IRIS
MARGAGLIONE, MAURIZIO
 Distribuzione geografica
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Continente #
NA - Nord America 10.526
EU - Europa 10.516
AS - Asia 8.473
SA - Sud America 1.474
AF - Africa 118
Continente sconosciuto - Info sul continente non disponibili 29
OC - Oceania 17
Totale 31.153
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Nazione #
US - Stati Uniti d'America 10.385
CN - Cina 3.544
IE - Irlanda 3.271
SG - Singapore 2.510
UA - Ucraina 2.175
SE - Svezia 1.390
BR - Brasile 1.208
RU - Federazione Russa 993
HK - Hong Kong 790
IT - Italia 771
FI - Finlandia 496
IN - India 484
DE - Germania 466
VN - Vietnam 455
TR - Turchia 371
FR - Francia 356
GB - Regno Unito 257
AR - Argentina 117
NL - Olanda 70
AT - Austria 61
CA - Canada 61
BE - Belgio 59
IQ - Iraq 56
BD - Bangladesh 46
CZ - Repubblica Ceca 45
MX - Messico 41
EC - Ecuador 37
ZA - Sudafrica 35
ID - Indonesia 29
PK - Pakistan 27
EU - Europa 26
CO - Colombia 25
VE - Venezuela 24
ES - Italia 23
JP - Giappone 23
AE - Emirati Arabi Uniti 20
MA - Marocco 20
UZ - Uzbekistan 19
PL - Polonia 18
CL - Cile 17
IR - Iran 17
TN - Tunisia 17
LT - Lituania 15
PE - Perù 14
EG - Egitto 13
PY - Paraguay 12
SA - Arabia Saudita 12
JO - Giordania 11
UY - Uruguay 11
AU - Australia 9
BO - Bolivia 9
RO - Romania 9
AZ - Azerbaigian 8
DZ - Algeria 8
KE - Kenya 8
NZ - Nuova Zelanda 7
BY - Bielorussia 6
CH - Svizzera 6
NI - Nicaragua 6
OM - Oman 6
PA - Panama 6
CR - Costa Rica 5
HN - Honduras 5
MY - Malesia 5
NP - Nepal 5
LB - Libano 4
PS - Palestinian Territory 4
RS - Serbia 4
TT - Trinidad e Tobago 4
BB - Barbados 3
BG - Bulgaria 3
DO - Repubblica Dominicana 3
ET - Etiopia 3
GE - Georgia 3
GR - Grecia 3
HR - Croazia 3
KG - Kirghizistan 3
KZ - Kazakistan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AL - Albania 2
BA - Bosnia-Erzegovina 2
BH - Bahrain 2
DK - Danimarca 2
JM - Giamaica 2
KR - Corea 2
KW - Kuwait 2
LV - Lettonia 2
MK - Macedonia 2
NG - Nigeria 2
NO - Norvegia 2
PT - Portogallo 2
SV - El Salvador 2
TH - Thailandia 2
AM - Armenia 1
AO - Angola 1
BF - Burkina Faso 1
BN - Brunei Darussalam 1
BS - Bahamas 1
CG - Congo 1
CI - Costa d'Avorio 1
Totale 31.131
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Città #
Dublin 3.270
Jacksonville 1.533
Chandler 1.268
Dearborn 1.097
Singapore 1.039
Nanjing 791
Hong Kong 790
Nyköping 763
Ashburn 664
Beijing 573
Wilmington 495
Santa Clara 408
Princeton 362
Nanchang 345
San Mateo 300
Ann Arbor 251
Dallas 239
New York 183
Shenyang 179
Moscow 173
Helsinki 171
Boardman 168
The Dalles 165
Munich 162
Ho Chi Minh City 149
Tianjin 140
Woodbridge 140
Kunming 126
Hebei 122
Foggia 121
Changsha 114
Jiaxing 114
Hanoi 110
Los Angeles 106
Hilden 104
Jinan 102
Des Moines 100
São Paulo 99
Shanghai 96
Hangzhou 77
Bari 71
Guangzhou 65
Zhengzhou 62
Ningbo 55
Rio de Janeiro 50
Brussels 49
Lanzhou 43
Vienna 42
Changchun 40
Milan 37
Turku 35
Brno 34
Nuremberg 33
Pune 31
San Francisco 29
Rome 28
London 27
Taizhou 27
Baghdad 26
Brasília 25
Brooklyn 25
Norwalk 25
Belo Horizonte 24
Buenos Aires 24
Council Bluffs 24
Haiphong 24
Seattle 23
Orange 22
Auburn Hills 21
Fuzhou 21
Augusta 20
Boston 20
San Severo 20
Tokyo 20
Toronto 20
Charlotte 19
Borås 18
Manfredonia 18
Stevenage 18
Chicago 17
Porto Alegre 17
Salvador 17
Tashkent 16
Wuhan 16
Ankara 15
Haikou 15
Biên Hòa 14
Da Nang 14
Frankfurt am Main 14
Ninh Bình 14
Philadelphia 14
Shenzhen 14
Chennai 13
Curitiba 13
Johannesburg 13
Montreal 13
Thái Bình 13
Warsaw 13
Hefei 12
Jakarta 12
Totale 18.723
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Nome #
A Novel Mutation In HERG Gene, A490P, Found In A Large Family With Autosomal Dominant Long QT Syndrome 171
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 146
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo 142
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers. 138
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema. 138
In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU 137
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 135
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 135
A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing 134
Serum Albumin Is Inversely Associated With Portal Vein Thrombosis in Cirrhosis 133
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 132
Preventing adverse obstetric outcomes in women with genetic thrombophilia. 132
Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings 131
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 131
Detection of the factor V Leiden using SSCP 130
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 129
A successful pregnancy in a woman with late-onset combined homocystinuria and methylmalonic aciduria 129
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. 128
"Genetic modulation of oral anticoagulantion with warfarin " 127
Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis. 126
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 126
A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis 125
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 124
How to handle low-molecular-weight heparins in patients with decreased renal function: an open issue. 123
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 123
A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen. 122
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism. 121
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 121
Small Supernumerary Marker Chromosome Originating From Chromosome 10 Associated With an Apparently Normal Phenotype’ 121
Occurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome 120
Structural analysis of protein Z gene variants in patients with foetal losses 119
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 119
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 119
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 118
A novel mutation of gene CBFA1/RUNX2 in Cleidocranial Dysplasia 117
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. 116
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 116
Characterization of patients with angioedema without wheals: the importance of F12 gene screening 116
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 114
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 114
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 114
Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema 114
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 114
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 113
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 113
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 112
FXI deficiency: two novel mutations in asymptomatic Italian patients 110
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 110
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype 109
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 108
A novel mutation in HERG gene, a490p, found in a large family with autosomal dominant long QT syndrome 108
The Genetics of Hereditary Angioedema: A Review 108
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 107
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 107
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 107
Low-dose aspirin for in vitro fertilization or intracytoplasmic sperm injection: a systematic review and a meta-analysis of the literature 107
The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study. 106
A novel congenital dysprothrombinemia leading to defective prothrombin maturation 106
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 106
Venous thromboembolism in assisted reproductive technologies: comparison between unsuccessful versus successful cycles in an Italian cohort. 106
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism 106
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 106
A six month mitotane course induced sustained correctio of hypercortisolism in a young womam with PPNAD and Carney Complex. 105
Role of thrombophilia in adverse obstetric outcomes and their prevention using antithrombotic therapy. 105
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 105
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 105
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin 105
Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations 105
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 105
Identification of six novel mutations in type I antithrombin deficient Italian families 104
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 104
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 104
Mutation analysis in hyperphenylalaninemia patients from South Italy. 104
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 103
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 103
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. 103
A description of a new case of combined Factor V and Factor VIII deficiency: the LMAN1 M1T is a frequent cause in Italian patients. 103
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 103
A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis. 102
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 102
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 101
Coexistence of beta-thalassemia and hereditary hemochromatosis in homozygosity: a possible synergic effect? 101
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 101
C-reactive protein in offspring is associated with the occurrence of myocardial infarction in first-degree relatives. 101
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema 101
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 101
A PC-1 amino acid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuria. 100
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia 100
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology. 100
Lo sport come mediatore tra mente e corpo 100
Survival in primary antiphospholipid syndrome: A single-centre cohort study 100
Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group. 99
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 99
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 99
Family history of VTE: an easy tool to score the individual risk 98
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 98
Chronic thromboembolic pulmonary hypertension. 97
Thrombophilic genotypes, natural anticoagulants, and plasma homocysteine in myeloproliferative disorders: relationship with splanchnic vein thrombosis and arterial disease. 96
Clinical counselling in congenital fibrinogen disorders 96
The C677T methylenetetrahydrofolate reductase gene mutation does not influence cardiovascular risk in the dialysis population: results of a multicentre prospective study 96
Totale 11.349
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Categoria #
all - tutte 178.476
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 178.476
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.541 0 0 0 0 0 168 364 103 468 411 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
2024/20255.546 321 66 130 200 157 646 610 349 1.599 342 528 598
2025/20264.697 643 689 1.082 1.600 401 282 0 0 0 0 0 0
Totale 31.963