Research Topics
Species | M FranchiniSummaryAffiliation: University of Parma Country: Italy Publications
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Publications
Acquired hemophilia AMassimo Franchini
Department of Pathology and Laboratory Medicine, Immunohematology and Transfusion Center, University Hospital of Parma, Parma, Italy
Adv Clin Chem 54:71-80. 2011..In this review the actual knowledge on diagnostic and therapeutic aspects of this disease will be summarized...
Multiple gene interaction and modulation of hemostatic balanceMassimo Franchini
Department of Pathology and Laboratory Medicine, Immunohematology and Transfusion Center, University Hospital of Parma, Parma, Italy
Clin Chem Lab Med 47:1455-60. 2009..The role of genetic factors on the modulation of the phenotypic expression of coagulation disorders will be addressed in this review, with particular emphasis on the underlying pathogenic mechanisms and clinical implications...
Hepcidin and iron metabolism: from laboratory to clinical implicationsMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Italy
Clin Chim Acta 411:1565-9. 2010..The most important advances on the role of hepcidin in normal and abnormal iron metabolism and the main clinical and diagnostic implications are summarized in this review...
Disseminated intravascular coagulation in hematologic malignanciesMassimo Franchini
Department of Pathology and Laboratory Medicine, Immunohematology and Transfusion Center, University Hospital, Parma, Italy
Semin Thromb Hemost 36:388-403. 2010..Current approaches and open issues for the management and treatment of these patients are also reviewed...
Acquired hemophilia in pediatrics: a systematic reviewMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Pediatr Blood Cancer 55:606-11. 2010..The epidemiology, diagnosis, clinical course, and management of this hemorrhagic disorder in children will be addressed in this systematic review...
Errors in transfusion: causes and measures to avoid themMassimo Franchini
Department of Pathology and Laboratory Medicine, Immunohematology and Transfusion Center, University Hospital of Parma, Parma, Italy
Clin Chem Lab Med 48:1075-7. 2010..In this review, the errors related to blood transfusion are briefly summarized along with new technologies developed for improving blood safety...
Serum bilirubin levels and cardiovascular disease risk: a Janus Bifrons?Massimo Franchini
Servizio di Immuno ematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Adv Clin Chem 50:47-63. 2010....
Hyperthyroidism and venous thrombosis: a casual or causal association? A systematic literature reviewMassimo Franchini
Immunohematology and Transfusion Center, Department of Pathology and Laboratory Medicine, University Hospital of Parma, Parma, Italy
Clin Appl Thromb Hemost 17:387-92. 2011....
Recent improvements in the clinical treatment of coagulation factor inhibitorsMassimo Franchini
Immunohematology and Transfusion Center, University Hospital of Parma, Parma, Italy
Semin Thromb Hemost 35:806-13. 2009..The most recent options available for treating patients with acquired hemophilia and congenital hemophilia with inhibitors are addressed in this review...
The use of recombinant activated FVII in postpartum hemorrhageMassimo Franchini
Department of Pathology and Laboratory Medicine, University Hospital of Parma, Immunohematology and Transfusion Center, Parma, Italy
Clin Obstet Gynecol 53:219-27. 2010..Finally, on the basis of the evidence from the literature and on own experience, we included some recommendations and an algorithm on the therapeutic role of rFVIIa in the management of PPH...
Particulate air pollution and cardiovascular risk: short-term and long-term effectsMassimo Franchini
Immunohematology and Transfusion Center, Department of Pathology and Laboratory Medicine, University Hospital of Parma, Italy
Semin Thromb Hemost 35:665-70. 2009..The literature data on the short-term and long-term cardiovascular effects of particulate air pollutants are discussed in this review from a clinical and mechanistic point of view...
Mild hemophilia AM Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
J Thromb Haemost 8:421-32. 2010..Many aspects concerning mild HA remain to be clarified, including the molecular basis, the natural history and the optimal diagnostic and therapeutic strategies. Only large prospective studies will shed light on this condition...
Hemostatic abnormalities in endocrine and metabolic disordersMassimo Franchini
Servizio di Immuno ematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria, 43100 Parma, Italy
Eur J Endocrinol 162:439-51. 2010..Further larger and high-quality studies are needed to provide more definitive information on the effects of endocrine disorders on coagulation and fibrinolysis...
