G. Tagariello

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High rate of spontaneous inhibitor clearance during the long term observation study of a single cohort of 524 haemophilia A patients not undergoing immunotolerance

A. Iorio, D. Matino, G. Tagariello, 2013, Journal of Hematology & Oncology.

Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A

M. Margaglione, F. Sessa, D. Pisanelli, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

In vitro reactivity of factor VIII inhibitors with von Willebrand factor in different commercial factor VIII concentrates

G. Tagariello, D. Belvini, R. Salviato, 2007, American journal of hematology.

Occurrence of inhibitors in previously untreated or minimally treated patients with haemophilia A after exposure to a plasma‐derived solvent‐detergent factor VIII concentrate

A. Gringeri, G. Tagariello, P. Mannucci, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Efficacy and inhibitor development in previously treated patients with haemophilia A switched to a B domain‐deleted recombinant factor VIII

M. Morfini, E. Santagostino, P. Mannucci, 2004, British journal of haematology.

Experience of a single Italian center in genetic counseling for hemophilia: from linkage analysis to molecular diagnosis.

G. Tagariello, D. Belvini, R. Salviato, 2000, Haematologica.

Orthopedic Surgery in HIV-Positive Hemophiliac Patients

G. Tagariello, P. Radossi, 2008 .

Clinical Factors Associated with Progression to AIDS in the Italian Cohort of HIV-Positive Hemophiliacs

M. Morfini, F. Chiarotti, M. Mazzucconi, 1994, Thrombosis and Haemostasis.

Mild bleeding diathesis in a boy with combined severe haemophilia B (C10400→T) and heterozygous factor V Leiden

A. Lombardi, A. Girolami, E. Zanon, 2001, Haemophilia : the official journal of the World Federation of Hemophilia.

Autologous chondrocytes as a novel source for neo-chondrogenesis in haemophiliacs

C. Grandi, P. Parnigotto, G. Tagariello, 2016, Cell and Tissue Research.

The JAK2(V617F) tyrosine kinase mutation in blood donors with upper-limit haematocrit levels.

G. Tagariello, D. Belvini, R. Salviato, 2009, Blood transfusion = Trasfusione del sangue.

High resolution melting for F9 gene mutation analysis in patients with haemophilia B.

G. Tagariello, D. Belvini, R. Salviato, 2019, Blood transfusion = Trasfusione del sangue.

Phase 1, single‐dose escalating study of marzeptacog alfa (activated), a recombinant factor VIIa variant, in patients with severe hemophilia

L. Boggio, S. Arkin, M. Mancuso, 2018, Journal of thrombosis and haemostasis : JTH.

“In vitro” correction of the severe factor V deficiency‐related coagulopathy by a novel plasma‐derived factor V concentrate

P. Simioni, F. Peyvandi, G. Tagariello, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

IDO1 suppresses inhibitor development in hemophilia A treated with factor VIII.

D. Fuchs, L. Boon, A. Iorio, 2015, The Journal of clinical investigation.

Hepatitis C virus genotypes and severity of chronic liver disease in haemophiliacs

A. Alberti, P. Pontisso, G. Tagariello, 1995, British journal of haematology.

Tyr2105Cys mutation in exon 22 of FVIII gene is a risk factor for the development of inhibitors in patients with mild/moderate haemophilia A

D. Girelli, O. Olivieri, G. Lippi, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

ANTIBODY RESPONSE TO PRE-S2 AND HEPATITIS B VIRUS INDUCED LIVER DAMAGE

A. Alberti, P. Pontisso, G. Tagariello, 1988, The Lancet.

Markers of Hypercoagulability in Patients with Hemophilia B Given Repeated, Large Doses of Factor IX Concentrates during and after Surgery

P. Mannucci, E. Santagostino, K. Bauer, 1994, Thrombosis and Haemostasis.

Flow cytometry CD4+CD26−CD38+ lymphocyte subset in the microenvironment of Hodgkin lymphoma-affected lymph nodes

