IRIS
MARGAGLIONE, MAURIZIO
 Distribuzione geografica
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Continente #
EU - Europa 9.382
NA - Nord America 8.983
AS - Asia 5.269
SA - Sud America 156
Continente sconosciuto - Info sul continente non disponibili 28
AF - Africa 18
OC - Oceania 13
Totale 23.849
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Nazione #
US - Stati Uniti d'America 8.940
IE - Irlanda 3.270
CN - Cina 3.200
UA - Ucraina 2.166
SE - Svezia 1.380
HK - Hong Kong 624
IT - Italia 618
SG - Singapore 593
FI - Finlandia 459
IN - India 426
RU - Federazione Russa 367
DE - Germania 345
TR - Turchia 345
FR - Francia 338
GB - Regno Unito 196
BR - Brasile 116
BE - Belgio 59
NL - Olanda 52
AT - Austria 46
CZ - Repubblica Ceca 43
CA - Canada 30
EU - Europa 26
AR - Argentina 19
IR - Iran 15
AE - Emirati Arabi Uniti 12
LT - Lituania 9
MX - Messico 8
JP - Giappone 7
NZ - Nuova Zelanda 7
TN - Tunisia 7
AU - Australia 6
PK - Pakistan 6
RO - Romania 6
CH - Svizzera 5
CL - Cile 5
ID - Indonesia 5
IQ - Iraq 5
PE - Perù 5
UZ - Uzbekistan 5
BD - Bangladesh 4
CO - Colombia 4
PL - Polonia 4
ZA - Sudafrica 4
BO - Bolivia 3
ES - Italia 3
JO - Giordania 3
MA - Marocco 3
MY - Malesia 3
PA - Panama 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AZ - Azerbaigian 2
EC - Ecuador 2
EG - Egitto 2
HR - Croazia 2
LV - Lettonia 2
NO - Norvegia 2
PT - Portogallo 2
RS - Serbia 2
TH - Thailandia 2
VN - Vietnam 2
AL - Albania 1
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BY - Bielorussia 1
CY - Cipro 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GR - Grecia 1
GT - Guatemala 1
KG - Kirghizistan 1
KR - Corea 1
MD - Moldavia 1
MN - Mongolia 1
NP - Nepal 1
PH - Filippine 1
PS - Palestinian Territory 1
QA - Qatar 1
SD - Sudan 1
TW - Taiwan 1
UY - Uruguay 1
VE - Venezuela 1
Totale 23.849
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Città #
Dublin 3.269
Jacksonville 1.532
Chandler 1.268
Dearborn 1.096
Nanjing 791
Nyköping 763
Hong Kong 624
Wilmington 495
Santa Clara 392
Princeton 362
Nanchang 345
Beijing 342
San Mateo 300
Ann Arbor 251
Singapore 249
Ashburn 206
Shenyang 179
Helsinki 169
Boardman 162
New York 158
Tianjin 140
Woodbridge 140
Kunming 126
Hebei 122
Foggia 116
Changsha 114
Jiaxing 114
Moscow 105
Hilden 104
Jinan 102
Des Moines 100
Shanghai 93
Hangzhou 76
Bari 65
Guangzhou 65
Munich 63
Zhengzhou 62
Los Angeles 59
Ningbo 55
Brussels 49
Lanzhou 42
Changchun 40
Vienna 40
Brno 34
Pune 30
Nuremberg 29
Taizhou 27
Norwalk 25
Rome 24
Orange 22
Auburn Hills 21
Fuzhou 21
London 21
Augusta 20
San Severo 20
Borås 18
Manfredonia 18
Stevenage 18
Seattle 16
Wuhan 16
Haikou 15
Milan 15
Toronto 15
Shenzhen 14
Buenos Aires 12
Hefei 12
Redwood City 12
Falls Church 11
Lucera 11
Cedar Knolls 10
Frankfurt am Main 10
Philadelphia 10
Saint Petersburg 10
Waanrode 10
Florence 9
Olomouc 9
Washington 9
Cutrofiano 8
Leawood 8
Palermo 8
Taiyuan 8
Bangalore 7
Hanover 7
Naples 7
Rui'an 7
Taranto 7
Dongyang 6
Falkenstein 6
Meda 6
Redmond 6
Shaoxing 6
São Paulo 6
Amsterdam 5
Ankara 5
Cepagatti 5
Chicago 5
Jakarta 5
Lecce 5
Lima 5
Ottawa 5
Totale 15.662
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Nome #
A Novel Mutation In HERG Gene, A490P, Found In A Large Family With Autosomal Dominant Long QT Syndrome 144
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 124
Detection of the factor V Leiden using SSCP 121
How to handle low-molecular-weight heparins in patients with decreased renal function: an open issue. 116
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 116
Preventing adverse obstetric outcomes in women with genetic thrombophilia. 114
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers. 111
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 109
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 108
Structural analysis of protein Z gene variants in patients with foetal losses 107
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 106
Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis. 106
Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings 106
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 106
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 106
A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing 106
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo 105
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 104
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema. 104
"Genetic modulation of oral anticoagulantion with warfarin " 103
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 101
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 101
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 100
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 99
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 98
Characterization of patients with angioedema without wheals: the importance of F12 gene screening 98
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 97
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism. 97
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 97
A successful pregnancy in a woman with late-onset combined homocystinuria and methylmalonic aciduria 97
A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen. 96
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 96
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 96
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 95
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. 95
Occurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome 95
Identification of six novel mutations in type I antithrombin deficient Italian families 94
FXI deficiency: two novel mutations in asymptomatic Italian patients 94
The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study. 94
Role of thrombophilia in adverse obstetric outcomes and their prevention using antithrombotic therapy. 93
In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU 93
A novel mutation of gene CBFA1/RUNX2 in Cleidocranial Dysplasia 92
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 91
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. 91
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 91
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 90
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 90
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 90
Coexistence of beta-thalassemia and hereditary hemochromatosis in homozygosity: a possible synergic effect? 89
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 89
Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations 89
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 89
A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis 89
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 88
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. 88
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 88
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype 88
Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group. 87
A PC-1 amino acid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuria. 87
Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema 87
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 86
C-reactive protein in offspring is associated with the occurrence of myocardial infarction in first-degree relatives. 86
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 86
A novel mutation in HERG gene, a490p, found in a large family with autosomal dominant long QT syndrome 86
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 85
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia 85
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology. 85
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 85
Thrombophilic genotypes, natural anticoagulants, and plasma homocysteine in myeloproliferative disorders: relationship with splanchnic vein thrombosis and arterial disease. 84
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 84
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 84
Lo sport come mediatore tra mente e corpo 84
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema 84
A novel congenital dysprothrombinemia leading to defective prothrombin maturation 84
The Genetics of Hereditary Angioedema: A Review 84
A six month mitotane course induced sustained correctio of hypercortisolism in a young womam with PPNAD and Carney Complex. 83
A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis. 83
Clinical counselling in congenital fibrinogen disorders 83
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 83
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 83
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 83
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 82
Inherited thrombophilia and in vitro fertilization implantation failure. 82
The C677T methylenetetrahydrofolate reductase gene mutation does not influence cardiovascular risk in the dialysis population: results of a multicentre prospective study 82
Mutation analysis in hyperphenylalaninemia patients from South Italy. 82
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 81
Chronic thromboembolic pulmonary hypertension. 81
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 81
Congenital nephrotic syndrome of Finnish type: detection of new nephrin mutations and prenatal diagnosis in an Italian family. 80
Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation. 80
Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance. 80
Survival in primary antiphospholipid syndrome: A single-centre cohort study 80
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism 80
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 80
The haplotype M2 within the ANXA5 gene is independently associated with the occurrence of deep venous thrombosis. 79
Bleeding and re-thrombosis in primary antiphospholipid syndrome on oral anticoagulation: an 8-year longitudinal comparison with mitral valve replacement and inherited thrombophilia. 79
A description of a new case of combined Factor V and Factor VIII deficiency: the LMAN1 M1T is a frequent cause in Italian patients. 79
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 79
Inherited platelet disorders>thrombocytopenias and thrombocytopathies. 78
The assessment of the relationship between personality, the presence of the 5htt polymorphism, and the occurrence of anxiety and depressive symptoms in elite athletes 78
Totale 9.234
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Categoria #
all - tutte 136.669
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 136.669
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020928 0 0 0 0 0 0 0 0 402 76 403 47
2020/20212.594 349 21 331 22 330 168 364 103 468 411 11 16
2021/20222.086 302 8 35 38 287 41 49 153 268 253 158 494
2022/20236.961 735 196 268 371 363 532 35 486 3.678 37 114 146
2023/20241.139 185 70 87 41 83 283 75 74 10 21 13 197
2024/20252.927 321 66 130 200 157 646 610 349 448 0 0 0
Totale 24.647