Factor V Leiden and hemophiliaMassimo Franchini
Immunohematology and Transfusion Center, Department of Pathology and Laboratory Medicine, University Hospital of Parma, Parma, Italy
Thromb Res 125:119-23. 2010....
Glanzmann thrombasthenia: an updateMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Clin Chim Acta 411:1-6. 2010..In this review we discuss the main characteristics of GT, focusing on molecular defects, diagnostic evaluation and treatment strategies...
The use of desmopressin in mild hemophilia AMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Blood Coagul Fibrinolysis 21:615-9. 2010..In this paper, we summarize the current knowledge on the mechanisms of action as well as its biological effects in patients with mild hemophilia A. The results of the most important clinical trials in this setting are also reviewed...
Von Willebrand factor-containing factor VIII concentrates and inhibitors in haemophilia A. A critical literature reviewMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Thromb Haemost 104:931-40. 2010..As a result, we have not found definitive evidence supporting a role for product type on inhibitor incidence and inhibitor eradication in haemophilia A patients...
Evaluation of cryopreserved donor skin viability: the experience of the regional tissue bank of VeronaMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Blood Transfus 7:100-5. 2009..In this study we evaluated the cellular viability of cryopreserved skin at the regional tissue bank of Verona (Italy)...
[Acquired hemophilia: update on diagnosis and treatment]Massimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria, Parma
Recenti Prog Med 102:286-9. 2011..In this paper, current knowledgs on diagnostic and therapeutic aspects of this disease are summarized...
Acquired factor V inhibitors: a systematic reviewMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
J Thromb Thrombolysis 31:449-57. 2011..However, since this preparation is no longer used, in this systematic review we have only focused on non-bovine thrombin-related FV inhibitor cases...
Cumulative inhibitor incidence in previously untreated patients with severe hemophilia A treated with plasma-derived versus recombinant factor VIII concentrates: a critical systematic reviewMassimo Franchini
Immunohematology and Transfusion Center, Department of Laboratory and Pathology Medicine, University Hospital of Parma, Via Gramsci 14, Parma, Italy
Crit Rev Oncol Hematol 81:82-93. 2012..e., plasma-derived versus recombinant FVIII concentrates) does not seem to influence the inhibitor rate in PUPs with severe hemophilia A...
Pathogenesis, laboratory, and clinical characteristics of Helicobacter pylori-associated immune thrombocytopenic purpuraMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Italy
Adv Clin Chem 52:131-44. 2010..The aim of this review is to analyze the current knowledge on the pathogenic, diagnostic, clinical, and therapeutic characteristics of H. pylori-associated ITP...
Factor V Leiden in women: a thrombotic risk factor or an evolutionary advantage?Massimo Franchini
Immunohematology and Transfusion Center, Department of Pathology and Laboratory Medicine, University Hospital of Parma, Parma, Italy
Semin Thromb Hemost 37:275-9. 2011..The results of the most important meta-analyses on the relationship between inherited (factor V Leiden) and acquired thrombophilia in women are analyzed in this review, along with the possible evolutionary role of this mutation...
Low-density lipoprotein receptor-related protein 1: new functions for an old moleculeMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Clin Chem Lab Med 49:967-70. 2011..More recently, LRP1 has been implicated in the catabolism of factor VIII and regulation of its plasma concentrations. The pathophysiology of the role of LRP1 in hemostasis will be summarized in this review...
The natural history of chronic hepatitis C in a cohort of HIV-negative Italian patients with hereditary bleeding disordersM Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Verona, Italy
Blood 98:1836-41. 2001..The results confirm the slow progression of HCV infection in HIV-negative hemophiliacs...
The natural history of mild haemophilia: a 30-year single centre experienceA Tagliaferri
Regional Reference Centre for Inherited Bleeding Disorders, Department of Medicine, University Hospital of Parma, Parma, Italy
Haemophilia 18:166-74. 2012..The HTCs should improve patients' knowledge and consideration of their disease and encourage them to maintain regular contact with their haemophilia care provider...
Effects of secondary prophylaxis started in adolescent and adult haemophiliacsA Tagliaferri
Regional Reference Centre for Inherited Bleeding Disorders, University Hospital, Parma, Italy
Haemophilia 14:945-51. 2008..With respect to on-demand treatment, higher factor consumption and cost of secondary prophylaxis were balanced by marked clinical benefits and greater well-being in this cohort of adolescent/adult haemophiliacs...
