IRIS
MARGAGLIONE, MAURIZIO
 Distribuzione geografica
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Continente #
NA - Nord America 14.475
EU - Europa 11.894
AS - Asia 9.179
SA - Sud America 1.558
Continente sconosciuto - Info sul continente non disponibili 854
AF - Africa 145
OC - Oceania 18
Totale 38.123
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Nazione #
US - Stati Uniti d'America 14.254
CN - Cina 3.742
IE - Irlanda 3.279
SG - Singapore 2.759
UA - Ucraina 2.177
RU - Federazione Russa 1.731
SE - Svezia 1.391
BR - Brasile 1.246
IT - Italia 915
HK - Hong Kong 832
FR - Francia 737
VN - Vietnam 530
IN - India 507
FI - Finlandia 498
DE - Germania 496
TR - Turchia 376
GB - Regno Unito 275
AR - Argentina 126
CA - Canada 93
BD - Bangladesh 91
NL - Olanda 85
IQ - Iraq 71
AT - Austria 62
BE - Belgio 61
MX - Messico 61
CZ - Repubblica Ceca 46
EC - Ecuador 44
ZA - Sudafrica 37
CO - Colombia 35
PL - Polonia 34
ID - Indonesia 33
PK - Pakistan 33
ES - Italia 30
VE - Venezuela 30
JP - Giappone 28
EU - Europa 26
CL - Cile 24
MA - Marocco 24
UZ - Uzbekistan 24
AE - Emirati Arabi Uniti 22
JO - Giordania 21
TN - Tunisia 20
IR - Iran 17
PY - Paraguay 17
LT - Lituania 16
SA - Arabia Saudita 16
EG - Egitto 14
PE - Perù 14
CR - Costa Rica 13
DZ - Algeria 12
UY - Uruguay 12
AU - Australia 10
BO - Bolivia 10
KE - Kenya 10
RO - Romania 10
AZ - Azerbaigian 9
HN - Honduras 8
MY - Malesia 8
NI - Nicaragua 8
NP - Nepal 8
PA - Panama 8
CH - Svizzera 7
NZ - Nuova Zelanda 7
OM - Oman 7
BY - Bielorussia 6
ET - Etiopia 6
JM - Giamaica 6
PS - Palestinian Territory 6
TT - Trinidad e Tobago 6
AL - Albania 5
HR - Croazia 5
RS - Serbia 5
BB - Barbados 4
BH - Bahrain 4
GR - Grecia 4
KZ - Kazakistan 4
LB - Libano 4
BG - Bulgaria 3
DO - Repubblica Dominicana 3
GE - Georgia 3
KG - Kirghizistan 3
KW - Kuwait 3
NG - Nigeria 3
PT - Portogallo 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
BS - Bahamas 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
Totale 37.268
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Città #
Dublin 3.278
San Jose 2.437
Jacksonville 1.536
Chandler 1.268
Singapore 1.168
Dearborn 1.097
Ashburn 903
Hong Kong 832
Nanjing 791
Nyköping 763
Beijing 625
Wilmington 497
Santa Clara 453
Council Bluffs 379
Princeton 362
Lauterbourg 345
Nanchang 345
San Mateo 300
Columbus 263
Ann Arbor 251
Dallas 251
Moscow 245
The Dalles 208
New York 200
Shenyang 179
Ho Chi Minh City 174
Helsinki 173
Boardman 170
Munich 163
Tianjin 141
Woodbridge 140
Hanoi 127
Kunming 126
Hebei 122
Foggia 121
Los Angeles 116
Changsha 114
Jiaxing 114
Hilden 104
São Paulo 103
Jinan 102
Des Moines 101
Shanghai 100
Bari 78
Hangzhou 77
Guangzhou 65
Zhengzhou 62
Ningbo 55
Rio de Janeiro 50
Brussels 49
Milan 45
Lanzhou 43
Rome 42
Vienna 42
Changchun 40
Frankfurt am Main 37
Nuremberg 36
Turku 35
Brno 34
Hillsboro 32
London 32
Pune 31
Baghdad 30
Brooklyn 29
Orem 29
San Francisco 29
Taizhou 27
Warsaw 27
Brasília 26
Haiphong 26
Norwalk 26
Belo Horizonte 25
Buenos Aires 25
Tokyo 25
Toronto 25
Boston 24
Seattle 23
Mexico City 22
Orange 22
Auburn Hills 21
Charlotte 21
Chennai 21
Da Nang 21
Fuzhou 21
Augusta 20
San Severo 20
Tashkent 20
Chicago 19
Amman 18
Borås 18
Manfredonia 18
Philadelphia 18
Porto Alegre 18
Stevenage 18
Manchester 17
Salvador 17
Wuhan 17
Amsterdam 16
Ankara 16
Haikou 15
Totale 23.002
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Nome #
A Novel Mutation In HERG Gene, A490P, Found In A Large Family With Autosomal Dominant Long QT Syndrome 196
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 168
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers. 166
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo 163
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema. 160
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 158
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 157
A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis 155
A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing 154
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 153
"Genetic modulation of oral anticoagulantion with warfarin " 151
Serum Albumin Is Inversely Associated With Portal Vein Thrombosis in Cirrhosis 151
Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema 149
Preventing adverse obstetric outcomes in women with genetic thrombophilia. 148
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. 148
A successful pregnancy in a woman with late-onset combined homocystinuria and methylmalonic aciduria 148
Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis. 147
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 147
In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU 147
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 146
Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings 145
Detection of the factor V Leiden using SSCP 144
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 144
A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen. 143
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 143
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 143
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 142
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 142
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 142
Characterization of patients with angioedema without wheals: the importance of F12 gene screening 140
A novel mutation of gene CBFA1/RUNX2 in Cleidocranial Dysplasia 139
Occurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome 139
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism. 138
How to handle low-molecular-weight heparins in patients with decreased renal function: an open issue. 137
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. 136
The Genetics of Hereditary Angioedema: A Review 136
Structural analysis of protein Z gene variants in patients with foetal losses 135
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 135
Small Supernumerary Marker Chromosome Originating From Chromosome 10 Associated With an Apparently Normal Phenotype’ 135
FXI deficiency: two novel mutations in asymptomatic Italian patients 134
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 134
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 133
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 132
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 131
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 130
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype 130
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 130
A six month mitotane course induced sustained correctio of hypercortisolism in a young womam with PPNAD and Carney Complex. 128
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 128
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 127
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 127
A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis. 127
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 127
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 127
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 126
A novel congenital dysprothrombinemia leading to defective prothrombin maturation 125
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 124
The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study. 124
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 124
A novel mutation in HERG gene, a490p, found in a large family with autosomal dominant long QT syndrome 124
Venous thromboembolism in assisted reproductive technologies: comparison between unsuccessful versus successful cycles in an Italian cohort. 124
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 124
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 124
Identification of six novel mutations in type I antithrombin deficient Italian families 123
A description of a new case of combined Factor V and Factor VIII deficiency: the LMAN1 M1T is a frequent cause in Italian patients. 123
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism 123
THE MOLECULAR ORGANIZATION OF ENDOTHELIAL JUNCTIONS IN VASCULAR PERMEABILITY 123
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 122
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 121
Coexistence of beta-thalassemia and hereditary hemochromatosis in homozygosity: a possible synergic effect? 121
Mutation analysis in hyperphenylalaninemia patients from South Italy. 121
Low-dose aspirin for in vitro fertilization or intracytoplasmic sperm injection: a systematic review and a meta-analysis of the literature 121
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 120
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 120
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 120
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 120
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 119
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 119
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness 119
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 118
Role of thrombophilia in adverse obstetric outcomes and their prevention using antithrombotic therapy. 118
Chronic thromboembolic pulmonary hypertension. 118
Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations 118
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 118
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia 117
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. 117
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 117
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 117
Congenital nephrotic syndrome of Finnish type: detection of new nephrin mutations and prenatal diagnosis in an Italian family. 116
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin 116
Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group. 115
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology. 115
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 115
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 115
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients 115
C-reactive protein in offspring is associated with the occurrence of myocardial infarction in first-degree relatives. 114
Low protein Z levels and risk of occurrence of deep vein thrombosis 114
Lo sport come mediatore tra mente e corpo 114
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema 114
Inherited thrombophilia and in vitro fertilization implantation failure. 113
Totale 13.203
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Categoria #
all - tutte 202.102
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 202.102
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.784 0 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
2025/20269.921 643 689 1.082 1.600 401 414 2.132 1.099 691 590 250 330
2026/2027936 217 719 0 0 0 0 0 0 0 0 0 0
Totale 38.123