DAIDONE, VIVIANA
 Distribuzione geografica
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Continente #
NA - Nord America 3.577
AS - Asia 1.071
EU - Europa 817
SA - Sud America 327
AF - Africa 277
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 8
Totale 6.098
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Nazione #
US - Stati Uniti d'America 3.432
SG - Singapore 304
CN - Cina 255
BR - Brasile 218
IT - Italia 180
HK - Hong Kong 123
VN - Vietnam 104
DE - Germania 81
FI - Finlandia 75
SE - Svezia 73
GB - Regno Unito 48
PL - Polonia 35
FR - Francia 32
UA - Ucraina 32
NL - Olanda 30
RU - Federazione Russa 25
AT - Austria 24
MX - Messico 24
IN - India 23
CI - Costa d'Avorio 21
AR - Argentina 19
EC - Ecuador 17
ES - Italia 15
BE - Belgio 14
PE - Perù 14
SA - Arabia Saudita 14
TR - Turchia 14
TZ - Tanzania 14
AE - Emirati Arabi Uniti 13
CA - Canada 13
CO - Colombia 13
PK - Pakistan 13
DZ - Algeria 12
IQ - Iraq 12
JP - Giappone 12
PR - Porto Rico 12
CL - Cile 11
EE - Estonia 11
GF - Guiana Francese 11
IE - Irlanda 11
IL - Israele 11
LA - Repubblica Popolare Democratica del Laos 11
LY - Libia 11
ZA - Sudafrica 11
AL - Albania 10
CR - Costa Rica 10
HR - Croazia 10
JM - Giamaica 10
KH - Cambogia 10
KR - Corea 10
AM - Armenia 9
AO - Angola 9
GH - Ghana 9
IR - Iran 9
ML - Mali 9
RS - Serbia 9
VC - Saint Vincent e Grenadine 9
VE - Venezuela 9
ZM - Zambia 9
BD - Bangladesh 8
BY - Bielorussia 8
CH - Svizzera 8
CU - Cuba 8
KG - Kirghizistan 8
KZ - Kazakistan 8
MA - Marocco 8
ME - Montenegro 8
PY - Paraguay 8
UG - Uganda 8
BF - Burkina Faso 7
BW - Botswana 7
DJ - Gibuti 7
DK - Danimarca 7
GA - Gabon 7
GE - Georgia 7
KE - Kenya 7
LB - Libano 7
NG - Nigeria 7
NI - Nicaragua 7
NO - Norvegia 7
PH - Filippine 7
TH - Thailandia 7
TJ - Tagikistan 7
TN - Tunisia 7
AD - Andorra 6
AZ - Azerbaigian 6
CM - Camerun 6
EG - Egitto 6
GN - Guinea 6
ID - Indonesia 6
IS - Islanda 6
JO - Giordania 6
LV - Lettonia 6
MN - Mongolia 6
MR - Mauritania 6
NA - Namibia 6
RE - Reunion 6
RW - Ruanda 6
SK - Slovacchia (Repubblica Slovacca) 6
SY - Repubblica araba siriana 6
Totale 5.870
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Città #
Fairfield 507
Ashburn 364
Woodbridge 322
Chandler 287
Houston 222
Ann Arbor 207
Singapore 200
Wilmington 185
Seattle 183
Cambridge 166
Hong Kong 119
Jacksonville 91
Beijing 81
Santa Clara 81
Princeton 55
Boardman 54
San Diego 50
Padova 48
Dong Ket 35
Los Angeles 30
Des Moines 28
Roxbury 27
Medford 26
Munich 26
Bytom 24
Ho Chi Minh City 23
New York 23
Buffalo 22
Helsinki 22
Abidjan 21
Nanjing 19
Milan 16
São Paulo 16
Turku 16
Chicago 15
Hanoi 15
Dar es Salaam 13
London 13
Vienna 13
Nuremberg 12
Vientiane 11
Dublin 9
Hefei 9
Kingston 9
Kingstown 9
Luanda 9
Lusaka 9
Tallinn 9
Yerevan 9
Zagreb 9
Bamako 8
Chennai 8
Havana 8
Kampala 8
Lima 8
Phnom Penh 8
Phoenix 8
Tirana 8
Accra 7
Cayenne 7
Dushanbe 7
Guayaquil 7
Hebei 7
Managua 7
Nanchang 7
Ouagadougou 7
Shenyang 7
Warsaw 7
Amman 6
Andorra la Vella 6
Baghdad 6
Baku 6
Bishkek 6
Cagliari 6
Conakry 6
Djibouti 6
Harare 6
Jeddah 6
Johannesburg 6
Kigali 6
Lagos 6
Nairobi 6
Nouakchott 6
Podgorica 6
Rio de Janeiro 6
Tel Aviv 6
Ulan Bator 6
Washington 6
Abu Dhabi 5
Addis Ababa 5
Antananarivo 5
Bangkok 5
Belgrade 5
Boston 5
Casablanca 5
Castries 5
Changsha 5
Council Bluffs 5
Dakar 5
Dallas 5
Totale 4.083
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Nome #
Diagnostic Value of Measuring Platelet Von Willebrand Factor in Von Willebrand Disease. 218
Diagnosis and complications of Cushing's disease: gender-related differences. 216
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. 212
Type 2N von Willebrand disease: Characterization and diagnostic difficulties 200
A venous thromboembolism risk assessment model for patients with Cushing’s syndrome 191
Type 2B von Willebrand disease with or without large multimers: A distinction of the two sides of the disorder is long overdue 182
Haemostatic patterns and bleeding scores of a genetically characterised Italian family with combined haemophilia A and type 1 von Willebrand disease 176
