IRIS
NORIS, PATRIZIA
 Distribuzione geografica
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Continente #
NA - Nord America 7.380
AS - Asia 5.618
EU - Europa 4.291
SA - Sud America 691
Continente sconosciuto - Info sul continente non disponibili 439
AF - Africa 149
OC - Oceania 19
Totale 18.587
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Nazione #
US - Stati Uniti d'America 7.190
CN - Cina 2.832
SG - Singapore 1.197
IE - Irlanda 965
HK - Hong Kong 585
FI - Finlandia 514
BR - Brasile 504
DE - Germania 498
UA - Ucraina 486
VN - Vietnam 464
IT - Italia 432
RU - Federazione Russa 395
SE - Svezia 306
FR - Francia 258
GB - Regno Unito 205
IN - India 127
CA - Canada 111
AR - Argentina 86
BD - Bangladesh 83
ZA - Sudafrica 70
IQ - Iraq 53
MX - Messico 37
JP - Giappone 36
NL - Olanda 32
EC - Ecuador 30
PL - Polonia 30
TR - Turchia 30
ES - Italia 28
PK - Pakistan 26
ID - Indonesia 25
SA - Arabia Saudita 24
UZ - Uzbekistan 21
BE - Belgio 20
CO - Colombia 20
AU - Australia 18
PH - Filippine 18
RO - Romania 18
MA - Marocco 16
CZ - Repubblica Ceca 15
AT - Austria 13
EG - Egitto 13
IR - Iran 11
AZ - Azerbaigian 10
JO - Giordania 10
KE - Kenya 10
PE - Perù 10
PY - Paraguay 10
VE - Venezuela 10
AL - Albania 9
CL - Cile 9
ET - Etiopia 9
EU - Europa 9
GR - Grecia 9
LT - Lituania 9
MY - Malesia 9
CH - Svizzera 8
PA - Panama 8
TN - Tunisia 8
DO - Repubblica Dominicana 7
JM - Giamaica 7
UY - Uruguay 7
KG - Kirghizistan 6
NP - Nepal 6
DZ - Algeria 5
HU - Ungheria 5
KR - Corea 5
KZ - Kazakistan 5
LB - Libano 5
MU - Mauritius 5
PT - Portogallo 5
AE - Emirati Arabi Uniti 4
BO - Bolivia 4
IL - Israele 4
RS - Serbia 4
SK - Slovacchia (Repubblica Slovacca) 4
BB - Barbados 3
BH - Bahrain 3
DK - Danimarca 3
HN - Honduras 3
LU - Lussemburgo 3
MD - Moldavia 3
AO - Angola 2
BA - Bosnia-Erzegovina 2
BG - Bulgaria 2
CG - Congo 2
CR - Costa Rica 2
DM - Dominica 2
EE - Estonia 2
GE - Georgia 2
GH - Ghana 2
HR - Croazia 2
KH - Cambogia 2
LC - Santa Lucia 2
LK - Sri Lanka 2
LV - Lettonia 2
NG - Nigeria 2
NO - Norvegia 2
PS - Palestinian Territory 2
SN - Senegal 2
SV - El Salvador 2
Totale 18.133
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Città #
Dublin 965
Chandler 874
San Jose 839
Jacksonville 663
Singapore 658
Ashburn 654
Nanjing 615
Hong Kong 567
Dallas 527
Beijing 429
Boardman 284
Council Bluffs 241
Nanchang 224
Princeton 194
Shenyang 184
Wilmington 182
Lawrence 180
Medford 178
Munich 176
Changsha 165
Hebei 165
Lauterbourg 165
Ho Chi Minh City 160
Los Angeles 158
Helsinki 156
Jiaxing 128
Hanoi 125
New York 99
Tianjin 97
Hangzhou 91
Ann Arbor 89
Milan 88
Buffalo 77
Pavia 66
Shanghai 66
São Paulo 64
Johannesburg 57
Moscow 56
Redondo Beach 53
Houston 52
Santa Clara 52
Orem 47
Woodbridge 47
Turku 43
Chennai 35
Toronto 35
Guangzhou 33
Montreal 33
Tokyo 33
Verona 33
Brooklyn 28
Fairfield 28
The Dalles 28
Da Nang 27
Seattle 26
Denver 25
Frankfurt am Main 25
London 25
Norwalk 25
Atlanta 22
Columbus 22
San Francisco 21
Warsaw 21
Phoenix 20
Pune 20
Rome 20
Belo Horizonte 19
Zhengzhou 19
Ankara 18
Baghdad 18
Brussels 18
Chicago 18
Tashkent 18
Brasília 17
Falkenstein 17
Manchester 17
Mexico City 17
Haiphong 16
Jinan 16
Des Moines 15
Rio de Janeiro 15
Stockholm 15
Brno 13
Falls Church 12
Mumbai 12
Nuremberg 12
Timisoara 12
Auburn Hills 11
Paris 11
Quito 11
Secaucus 11
Amsterdam 10
Biên Hòa 10
Boston 10
Buenos Aires 10
Dhaka 10
Florence 10
Kunming 10
Sydney 10
Amman 9
Totale 12.052
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Nome #
Anemia in patients with Covid-19: pathogenesis and clinical significance 290
Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy 178
Abdominal lymphographic pattern in connective tissue diseases is quite similar to that observed in lymphocytic lymphoma. 168
A new variant of Bernard-Soulier syndrome characterized by dysfunctional glycoprotein (GP) IB and severely reduced amounts of GPIX and GPV. 166
Correction to: Anemia in patients with Covid-19: pathogenesis and clinical significance (Clinical and Experimental Medicine, (2021), 10.1007/s10238-020-00679-4) 164
Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia 162
Correction to: Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy (Internal and Emergency Medicine, (2021), 16, 5, (1141-1152), 10.1007/s11739-020-02550-6) 153
Activation of the haemostatic process in patients with unruptured aortic aneurysm before and after surgical repair 151
NOVEL PERSPECTIVES IN GENOTYPE-PHENOTYPE CORRELATIONS IN MYH9-RELATED DISEASE: NO LONGER JUST A MATTER OF HEAD OR TAIL 151
Bleeding risk of surgery and its prevention in patients with inherited platelet disorders. The Surgery in Platelet disorders And Therapeutic Approach (SPATA) study 143