Immune tolerance with rituximab in congenital haemophilia with inhibitors: a systematic literature review based on individual patients' analysisM Franchini
Immunohematology and Transfusion Center, City Hospital of Parma, Parma, Italy
Haemophilia 14:903-12. 2008..Large prospective randomized studies with an adequate follow-up are needed to confirm these preliminary findings...
[Menorrhagia and inherited disorders of coagulation]M Franchini
Centro Emofilia, Azienda Ospedaliera, Servizio di Immunoematologia e Trasfusione, Verona, Italy
Minerva Ginecol 54:453-60. 2002..Since inherited bleeding disorders are frequently associated with menorrhagia, the conclusion is drawn that an underlying congenital bleeding disorder should be ruled out in any woman with menorrhagia...
Interferon and ribavirin in HIV-negative haemophiliacs with chronic hepatitis C who were nonresponders to a previous interferon treatmentM Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Verona, Italy
Haemophilia 8:794-7. 2002..001). Our study shows that IFN and ribavirin combination therapy is effective in HIV-negative chronically HCV-infected haemophiliacs who do not respond to a previous IFN treatment...
Forum on: the role of recombinant factor VIII in children with severe haemophilia AM Franchini
Immunohaematology and Transfusion Centre, Department of Pathology and Laboratory Medicine, University Hospital of Parma, Parma, Italy
Haemophilia 15:578-86. 2009..These and other topics concerning rFVIII treatment of haemophilic children were discussed in a meeting held in Rome on 27 February 2008 and are summarized in this report...
Mortality and causes of death in Italian persons with haemophilia, 1990-2007A Tagliaferri
Regional Reference Centre for Inherited Bleeding Disorders, University Hospital, Parma, Italy
Haemophilia 16:437-46. 2010..The results of this retrospective study show that in Italian PWH improvements in the quality of treatment and global medical care provided by specialized haemophilia centres resulted in a significantly increased life expectancy...
The use of central venous catheters in haemophilia patientsG Izzi
Unità Operativa Pediatria e Oncoematologia, Dipartimento Materno Infantile, Parma, Italy
Haemophilia 16:29-31. 2010..Finally, we describe our personal experience on the use of the external tunnelled catheter Broviac...
Inherited and acquired factor V deficiencyGiuseppe Lippi
U O di Diagnostica Ematochimica, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Blood Coagul Fibrinolysis 22:160-6. 2011..The aim of the current review is to provide an overview on the physiopathology, diagnostics, and clinical management of both inherited and acquired factor V deficiency...
Prostate-specific antigen, prostate cancer, and disorders of hemostasisGiuseppe Lippi
U O Diagnostica Ematochimica, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospadaliero Universitaria di Parma, Parma, Italy
Semin Thromb Hemost 35:654-64. 2009....
Platelet gel in the treatment of cutaneous ulcers: the experience of the Immunohaematology and Transfusion Centre of ParmaGino Bernuzzi
U O Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Via Gramsci 14, Parma, Italy
Blood Transfus 8:237-47. 2010..Platelet gel is being ever more frequently used to promote healing of cutaneous ulcers. However, the factors that determine the often variable clinical outcome of this procedure are still incompletely understood...
Biochemical markers for the diagnosis of venous thromboembolism: the past, present and futureGiuseppe Lippi
U O di Diagnostica Ematochimica, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Via Gramsci 14, 43126 Parma, Italy
J Thromb Thrombolysis 30:459-71. 2010....
Glycoprotein IIb/IIIa inhibitors: an update on the mechanism of action and use of functional testing methods to assess antiplatelet efficacyGiuseppe Lippi
UO di Diagnostica Ematochimica, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Italy
Biomark Med 5:63-70. 2011..As such, the aim of this article is to provide an update on the mechanism of action and use of functional testing methods to assess antiplatelet efficacy in patients undergoing therapy with GPIIb/IIIa antagonists...
Venous thromboembolism in chronic liver diseaseGiuseppe Lippi
UO di Diagnostica Ematochimica, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Semin Thromb Hemost 37:66-76. 2011..The clinical significance of an increased risk of venous thromboembolism in CLD is an important topic for future research, and the initiation of new randomized studies of potential treatments for this complication is needed...
Shortened activated partial thromboplastin time: causes and managementGiuseppe Lippi
Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Italy
Blood Coagul Fibrinolysis 21:459-63. 2010..If the value is systematically confirmed in subsequent samples, please contact the laboratory to help assess the cause'...