Loss of cysteine 584 impairs the storage and release, but not the synthesis of von Willebrand factor 175
Usefulness of the Total Thrombus-Formation Analysis System (T-TAS) in the diagnosis and characterization of von Willebrand disease 174
The p.R1819_C1948delinsS mutation makes von Willebrand factor ADAMTS13-resistant and reduces its collagen-binding capacity 174
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 172
Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease. 164
Type 1 von Willebrand disease due to reduced von Willebrand factor synthesis and/or survival: observations from a case series. 163
Higher and lower active circulating VWF levels: different facets of von Willebrand disease 157
Cryptic noncanonical splice site activation is part of the mechanism that abolishes multimer organization in the c.2269_2270del von Willebrand factor 157
A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease: An elusive phenotype and a difficult diagnosis 152
New insight into the Hypercoagulability of Cushing's Syndrome 150
von Willebrand factor abnormalities in aortic valve stenosis:pathophysiology and impact on bleeding. 150
I polimorfismi del gene del fattore Von Willebrand (VWF) modulano l'aumento del VWF, indotto da corticosteroidi, nella sindrome di Cushing 150
C2362F mutation gives rise to an ADAMTS13-resistant von Willebrand factor 148
Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia. 146
The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge 146
Hypercortisolism and pregnancy upregulate von Willebrand factor through different mechanisms: report on a pregnant patient with Cushing's syndrome. 146
A Mechanistic Model to Quantify von Willebrand Factor Release, Survival and Proteolysis in Patients with von Willebrand Disease 144
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. 142
Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease. 142
Acquired von Willebrand Syndrome Hiding Inherited von Willebrand Disease Can Explain Severe Bleeding in Patients With Aortic Stenosis. 135
A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy. 130
Type 1 von Willebrand disease due to a vicinal cysteine loss (p.C524Y) disclosed after a thrombotic episode 128
Venous thromboembolism in patients with Cushing's syndrome: need of a careful investigation of the prothrombotic risk profile. 127
Two novel ITGA2B mutations in a Glanzmann thrombasthaenia family associated with different platelet phenotypic expression 126
Type 3 von Willebrand disease mistaken for moderate haemophilia A: a lesson still to be learned 126
Microsatellite (GT)(n) repeats and SNPs in the von Willebrand factor gene promoter do not influence circulating von Willebrand factor levels under normal conditions. 125
The Bleeding Assessment Tool and laboratory data in the characterisation of a female with inherited haemophilia A 120
Coagulopathy in Cushing's syndrome. 119
A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor 112
Haplotypes of Von Willebrand factor promoter predict thrombotic risk in Cushing's syndrome 111
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. 110
An apparent silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease. 107
Von Willebrand disease type Vicenza: In search of a classification for the archetype of reduced von Willebrand factor survival 76
Assessment of von Willebrand factor propeptide improves the diagnosis of von Willebrand disease. 68
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 56
null 28
Totale 6.151
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Categoria #
all - tutte 20.069
article - articoli 19.152
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 39.221
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021549 0 0 0 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
2024/20251.139 15 86 48 81 150 40 36 98 82 32 180 291
2025/20261.523 260 440 549 274 0 0 0 0 0 0 0 0
Totale 6.151