IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

MENEGATTI, MARZIA
 Distribuzione geografica
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Continente #
EU - Europa 1.664
NA - Nord America 1.247
AS - Asia 464
AF - Africa 38
SA - Sud America 25
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 1
Totale 3.454
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Nazione #
US - Stati Uniti d'America 1.203
IT - Italia 833
DE - Germania 389
CN - Cina 200
FR - Francia 90
GB - Regno Unito 90
IN - India 66
CA - Canada 37
RU - Federazione Russa 37
KR - Corea 33
IR - Iran 32
NL - Olanda 32
VN - Vietnam 24
CH - Svizzera 23
JP - Giappone 22
ES - Italia 21
UA - Ucraina 19
BE - Belgio 15
PK - Pakistan 15
AU - Australia 13
FI - Finlandia 13
IE - Irlanda 12
BR - Brasile 11
EU - Europa 10
LT - Lituania 10
ZA - Sudafrica 10
CZ - Repubblica Ceca 9
EG - Egitto 9
GR - Grecia 9
ID - Indonesia 9
PL - Polonia 9
HK - Hong Kong 8
TR - Turchia 8
IQ - Iraq 7
SA - Arabia Saudita 7
SD - Sudan 7
BG - Bulgaria 6
CL - Cile 5
DZ - Algeria 5
MX - Messico 5
NO - Norvegia 5
RO - Romania 5
SG - Singapore 5
AL - Albania 4
IL - Israele 4
JO - Giordania 4
PT - Portogallo 4
SE - Svezia 4
TH - Thailandia 4
AE - Emirati Arabi Uniti 3
AT - Austria 3
BY - Bielorussia 3
HU - Ungheria 3
MY - Malesia 3
RS - Serbia 3
VE - Venezuela 3
AR - Argentina 2
BA - Bosnia-Erzegovina 2
CO - Colombia 2
DK - Danimarca 2
KE - Kenya 2
KH - Cambogia 2
LY - Libia 2
MA - Marocco 2
MK - Macedonia 2
NZ - Nuova Zelanda 2
TW - Taiwan 2
UY - Uruguay 2
AM - Armenia 1
BD - Bangladesh 1
CU - Cuba 1
EE - Estonia 1
HR - Croazia 1
LV - Lettonia 1
ME - Montenegro 1
MQ - Martinica 1
MT - Malta 1
NP - Nepal 1
OM - Oman 1
PS - Palestinian Territory 1
QA - Qatar 1
SK - Slovacchia (Repubblica Slovacca) 1
SM - San Marino 1
TN - Tunisia 1
Totale 3.463
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Città #
Fairfield 120
Houston 94
Ashburn 80
Seattle 80
Woodbridge 78
Beijing 76
Milan 68
Buffalo 66
Ann Arbor 55
Wilmington 39
Rome 37
Cambridge 36
Mountain View 35
Santa Cruz 32
Nürnberg 29
Redmond 20
Shanghai 16
Southend 16
San Diego 15
Wuhan 15
Boardman 14
Helsinki 13
Napoli 13
Parma 13
Chicago 12
Paris 12
Kiez 11
New York 11
Reggio Nell'emilia 11
Hangzhou 10
Ottawa 10
Padova 10
Catania 9
Palermo 9
University Park 9
Bengaluru 8
Delhi 8
Hanoi 8
Los Angeles 8
Muizenberg 8
Tehran 8
Bologna 7
Bonn 7
Dublin 7
London 7
Provo 7
Toronto 7
Trieste 7
Chennai 6
Dong Ket 6
Duncan 6
Genova 6
Jakarta 6
Las Vegas 6
Naples 6
Bangalore 5
Barcelona 5
Capri 5
Castellammare Di Stabia 5
Centro 5
Cinisello Balsamo 5
Florence 5
Frankfurt am Main 5
Gambolò 5
Leawood 5
Neuchâtel 5
Phoenix 5
Riyadh 5
Seoul 5
Villaricca 5
Zurich 5
Altamura 4
Baghdad 4
Bari 4
Chapel Hill 4
Chengdu 4
Clearwater 4
Columbus 4
Frascati 4
Guangzhou 4
Hyderabad 4
Islamabad 4
Kemerovo 4
Keyport 4
Leipzig 4
Milpitas 4
Milwaukee 4
Montréal 4
New Delhi 4
Piemonte 4
Salerno 4
Singapore 4
Verona 4
Abington 3
Amsterdam 3
Ath 3
Athens 3
Atlanta 3
Boston 3
Brescia 3
Totale 1.502
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Nome #
Dalla diagnosi di portatrice di emofilia alla diagnosi prenatale, file dfa8b990-c7fe-748b-e053-3a05fe0a3a96 899
Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency, file dfa8b98f-0247-748b-e053-3a05fe0a3a96 642
Molecular characterization of an Italian patient with plasminogen deficiency and ligneous conjunctivitis, file dfa8b98e-f8db-748b-e053-3a05fe0a3a96 603
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age, file dfa8b98f-0242-748b-e053-3a05fe0a3a96 343
Establishment of a bleeding score as a diagnostic tool for patients with rare bleeding disorders, file dfa8b9a5-749d-748b-e053-3a05fe0a3a96 325
Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes, file dfa8b98f-dfce-748b-e053-3a05fe0a3a96 268
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease, file dfa8b9a2-8ee3-748b-e053-3a05fe0a3a96 122
Analysis of factor V in zebrafish demonstrates minimal levels needed for early hemostasis, file dfa8b9a0-1848-748b-e053-3a05fe0a3a96 114
An international registry of patients with plasminogen deficiency (HISTORY), file dfa8b9a1-80ac-748b-e053-3a05fe0a3a96 96
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency., file dfa8b99e-bec2-748b-e053-3a05fe0a3a96 94
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, file dfa8b9a9-cbc7-748b-e053-3a05fe0a3a96 24