Evaluation of cardiovascular risk in blood donors: results of the CARDIORISK study in the Parma Transfusion ServicePaolo Dell'anna
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laoratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Blood Transfus 8:155-8. 2010..In this study, called "Cardiorisk", we evaluated cardiovascular risk in the population of blood donors at the Service of Immunohaematology and Transfusion Medicine in Parma...
The role of anti-core antibody response in the detection of occult hepatitis B virus infectionSimona Urbani
Unità Operativa di Immunoematologia e Medicina Trasfusionale, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Clin Chem Lab Med 48:23-9. 2010..The risk of occult hepatitis associated with anti-HBc seropositivity has been demonstrated extensively, and the presence of antibody response to HBc can be considered a sentinel marker of occult HBV infection...
Potential role of recombinant activated factor VII for the treatment of severe bleeding associated with disseminated intravascular coagulation: a systematic reviewMassimo Franchini
Immunohematology and Transfusion Center, City Hospital of Verona, Italy
Blood Coagul Fibrinolysis 18:589-93. 2007..Large randomized trials are needed, however, to confirm the preliminary results and to assess the safety and dosing regimens of this agent in refractory bleeding associated with disseminated intravascular coagulation...
Von Willebrand factor: another janus-faced hemostasis proteinMassimo Franchini
Immunohematology and Transfusion Centre, Department of Pathology and Laboratory Medicine, University Hospital of Parma, Italy
Semin Thromb Hemost 34:663-9. 2008..In addition, high plasma levels of VWF have been associated with an increased risk of atherothrombosis. The current article reviews the literature and provides evidence for the two-faced character that VWF therefore represents...
Haemostasis and pregnancyMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Ospedale Policlinico, Piazzale L Scuro, 10, 37134 Verona, Italy
Thromb Haemost 95:401-13. 2006..Based on an analysis of the literature data, this review presents an overview of the main thrombotic and haemorrhagic disorders complicating pregnancy...
Clinical, laboratory and therapeutic aspects of platelet-type von Willebrand diseaseM Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Verona, Italy
Int J Lab Hematol 30:91-4. 2008..In this review, the main clinical, laboratory and therapeutic characteristics of PT-VWD are concisely reported...
Preoperative autologous blood donation in primary total knee arthroplasty: a single-centre experience on 214 consecutive patientsM Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Vox Sang 90:191-4. 2006....
Non-ABO red blood cell alloantibodies following allogeneic hematopoietic stem cell transplantationM Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Bone Marrow Transplant 33:1169-72. 2004....
Recombinant factor VIIa. An update on its clinical useMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Ospedale Policlinico, Piazzale Ludovico Scuro, 37134 Verona, Italy
Thromb Haemost 93:1027-35. 2005..Based on a literature search, this review examines the current knowledge on therapy with rFVIIa, from the now well-standardized uses to the newer and less well-characterised clinical applications...
Recombinant activated factor VII: mechanisms of action and current indicationsMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Semin Thromb Hemost 36:485-92. 2010..The agent's safety profile is also examined, along with recent advances in rFVIIa dosing and storage that may help to improve both clinical outcomes and patient quality of life...
Postpartum acquired factor VIII inhibitorsMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Verona, Italy
Am J Hematol 81:768-73. 2006..Based on an analysis of the literature, this review presents the current knowledge on the pathogenesis, diagnosis, epidemiology, natural history, clinical manifestations, and therapeutic management of postpartum acquired hemophilia A...
Acquired factor VIII inhibitorsMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera Universitaria di Parma, Parma, Italy
Blood 112:250-5. 2008..If confirmed by large controlled studies, these innovative therapies might become a valid option for long-term eradication of factor VIII inhibitors...
Prophylaxis in congenital hemophilia with inhibitors: the role of recombinant activated factor VIIMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Semin Thromb Hemost 35:814-9. 2009..The published data on the use of rFVIIa as a prophylactic treatment in hemophilia patients with inhibitors are reviewed in this article...
Thyroid dysfunction and hemostasis: an issue still unresolvedMassimo Franchini
Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Italy
Semin Thromb Hemost 35:288-94. 2009..Further trials on larger series of patients are needed to confirm these preliminary findings and to elucidate the pathogenic mechanisms regulating the complex interaction between thyroid disorders and hemostasis...
