DAIDONE, VIVIANA
 Distribuzione geografica
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Continente #
NA - Nord America 3.671
AS - Asia 1.289
EU - Europa 868
AF - Africa 376
SA - Sud America 347
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 9
Totale 6.587
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Nazione #
US - Stati Uniti d'America 3.500
SG - Singapore 459
CN - Cina 272
BR - Brasile 231
IT - Italia 183
HK - Hong Kong 124
VN - Vietnam 107
DE - Germania 81
FI - Finlandia 79
SE - Svezia 73
BJ - Benin 49
GB - Regno Unito 49
PL - Polonia 36
UA - Ucraina 35
FR - Francia 32
NL - Olanda 30
RU - Federazione Russa 27
AT - Austria 26
IN - India 25
MX - Messico 25
CI - Costa d'Avorio 24
AR - Argentina 19
EC - Ecuador 18
SA - Arabia Saudita 17
TR - Turchia 17
ES - Italia 16
TZ - Tanzania 16
BE - Belgio 15
CO - Colombia 15
PK - Pakistan 15
ZA - Sudafrica 15
CA - Canada 14
DZ - Algeria 14
PE - Perù 14
PR - Porto Rico 14
AE - Emirati Arabi Uniti 13
IL - Israele 13
RS - Serbia 13
AL - Albania 12
AO - Angola 12
BY - Bielorussia 12
CL - Cile 12
DK - Danimarca 12
EE - Estonia 12
IQ - Iraq 12
JP - Giappone 12
KR - Corea 12
LA - Repubblica Popolare Democratica del Laos 12
ML - Mali 12
ZM - Zambia 12
GF - Guiana Francese 11
GH - Ghana 11
HR - Croazia 11
IE - Irlanda 11
JM - Giamaica 11
KH - Cambogia 11
LY - Libia 11
VC - Saint Vincent e Grenadine 11
AM - Armenia 10
CH - Svizzera 10
CR - Costa Rica 10
IR - Iran 10
MA - Marocco 10
VE - Venezuela 10
CU - Cuba 9
DJ - Gibuti 9
EG - Egitto 9
GE - Georgia 9
JO - Giordania 9
KG - Kirghizistan 9
ME - Montenegro 9
NO - Norvegia 9
TN - Tunisia 9
AD - Andorra 8
BD - Bangladesh 8
BF - Burkina Faso 8
GN - Guinea 8
ID - Indonesia 8
KZ - Kazakistan 8
LB - Libano 8
MG - Madagascar 8
MN - Mongolia 8
NI - Nicaragua 8
PH - Filippine 8
PY - Paraguay 8
RE - Reunion 8
TH - Thailandia 8
TJ - Tagikistan 8
UG - Uganda 8
AZ - Azerbaigian 7
BW - Botswana 7
CM - Camerun 7
ET - Etiopia 7
GA - Gabon 7
IS - Islanda 7
KE - Kenya 7
MR - Mauritania 7
MW - Malawi 7
NG - Nigeria 7
SK - Slovacchia (Repubblica Slovacca) 7
Totale 6.303
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Città #
Fairfield 507
Ashburn 385
Woodbridge 322
Singapore 294
Chandler 287
Houston 223
Ann Arbor 207
Wilmington 185
Seattle 183
Cambridge 166
Hong Kong 119
Jacksonville 91
Beijing 87
Santa Clara 81
Princeton 55
Boardman 54
San Diego 50
Cotonou 48
Padova 48
Dong Ket 35
Los Angeles 33
Des Moines 28
New York 28
Roxbury 27
Medford 26
Munich 26
Abidjan 24
Buffalo 24
Bytom 24
Helsinki 23
Ho Chi Minh City 23
Nanjing 19
São Paulo 19
Turku 17
Chicago 16
Hanoi 16
Milan 16
Vienna 15
Dar es Salaam 14
London 13
Lusaka 12
Nuremberg 12
Vientiane 12
Kingstown 11
Bamako 10
Tallinn 10
Yerevan 10
Zagreb 10
Accra 9
Amman 9
Dublin 9
Havana 9
Hefei 9
Johannesburg 9
Kingston 9
Luanda 9
Phnom Penh 9
Andorra la Vella 8
Antananarivo 8
Chennai 8
Conakry 8
Dallas 8
Dushanbe 8
Kampala 8
Lima 8
Managua 8
Ouagadougou 8
Phoenix 8
Tirana 8
Ulan Bator 8
Baku 7
Belgrade 7
Bishkek 7
Casablanca 7
Cayenne 7
Guayaquil 7
Hebei 7
Jeddah 7
Minsk 7
Nanchang 7
Nouakchott 7
Podgorica 7
Redondo Beach 7
Shenyang 7
Warsaw 7
Addis Ababa 6
Apia 6
Baghdad 6
Bridgetown 6
Cagliari 6
Castries 6
Dakar 6
Djibouti 6
Harare 6
Kigali 6
Lagos 6
Nairobi 6
Praia 6
Rio de Janeiro 6
Tel Aviv 6
Totale 4.325
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Nome #
Diagnostic Value of Measuring Platelet Von Willebrand Factor in Von Willebrand Disease. 234
Diagnosis and complications of Cushing's disease: gender-related differences. 228
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. 222
Type 2N von Willebrand disease: Characterization and diagnostic difficulties 216
A venous thromboembolism risk assessment model for patients with Cushing’s syndrome 201
Type 2B von Willebrand disease with or without large multimers: A distinction of the two sides of the disorder is long overdue 196
Loss of cysteine 584 impairs the storage and release, but not the synthesis of von Willebrand factor 189
