DAIDONE, VIVIANA
 Distribuzione geografica
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Continente #
NA - Nord America 3.119
EU - Europa 461
AS - Asia 434
SA - Sud America 5
OC - Oceania 2
AF - Africa 1
Totale 4.022
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Nazione #
US - Stati Uniti d'America 3.114
CN - Cina 191
SG - Singapore 185
IT - Italia 158
SE - Svezia 65
FI - Finlandia 50
DE - Germania 47
GB - Regno Unito 37
VN - Vietnam 36
UA - Ucraina 24
FR - Francia 22
RU - Federazione Russa 16
NL - Olanda 14
HK - Hong Kong 10
BE - Belgio 7
IE - Irlanda 7
AT - Austria 5
CA - Canada 4
IN - India 4
CH - Svizzera 3
ES - Italia 3
BR - Brasile 2
EC - Ecuador 2
NZ - Nuova Zelanda 2
PK - Pakistan 2
BG - Bulgaria 1
CO - Colombia 1
DK - Danimarca 1
HU - Ungheria 1
IL - Israele 1
IQ - Iraq 1
IR - Iran 1
JP - Giappone 1
LA - Repubblica Popolare Democratica del Laos 1
NG - Nigeria 1
PA - Panama 1
PH - Filippine 1
Totale 4.022
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Città #
Fairfield 507
Woodbridge 322
Chandler 287
Ashburn 233
Houston 222
Ann Arbor 207
Seattle 183
Wilmington 183
Cambridge 166
Singapore 110
Jacksonville 90
Santa Clara 75
Princeton 55
Boardman 54
San Diego 50
Padova 48
Beijing 45
Dong Ket 35
Des Moines 27
Roxbury 27
Medford 26
Helsinki 20
Nanjing 19
New York 15
Milan 13
London 11
Los Angeles 11
Hong Kong 10
Dublin 7
Hebei 7
Nanchang 7
Shenyang 7
Cagliari 6
Washington 6
Jiaxing 5
Las Vegas 5
Changsha 4
Clifton 4
Fuzhou 4
Hefei 4
Nuremberg 4
Redwood City 4
Trieste 4
Waanrode 4
Borås 3
Brescia 3
Brussels 3
Florence 3
Frankfurt am Main 3
Indiana 3
Kharkiv 3
Kunming 3
Norwalk 3
Amsterdam 2
Auburn Hills 2
Baoding 2
Carmignano Di Brenta 2
Chongqing 2
Council Bluffs 2
Dallas 2
Falls Church 2
Genoa 2
Guangzhou 2
Guardiagrele 2
Hangzhou 2
Hounslow 2
Kilburn 2
Mediglia 2
Montecchio Maggiore 2
Ningbo 2
Parma 2
Phoenix 2
Quito 2
Rockville 2
Rome 2
Shanghai 2
Southwark 2
Tianjin 2
Toronto 2
Venice 2
Vienna 2
Vivaro 2
Zhengzhou 2
Ürümqi 2
Asir 1
Baghdad 1
Bologna 1
Brendola 1
Charlotte 1
Chiswick 1
Christchurch 1
Deiva Marina 1
Elk Grove Village 1
Enschede 1
Falkenstein 1
Ferentino 1
Geneva 1
Haikou 1
Handan 1
Harbin 1
Totale 3.238
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Nome #
Diagnosis and complications of Cushing's disease: gender-related differences. 166
Diagnostic Value of Measuring Platelet Von Willebrand Factor in Von Willebrand Disease. 160
A venous thromboembolism risk assessment model for patients with Cushing’s syndrome 141
Type 2B von Willebrand disease with or without large multimers: A distinction of the two sides of the disorder is long overdue 136
Usefulness of the Total Thrombus-Formation Analysis System (T-TAS) in the diagnosis and characterization of von Willebrand disease 131
Haemostatic patterns and bleeding scores of a genetically characterised Italian family with combined haemophilia A and type 1 von Willebrand disease 131
New insight into the Hypercoagulability of Cushing's Syndrome 125
The p.R1819_C1948delinsS mutation makes von Willebrand factor ADAMTS13-resistant and reduces its collagen-binding capacity 125
Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease. 123
Loss of cysteine 584 impairs the storage and release, but not the synthesis of von Willebrand factor 122
Severe, recessive type 1 is a discrete form of von Willebrand disease: The lesson learned from the c.1534-3C>A von Willebrand factor mutation 121
von Willebrand factor propeptide makes it easy to identify the shorter von Willebrand factor survival in patients with type 1 and type Vicenza von Willebrand disease. 116
von Willebrand factor abnormalities in aortic valve stenosis:pathophysiology and impact on bleeding. 110
