IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

MENEGATTI, MARZIA
 Distribuzione geografica
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Continente #
EU - Europa 4154
NA - Nord America 2517
AS - Asia 992
SA - Sud America 60
AF - Africa 22
OC - Oceania 17
Continente sconosciuto - Info sul continente non disponibili 7
Totale 7769
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Nazione #
US - Stati Uniti d'America 2428
GB - Regno Unito 1743
IT - Italia 581
CN - Cina 562
DE - Germania 511
SE - Svezia 508
UA - Ucraina 150
IE - Irlanda 146
TR - Turchia 124
FR - Francia 108
RU - Federazione Russa 106
KR - Corea 93
CA - Canada 83
EU - Europa 82
NL - Olanda 73
FI - Finlandia 71
IN - India 70
IR - Iran 35
CO - Colombia 34
DK - Danimarca 34
BE - Belgio 29
ID - Indonesia 23
VN - Vietnam 22
GR - Grecia 17
AU - Australia 16
ES - Italia 16
JP - Giappone 14
CH - Svizzera 11
BG - Bulgaria 10
AR - Argentina 9
BR - Brasile 9
EG - Egitto 9
HK - Hong Kong 9
DZ - Algeria 6
RO - Romania 6
SA - Arabia Saudita 6
SG - Singapore 6
PL - Polonia 5
PT - Portogallo 5
SK - Slovacchia (Repubblica Slovacca) 5
LT - Lituania 4
MX - Messico 4
TH - Thailandia 4
TW - Taiwan 4
UZ - Uzbekistan 4
AE - Emirati Arabi Uniti 3
CL - Cile 3
HR - Croazia 3
NO - Norvegia 3
BZ - Belize 2
CZ - Repubblica Ceca 2
HU - Ungheria 2
IL - Israele 2
IQ - Iraq 2
KW - Kuwait 2
LV - Lettonia 2
PK - Pakistan 2
TN - Tunisia 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AT - Austria 1
EC - Ecuador 1
LU - Lussemburgo 1
MA - Marocco 1
MM - Myanmar 1
MU - Mauritius 1
MY - Malesia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
OM - Oman 1
PE - Perù 1
PS - Palestinian Territory 1
SC - Seychelles 1
SD - Sudan 1
SI - Slovenia 1
UY - Uruguay 1
ZA - Sudafrica 1
Totale 7845
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Città #
Southend 1641
Chandler 339
Seattle 264
Hanover 241
Milan 226
Princeton 183
Wilmington 153
Dublin 146
Beijing 140
Jacksonville 139
Fairfield 128
Ann Arbor 100
Woodbridge 86
Mountain View 85
Nanjing 75
Redmond 72
Des Moines 68
Ottawa 61
Dearborn 58
Ashburn 55
Houston 55
Shanghai 49
Boardman 44
Cambridge 43
Sakarya 43
Serra 42
Somerville 42
Centro 38
Bogotá 34
Pisa 34
Andover 33
Phoenix 33
Jinan 32
Redwood City 32
Shenyang 29
Roxbury 27
Guangzhou 21
San Diego 21
Brussels 18
Saint Petersburg 18
Nanchang 17
Turin 17
Bitonto 16
Hebei 16
Jiaxing 16
Kunming 16
Medford 16
Rome 15
Athens 14
Changsha 13
Zhengzhou 13
Hangzhou 12
Dong Ket 11
Tianjin 11
Toronto 11
Berlin 10
Kiez 10
Istanbul 9
Lanzhou 8
Verona 8
Falls Church 7
Ningbo 7
Nürnberg 7
Auburn Hills 6
Bangalore 6
Bologna 6
Grafing 6
London 6
Paris 6
Taizhou 6
Waanrode 6
Ankara 5
Delhi 5
Ferrara 5
Florence 5
Haikou 5
Hefei 5
Lincoln 5
Melbourne 5
Munich 5
Noginsk 5
Qualiano 5
Seoul 5
Silver Spring 5
Warsaw 5
Central 4
Central District 4
Chennai 4
Cupertino 4
Gussago 4
Margão 4
Medicine Hat 4
Milwaukee 4
Norwalk 4
Pars 4
San Francisco 4
San Jose 4
São Paulo 4
Tehran 4
Tennyson 4
Totale 5406
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Nome #
Treatment of rare factor deficiencies other than hemophilia 288
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age 268
Molecular characterization of an Italian patient with plasminogen deficiency and ligneous conjunctivitis 248
Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency 241
Establishment of a bleeding score as a diagnostic tool for patients with rare bleeding disorders 224
Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes 185
International Rare Bleeding Disorders Database 171
Genetics of rare bleeding disorders 167
European Network of Rare Bleeding Disorders (EN-RBD) 158
Effect of adenosine derivatives on in vitro thrombus formation induced by shear stress 153
Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein 143
Genetic diagnosis of haemophilia and other inherited bleeding disorders 142
Future perspective of international registry on rare inherited bleeding disorder 142
A rare inherited coagulation disorder : combined homozygous factor VII and factor X deficiency 139
Database on rare bleeding disorder (RBDS) : phenotype and genotype analysis on 400 affected patients 139
International Registry of rare bleeding disorders (RBD) 132
Rare bleeding disorders 131
Recurrent mutations identified on LMAN1 and coagulation factors VII, X, XIII genes 120
Performance of clinical laboratories for DNA analyses to detect thrombophilia mutations 116
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 115
Relatively poor performance of clinical laboratories for DNA analyses in the detection of two thrombophilic mutations : a cause for concern 114
Establishment of a European network of Rare Bleeding Disorders (RBDs) 114
Analysis of factor V in zebrafish demonstrates minimal levels needed for early hemostasis 113
Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency 111
Two adjacent homozygous mutations on EGF2 domain of factor X (FX) gene lead to severe FX deficiency 111
Oxidative stress is increased in primary and post-polycythemia vera myelofibrosis 109
Molecular evaluation of a naturally occuring mutation on Factor X gene (Gly222Asp) causing severe FX deficiency 106
Kinetics studies of a naturally occurring mutation on Factor X (FX) gene (G222D) 106
Dalla diagnosi di portatrice di emofilia alla diagnosi prenatale 106
Molecular characterization in an Italian patient with plasminogen deficiency and ligneous conjunctivitis 104
Genotype analysis of rare coagulation factor deficiency cases from India 104
State of the art of rare bleeding disorders database (RBDD) 100