G. Tagariello, A. Padoan, Laura Candiotto, 2014, Annals of Hematology.

In Vitro Conditioning of Adipose-Derived Mesenchymal Stem Cells by the Endothelial Microenvironment: Modeling Cell Responsiveness towards Non-Genetic Correction of Haemophilia A

C. Grandi, P. Parnigotto, G. Tagariello, 2022, International journal of molecular sciences.

Anticardiolipin Antibodies in Hemophiliac and Nonhemophiliac Patients with Chronic Hepatitis C

A. Girolami, E. Zanon, G. Tagariello, 1998 .

Antibody to hepatitis C virus and liver disease in volunteer blood donors.

A. Alberti, A. Ruol, A. Dal Canton, 1991, Annals of internal medicine.

Cases of surgery in high‐responder haemophilia patients

J. Goudemand, G. Tagariello, F. Lopaciuk, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

Persistence of parvovirus B19 DNA in synovium of patients with haemophilic arthritis

K. Zakrzewska, A. Azzi, G. Tagariello, 2001, Journal of medical virology.

Immune thrombocytopenia successfully treated with eltrombopag following multiple therapies including romiplostim.

G. Tagariello, R. Sartori, M. Ruggeri, 2014, Blood transfusion = Trasfusione del sangue.

A multicenter controlled, randomized, open trial of interferon alpha2b treatment of anti-human immunodeficiency virus-negative hemophilic patients with chronic hepatitis C. Hepatitis Study Group of the Association of Italian Hemophilia Centers.

P. Pontisso, M. Morfini, E. Santagostino, 1997, Blood.

Intra‐articular rifamycin in haemophilic arthropathy

G. Tagariello, P. Radossi, P. Davoli, 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

European Study on Orthopaedic Status of haemophilia patients with inhibitors

G. Dolan, M. Morfini, S. Haya, 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

Concurrent total hip and knee replacements in a patient with haemophilia with inhibitors using recombinant factor VIIa by continuous infusion

G. Tagariello, P. Radossi, E. De Biasi, 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

Comparison of the rates of joint arthroplasty in patients with severe factor VIII and IX deficiency: an index of different clinical severity of the 2 coagulation disorders.

A. Iorio, P. Mannucci, M. Morfini, 2009, Blood.

One‐stage replacement of infected knee prosthesis in a patient with haemophilia A and high titre of inhibitors

G. Tagariello, R. Sartori, P. Radossi, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

Consensus perspectives on surgery in haemophilia patients with inhibitors: summary statement

J. Goudemand, C. Négrier, E. Rodríguez‐Merchán, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

Prevalence of anti‐FVIII antibodies in severe haemophilia A patients with inversion of intron 22

A. Girolami, F. Dazzi, G. Tagariello, 1997, British journal of haematology.

Interleukin-1 in haemophilic arthritis.

G. Tagariello, F. D. di Giovine, 1996, Thrombosis and Haemostasis.

Autologous chondrocytes as a novel source for neo-chondrogenesis in haemophiliacs

C. Grandi, P. Parnigotto, G. Tagariello, 2016, Cell and Tissue Research.

Correlation between FIX genotype and pharmacokinetics of Nonacog alpha according to a multicentre Italian study

G. Barillari, G. Di Minno, M. Napolitano, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of the Profile of the Patients with Hemophilia B Eligible for Treatment with Nonacog Alfa Once-Weekly

M. Morfini, C. Santoro, R. De Cristofaro, 2020 .

2 coagulation disorders factor VIII and IX deficiency: an index of different clinical severity of the Comparison of the rates of joint arthroplasty in patients with severe

A. Iorio, P. Mannucci, M. Morfini, 2013 .

Use of factor IX concentrates in active teenagers with hemophilia B

G. Tagariello, 2004, Blood Coagulation and Fibrinolysis.

F8 gene mutation profile and ITT response in a cohort of Italian haemophilia A patients with inhibitors

G. Castaman, E. Zanon, G. Tagariello, 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

Outcome in moderate haemophilia: back to the past? Remarks on haemophilia A classification and treatment.

