IRIS
MARGAGLIONE, MAURIZIO
 Distribuzione geografica
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Continente #
NA - Nord America 16.286
EU - Europa 12.003
AS - Asia 9.197
SA - Sud America 1.577
Continente sconosciuto - Info sul continente non disponibili 854
AF - Africa 145
OC - Oceania 18
Totale 40.080
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Nazione #
US - Stati Uniti d'America 15.998
CN - Cina 3.743
IE - Irlanda 3.279
SG - Singapore 2.762
UA - Ucraina 2.178
RU - Federazione Russa 1.736
SE - Svezia 1.391
BR - Brasile 1.265
IT - Italia 976
HK - Hong Kong 833
FR - Francia 741
VN - Vietnam 530
IN - India 507
DE - Germania 498
FI - Finlandia 498
TR - Turchia 376
GB - Regno Unito 304
CA - Canada 136
AR - Argentina 126
BD - Bangladesh 93
NL - Olanda 85
IQ - Iraq 71
AT - Austria 63
BE - Belgio 61
MX - Messico 61
CZ - Repubblica Ceca 46
EC - Ecuador 44
ID - Indonesia 39
ZA - Sudafrica 37
CO - Colombia 35
PL - Polonia 34
PK - Pakistan 33
ES - Italia 31
VE - Venezuela 30
JP - Giappone 28
EU - Europa 26
UZ - Uzbekistan 25
CL - Cile 24
MA - Marocco 24
AE - Emirati Arabi Uniti 22
JO - Giordania 21
TN - Tunisia 20
CR - Costa Rica 19
IR - Iran 17
PY - Paraguay 17
LT - Lituania 16
SA - Arabia Saudita 16
EG - Egitto 14
HN - Honduras 14
PE - Perù 14
DZ - Algeria 12
UY - Uruguay 12
AU - Australia 10
BO - Bolivia 10
KE - Kenya 10
NI - Nicaragua 10
RO - Romania 10
TT - Trinidad e Tobago 10
AZ - Azerbaigian 9
MY - Malesia 8
NP - Nepal 8
PA - Panama 8
CH - Svizzera 7
JM - Giamaica 7
NZ - Nuova Zelanda 7
OM - Oman 7
BY - Bielorussia 6
ET - Etiopia 6
PS - Palestinian Territory 6
AL - Albania 5
GR - Grecia 5
HR - Croazia 5
RS - Serbia 5
BB - Barbados 4
BG - Bulgaria 4
BH - Bahrain 4
IL - Israele 4
KZ - Kazakistan 4
LB - Libano 4
PR - Porto Rico 4
SV - El Salvador 4
DO - Repubblica Dominicana 3
EE - Estonia 3
GE - Georgia 3
KG - Kirghizistan 3
KW - Kuwait 3
NG - Nigeria 3
PT - Portogallo 3
SN - Senegal 3
TH - Thailandia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AO - Angola 2
BA - Bosnia-Erzegovina 2
BS - Bahamas 2
CG - Congo 2
CI - Costa d'Avorio 2
CY - Cipro 2
DK - Danimarca 2
GT - Guatemala 2
KH - Cambogia 2
Totale 39.219
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Città #
Dublin 3.279
San Jose 2.618
Jacksonville 1.536
Chandler 1.268
Singapore 1.169
Dearborn 1.098
Ashburn 1.047
Hong Kong 833
Nanjing 791
Nyköping 763
Beijing 626
Wilmington 498
Santa Clara 489
Council Bluffs 444
Princeton 371
Columbus 365
Lauterbourg 345
Nanchang 345
San Mateo 300
New York 272
Dallas 268
Ann Arbor 251
Moscow 245
The Dalles 208
Shenyang 179
Los Angeles 178
Ho Chi Minh City 174
Helsinki 173
Boardman 170
Munich 163
Tianjin 141
Woodbridge 140
Hanoi 127
Kunming 126
Hebei 122
Foggia 121
Changsha 114
Jiaxing 114
Hilden 104
São Paulo 103
Jinan 102
Des Moines 101
Shanghai 100
Bari 78
Hangzhou 77
Guangzhou 65
Zhengzhou 62
Phoenix 60
Long Beach 57
Ningbo 55
Milan 51
Rio de Janeiro 50
Rome 50
Brussels 49
Lanzhou 43
Vienna 43
Buffalo 41
Changchun 40
New Providence 38
Frankfurt am Main 37
Nuremberg 36
Seattle 35
Turku 35
Brno 34
Hillsboro 33
London 33
Pune 31
San Francisco 31
Toronto 31
Baghdad 30
Atlanta 29
Brooklyn 29
Orem 29
Fresno 28
Brasília 27
Chicago 27
Taizhou 27
Warsaw 27
Haiphong 26
Norwalk 26
Belo Horizonte 25
Boston 25
Buenos Aires 25
Tokyo 25
Charlotte 22
Mexico City 22
Orange 22
Auburn Hills 21
Chennai 21
Da Nang 21
Fuzhou 21
Philadelphia 21
Tashkent 21
Augusta 20
San Severo 20
Montreal 19
Amman 18
Borås 18
Manchester 18
Manfredonia 18
Totale 23.904
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Nome #
A Novel Mutation In HERG Gene, A490P, Found In A Large Family With Autosomal Dominant Long QT Syndrome 199
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 173
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers. 173
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo 168
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema. 168
Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings 163
A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing 163
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 162
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 161
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 161
Serum Albumin Is Inversely Associated With Portal Vein Thrombosis in Cirrhosis 161
A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis 160
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 159
"Genetic modulation of oral anticoagulantion with warfarin " 157
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 156
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. 155
In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU 154
A successful pregnancy in a woman with late-onset combined homocystinuria and methylmalonic aciduria 154
Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema 154
Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis. 153
Preventing adverse obstetric outcomes in women with genetic thrombophilia. 151
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 151
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 150
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 150
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 150
A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen. 148
Detection of the factor V Leiden using SSCP 147
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 147
The Genetics of Hereditary Angioedema: A Review 147
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 146
Characterization of patients with angioedema without wheals: the importance of F12 gene screening 144
