington 2
Jiaxing 2
Kilburn 2
Nanjing 2
Paris 2
Toronto 2
Waanrode 2
Belize City 1
Boardman 1
Borås 1
Brindisi 1
Chicago 1
Dublin 1
Frankfurt am Main 1
Guangzhou 1
Hangzhou 1
Kunming 1
Leawood 1
Milan 1
Nanchang 1
Napoli 1
Sabbio Chiese 1
San Jose 1
Sarajevo 1
Warsaw 1
Totale 1.144
Salva come PNG Salva come JPEG
Nome #
The Janus-faced manifestations of homozygous familial hypobetalipoproteinemia due to apolipoprotein B truncations 228
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia. 182
Identification of patients with abetalipoproteinemia and homozygous familial hypobetalipoproteinemia in Tunisia 170
Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia 156
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia. 138
Characterization of Three Kindreds with Familial Combined Hypolipidemia Due to Loss of Function Mutations of ANGPTL3. 137
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations 134
Novel mutations of CETP gene in Italian subjects with hyeralphalipoproteinemia 120
Molecular diagnosis of hypobetalipoproteinemia: an ENID Review 120
Totale 1.385
Salva come PNG Salva come JPEG
Categoria #
all - tutte 5.315
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 5.315
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020369 35 14 12 21 46 59 66 39 32 12 18 15
2020/2021260 27 7 22 62 18 23 16 26 9 23 17 10
2021/2022200 3 31 21 10 5 21 18 4 21 12 38 16
2022/2023159 14 22 15 12 24 24 2 13 21 2 7 3
2023/202499 4 3 7 17 23 13 4 10 4 3 2 9
2024/20251 1 0 0 0 0 0 0 0 0 0 0 0
Totale 1.385