IRIS
MARGAGLIONE, MAURIZIO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 8.477
NA - Nord America 8.288
AS - Asia 3.589
Continente sconosciuto - Info sul continente non disponibili 27
SA - Sud America 22
OC - Oceania 13
AF - Africa 3
Totale 20.419
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 8.265
IE - Irlanda 3.084
CN - Cina 2.787
UA - Ucraina 2.166
SE - Svezia 1.344
IT - Italia 524
IN - India 424
FI - Finlandia 419
FR - Francia 338
TR - Turchia 338
DE - Germania 227
GB - Regno Unito 181
BE - Belgio 57
NL - Olanda 41
RU - Federazione Russa 40
AT - Austria 31
EU - Europa 26
CA - Canada 20
AR - Argentina 12
IR - Iran 12
JP - Giappone 7
NZ - Nuova Zelanda 7
AU - Australia 6
RO - Romania 6
SG - Singapore 6
CL - Cile 5
CH - Svizzera 4
PL - Polonia 4
ES - Italia 3
IQ - Iraq 3
BR - Brasile 2
CO - Colombia 2
MX - Messico 2
MY - Malesia 2
NO - Norvegia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BD - Bangladesh 1
CZ - Repubblica Ceca 1
EG - Egitto 1
GR - Grecia 1
GT - Guatemala 1
HR - Croazia 1
KR - Corea 1
MD - Moldavia 1
MN - Mongolia 1
PK - Pakistan 1
PT - Portogallo 1
QA - Qatar 1
SD - Sudan 1
TH - Thailandia 1
TW - Taiwan 1
VE - Venezuela 1
VN - Vietnam 1
ZA - Sudafrica 1
Totale 20.419
Salva come PNG Salva come JPEG
Città #
Dublin 3.083
Jacksonville 1.532
Chandler 1.259
Dearborn 1.096
Nanjing 789
Nyköping 735
Wilmington 485
Nanchang 345
Princeton 340
Beijing 316
San Mateo 300
Ann Arbor 251
Ashburn 193
Shenyang 178
New York 158
Woodbridge 140
Tianjin 139
Helsinki 133
Kunming 126
Hebei 122
Boardman 118
Foggia 116
Changsha 114
Hilden 104
Jinan 100
Jiaxing 99
Des Moines 95
Hangzhou 75
Zhengzhou 61
Ningbo 55
Bari 51
Brussels 47
Lanzhou 42
Changchun 40
Los Angeles 31
Shanghai 31
Vienna 31
Pune 30
Guangzhou 26
Taizhou 26
Norwalk 22
Orange 22
Auburn Hills 21
Augusta 20
Rome 19
San Severo 19
Borås 18
Fuzhou 18
Seattle 17
Stevenage 17
London 16
Haikou 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
Toronto 9
Cutrofiano 8
Florence 8
Leawood 8
Taiyuan 8
Bangalore 7
Washington 7
Meda 6
Palermo 6
Cepagatti 5
Chicago 5
Hanover 5
Lecce 5
Paris 5
Redmond 5
Shaoxing 5
Strasbourg 5
Tappahannock 5
Taranto 5
Tokyo 5
Amsterdam 4
Auckland 4
Aurora 4
Candiolo 4
Houston 4
Walnut 4
Baghdad 3
Bologna 3
Brescia 3
Castelvetrano 3
Genoa 3
Grottaglie 3
Mola di Bari 3
Mountain View 3
Naples 3
Nutley 3
Ottawa 3
Padova 3
Totale 13.525
Salva come PNG Salva come JPEG
Nome #
A Novel Mutation In HERG Gene, A490P, Found In A Large Family With Autosomal Dominant Long QT Syndrome 131
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 119
Detection of the factor V Leiden using SSCP 111
How to handle low-molecular-weight heparins in patients with decreased renal function: an open issue. 108
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 107
Preventing adverse obstetric outcomes in women with genetic thrombophilia. 103
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers. 103
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 101
Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings 100
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 100
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 98
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema. 98
Structural analysis of protein Z gene variants in patients with foetal losses 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 95
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo 94
Characterization of patients with angioedema without wheals: the importance of F12 gene screening 94
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 94
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 93
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 93
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 92
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 92
A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing 92
Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis. 90
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 90
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 88
The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study. 88
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 88
Identification of six novel mutations in type I antithrombin deficient Italian families 87
"Genetic modulation of oral anticoagulantion with warfarin " 87
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 87
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 87
In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU 87
FXI deficiency: two novel mutations in asymptomatic Italian patients 86
Role of thrombophilia in adverse obstetric outcomes and their prevention using antithrombotic therapy. 85
A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen. 85
Occurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome 85
Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations 85
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 84
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 84
A successful pregnancy in a woman with late-onset combined homocystinuria and methylmalonic aciduria 84
