IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

MENEGATTI, MARZIA
 Distribuzione geografica
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Continente #
EU - Europa 5.513
NA - Nord America 4.654
AS - Asia 4.125
SA - Sud America 414
AF - Africa 124
OC - Oceania 37
Continente sconosciuto - Info sul continente non disponibili 8
Totale 14.875
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Nazione #
US - Stati Uniti d'America 4.456
GB - Regno Unito 1.823
SG - Singapore 1.270
CN - Cina 1.240
IT - Italia 841
DE - Germania 709
SE - Svezia 520
RU - Federazione Russa 452
HK - Hong Kong 333
BR - Brasile 273
BD - Bangladesh 259
FR - Francia 237
VN - Vietnam 222
IN - India 221
NL - Olanda 218
TR - Turchia 169
UA - Ucraina 158
IE - Irlanda 147
CA - Canada 125
FI - Finlandia 121
KR - Corea 113
EU - Europa 82
ID - Indonesia 65
ES - Italia 51
CO - Colombia 47
JP - Giappone 47
IR - Iran 46
DK - Danimarca 45
MX - Messico 41
AR - Argentina 38
AU - Australia 30
BE - Belgio 30
TN - Tunisia 24
PL - Polonia 23
GR - Grecia 20
IQ - Iraq 20
CI - Costa d'Avorio 19
EG - Egitto 18
CH - Svizzera 17
PK - Pakistan 16
AT - Austria 14
SA - Arabia Saudita 14
TH - Thailandia 14
VE - Venezuela 14
CL - Cile 13
ZA - Sudafrica 13
BG - Bulgaria 12
PT - Portogallo 12
UZ - Uzbekistan 12
PE - Perù 11
DZ - Algeria 10
RO - Romania 9
AE - Emirati Arabi Uniti 8
EC - Ecuador 8
HU - Ungheria 8
KE - Kenya 8
MA - Marocco 8
JO - Giordania 7
SK - Slovacchia (Repubblica Slovacca) 7
NZ - Nuova Zelanda 6
PA - Panama 6
PH - Filippine 6
CR - Costa Rica 5
LT - Lituania 5
MY - Malesia 5
TW - Taiwan 5
AL - Albania 4
CZ - Repubblica Ceca 4
GT - Guatemala 4
HR - Croazia 4
IL - Israele 4
NO - Norvegia 4
NP - Nepal 4
UY - Uruguay 4
AZ - Azerbaigian 3
DO - Repubblica Dominicana 3
ET - Etiopia 3
JM - Giamaica 3
LU - Lussemburgo 3
MD - Moldavia 3
NG - Nigeria 3
NI - Nicaragua 3
OM - Oman 3
PS - Palestinian Territory 3
PY - Paraguay 3
SN - Senegal 3
AF - Afghanistan, Repubblica islamica di 2
BH - Bahrain 2
BO - Bolivia 2
BY - Bielorussia 2
BZ - Belize 2
EE - Estonia 2
GA - Gabon 2
KW - Kuwait 2
LV - Lettonia 2
ML - Mali 2
MU - Mauritius 2
RS - Serbia 2
SV - El Salvador 2
SY - Repubblica araba siriana 2
Totale 14.922
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Città #
Southend 1.641
Singapore 754
Ashburn 445
Chandler 339
Hong Kong 309
San Jose 286
Seattle 279
Milan 273
Beijing 245
Hanover 242
Dallas 197
Princeton 183
Council Bluffs 158
Wilmington 154
Dublin 147
Jacksonville 139
Fairfield 128
Frankfurt am Main 113
Los Angeles 109
Ann Arbor 101
Bengaluru 90
Shanghai 90
Woodbridge 86
Mountain View 85
Lauterbourg 84
New York 82
Nanjing 79
Santa Clara 76
Redmond 72
Des Moines 69
Moscow 67
Boardman 64
Ottawa 64
Houston 60
Buffalo 58
Dearborn 58
Ho Chi Minh City 55
Guangzhou 54
Hanoi 53
Rome 47
Cambridge 46
Cangzhou 43
Sakarya 43
Serra 43
Phoenix 42
Somerville 42
Bogotá 40
São Paulo 39
Centro 38
Jakarta 37
Jinan 36
Andover 34
Hefei 34
Pisa 34
Helsinki 32
Redwood City 32
Columbus 31
Tokyo 31
Shenyang 30
Roxbury 27
The Dalles 26
San Diego 25
Tianjin 25
Turin 25
Seoul 24
Hangzhou 23
Berlin 21
Istanbul 19
Nanchang 19
Abidjan 18
Saint Petersburg 18
Shenzhen 18
Brussels 17
Medford 17
Warsaw 17
Athens 16
Bitonto 16
Changsha 16
Eitensheim 16
Hebei 16
Jiaxing 16
Kunming 16
Zhengzhou 16
Ankara 15
Orem 15
Paris 15
Bristol 14
Chennai 14
Da Nang 14
London 14
Bologna 13
Munich 13
Toronto 13
Düsseldorf 12
Mumbai 12
Dong Ket 11
Montreal 11
Naples 11
Nuremberg 11
Turku 11
Totale 9.028
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Nome #
Establishment of a bleeding score as a diagnostic tool for patients with rare bleeding disorders 516
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age 395
European Network of Rare Bleeding Disorders (EN-RBD) 384
Treatment of rare factor deficiencies other than hemophilia 379
Molecular characterization of an Italian patient with plasminogen deficiency and ligneous conjunctivitis 367
Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency 360
Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes 318
Oxidative stress is increased in primary and post-polycythemia vera myelofibrosis 276
Genetic diagnosis of haemophilia and other inherited bleeding disorders 267
International Rare Bleeding Disorders Database 262
Genetics of rare bleeding disorders 245
An international registry of patients with plasminogen deficiency (HISTORY) 242
Analysis of factor V in zebrafish demonstrates minimal levels needed for early hemostasis 237
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 232
Database on rare bleeding disorder (RBDS) : phenotype and genotype analysis on 400 affected patients 229
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency. 216
Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein 209
A rare inherited coagulation disorder : combined homozygous factor VII and factor X deficiency 205
Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency 205
Dalla diagnosi di portatrice di emofilia alla diagnosi prenatale 203
State of the art of rare bleeding disorders database (RBDD) 202
Effect of adenosine derivatives on in vitro thrombus formation induced by shear stress 201
Rare bleeding disorders 200
Future perspective of international registry on rare inherited bleeding disorder 196
Establishment of a European network of Rare Bleeding Disorders (RBDs) 193
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 193
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database 190
International Registry of rare bleeding disorders (RBD) 188
Recurrent mutations identified on LMAN1 and coagulation factors VII, X, XIII genes 187
Molecular characterization in an Italian patient with plasminogen deficiency and ligneous conjunctivitis 180
Introduction. Rare bleeding disorders : general aspects of clinical features, diagnosis, and management 174
Performance of clinical laboratories for DNA analyses to detect thrombophilia mutations 173
Kinetics studies of a naturally occurring mutation on Factor X (FX) gene (G222D) 173
Factor X deficiency 168
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders : results from the European Network of Rare Bleeding Disorders 167
Relatively poor performance of clinical laboratories for DNA analyses in the detection of two thrombophilic mutations : a cause for concern 164
Association between thrombin generation and bleeding severity in 41 patients with coagulation factor VII deficiency 160
Molecular characterization in an Italian patient with plasminogen deficiency and ligneous conjunctivitis 159
Italian experience in the assessment of performance of clinical laboratories for DNA analyses to detect three thrombophilic mutations 158
Post-partum haemorrhage in women with rare bleeding disorders 158
Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency 155
Two adjacent homozygous mutations on EGF2 domain of factor X (FX) gene lead to severe FX deficiency 155
European registry of rare bleeding disorders 155
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene 155
Establishment of a European network of rare bleeding disorders 152
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene 152
Diagnosis of FXIII deficiency: data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories 150
Rare bleeding disorders: worldwide efforts for classification, diagnosis, and management 149
Factor XIII deficiency : preliminary results of the PRO-RBDD project 149
Genotype analysis of rare coagulation factor deficiency cases from India 146
Thrombin Generation in Patients with Idiopathic Sudden Sensorineural Hearing Loss 145
Diagnostic utility of bleeding assessment tools in congenital fibrinogen deficiencies 144
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran 144
The role of factor X in blood coagulation : clinical, phenotypic and molecular analysis of a severe rare bleeding disorder 144
Effect of prothrombin 19911 A>G polymorphism on the risk of cerebral sinus-venous thrombosis 144