G. Castaman, G. Tagariello, P. Radossi, 2014, Blood transfusion = Trasfusione del sangue.

Total ankle replacement for end‐stage arthropathy in patients with haemophilia

G. Tagariello, R. Sartori, P. Radossi, 2008, Haemophilia.

Radiosynoviorthesis in people with haemophilia.

F. Pozza, G. Tagariello, P. Radossi, 2013, Blood transfusion = Trasfusione del sangue.

The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype

M. Margaglione, E. Grandone, F. Torricelli, 2008, Haematologica.

The Italian haemophilia B mutation database: a tool for genetic counselling, carrier detection and prenatal diagnosis.

G. Tagariello, D. Belvini, R. Salviato, 2007, Blood transfusion = Trasfusione del sangue.

Haematological Care in Patients with Haemophilia and Inhibitors Candidate to Orthopaedic Surgery

G. Tagariello, P. Radossi, M. Basso, 2017 .

Correction of knee flexion contracture at the time of surgical fixation of a femoral supracondylar fracture in a haemophiliac with inhibitors.

G. Tagariello, P. Radossi, Laura Candiotto, 2015, Blood transfusion = Trasfusione del sangue.

Large FVIII gene deletion confers very high risk of inhibitor development in three related severe haemophiliacs

G. Tagariello, D. Belvini, R. Salviato, 2002, Haemophilia : the official journal of the World Federation of Hemophilia.

The Management of the Haemophilic Arthropathy

G. Roselli, M. Makris, M. Matucci-Cerinic, 2017 .

Molecular genotyping of the Italian cohort of patients with hemophilia B.

G. Castaldo, G. Tagariello, D. Belvini, 2005, Haematologica.

Response: Comparing joint arthroplasties in severe hemophilia A with severe hemophilia B

A. Iorio, P. Mannucci, G. Tagariello, 2009 .

Ribosome readthrough accounts for secreted full‐length factor IX in hemophilia B patients with nonsense mutations

F. Bernardi, M. Pinotti, A. Canella, 2012, Human mutation.

Inhibitors in haemophilia B: the Italian experience

M. Morfini, G. Castaman, A. Rocino, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

Pharmacokinetics of a new human plasma‐derived double virus inactivated and nanofiltered factor IX concentrate in previously treated severe or moderately severe haemophilia B patients

M. Morfini, E. Santagostino, G. Castaman, 2019, Haemophilia : the official journal of the World Federation of Hemophilia.

Multiplex ligation‐dependent probe amplification as first mutation screening for large deletions and duplications in haemophilia

G. Tagariello, D. Belvini, R. Salviato, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Prenatal diagnosis of haemophilia B: the Italian experience

M. Bicocchi, I. Garagiola, A. Rocino, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

Acquired haemophilia A as a blood transfusion emergency.

M. Franchini, G. Tagariello, R. Sartori, 2008, Blood transfusion = Trasfusione del sangue.

Clinical heterogeneity and predictors of outcome in primary autoimmune hemolytic anemia: a GIMEMA study of 308 patients.

D. Consonni, A. Zanella, G. Gaidano, 2014, Blood.

Hepatitis B core antigen in serum during acute hepatitis B

P. Pontisso, G. Tagariello, L. Chemello, 1988, Journal of medical virology.

Hepatitis C virus quasispecies in the natural course of HCV‐related disease in patients with haemophilia

A. Alberti, P. Pontisso, G. Tagariello, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

Hepatitis G viral RNA in Italian haemophiliacs with and without hepatitis C infection

M. Biasin, G. Tagariello, P. Davoli, 1996, The Lancet.

Romiplostim for the early management of severe immune thrombocytopenia unresponsive to conventional treatment

G. Tagariello, R. Sartori, P. Radossi, 2012, British journal of haematology.

Homozygous F5 deep‐intronic splicing mutation resulting in severe factor V deficiency and undetectable thrombin generation in platelet‐rich plasma

J. Rosing, P. Simioni, G. Tagariello, 2011, Journal of thrombosis and haemostasis : JTH.

P. Pontisso, M. Morfini, E. Santagostino, 1997, Blood.

Clinical factors associated with progression to AIDS in the Italian cohort of HIV-positive hemophiliacs. G.I.C.C. Gruppo Italiano Coagulopatie Congenite.