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. 83
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 83
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 83
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism. 82
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 81
A PC-1 amino acid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuria. 81
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. 81
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 81
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 80
Coexistence of beta-thalassemia and hereditary hemochromatosis in homozygosity: a possible synergic effect? 80
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype 80
Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group. 79
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 79
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 78
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. 78
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology. 78
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema 78
A novel congenital dysprothrombinemia leading to defective prothrombin maturation 78
Thrombophilic genotypes, natural anticoagulants, and plasma homocysteine in myeloproliferative disorders: relationship with splanchnic vein thrombosis and arterial disease. 77
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia 77
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 77
A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis 77
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 76
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 76
A novel mutation of gene CBFA1/RUNX2 in Cleidocranial Dysplasia 76
Clinical counselling in congenital fibrinogen disorders 76
A novel mutation in HERG gene, a490p, found in a large family with autosomal dominant long QT syndrome 76
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 76
The C677T methylenetetrahydrofolate reductase gene mutation does not influence cardiovascular risk in the dialysis population: results of a multicentre prospective study 75
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 75
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 75
Lo sport come mediatore tra mente e corpo 75
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 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 74
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 73
A six month mitotane course induced sustained correctio of hypercortisolism in a young womam with PPNAD and Carney Complex. 73
A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis. 73
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 73
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 73
Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance. 73
Polymorphism of the angiotensin-converting enzyme gene in end-stage renal failure patients. 72
The haplotype M2 within the ANXA5 gene is independently associated with the occurrence of deep venous thrombosis. 72
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 72
Mutation analysis in hyperphenylalaninemia patients from South Italy. 72
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 72
Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema 72
Bleeding and re-thrombosis in primary antiphospholipid syndrome on oral anticoagulation: an 8-year longitudinal comparison with mitral valve replacement and inherited thrombophilia. 71
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 71
Congenital nephrotic syndrome of Finnish type: detection of new nephrin mutations and prenatal diagnosis in an Italian family. 71
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 71
Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation. 71
TET2 mutations in Ph-negative myeloproliferative neoplasms: identification of three novel mutations and relationship with clinical and laboratory findings 71
Chronic thromboembolic pulmonary hypertension. 71
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 71
The Genetics of Hereditary Angioedema: A Review 71
Inherited platelet disorders>thrombocytopenias and thrombocytopathies. 70
Antithrombotic prophylaxis during pregnancy in women with deficiency of natural anticoagulants 70
Association of a sequence variant in DAB2IP with coronary heart disease 70
Small Supernumerary Marker Chromosome Originating From Chromosome 10 Associated With an Apparently Normal Phenotype’ 70
Survival in primary antiphospholipid syndrome: A single-centre cohort study 70
Totale 8.287
Salva come PNG Salva come JPEG
Categoria #
all - tutte 91.744
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 91.744
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019522 0 0 0 0 0 0 0 0 0 68 110 344
2019/20204.889 1.046 552 162 89 543 657 859 53 402 76 403 47
2020/20212.594 349 21 331 22 330 168 364 103 468 411 11 16
2021/20221.954 302 8 35 38 216 40 44 143 257 246 158 467
2022/20236.703 703 192 259 367 359 521 33 478 3.496 37 112 146
2023/2024907 182 68 83 40 81 273 75 74 10 21 0 0
Totale 21.098