P. Radossi

发表

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.

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.

Orthopedic Surgery in HIV-Positive Hemophiliac Patients

G. Tagariello, P. Radossi, 2008 .

Heparin Induces Apoptosis in Lymphocytes from B-cell Chronic Lymphocytic Leukemia.

A. Girolami, F. Dazzi, P. Radossi, 1998, Hematology.

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.

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

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

“Pseudo Homozygous” Activated Protein C Resistance due to Double Heterozygous Factor V Defects (Factor V Leiden Mutation and Type I Quantitative Factor V Defect) Associated with Thrombosis: Report of Two Cases Belonging to Two Unrelated Kindreds

P. Simioni, A. Girolami, P. Radossi, 1996, Thrombosis and Haemostasis.

Treatment With Efmoroctocog Alfa (Elocta®) in Hemophilia: A Case Series

A. Tosetto, S. Pasca, E. Zanon, 2020 .

CD25‐negative hairy cell leukaemia: Intracytoplasmic detection of Tac antigen and interferon‐induced surface expression

A. Girolami, F. Dazzi, P. Radossi, 1995, The Journal of pathology.

Intractable pruritus in non-Hodgkin lymphoma/CLL: rapid response to IFN alpha.

F. Dazzi, P. Radossi, F. Vianello, 1996, British journal of haematology.

Homozygous patients with APC resistance may remain paucisymptomatic or asymptomatic during oral contraception.

P. Simioni, A. Girolami, P. Radossi, 1996, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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.

Promoting physical activity in people with haemophilia: the MEMO (Movement for persons with haEMOphilia) expert consensus project.

G. Di Minno, A. Coppola, R. De Cristofaro, 2021, Blood transfusion = Trasfusione del sangue.

Non-Compartment and Compartmental Pharmacokinetics, Efficacy, and Safety of Kedrion FIX concentrate.

E. Santagostino, S. Aksu, G. Castaman, 2020, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

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

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

Detection of B-cell monoclonality in fine needle aspiration by PCR analysis.

A. Girolami, F. Dazzi, P. Radossi, 1998, Leukemia & lymphoma.

Intra‐articular rifamycin in haemophilic arthropathy

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

Effects of secondary prophylaxis started in adolescent and adult haemophiliacs

P. Mannucci, M. Franchini, C. Santoro, 2008, 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.

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.

High incidence of anti‐FVIII antibodies against non‐coagulant epitopes in haemophilia A patients: a possible role for the half‐life of transfused FVIII

A. Girolami, F. Dazzi, P. Radossi, 1996, British journal of haematology.

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.

F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes

M. Morfini, M. Pinotti, A. Branchini, 2021, Journal of thrombosis and haemostasis : JTH.

IDEAL study: A real‐world assessment of pattern of use and clinical outcomes with recombinant coagulation factor IX albumin fusion protein (rIX‐FP) in patients with haemophilia B in Italy

M. Margaglione, A. Tosetto, C. Santoro, 2022, Haemophilia : the official journal of the World Federation of Hemophilia.

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 .

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 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.

Rate and appropriateness of polypharmacy in older patients with hemophilia compared with age‐matched controls

A. Iorio, A. Nobili, E. Santagostino, 2018, 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.

Systematic Review of the Published Evidence on the Pharmacokinetic Characteristics of Factor VIII and IX Concentrates

E. Neufeld, A. Iorio, C. Hermans, 2014 .

Acquired haemophilia A as a blood transfusion emergency.

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

Translational readthrough at F8 nonsense variants in the factor VIII B domain contributes to residual expression and lowers inhibitor association

M. Pinotti, A. Branchini, G. Castaman, 2022, Haematologica.

Comorbidities in persons with haemophilia aged 60 years or more compared with age‐matched people from the general population

A. Iorio, E. Santagostino, P. Mannucci, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

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.

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

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

Undetected vitamin B12 deficiency due to false normal assay results.

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

Primary breast lymphoma.

A. Girolami, R. Sartori, P. Radossi, 1998, Forum.

Remission in hairy cell leukemia-variant following splenic radiotherapy alone.

A. Girolami, R. Sartori, P. Radossi, 1997, Leukemia & lymphoma.

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.

Comparison of quality of life, and emotional and functional profiles in older people with and without severe haemophilia

A. Iorio, E. Santagostino, P. Mannucci, 2021, Haemophilia : the official journal of the World Federation of Hemophilia.

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.

Risk of bleeding and thrombosis in inherited qualitative fibrinogen disorders

G. Castaman, P. Radossi, S. Giacomelli, 2019, European journal of haematology.

Marked but transitory elevation of hepatic transaminases after subcutaneous calcium heparin administration.

A. Girolami, F. Dazzi, P. Radossi, 1994, Acta haematologica.

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.

Modifications of erythropoiesis in myelodysplastic syndromes treated with recombinant erythropoietin as evaluated by soluble transferrin receptor, high fluorescence reticulocytes and hypochromic erythrocytes.

M. Boccadoro, E. Barbieri, A. Longo, 1994, Haematologica.

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.

Myelodysplastic syndrome and thrombocytosis: a random association?

A. Girolami, F. Dazzi, P. Radossi, 1994, Haematologica.