A novel mutation of gene CBFA1/RUNX2 in Cleidocranial Dysplasia 143
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism. 143
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype 142
How to handle low-molecular-weight heparins in patients with decreased renal function: an open issue. 142
A six month mitotane course induced sustained correctio of hypercortisolism in a young womam with PPNAD and Carney Complex. 141
Structural analysis of protein Z gene variants in patients with foetal losses 141
Occurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome 141
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 140
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 140
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. 139
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 138
Small Supernumerary Marker Chromosome Originating From Chromosome 10 Associated With an Apparently Normal Phenotype’ 138
FXI deficiency: two novel mutations in asymptomatic Italian patients 137
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 137
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 136
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 134
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 134
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 134
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 132
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism 132
A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis. 131
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 130
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 130
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 130
Mutation analysis in hyperphenylalaninemia patients from South Italy. 130
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 129
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 129
Low protein Z levels and risk of occurrence of deep vein thrombosis 129
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 129
Venous thromboembolism in assisted reproductive technologies: comparison between unsuccessful versus successful cycles in an Italian cohort. 129
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 129
A description of a new case of combined Factor V and Factor VIII deficiency: the LMAN1 M1T is a frequent cause in Italian patients. 128
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 128
A novel congenital dysprothrombinemia leading to defective prothrombin maturation 128
THE MOLECULAR ORGANIZATION OF ENDOTHELIAL JUNCTIONS IN VASCULAR PERMEABILITY 128
The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study. 127
A novel mutation in HERG gene, a490p, found in a large family with autosomal dominant long QT syndrome 127
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 127
Identification of six novel mutations in type I antithrombin deficient Italian families 126
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 126
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 126
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 125
Low-dose aspirin for in vitro fertilization or intracytoplasmic sperm injection: a systematic review and a meta-analysis of the literature 125
Chronic thromboembolic pulmonary hypertension. 125
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 125
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients 125
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 124
Coexistence of beta-thalassemia and hereditary hemochromatosis in homozygosity: a possible synergic effect? 124
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness 124
Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group. 123
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 123
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 123
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 123
Role of thrombophilia in adverse obstetric outcomes and their prevention using antithrombotic therapy. 123
Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations 123
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 122
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia 121
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. 121
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 121
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology. 120
Functional and clinical data of Best vitelliform macular dystrophy patients with mutations in the BEST1 gene 120
Lo sport come mediatore tra mente e corpo 120
Identification of GLA gene deletions in Fabry patients by Multiplex Ligation-dependent Probe Amplification (MLPA) 120
C-reactive protein in offspring is associated with the occurrence of myocardial infarction in first-degree relatives. 119
Congenital nephrotic syndrome of Finnish type: detection of new nephrin mutations and prenatal diagnosis in an Italian family. 119
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 119
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 119
Associations Between Personality Traits, Perceived Stress and Depressive Symptoms in Gynecological Cancer Patients Characterized by the Short and Long Allele Variant of the 5-HTTLPR Genotype: Preliminary Results 118
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 118
Totale 13.757
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Categoria #
all - tutte 211.050
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 211.050
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.741 0 0 0 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
2025/20269.921 643 689 1.082 1.600 401 414 2.132 1.099 691 590 250 330
2026/20272.893 217 937 763 976 0 0 0 0 0 0 0 0
Totale 40.080