Search Results - "MANNUCCI, P"
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Miracle of haemophilia drugs: Personal views about a few main players
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-07-2018)“…Introduction In the second decade of the third millennium there have been dramatic developments pertaining to the availability of highly innovative drugs for…”
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Viral safety of coagulation factor concentrates: memoirs from an insider
Published in Journal of thrombosis and haemostasis (01-04-2018)“…Summary The purpose of this essay is to recall the actions taken globally to improve the viral safety of coagulation factor concentrates, mainly in the years…”
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Is haemophilia B less severe than haemophilia A?
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-07-2013)“…Summary A number of observations suggest that severe factor IX deficiency (<1%) may be less clinically severe than the corresponding factor VIII deficiency:…”
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Airborne pollution and cardiovascular disease: burden and causes of an epidemic
Published in European heart journal (01-05-2013)Get full text
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Back to the future: a recent history of haemophilia treatment
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-07-2008)“…In the last few decades, the management of patients with haemophilia has witnessed dramatic improvements, through the larger availability of safe…”
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Use and prescription appropriateness of drugs for peptic ulcer and gastrooesophageal reflux disease in hospitalized older people
Published in European journal of clinical pharmacology (01-03-2020)“…Purpose The aims of this study were to assess the prevalence of use and prescription appropriateness of drugs for peptic ulcer and gastrooesophageal reflux…”
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7
Laboratory monitoring of replacement therapy for major surgery in von Willebrand disease
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-03-2017)“…Von Willebrand disease (VWD) is an inherited haemorrhagic disorder caused by a quantitative or qualitative defect of von Willebrand factor (VWF), a multimeric…”
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8
Venous thromboembolism in von Willebrand disease
Published in Thrombosis and haemostasis (01-09-2002)Get more information
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9
A randomized clinical trial of prophylaxis in children with hemophilia A (the ESPRIT Study)
Published in Journal of thrombosis and haemostasis (01-04-2011)“…Background: Prevention of arthropathy is a major goal of hemophilia treatment. While studies in adults have demonstrated an impact of prophylaxis on the…”
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Health technology assessment for pharmaceuticals in the European Union: what lessons after two decades?
Published in Internal and emergency medicine (01-08-2022)Get full text
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SIPPET: methodology, analysis and generalizability
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-05-2017)“…The development of anti‐FVIII neutralizing alloantibodies (inhibitors), occurring in about one‐third of previously untreated patients (PUPs) with severe…”
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Prevalence of potentially inappropriate medications and risk of adverse clinical outcome in a cohort of hospitalized elderly patients: results from the REPOSI Study
Published in Journal of clinical pharmacy and therapeutics (01-10-2014)“…Summary What is known and objective Inappropriate prescribing is highly prevalent for older people and has become a global healthcare concern because of its…”
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Long COVID: A patient perspective
Published in European journal of internal medicine (01-01-2022)Get full text
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Severe hemophilia with mild bleeding phenotype: molecular characterization and global coagulation profile
Published in Journal of thrombosis and haemostasis (01-04-2010)“…Background: Patients with severe hemophilia may show very varied bleeding tendencies, and the reasons for this heterogeneous clinical expression are unclear…”
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Recombinant porcine factor VIII: a new instalment of a long story
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-03-2015)Get full text
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The complex differential diagnosis between thrombotic thrombocytopenic purpura and the atypical hemolytic uremic syndrome: Laboratory weapons and their impact on treatment choice and monitoring
Published in Thrombosis research (01-11-2015)“…Abstract Thrombocytopenia and microangiopathic hemolytic anemia are the hallmark of the thrombotic microangiopathies (TMAs) thrombotic thrombocytopenic purpura…”
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Sustainable and personalized nutrition: From earth health to public health
Published in European journal of internal medicine (01-04-2021)“…•The main dietary recommendations currently suggest to limit the intake of satured fats.•Yet, recent data fail to demonstrate harm of saturated fats for the…”
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Pharmacokinetics and safety of fibrinogen concentrate
Published in Journal of thrombosis and haemostasis (01-12-2009)“…Background: Although fibrinogen concentrate has been available for the treatment of congenital fibrinogen deficiency for years, knowledge of its…”
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Tailoring hemostatic therapies to lower inhibitor development in previously untreated patients with severe hemophilia A
Published in Journal of thrombosis and haemostasis (01-07-2016)“…Summary After technological progress provided safer therapeutic products for patients with hemophilia A, the development of alloantibodies (inhibitors)…”
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Effects on bleeding complications of pharmacogenetic testing for initial dosing of vitamin K antagonists: a systematic review and meta‐analysis
Published in Journal of thrombosis and haemostasis (01-09-2014)“…Summary Background Although warfarin and other vitamin K antagonists (VKAs) are the most widely used oral anticoagulants for the prevention and treatment of…”
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