A Leu40Pro substitution in the leucine rich motif (LRM) of glycoprotein (GP) IX is responsible for dysfunction of a normally expressed GPIB alpha in Bernard-Soulier syndrome (BSS) 142
Clinical and pathogenetic characterization of ETV6-related thrombocytopenia (ETV6-RT), an inherited thrombocytopenia (IT) predisposing to childhood acute lymphoblastic leukemia (ALL) 142
Antigeni minori di istocompatibilità 141
Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia 141
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. 141
Impact of COVID-19 on liver function: results from an internal medicine unit in Northern Italy 141
Altered cytoskeleton organization in platelets from patients with MYH9-related disease. 140
A HOMOZYGOUS POINT MUTATION IN A LEUCINE-RICH MOTIF OF PLATELET GLYCOPROTEIN-IX ASSOCIATED WITH BERNARD-SOULIER SYNDROME (BSS) 135
Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia 135
Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy 134
Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders 133
A MONOALLELIC LOSS-FUNCTION MUTATION IN THE THROMBOPOIETIN (THPO) GENE IS RESPONSIBLE FOR A NEW FORM OF INHERITED THROMBOCYTOPENIA (IT) 131
Thrombocytopenia, giant platelets, and leukocyte inclusion bodies (May-Hegglin anomaly). Clinical and laboratory findings. 130
Confronto di due metodi di criopreservazione piastrinica basati sull'impiego di glicerolo-glucosio o DMSO: studio della funzionalità piastrinica in vitro. 129
Screening for congenital bleeding disorders with platelet function analyzer (PFA-100) in women with menorrhagia 127
Spectrum of the mutations in Bernard-Soulier syndrome. 126
Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombo-cytopenia. 126
Autosomal dominant thrombocytopenias with reduced expression of glycoprotein Ia 126
Activation of the haemostatic process in patients with unruptured aortic aneurysm before and in the first week after surgical repair. 122
Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders. 121
IN VIVO AND IN VITRO EFFECTS OF THROMBOLYTIC AGENTS ON PLATELET COMPOSITION AND FUNCTION 121
Alteration of Liver Enzymes Is a Feature of the Myh9-Related Disease Syndrome. 121
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene 120
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIb{alpha} (Bolzano mutation). 120
Thrombopoietin is not uniquely responsible for thrombocytosis in inflammatory disorders 119
NITROGLYCERIN INFUSION - HEMODYNAMIC AND ANTI-PLATELETS EFFECTS IN PATIENTS WITH CARDIOMYOPATHY 119
Effect of low molecular weight heparin on some markers of platelet and thrombin activation in patients with inflammatory bowel diseasesnresponsive to the standard therapy 119
Platelet function after 'in vivo' and 'in vitro' treatment with thrombolytic agents. 119
Clinical and genetic aspects Bernard-Soulier syndrome: searching for genotype/phenotype correlations. 119
Heparin modifies platelet count and function in patients who have undergone thrombolytic therapy for acute myocardial infarction. 118
Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown origin. 118
Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders. 117
Factor V Leiden mutation and risk of thrombotic complications in children treated for lynphoprolipherative diseases 117
A phenylalanine-55 to serine amino-acid substitution in the human glycoprotein IX leucine-rich repeat is associated with Bernard-Soulier syndrome. 116
Cryopreservation of human platelets using dimethyl sulfoxide and glycerol-glucose: effects on "in vitro" platelet function. 116
Particulate cytoplasmic structures with high concentration of ubiquitin-proteasome accumulate in myeloid neoplasms 116
Both haploinsufficiency and dominant negative effects are responsible for abnormalities of patiens with MHY9-related disease. 116
A novel mutation in gp1bb reveals the role of the cytoplasmic domain of gpibβ in the pathophysiology of bernard‐soulier syndrome and gpib‐ix complex assembly 116
Inherited thrombocytopenias. The evolving spectrum. 115
X-linked thrombocytopenia with thalassemia: Clinical and biological features of a second family 113
β-1 tubulin R307H SNP alters microtubule dynamics and affects severity of a hereditary thrombocytopenia. 112
Platelet-independent defect in hemostasis associated with sirolimus use 112
Effetti sistemici della terapia trombolitica.[Systemic effects of thrombolytic therapy]. 111
Acquired cyclic thrombocytopenia-thrombocytosis with periodic defect of platelet function. 111
Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia 110
Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk disorders. In patients the SPATA-DVT with inherited Study platelet 108
Autoimmunità e piastrinopatie [Autoimmunity and platelet disorders] 107
MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations. 107