Higher and lower active circulating VWF levels: different facets of von Willebrand disease 109
Cryptic noncanonical splice site activation is part of the mechanism that abolishes multimer organization in the c.2269_2270del von Willebrand factor 106
Type 1 von Willebrand disease due to reduced von Willebrand factor synthesis and/or survival: observations from a case series. 103
Hypercortisolism and pregnancy upregulate von Willebrand factor through different mechanisms: report on a pregnant patient with Cushing's syndrome. 102
I polimorfismi del gene del fattore Von Willebrand (VWF) modulano l'aumento del VWF, indotto da corticosteroidi, nella sindrome di Cushing 101
A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease: An elusive phenotype and a difficult diagnosis 99
Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia. 97
The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge 97
C2362F mutation gives rise to an ADAMTS13-resistant von Willebrand factor 95
A Mechanistic Model to Quantify von Willebrand Factor Release, Survival and Proteolysis in Patients with von Willebrand Disease 95
Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease. 95
Type 2N von Willebrand disease: Characterization and diagnostic difficulties 91
Coagulopathy in Cushing's syndrome. 90
Venous thromboembolism in patients with Cushing's syndrome: need of a careful investigation of the prothrombotic risk profile. 90
Microsatellite (GT)(n) is part of the von Willebrand factor (VWF) promoter region that influences the glucocorticoid-induced increase in VWF in Cushing's syndrome. 88
Acquired von Willebrand Syndrome Hiding Inherited von Willebrand Disease Can Explain Severe Bleeding in Patients With Aortic Stenosis. 88
Type 3 von Willebrand disease mistaken for moderate haemophilia A: a lesson still to be learned 87
A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy. 86
Microsatellite (GT)(n) repeats and SNPs in the von Willebrand factor gene promoter do not influence circulating von Willebrand factor levels under normal conditions. 84
Type 1 von Willebrand disease due to a vicinal cysteine loss (p.C524Y) disclosed after a thrombotic episode 81
Two novel ITGA2B mutations in a Glanzmann thrombasthaenia family associated with different platelet phenotypic expression 79
Haplotypes of Von Willebrand factor promoter predict thrombotic risk in Cushing's syndrome 73
A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor 68
The Bleeding Assessment Tool and laboratory data in the characterisation of a female with inherited haemophilia A 64
An apparent silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease. 58
Assessment of von Willebrand factor propeptide improves the diagnosis of von Willebrand disease. 33
The lesson learned from the new c.2547-1G>T mutation combined with p.R854Q:when a type 2N mutation reveals a quantitative von Willebrand factor defect. 33
Von Willebrand disease type Vicenza: In search of a classification for the archetype of reduced von Willebrand factor survival 31
null 28
The Lesson Learned from the New c.2547-1G>T Mutation Combined with p.R854Q: When a Type 2N Mutation Reveals a Quantitative von Willebrand Factor Defect 17
Totale 4.075
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Categoria #
all - tutte 15.590
article - articoli 14.880
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 30.470
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020223 0 0 0 0 0 0 0 0 80 63 54 26
2020/2021618 28 23 18 49 27 58 47 40 103 89 58 78
2021/2022648 18 46 98 63 47 45 28 81 24 8 59 131
2022/2023502 92 75 3 73 71 66 4 34 54 3 22 5
2023/2024259 13 33 30 24 20 33 22 16 5 15 21 27
2024/2025586 15 86 48 81 150 40 36 98 32 0 0 0
Totale 4.075