M. Morfini, F. Chiarotti, M. Mazzucconi, 1994, Thrombosis and haemostasis.

Undetected vitamin B12 deficiency due to false normal assay results.

G. Tagariello, R. Sartori, P. Radossi, 2013, Blood transfusion = Trasfusione del sangue.

Outcome of Patients with Relapsed/Refractory (R/R) Chronic Lymphocytic Leukemia (CLL) and/or 17p Deletion/TP53 Mutations Treated with Ibrutinib According to a Named Patient Program (NPP) in Italy: Preliminary Analysis of a Real Life Retrospective Study

R. Foà, S. Molica, M. Vignetti, 2016 .

Unbiased pro-thrombotic features at diagnosis in 977 thrombocythemic patients with Philadelphia-negative chronic myeloproliferative neoplasms.

M. Vignetti, G. Gaidano, V. Martinelli, 2016, Leukemia research.

Dramatic post-splenectomy onset of malaria caused by latent Plasmodium vivax in a female immigrant with severe immunological anaemia.

G. Tagariello, R. Sartori, P. Radossi, 2014, Blood transfusion = Trasfusione del sangue.

Complications after stapled hemorrhoidectomy: can they be prevented?

G. Tagariello, G. Milito, D. Mascagni, 2002, Techniques in Coloproctology.

Clinical relevance of isolated prolongation of the activated partial thromboplastin time in a cohort of adults undergoing surgical procedures.

G. Castaman, G. Tagariello, R. Salviato, 2017, Blood transfusion = Trasfusione del sangue.

Challenges in the Management of Hemophilia B with Inhibitor

G. Tagariello, J. Horáková, Denisa Jankovičová, 2013, Seminars in Thrombosis & Hemostasis.

Outcome of 472 Chronic Myeloid Leukemia Patients Treated with Frontline Nilotinib: A Gimema CML WP Analysis

R. Foà, M. Baccarani, G. Rosti, 2018, Blood.

Italian daily platelet transfusion practice for haematological patients undergoing high dose chemotherapy with or without stem cell transplantation: a survey by the GIMEMA Haemostasis and Thrombosis Working Party.

V. De Stefano, A. Falanga, G. Castaman, 2016, Blood transfusion = Trasfusione del sangue.

Prenatal diagnosis of haemophilia A by using intron 1 inversion detection

G. Tagariello, D. Belvini, R. Salviato, 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

Factor VIII gene intron 1 inversion: lower than expected prevalence in Italian haemophiliac severe patients

G. Tagariello, D. Belvini, R. Salviato, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

Rapid prenatal diagnosis of haemophilia

G. Tagariello, D. Belvini, R. Salviato, 2001, Haemophilia.

Mortality and causes of death in Italian persons with haemophilia, 1990–2007

M. Morfini, E. Santagostino, M. Franchini, 2010, Haemophilia : the official journal of the World Federation of Hemophilia.

Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)

J. Esser, G. Tiscia, M. N. D. Minno, 2012, Journal of thrombosis and haemostasis : JTH.

Differences among young adults, adults and elderly chronic myeloid leukemia patients.

G. Specchia, M. Gobbi, R. Fanin, 2015, Annals of oncology : official journal of the European Society for Medical Oncology.

A rapid and cost effective method for analysis of dinucleotide repeat polymorphisms in the factor VIII gene

A. Chuansumrit, G. Tagariello, F. Preston, 1996, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.