IRIS
MARGAGLIONE, MAURIZIO
 Distribuzione geografica
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Continente #
EU - Europa 8.826
NA - Nord America 8.480
AS - Asia 4.078
Continente sconosciuto - Info sul continente non disponibili 28
SA - Sud America 25
OC - Oceania 13
AF - Africa 4
Totale 21.454
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Nazione #
US - Stati Uniti d'America 8.453
IE - Irlanda 3.256
CN - Cina 3.050
UA - Ucraina 2.166
SE - Svezia 1.378
IT - Italia 547
FI - Finlandia 443
IN - India 425
FR - Francia 338
TR - Turchia 338
DE - Germania 271
SG - Singapore 221
GB - Regno Unito 186
BE - Belgio 57
CZ - Repubblica Ceca 43
NL - Olanda 42
RU - Federazione Russa 42
AT - Austria 31
EU - Europa 26
CA - Canada 22
IR - Iran 14
AR - Argentina 12
JP - Giappone 7
NZ - Nuova Zelanda 7
AU - Australia 6
RO - Romania 6
CL - Cile 5
CH - Svizzera 4
PL - Polonia 4
ES - Italia 3
IQ - Iraq 3
MY - Malesia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
BR - Brasile 2
CO - Colombia 2
MX - Messico 2
NO - Norvegia 2
PA - Panama 2
PE - Perù 2
PT - Portogallo 2
TH - Thailandia 2
VN - Vietnam 2
BA - Bosnia-Erzegovina 1
BD - Bangladesh 1
BO - Bolivia 1
CY - Cipro 1
DK - Danimarca 1
EG - Egitto 1
GR - Grecia 1
GT - Guatemala 1
HR - Croazia 1
JO - Giordania 1
KR - Corea 1
MA - Marocco 1
MD - Moldavia 1
MN - Mongolia 1
NP - Nepal 1
PK - Pakistan 1
QA - Qatar 1
SD - Sudan 1
TW - Taiwan 1
VE - Venezuela 1
ZA - Sudafrica 1
Totale 21.454
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Città #
Dublin 3.255
Jacksonville 1.532
Chandler 1.268
Dearborn 1.096
Nanjing 791
Nyköping 761
Wilmington 494
Princeton 360
Nanchang 345
Beijing 320
San Mateo 300
Ann Arbor 251
Ashburn 203
Shenyang 178
Boardman 162
New York 160
Helsinki 157
Woodbridge 140
Tianjin 139
Singapore 135
Kunming 126
Hebei 122
Foggia 116
Changsha 114
Jiaxing 111
Hilden 104
Jinan 102
Des Moines 99
Hangzhou 75
Shanghai 74
Bari 62
Zhengzhou 61
Guangzhou 55
Ningbo 55
Los Angeles 53
Brussels 47
Lanzhou 42
Changchun 40
Munich 35
Brno 34
Vienna 31
Pune 30
Taizhou 26
Norwalk 25
Orange 22
Auburn Hills 21
Augusta 20
San Severo 20
London 19
Rome 19
Borås 18
Fuzhou 18
Stevenage 18
Seattle 17
Haikou 15
Wuhan 15
Milan 13
Buenos Aires 11
Falls Church 11
Hefei 11
Redwood City 11
Cedar Knolls 10
Lucera 10
Philadelphia 10
Saint Petersburg 10
Waanrode 10
Olomouc 9
Toronto 9
Washington 9
Cutrofiano 8
Florence 8
Leawood 8
Taiyuan 8
Bangalore 7
Hanover 7
Rui'an 7
Shenzhen 7
Dongyang 6
Frankfurt am Main 6
Meda 6
Palermo 6
Redmond 6
Shaoxing 6
Cepagatti 5
Chicago 5
Lecce 5
Paris 5
Strasbourg 5
Tappahannock 5
Taranto 5
Tokyo 5
Xuzhou 5
Amsterdam 4
Auckland 4
Aurora 4
Candiolo 4
Houston 4
Jinhua 4
Ottawa 4
Walnut 4
Totale 14.215
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Nome #
A Novel Mutation In HERG Gene, A490P, Found In A Large Family With Autosomal Dominant Long QT Syndrome 140
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 120
Detection of the factor V Leiden using SSCP 113
How to handle low-molecular-weight heparins in patients with decreased renal function: an open issue. 111
Preventing adverse obstetric outcomes in women with genetic thrombophilia. 107
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers. 107
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 107
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 102
Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings 102
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 101
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 100
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema. 100
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 99
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 98
Structural analysis of protein Z gene variants in patients with foetal losses 98
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo 97
In the presence of other inherited or acquired high-risk situations, the Factor V Cambridge mutation may be an additional thrombophilic risk, through its effect on APC sensitivity 96
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 95
Characterization of patients with angioedema without wheals: the importance of F12 gene screening 95
A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing 95
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 94
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 94
"Genetic modulation of oral anticoagulantion with warfarin " 91
Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis. 91
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 91
In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU 90
The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study. 89
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 89
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 88
Identification of six novel mutations in type I antithrombin deficient Italian families 88
Role of thrombophilia in adverse obstetric outcomes and their prevention using antithrombotic therapy. 88
A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency. 88
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 88
The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in presence of the FV Leiden mutation 88
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 88
A successful pregnancy in a woman with late-onset combined homocystinuria and methylmalonic aciduria 88
A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen. 87
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 87
Occurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome 87
Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations 87
FXI deficiency: two novel mutations in asymptomatic Italian patients 86
A new case of combined factor V and factor VIII deficiency further suggests that the LMAN1 M1T mutation is a frequent cause in Italian patients. 86
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 85
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 84
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 83
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 83
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism. 83
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype 83
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 83
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 82
A PC-1 amino acid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuria. 82
Coexistence of beta-thalassemia and hereditary hemochromatosis in homozygosity: a possible synergic effect? 82
A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis 82
A novel mutation of gene CBFA1/RUNX2 in Cleidocranial Dysplasia 81
A novel congenital dysprothrombinemia leading to defective prothrombin maturation 81
Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group. 80
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. 80
Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema 80
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 79
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia 79
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology. 79
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema 79
Thrombophilic genotypes, natural anticoagulants, and plasma homocysteine in myeloproliferative disorders: relationship with splanchnic vein thrombosis and arterial disease. 78
Clinical counselling in congenital fibrinogen disorders 78
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 78
A novel mutation in HERG gene, a490p, found in a large family with autosomal dominant long QT syndrome 78
Lo sport come mediatore tra mente e corpo 78
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 77
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 77
The C677T methylenetetrahydrofolate reductase gene mutation does not influence cardiovascular risk in the dialysis population: results of a multicentre prospective study 77
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 77
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 77
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 77
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 77
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 76
A six month mitotane course induced sustained correctio of hypercortisolism in a young womam with PPNAD and Carney Complex. 75
Chronic thromboembolic pulmonary hypertension. 75
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 75
The assessment of the relationship between personality, the presence of the 5htt polymorphism, and the occurrence of anxiety and depressive symptoms in elite athletes 75
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 74
The haplotype M2 within the ANXA5 gene is independently associated with the occurrence of deep venous thrombosis. 74
A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis. 74
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 74
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 74
Congenital nephrotic syndrome of Finnish type: detection of new nephrin mutations and prenatal diagnosis in an Italian family. 74
Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance. 74
Identification of GLA gene deletions in Fabry patients by Multiplex Ligation-dependent Probe Amplification (MLPA) 74
The Genetics of Hereditary Angioedema: A Review 74
Inherited platelet disorders>thrombocytopenias and thrombocytopathies. 73
Polymorphism of the angiotensin-converting enzyme gene in end-stage renal failure patients. 73
Bleeding and re-thrombosis in primary antiphospholipid syndrome on oral anticoagulation: an 8-year longitudinal comparison with mitral valve replacement and inherited thrombophilia. 73
Mutation analysis in hyperphenylalaninemia patients from South Italy. 73
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism 73
preliminary Data From the Study of Coagulative Profile of HIV infected Individuals suggest a role for point mutations in the Gene in protein S deficiency in Individuals undergoing Higly Antiretroviral therapy 73
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 73
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 72
C-reactive protein in offspring is associated with the occurrence of myocardial infarction in first-degree relatives. 72
Gene polymorphisms and sport attitude in italian athletes. 72
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 72
Survival in primary antiphospholipid syndrome: A single-centre cohort study 72
Totale 8.508
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Categoria #
all - tutte 115.790
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 115.790
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.129 0 0 0 89 543 657 859 53 402 76 403 47
2020/20212.594 349 21 331 22 330 168 364 103 468 411 11 16
2021/20222.068 302 8 35 38 276 41 47 152 267 253 158 491
2022/20236.940 732 195 268 369 363 531 33 485 3.663 37 114 150
2023/20241.143 184 70 87 41 84 285 75 75 10 21 13 198
2024/2025520 320 66 130 4 0 0 0 0 0 0 0 0
Totale 22.205