Establishment of a European network of rare bleeding disorders 99
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders : results from the European Network of Rare Bleeding Disorders 99
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene 99
Association between thrombin generation and bleeding severity in 41 patients with coagulation factor VII deficiency 99
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency. 99
Post-partum haemorrhage in women with rare bleeding disorders 98
Italian experience in the assessment of performance of clinical laboratories for DNA analyses to detect three thrombophilic mutations 97
Molecular characterization in an Italian patient with plasminogen deficiency and ligneous conjunctivitis 97
Effect of prothrombin 19911 A>G polymorphism on the risk of cerebral sinus-venous thrombosis 97
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene 97
A recurrent Gly43Asp substitution of coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking 93
An international registry of patients with plasminogen deficiency (HISTORY) 92
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran 89
Introduction. Rare bleeding disorders : general aspects of clinical features, diagnosis, and management 87
In Vitro Expression Studies And Immunofluorescence Microscopy Analysis Of Two Naturally Occurring Mutations On Factor X (FX) Gene (G94R And D95E) 87
In vitro expression studies and immunofluorescence microscopy analysis of two naturally occuring mutations on Factor X (FX) gene (G94R and D95E) 85
Factor X deficiency 84
Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency 84
European registry of rare bleeding disorders 84
Rare bleeding disorders: worldwide efforts for classification, diagnosis, and management 83
Diagnosis of FXIII deficiency: data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories 82
Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran 80
The role of factor X in blood coagulation : clinical, phenotypic and molecular analysis of a severe rare bleeding disorder 80
Rare bleeding disorders 75
Registri nazionali ed internazionali sulle malattie rare della coagulazione 75
Prevalence of gain-of-function factor V Leiden and prothrombin G20210A in a large cohort of patients with rare bleeding disorders 70
Gynecological and obstetrical manifestations of inherited bleeding disorders in women 68
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 68
Factor XIII deficiency : preliminary results of the PRO-RBDD project 67
Thrombin Generation in Patients with Idiopathic Sudden Sensorineural Hearing Loss 65
Combined Factor V and Factor VIII Deficiency in Rare Coagulation Disorders 65
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 62
Retrospective evaluation of bleeding tendency and simultaneous thrombin and plasmin generation in patients with rare bleeding disorders 61
Inherited bleeding disorders in pregnancy : rare coagulation factor defects 61
Recurrent mutations identified on LMAN1 and coagulation factors VII, X, XIII genes 60
Patients Informative Booklet on the Establishment of a European Network of Rare Bleeding Disorders (EN-RBD) project funded by EC (downloadable at www.rbdd.eu) 59
Report on ten new patients with congenital Factor X deficiency and the associated mutations 58
Disseminated intravascular coagulation with positive D-dimer : a controversial clinical feature in severe congenital factor XIII deficiency in southeast Iran 55
Detection of Factor XIII deficiency: data from multicentre exercises amongst UK NEQAS and PRO-RBDD project laboratories 55
A recurrent Gly43Asp substitution in coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking 54
Inherited bleeding disorders in pregnancy: rare coagulation factor defects 48
Neonatal onset of congenital factor X deficiency : a description of two novel mutations with 6-year follow-up 47
Minimal residual FXIII coagulant activity to prevent spontaneous major bleeding, on behalf of the PRO-RBDD group 46
Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran 45
Reduced fibrinolytic resistance in patients with factor XI deficiency : Evidence of a thrombin-independent impairment of the thrombin-activatable fibrinolysis inhibitor pathway 44
Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories 44
Rare bleeding disorders 41
Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency 39
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 36
Minimal factor XIII activity level to prevent major spontaneous bleeds : reply 34
Genome editing of factor X in zebrafish reveals unexpected tolerance of severe defects in the common pathway 28
Recombinant factor XIII A-subunit in a patient with factor XIII deficiency and recurrent pregnancy loss 22
A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family 20
Treatment of rare factor deficiencies in 2016 15
Recurrent mutations identified on LMAN1 and coagulation factors VII, X, XIII genes 6
Two adjacent homozygous mutations on EGF2 domain of factor X (FX) gene lead to severe FX deficiency 6
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Rare coagulation defects 1
Totale 8425
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Categoria #
all - tutte 13197
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 13197
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/2018114 0000 00 00 009123
2018/20191082 2366775111 1095 13059 835911839
2019/2020998 135214861 56128 9534 1721525937
2020/20211106 749111417 11488 8958 949020473
2021/20221196 81603776 8873 11175 10614194254
2022/20231372 173133118137 155267 38137 14025490
Totale 8425