Molecular evaluation of a naturally occuring mutation on Factor X gene (Gly222Asp) causing severe FX deficiency 139
A recurrent Gly43Asp substitution of coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking 137
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 135
Gynecological and obstetrical manifestations of inherited bleeding disorders in women 133
In vitro expression studies and immunofluorescence microscopy analysis of two naturally occuring mutations on Factor X (FX) gene (G94R and D95E) 131
Rare inherited coagulation disorders: no longer orphan and neglected 130
Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran 128
Detection of Factor XIII deficiency: data from multicentre exercises amongst UK NEQAS and PRO-RBDD project laboratories 128
Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories 125
Recurrent mutations identified on LMAN1 and coagulation factors VII, X, XIII genes 124
In Vitro Expression Studies And Immunofluorescence Microscopy Analysis Of Two Naturally Occurring Mutations On Factor X (FX) Gene (G94R And D95E) 122
Prevalence of gain-of-function factor V Leiden and prothrombin G20210A in a large cohort of patients with rare bleeding disorders 118
Reduced fibrinolytic resistance in patients with factor XI deficiency : Evidence of a thrombin-independent impairment of the thrombin-activatable fibrinolysis inhibitor pathway 117
Inherited bleeding disorders in pregnancy : rare coagulation factor defects 117
Retrospective evaluation of bleeding tendency and simultaneous thrombin and plasmin generation in patients with rare bleeding disorders 116
Disseminated intravascular coagulation with positive D-dimer : a controversial clinical feature in severe congenital factor XIII deficiency in southeast Iran 116
Registri nazionali ed internazionali sulle malattie rare della coagulazione 112
Combined Factor V and Factor VIII Deficiency in Rare Coagulation Disorders 112
Recombinant factor XIII A-subunit in a patient with factor XIII deficiency and recurrent pregnancy loss 112
Rare bleeding disorders 111
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) 111
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 108
Genome editing of factor X in zebrafish reveals unexpected tolerance of severe defects in the common pathway 105
Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database 98
Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency 97
A recurrent Gly43Asp substitution in coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking 97
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 95
Report on ten new patients with congenital Factor X deficiency and the associated mutations 94
Minimal residual FXIII coagulant activity to prevent spontaneous major bleeding, on behalf of the PRO-RBDD group 92
Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran 90
Inherited bleeding disorders in pregnancy: rare coagulation factor defects 88
Minimal factor XIII activity level to prevent major spontaneous bleeds : reply 88
Rare bleeding disorders 81
The genetic spectrum of rare bleeding disorders 79
Treatment of rare factor deficiencies in 2016 79
Neonatal onset of congenital factor X deficiency : a description of two novel mutations with 6-year follow-up 78
Clinical, Laboratory Aspects and Management of Factor X Deficiency 76
Management of rare acquired bleeding disorders 37
Rare coagulation defects 27
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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Totale 15.676
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Categoria #
all - tutte 40.286
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 40.286
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202173 0 0 0 0 0 0 0 0 0 0 0 73
2021/20221.196 81 60 37 76 88 73 111 75 106 141 94 254
2022/20231.388 173 133 118 137 155 267 37 136 139 23 59 11
2023/2024807 30 78 34 32 175 95 42 68 22 41 75 115
2024/20252.107 102 208 59 171 159 80 78 234 131 233 180 472
2025/20264.324 452 214 421 412 493 305 416 186 435 354 475 161
Totale 15.679