IRIS
MARGAGLIONE, MAURIZIO
 Distribuzione geografica
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Continente #
NA - Nord America 12.975
EU - Europa 11.780
AS - Asia 9.068
SA - Sud America 1.542
AF - Africa 145
Continente sconosciuto - Info sul continente non disponibili 29
OC - Oceania 18
Totale 35.557
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Nazione #
US - Stati Uniti d'America 12.808
CN - Cina 3.699
IE - Irlanda 3.274
SG - Singapore 2.736
UA - Ucraina 2.177
RU - Federazione Russa 1.731
SE - Svezia 1.390
BR - Brasile 1.241
IT - Italia 832
HK - Hong Kong 822
FR - Francia 733
VN - Vietnam 528
IN - India 506
FI - Finlandia 498
DE - Germania 495
TR - Turchia 376
GB - Regno Unito 273
AR - Argentina 125
NL - Olanda 80
IQ - Iraq 71
CA - Canada 67
AT - Austria 62
BE - Belgio 61
BD - Bangladesh 59
MX - Messico 55
CZ - Repubblica Ceca 45
EC - Ecuador 43
ZA - Sudafrica 37
CO - Colombia 33
ID - Indonesia 33
PK - Pakistan 33
PL - Polonia 33
VE - Venezuela 30
JP - Giappone 28
EU - Europa 26
ES - Italia 25
MA - Marocco 24
UZ - Uzbekistan 24
AE - Emirati Arabi Uniti 22
CL - Cile 22
JO - Giordania 21
TN - Tunisia 20
IR - Iran 17
SA - Arabia Saudita 16
LT - Lituania 15
EG - Egitto 14
PE - Perù 14
PY - Paraguay 13
DZ - Algeria 12
UY - Uruguay 11
AU - Australia 10
BO - Bolivia 10
KE - Kenya 10
AZ - Azerbaigian 9
RO - Romania 9
MY - Malesia 8
NP - Nepal 8
NI - Nicaragua 7
NZ - Nuova Zelanda 7
OM - Oman 7
PA - Panama 7
BY - Bielorussia 6
CH - Svizzera 6
ET - Etiopia 6
PS - Palestinian Territory 6
CR - Costa Rica 5
HN - Honduras 5
HR - Croazia 5
RS - Serbia 5
AL - Albania 4
BH - Bahrain 4
KZ - Kazakistan 4
LB - Libano 4
TT - Trinidad e Tobago 4
BB - Barbados 3
BG - Bulgaria 3
DO - Repubblica Dominicana 3
GE - Georgia 3
GR - Grecia 3
JM - Giamaica 3
KG - Kirghizistan 3
KW - Kuwait 3
NG - Nigeria 3
SN - Senegal 3
SV - El Salvador 3
TH - Thailandia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AO - Angola 2
BA - Bosnia-Erzegovina 2
CG - Congo 2
CI - Costa d'Avorio 2
CY - Cipro 2
DK - Danimarca 2
KH - Cambogia 2
KR - Corea 2
LV - Lettonia 2
MD - Moldavia 2
MK - Macedonia 2
NO - Norvegia 2
PT - Portogallo 2
Totale 35.530
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Città #
Dublin 3.273
San Jose 1.912
Jacksonville 1.533
Chandler 1.268
Singapore 1.153
Dearborn 1.097
Ashburn 889
Hong Kong 822
Nanjing 791
Nyköping 763
Beijing 602
Wilmington 495
Santa Clara 423
Princeton 362
Lauterbourg 345
Nanchang 345
San Mateo 300
Ann Arbor 251
Moscow 245
Dallas 242
The Dalles 205
New York 188
Shenyang 179
Helsinki 173
Ho Chi Minh City 173
Boardman 169
Munich 163
Tianjin 141
Woodbridge 140
Hanoi 127
Kunming 126
Hebei 122
Foggia 121
Changsha 114
Jiaxing 114
Los Angeles 110
Hilden 104
Jinan 102
São Paulo 102
Des Moines 101
Shanghai 96
Hangzhou 77
Bari 76
Guangzhou 65
Zhengzhou 62
Ningbo 55
Rio de Janeiro 50
Brussels 49
Lanzhou 43
Vienna 42
Changchun 40
Milan 40
Frankfurt am Main 37
Nuremberg 36
Council Bluffs 35
Turku 35
Brno 34
Rome 34
Hillsboro 32
London 32
Pune 31
Baghdad 30
San Francisco 29
Orem 28
Taizhou 27
Warsaw 27
Brasília 26
Brooklyn 26
Belo Horizonte 25
Buenos Aires 25
Haiphong 25
Norwalk 25
Tokyo 25
Seattle 23
Toronto 23
Orange 22
Auburn Hills 21
Boston 21
Chennai 21
Da Nang 21
Fuzhou 21
Augusta 20
San Severo 20
Tashkent 20
Charlotte 19
Amman 18
Borås 18
Manfredonia 18
Porto Alegre 18
Stevenage 18
Chicago 17
Manchester 17
Salvador 17
Wuhan 17
Amsterdam 16
Ankara 16
Mexico City 16
Haikou 15
Biên Hòa 14
Curitiba 14
Totale 21.705
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Nome #
A Novel Mutation In HERG Gene, A490P, Found In A Large Family With Autosomal Dominant Long QT Syndrome 187
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 163
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers. 160
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo 157
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema. 152
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 150
A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing 149
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 148
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 148
A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis 147
Serum Albumin Is Inversely Associated With Portal Vein Thrombosis in Cirrhosis 145
"Genetic modulation of oral anticoagulantion with warfarin " 144
Preventing adverse obstetric outcomes in women with genetic thrombophilia. 144
In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU 144
A successful pregnancy in a woman with late-onset combined homocystinuria and methylmalonic aciduria 144
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 143
Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis. 142
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. 142
Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings 141
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 141
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 141
Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema 141
Detection of the factor V Leiden using SSCP 140
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 139
A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen. 138
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 137
Structural analysis of protein Z gene variants in patients with foetal losses 133
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism. 133
How to handle low-molecular-weight heparins in patients with decreased renal function: an open issue. 133
Occurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome 133
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 133
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. 132
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 132
A novel mutation of gene CBFA1/RUNX2 in Cleidocranial Dysplasia 131
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 130
Small Supernumerary Marker Chromosome Originating From Chromosome 10 Associated With an Apparently Normal Phenotype’ 130
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 129
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 129
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 129
FXI deficiency: two novel mutations in asymptomatic Italian patients 128
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 128
Characterization of patients with angioedema without wheals: the importance of F12 gene screening 128
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 125
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 125
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 125
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype 124
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 124
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 124
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 124
The Genetics of Hereditary Angioedema: A Review 123
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 122
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 122
A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis. 122
A six month mitotane course induced sustained correctio of hypercortisolism in a young womam with PPNAD and Carney Complex. 121
A novel mutation in HERG gene, a490p, found in a large family with autosomal dominant long QT syndrome 121
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 121
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 120
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 120
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism 120
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 120
Identification of six novel mutations in type I antithrombin deficient Italian families 119
The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study. 119
A description of a new case of combined Factor V and Factor VIII deficiency: the LMAN1 M1T is a frequent cause in Italian patients. 119
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 119
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 118
A novel congenital dysprothrombinemia leading to defective prothrombin maturation 118
Venous thromboembolism in assisted reproductive technologies: comparison between unsuccessful versus successful cycles in an Italian cohort. 118
Low-dose aspirin for in vitro fertilization or intracytoplasmic sperm injection: a systematic review and a meta-analysis of the literature 117
Role of thrombophilia in adverse obstetric outcomes and their prevention using antithrombotic therapy. 116
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 116
Coexistence of beta-thalassemia and hereditary hemochromatosis in homozygosity: a possible synergic effect? 116
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 116
Mutation analysis in hyperphenylalaninemia patients from South Italy. 116
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 115
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 115
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 115
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 115
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 115
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 114
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. 114
Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations 113
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 113
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 112
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia 112
Chronic thromboembolic pulmonary hypertension. 112
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin 112
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness 112
Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group. 111
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 111
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 111
Lo sport come mediatore tra mente e corpo 111
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema 111
Inherited thrombophilia and in vitro fertilization implantation failure. 110
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology. 110
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 110
Congenital nephrotic syndrome of Finnish type: detection of new nephrin mutations and prenatal diagnosis in an Italian family. 110
A PC-1 amino acid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuria. 109
C-reactive protein in offspring is associated with the occurrence of myocardial infarction in first-degree relatives. 109
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 108
The C677T methylenetetrahydrofolate reductase gene mutation does not influence cardiovascular risk in the dialysis population: results of a multicentre prospective study 107
Totale 12.665
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Categoria #
all - tutte 185.930
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 185.930
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021438 0 0 0 0 0 0 0 0 0 411 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
2025/20269.107 643 689 1.082 1.600 401 414 2.132 1.099 691 356 0 0
Totale 36.373