MAGNOLO, Antonia Lucia
 Distribuzione geografica
Continente #
NA - Nord America 947
EU - Europa 350
AS - Asia 59
Continente sconosciuto - Info sul continente non disponibili 6
Totale 1.362
Nazione #
US - Stati Uniti d'America 944
GB - Regno Unito 152
SE - Svezia 56
DE - Germania 44
CN - Cina 36
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
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 1.362
Città #
Fairfield 149
Southend 129
Woodbridge 107
Ashburn 88
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
New York 4
Des Moines 3
Hefei 3
London 3
Washington 3
Hounslow 2
Islington 2
Kilburn 2
Los Angeles 2
Nanjing 2
Paris 2
Toronto 2
Waanrode 2
Belize City 1
Boardman 1
Borås 1
Brindisi 1
Chicago 1
Dublin 1
Hangzhou 1
Jiaxing 1
Kunming 1
Leawood 1
Milan 1
Nanchang 1
Napoli 1
Sabbio Chiese 1
San Jose 1
Sarajevo 1
Warsaw 1
Totale 1.137
Nome #
The Janus-faced manifestations of homozygous familial hypobetalipoproteinemia due to apolipoprotein B truncations 225
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia. 181
Identification of patients with abetalipoproteinemia and homozygous familial hypobetalipoproteinemia in Tunisia 167
Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia 155
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. 135
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations 132
Novel mutations of CETP gene in Italian subjects with hyeralphalipoproteinemia 119
Molecular diagnosis of hypobetalipoproteinemia: an ENID Review 118
Totale 1.370
Categoria #
all - tutte 5.100
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 5.100


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019107 0 0 0 0 0 0 0 0 0 25 40 42
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
2023/202485 4 3 7 17 23 13 4 10 4 0 0 0
Totale 1.370