Haemostatic patterns and bleeding scores of a genetically characterised Italian family with combined haemophilia A and type 1 von Willebrand disease 188
The p.R1819_C1948delinsS mutation makes von Willebrand factor ADAMTS13-resistant and reduces its collagen-binding capacity 187
Usefulness of the Total Thrombus-Formation Analysis System (T-TAS) in the diagnosis and characterization of von Willebrand disease 185
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 185
Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease. 175
Type 1 von Willebrand disease due to reduced von Willebrand factor synthesis and/or survival: observations from a case series. 173
Higher and lower active circulating VWF levels: different facets of von Willebrand disease 172
Cryptic noncanonical splice site activation is part of the mechanism that abolishes multimer organization in the c.2269_2270del von Willebrand factor 169
A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease: An elusive phenotype and a difficult diagnosis 167
von Willebrand factor abnormalities in aortic valve stenosis:pathophysiology and impact on bleeding. 166
New insight into the Hypercoagulability of Cushing's Syndrome 162
C2362F mutation gives rise to an ADAMTS13-resistant von Willebrand factor 161
I polimorfismi del gene del fattore Von Willebrand (VWF) modulano l'aumento del VWF, indotto da corticosteroidi, nella sindrome di Cushing 161
The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge 160
Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia. 158
Hypercortisolism and pregnancy upregulate von Willebrand factor through different mechanisms: report on a pregnant patient with Cushing's syndrome. 157
A Mechanistic Model to Quantify von Willebrand Factor Release, Survival and Proteolysis in Patients with von Willebrand Disease 154
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. 149
Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease. 149
Acquired von Willebrand Syndrome Hiding Inherited von Willebrand Disease Can Explain Severe Bleeding in Patients With Aortic Stenosis. 146
Microsatellite (GT)(n) repeats and SNPs in the von Willebrand factor gene promoter do not influence circulating von Willebrand factor levels under normal conditions. 139
A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy. 139
Venous thromboembolism in patients with Cushing's syndrome: need of a careful investigation of the prothrombotic risk profile. 139
Type 1 von Willebrand disease due to a vicinal cysteine loss (p.C524Y) disclosed after a thrombotic episode 139
Type 3 von Willebrand disease mistaken for moderate haemophilia A: a lesson still to be learned 139
Two novel ITGA2B mutations in a Glanzmann thrombasthaenia family associated with different platelet phenotypic expression 134
The Bleeding Assessment Tool and laboratory data in the characterisation of a female with inherited haemophilia A 134
Coagulopathy in Cushing's syndrome. 128
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. 126
A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor 124
An apparent silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease. 119
Haplotypes of Von Willebrand factor promoter predict thrombotic risk in Cushing's syndrome 118
Von Willebrand disease type Vicenza: In search of a classification for the archetype of reduced von Willebrand factor survival 83
Assessment of von Willebrand factor propeptide improves the diagnosis of von Willebrand disease. 73
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 68
null 28
Totale 6.640
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Categoria #
all - tutte 20.822
article - articoli 19.882
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 40.704
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021500 0 0 0 0 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
2025/20262.012 260 440 549 720 43 0 0 0 0 0 0 0
Totale 6.640