LOMBARDI, ANNA-MARIA
 Distribuzione geografica
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Continente #
NA - Nord America 1.280
AS - Asia 137
EU - Europa 110
AF - Africa 2
OC - Oceania 1
Totale 1.530
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Nazione #
US - Stati Uniti d'America 1.279
CN - Cina 74
SG - Singapore 44
FI - Finlandia 21
SE - Svezia 18
IT - Italia 17
FR - Francia 14
DE - Germania 13
VN - Vietnam 12
UA - Ucraina 9
NL - Olanda 8
JP - Giappone 6
GB - Regno Unito 5
IE - Irlanda 2
LY - Libia 2
BE - Belgio 1
CA - Canada 1
CZ - Repubblica Ceca 1
IN - India 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
Totale 1.530
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Città #
Fairfield 240
Houston 137
Woodbridge 117
Ann Arbor 92
Cambridge 92
Seattle 88
Ashburn 78
Wilmington 74
Chandler 70
Jacksonville 44
Santa Clara 43
Singapore 38
Beijing 21
Princeton 21
Boardman 18
San Diego 18
Dong Ket 12
Helsinki 10
Des Moines 9
Medford 9
Padova 7
Roxbury 7
Nanjing 6
Osaka 6
Guangzhou 5
Changsha 4
Florence 4
Hebei 4
Nanchang 4
Norwalk 4
Redwood City 4
Plaidt 3
Dublin 2
Kilburn 2
Las Vegas 2
Munich 2
Philadelphia 2
Phoenix 2
Shenyang 2
Tianjin 2
Tripoli 2
Almada 1
Brno 1
Chiswick 1
Fontenay-sous-bois 1
Hangzhou 1
Jiaxing 1
Jinan 1
Kharkiv 1
Kitchener 1
London 1
Nashville 1
Olbia 1
Orange 1
Paraparaumu 1
Rockville 1
Rovereto 1
Saint Paul 1
Taiyuan 1
Waanrode 1
Washington 1
Wuhan 1
Totale 1.328
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Nome #
Comparison of three different immunoassays in the diagnosis of heparin-induced thrombocytopenia. 161
Weight loss reduces anti-ADAMTS13 autoantibodies and improves inflammatory and coagulative parameters in obese patients 155
Correlation between ADAMTS13 activity and neurological impairment in acute thrombotic microangiopathy patients 133
A large deletion due to a new mutation (intron 13/exon 23) in a sporadic case of severe hemophilia A 125
A novel germ-line mutation of c-mpl gene in a sporadic case of essential thrombocythemia 125
A novel type I factor X variant (factor X Cys350Phe) due to loss of a disulfide bond in the catalytic domain 105
Spectrum of 5’UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected 104
Conformation sensitive gel electrophoresis for detection of factor X gene mutations 103
Relevance of antiphospholipid antibody profile in the clinical outcome of ITP: a single-centre study 95
Mild bleeding diathesis in a boy with combined severe haemophilia B (C(10400)-->T) and heterozygous factor V Leiden 92
Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders 90
A NEW MUTATION (ARG 251TRP) IN THE CA2+ BINDING SITE OF FACTOR XPROTEASE DOMAIN APPEARS BE THE RESPONSIBLE FOR THE DEFECT IN THE EXTRINSIC PATHWAY ACTIVATION OF FACTORX PADUA. 85
Relapsing thrombotic thrombocytopenic purpura with low ADAMTS13 antigen levels: An indication for splenectomy? 85
A new Factor X defect (Factor X Padua 3) A compound heterozygous between true deficiency (Gly 380-Arg) and an abnormality (Der334 -Pro) 64
Hyperlactatemia reduces muscle glucose uptake and GLUT-4 mRNA while increasing (E1alpha)PDH gene expression in rat 33
Totale 1.555
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Categoria #
all - tutte 5.784
article - articoli 5.784
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 11.568
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020263 0 0 0 0 0 24 37 44 63 42 39 14
2020/2021278 28 30 20 8 11 20 7 22 47 43 23 19
2021/2022207 5 22 23 8 8 30 9 17 15 7 22 41
2022/2023146 27 25 4 9 22 13 0 10 20 9 5 2
2023/202486 2 17 18 6 8 7 3 1 5 3 9 7
2024/2025136 4 20 11 25 66 10 0 0 0 0 0 0
Totale 1.555