GALLINARO, LISA
 Distribuzione geografica
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Continente #
NA - Nord America 926
AS - Asia 143
EU - Europa 117
Totale 1.186
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Nazione #
US - Stati Uniti d'America 923
CN - Cina 67
SG - Singapore 49
IT - Italia 26
VN - Vietnam 23
FI - Finlandia 19
GB - Regno Unito 15
SE - Svezia 12
DE - Germania 9
NL - Olanda 8
UA - Ucraina 8
FR - Francia 7
RU - Federazione Russa 7
CA - Canada 3
BE - Belgio 2
HK - Hong Kong 2
IE - Irlanda 2
TR - Turchia 2
ES - Italia 1
HU - Ungheria 1
Totale 1.186
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Città #
Fairfield 152
Woodbridge 83
Chandler 81
Houston 73
Ashburn 58
Seattle 58
Cambridge 57
Wilmington 54
Jacksonville 46
Singapore 40
Ann Arbor 30
Princeton 29
Dong Ket 23
Santa Clara 23
Boardman 15
San Diego 15
Beijing 11
Padova 10
Roxbury 9
Guangzhou 8
Nanjing 8
Helsinki 5
Washington 5
Changsha 4
Hebei 4
Milan 4
Norwalk 3
Brussels 2
Dublin 2
Hong Kong 2
Indiana 2
Istanbul 2
London 2
New York 2
Southwark 2
Budapest 1
Chongqing 1
Dallas 1
Des Moines 1
Edinburgh 1
Florence 1
Hefei 1
Islington 1
Jiaxing 1
Linyi 1
Los Angeles 1
Madrid 1
Medford 1
Nanchang 1
Prescot 1
Redwood City 1
Shanghai 1
Shenyang 1
Simi Valley 1
Stockholm 1
Toronto 1
Trento 1
Totale 946
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Nome #
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. 113
Type 1 von Willebrand disease due to reduced von Willebrand factor synthesis and/or survival: observations from a case series. 99
A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease: An elusive phenotype and a difficult diagnosis 97
Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia. 94
Diagnosis and follow-up of thrombotic thrombocytopenic purpura by means of von Willebrand factor collagen binding assay. 94
Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease. 91
Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease. 87
Uneventful coronary artery bypass surgery without prophylatic replacement therapy in a patient with a novel heterozygous FVII gene deletion 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. 82
Combined exon skipping and cryptic splice activation as a new molecular mechanism for recessive type 1 von Willebrand disease. 81
A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy. 81
Altered von Willebrand factor subunit proteolysis and multimer processing associated with the Cys236Phe mutation in the B2 domain 76
An apparent silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease. 55
Identifying carriers of type 2N von Willebrand disease: procedures and significance. 51
Totale 1.187
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Categoria #
all - tutte 5.009
article - articoli 5.009
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 10.018
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020100 0 0 0 0 0 0 18 27 22 14 9 10
2020/2021188 7 9 0 24 6 34 8 13 31 11 15 30
2021/2022191 6 17 38 11 5 10 11 20 8 1 33 31
2022/2023160 30 17 2 16 27 18 0 13 24 0 12 1
2023/202486 7 15 17 2 12 7 7 3 1 1 5 9
2024/2025153 0 33 21 27 48 15 9 0 0 0 0 0
Totale 1.187