AVEMARIA, FRANCESCA
 Distribuzione geografica
Continente #
EU - Europa 291
NA - Nord America 231
AS - Asia 92
AF - Africa 5
SA - Sud America 3
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 624
Nazione #
US - Stati Uniti d'America 229
GB - Regno Unito 154
CN - Cina 49
IT - Italia 37
DE - Germania 32
SE - Svezia 22
KR - Corea 14
IN - India 10
FI - Finlandia 9
CZ - Repubblica Ceca 8
BE - Belgio 6
JP - Giappone 5
UA - Ucraina 5
ID - Indonesia 4
NL - Olanda 4
IQ - Iraq 3
PE - Perù 3
RU - Federazione Russa 3
ZA - Sudafrica 3
CA - Canada 2
CH - Svizzera 2
DK - Danimarca 2
FR - Francia 2
HK - Hong Kong 2
IE - Irlanda 2
KZ - Kazakistan 2
RO - Romania 2
TR - Turchia 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
BJ - Benin 1
ES - Italia 1
EU - Europa 1
SC - Seychelles 1
Totale 624
Città #
Southend 140
Seattle 37
Wilmington 37
Fairfield 21
Milan 19
Princeton 18
Woodbridge 16
Houston 14
Wolverhampton 9
Ann Arbor 8
Beijing 7
Cambridge 7
Tianjin 7
Ashburn 6
Chandler 6
Des Moines 6
Falls Church 6
Nanjing 6
Changsha 5
Greifswald 4
Jakarta 4
Ningbo 4
Norwalk 4
Shanghai 4
Waanrode 4
Absecon 3
Hangzhou 3
Ipswich 3
Menlo Park 3
San Diego 3
Shenyang 3
Atlanta 2
Bitonto 2
Dearborn 2
Hebei 2
Karbala 2
Kokshetau 2
Novosibirsk 2
Redwood City 2
Tokyo 2
Toronto 2
Trujillo 2
Baghdad 1
Bari 1
Berlin 1
Brooklyn 1
Canberra 1
Cape Town 1
Central 1
Chengdu 1
Dubai 1
El Paso 1
Glen Ellyn 1
Guangzhou 1
Haikou 1
Hanover 1
Hefei 1
Helsinki 1
Jinan 1
Johannesburg 1
Kofu 1
Lecce 1
Lima 1
Mahé 1
Medford 1
Mountain View 1
Nanchang 1
New Haven 1
Osaka 1
Phoenix 1
Piano Di Sorrento 1
Rho 1
Richmond 1
Rochester 1
Seoul 1
Stellenbosch 1
Voerde 1
Zhengzhou 1
Zurich 1
Totale 476
Nome #
DIABETES MELLITUS: A COMPLEX METABOLIC DISORDER.EXPLORING THE DISEASE THROUGH FRUCTOSAMINE 3-KINASE GENE ANALYSIS 175
PDCD10 gene mutations in multiple cerebral cavernous malformations 120
Role of fructosamine-3-kinase in protecting against the onset of microvascular and macrovascular complications in patients with T2DM 71
Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype 66
De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations 64
Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression 53
Phenotypic heterogeneity in a SOD1 G93D Italian ALS family : an example of human model to study a complex disease 50
Wide phenotypic spectrum of the TARDBP gene : homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject 48
Possible role of fructosamine 3-kinase genotyping for the management of diabetic patients 46
Totale 693
Categoria #
all - tutte 1065
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 1065


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/201889 00196 815 27 125105
2018/2019107 258117 711 53 83712
2019/202087 13435 115 55 181152
2020/2021100 72023 1111 88 64155
2021/2022115 8782 1511 51 917329
2022/202339 1313130 00 00 0000
Totale 693