MAGNOLO, Antonia Lucia
 Distribuzione geografica
Continente #
NA - Nord America 870
EU - Europa 329
AS - Asia 27
Continente sconosciuto - Info sul continente non disponibili 6
Totale 1232
Nazione #
US - Stati Uniti d'America 867
GB - Regno Unito 144
SE - Svezia 53
DE - Germania 40
UA - Ucraina 26
FR - Francia 18
IT - Italia 17
CN - Cina 14
TR - Turchia 11
FI - Finlandia 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
IN - India 1
JP - Giappone 1
RO - Romania 1
RU - Federazione Russa 1
Totale 1232
Città #
Fairfield 149
Southend 129
Woodbridge 107
Houston 71
Ashburn 65
Seattle 63
Jacksonville 60
Wilmington 59
Ann Arbor 57
Cambridge 53
Chandler 47
Dearborn 47
Nyköping 29
Modena 12
Falls Church 11
Grafing 11
Eugene 10
Princeton 10
Bremen 9
Sofia 9
Izmir 7
San Diego 6
Brussels 5
Beijing 4
Des Moines 3
Hefei 3
London 2
Los Angeles 2
Nanjing 2
Paris 2
Toronto 2
Waanrode 2
Belize City 1
Boardman 1
Borås 1
Brindisi 1
Chicago 1
Hangzhou 1
Helsinki 1
Jiaxing 1
Kunming 1
Leawood 1
Milan 1
Nanchang 1
Napoli 1
Sabbio Chiese 1
San Jose 1
Sarajevo 1
Totale 1064
Nome #
The Janus-faced manifestations of homozygous familial hypobetalipoproteinemia due to apolipoprotein B truncations 207
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia. 161
Identification of patients with abetalipoproteinemia and homozygous familial hypobetalipoproteinemia in Tunisia 150
Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia 142
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia. 132
Characterization of Three Kindreds with Familial Combined Hypolipidemia Due to Loss of Function Mutations of ANGPTL3. 121
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations 116
Molecular diagnosis of hypobetalipoproteinemia: an ENID Review 109
Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemia. 102
Totale 1240
Categoria #
all - tutte 2064
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 2064


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/20187 0000 00 04 0210
2018/2019183 12085 109 112 10254042
2019/2020369 35141221 4659 6639 32121815
2020/2021260 2772262 1823 1626 9231710
2021/2022200 3312110 521 184 21123816
2022/2023114 14221512 2424 30 0000
Totale 1240