Defect of platelet aggregation and adhesion induced by autoantibody against glycoprotein IIIa. 106
Application of a diagnostic algorithm to 50 consecutive patients with inherited thrombocytopenias 106
Autologous cryopreserved platelets can efficiently support patients with breast cancer after high-dose chemotherapy and circulating progenitor cell transplantation 105
Heparin infusion facilitates ex vivo platelet aggregation in patients with acute myocardial infarction who have undergone thrombolytic therapy. 105
Thrombopoietin levels in patients with primary and reactive thrombocytosis. 104
Platelet composition and function in patients undergoing cardiopulmonary bypass for hearth surgery. 104
Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup 102
Splenectomia in corso di porpora trombocitopenica idiopatica: fattori prognostici e risultati clinici. 102
Autologous transfusion of thrombosol plus low-dose DMSO cryopreserved platelet concentrates (PCs) for severe thrombocytopenia following high-dose chemotherapy (HDC). 102
High versus standard dose methylprednisolone in the acute phase of idiopathic thrombotic thrombocytopenic purpura: a randomized study. 102
Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patients. 101
Platelet predeposit and transfusion in patients receiving high-dose chemotherapy and autologous transplant for breast cancer 101
In vitro and in vivo effects of desmopressin on platelet function 101
Eltrombopag for the treatment of inherited thrombocytopenias: A phase II clinical trial 101
null 100
Donor-recipient incompatibility at CD31-codon 563 is a major risk factor for acute graft-versus-host disease after allogeneic bone marrow transplantation from a human leucocyte antigen-matched donor. 100
Malattia di von Willebrand tipo IIb: descrizione di un caso clinico 100
High prevalence of fibrin formation defects in women with menorrhagia and congenital bleeding disorders 100
Effect of 52 monoclonal antibodies against platelet membrane on platelet aggregation and release reaction 98
NEONATAL ALLOIMMUNE THROMBOCYTOPENIA (NATP) CAUSED BY A NEW LOW-FREQUENCY PLATELET-SPECIFIC ALLOANTIGEN, MAXA, LOCATED ON GPIIB 98
Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome) 98
ETV6-RELATED THROMBOCYTOPENIA (ETV6-RT): CLINICAL AND PATHOGENETIC CHARACTERIZATION OF AN INHERITED THROMBOCYTOPENIA (IT) PREDISPOSING TO CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA (ALL) 98
Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel GFI1B germline mutation 98
Platelet count and aging 97
Effect of anagrelide on platelet count and function in patients with thrombocytosis and myeloproliferative disorders. 97
NOVEL RUNX1 MUTATIONS IN FAMILIES WITH INHERITED THROMBOCYTOPENIA 97
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC 97
The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology 96
Cryopreservation of human platelets using dimethyl sulfoxide and glycerol-glucose: effects on "in vitro" platelet function 95
Heavy chain myosin 9-related disease (MYH9-RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder. 95
ANKRD26-related thrombocytopenia and myeloid malignancies 95
ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia 95
Transfusion of platelet concentrates cryopreserved with thromboSol plus low-dose dimethilsulphoxide in patients with severe thrombocytopenia: a pilot study 94
The effect of red blood cells on platelet aggregation; a study with the whole blood aggregometer 94
Hyperhomocysteinemia and FV ARG 506 GLN in 81 consecutive patients with thrombosis. 94
Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia. 93
PLASMA PROTEIN-Z LEVELS AND HEMOSTASIS IN PATIENTS ON DICUMAROL TREATMENT AND IN PATIENTS WITH BLEEDING TENDENCY OF UNKNOWN ORIGIN 93
Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia 93
A review of platelet secretion assays for the diagnosis of inherited platelet secretion disorders 92
MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations. 91
New roles for mean platelet volume measurement in the clinical practice? 91
CYCLIC THROMBOCYTOPENIA-THROMBOCYTOSIS WITH A PERIODIC DEFECT OF PLATELET-FUNCTION - REPORT OF A CASE 90
Totale 11.743
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Categoria #
all - tutte 80.861
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 80.861
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022889 0 1 32 17 36 48 14 53 53 35 108 492
2022/20232.615 273 158 15 232 265 271 5 138 1.122 21 67 48
2023/2024890 113 125 33 82 107 240 19 58 11 39 37 26
2024/20252.556 48 230 53 84 52 178 141 201 534 89 321 625
2025/20266.430 499 432 827 731 716 305 1.296 287 524 436 212 165
2026/2027413 128 285 0 0 0 0 0 0 0 0 0 0
Totale 18.587