Relatively poor performance of clinical laboratories for DNA analyses in the detection of two thrombophilic mutations : a cause for concern, file dfa8b990-8029-748b-e053-3a05fe0a3a96 23
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease, file dfa8b9a3-7658-748b-e053-3a05fe0a3a96 17
Treatment of rare factor deficiencies in 2016, file dfa8b9aa-7244-748b-e053-3a05fe0a3a96 12
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran, file dfa8b990-7c58-748b-e053-3a05fe0a3a96 5
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency, file dfa8b992-2780-748b-e053-3a05fe0a3a96 5
Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency, file dfa8b995-ffa7-748b-e053-3a05fe0a3a96 5
Oxidative stress is increased in primary and post-polycythemia vera myelofibrosis, file dfa8b990-61fd-748b-e053-3a05fe0a3a96 4
Introduction. Rare bleeding disorders : general aspects of clinical features, diagnosis, and management, file dfa8b990-7add-748b-e053-3a05fe0a3a96 3
Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency, file dfa8b990-7b3f-748b-e053-3a05fe0a3a96 3
Post-partum haemorrhage in women with rare bleeding disorders, file dfa8b990-7ccc-748b-e053-3a05fe0a3a96 3
A rare inherited coagulation disorder : combined homozygous factor VII and factor X deficiency, file dfa8b990-83df-748b-e053-3a05fe0a3a96 3
Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories, file dfa8b99a-bb68-748b-e053-3a05fe0a3a96 3
Recurrent mutations identified on LMAN1 and coagulation factors VII, X, XIII genes, file dfa8b990-7d81-748b-e053-3a05fe0a3a96 2
Factor X deficiency, file dfa8b990-815a-748b-e053-3a05fe0a3a96 2
Recombinant factor XIII A-subunit in a patient with factor XIII deficiency and recurrent pregnancy loss, file dfa8b99d-dda1-748b-e053-3a05fe0a3a96 2
Gynecological and obstetrical manifestations of inherited bleeding disorders in women, file dfa8b990-7c64-748b-e053-3a05fe0a3a96 1
Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency, file dfa8b990-7fb5-748b-e053-3a05fe0a3a96 1
Performance of clinical laboratories for DNA analyses to detect thrombophilia mutations, file dfa8b990-8992-748b-e053-3a05fe0a3a96 1
Prevalence of gain-of-function factor V Leiden and prothrombin G20210A in a large cohort of patients with rare bleeding disorders, file dfa8b990-b965-748b-e053-3a05fe0a3a96 1
State of the art of rare bleeding disorders database (RBDD), file dfa8b990-b967-748b-e053-3a05fe0a3a96 1
Report on ten new patients with congenital Factor X deficiency and the associated mutations, file dfa8b990-bbb0-748b-e053-3a05fe0a3a96 1
Recurrent mutations identified on LMAN1 and coagulation factors VII, X, XIII genes, file dfa8b990-bbb2-748b-e053-3a05fe0a3a96 1
Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran, file dfa8b991-efc4-748b-e053-3a05fe0a3a96 1
Reduced fibrinolytic resistance in patients with factor XI deficiency : Evidence of a thrombin-independent impairment of the thrombin-activatable fibrinolysis inhibitor pathway, file dfa8b995-e28a-748b-e053-3a05fe0a3a96 1
Minimal residual FXIII coagulant activity to prevent spontaneous major bleeding, on behalf of the PRO-RBDD group, file dfa8b997-2718-748b-e053-3a05fe0a3a96 1
Disseminated intravascular coagulation with positive D-dimer : a controversial clinical feature in severe congenital factor XIII deficiency in southeast Iran, file dfa8b997-73db-748b-e053-3a05fe0a3a96 1
Minimal factor XIII activity level to prevent major spontaneous bleeds : reply, file dfa8b99a-bd7b-748b-e053-3a05fe0a3a96 1
Genome editing of factor X in zebrafish reveals unexpected tolerance of severe defects in the common pathway, file dfa8b99b-dad8-748b-e053-3a05fe0a3a96 1
Molecular investigation of 41 patients affected by coagulation factor XI deficiency, file dfa8b99c-07c1-748b-e053-3a05fe0a3a96 1
Treatment of rare factor deficiencies other than hemophilia, file dfa8b99e-2796-748b-e053-3a05fe0a3a96 1
Totale 3.637
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Categoria #
all - tutte 5.863
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 5.863
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019131 0 0 0 0 0 0 0 0 0 33 39 59
2019/2020416 36 17 29 49 31 41 36 29 44 36 41 27
2020/2021492 31 36 66 47 51 70 36 30 24 28 36 37
2021/2022498 45 24 31 63 72 17 36 18 47 28 82 35
2022/2023345 23 23 73 48 24 32 18 21 17 24 34 8
2023/2024234 10 19 21 24 30 17 43 28 21 21 0 0
Totale 3.637