LRP1/CD91 is up-regulated in monocytes from patients with haemophilia A: a single-centre analysisM Franchini
Immunohematology and Transfusion Center, Department of Hematology and Transfusion Medicine, Carlo Poma Hospital, Mantova, Italy
Haemophilia 19:e126-32. 2013..Further studies are needed to assess the clinical implications of these findings...
High prevalence of inherited prothrombotic risk factors in 134 consecutive patients with von Willebrand diseaseMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Am J Hematol 81:465-7. 2006..Three carriers of multiple prothrombotic gene mutations experienced a thrombotic event. Our study suggests that the recent evidence of an association between inherited thrombotic and hemorrhagic disorders also holds true in VWD patients...
Hemostasis and agingMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Ospedale Policlinico, Piazzale Ludovico Scuro, Azienda Ospedaliera di Verona, 37134 Verona, Italy
Crit Rev Oncol Hematol 60:144-51. 2006..The complex inter-relationships between inherited and acquired factors influencing the hemostatic system during aging are discussed in this review...
Extracorporeal immunoadsorption for the treatment of coagulation inhibitorsMassimo Franchini
Immunohematology and Transfusion Center, University Hospital of Parma, Parma, Italy
Semin Thromb Hemost 35:76-80. 2009..However, further randomized clinical trials are needed to better assess the cost-effectiveness of such procedures...
Recombinant factor VIII concentratesMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Semin Thromb Hemost 36:493-7. 2010..In this article we review the current knowledge on the commercially available rFVIII concentrates, analyzing their main characteristics. Moreover, results of the literature on their clinical hemostatic efficacy and safety are summarized...
Laboratory, clinical and therapeutic aspects of acquired hemophilia AMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Italy
Clin Chim Acta 395:14-8. 2008..Moreover, we focus on the most recent advances in the treatment of this disorder, which is primarily aimed to control bleeding episodes and to eradicate the autoantibody production...
The use of desmopressin as a hemostatic agent: a concise reviewMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Verona, Italy
Am J Hematol 82:731-5. 2007..This review briefly summarizes the current clinical indications on the use of desmopressin as a hemostatic agent...
Efficacy and safety of factor VIII/von Willebrand's factor concentrate (Haemate-P) in preventing bleeding during surgery or invasive procedures in patients with von Willebrand diseaseMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Verona, Italy
Haematologica 88:1279-83. 2003..To evaluate the efficacy and safety of the factor VIII/von Willebrand factor concentrate Haemate-P as replacement therapy in patients with von Willebrand's disease (VWD) undergoing surgical or invasive procedures...
Efficacy of desmopressin as surgical prophylaxis in patients with acquired von Willebrand disease undergoing thyroid surgeryM Franchini
Servizio di Immunoematologia e Trasfusione, Istituto di Chimica e Microscopia Clinica and Dipartimento di Chirurgia, Verona, Italy
Haemophilia 8:142-4. 2002..This study highlights the need for coagulation studies in patients with thyroid diseases undergoing thyroid surgery. Subcutaneous desmopressin may be used in these patients in order to prevent a surgically related bleeding risk...
Unrelated allogeneic bone marrow donation: short- and long-term follow-up of 103 consecutive volunteer donorsA Gandini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Bone Marrow Transplant 28:369-74. 2001..1 months). All donors signed a written informed consent for a further bone marrow collection, if needed. Our findings confirm the short- and long-term safety of allogeneic bone marrow collection in volunteer donors...
Biochemistry and physiology of anabolic androgenic steroids dopingG Lippi
UO Diagnostica Ematochimica, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Mini Rev Med Chem 11:362-73. 2011..The aim of this article is to review the biochemistry, physiology and the ergogenic effects of AASs...
Efficacy of desmopressin in preventing hemorrhagic complications in a patient with Marfan syndrome undergoing cardiac surgeryMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Blood Coagul Fibrinolysis 17:325-6. 2006..In this case report, we describe the successful use of desmopressin as prophylaxis against hemorrhage in a patient with a bleeding tendency associated with Marfan syndrome and a platelet function defect undergoing cardiovascular surgery...
Von Willebrand factor and thrombosisMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Ospedale Policlinico, Azienda Ospedaliera di Verona, Piazzale L Scuro, 10, 37134, Verona, Italy
Ann Hematol 85:415-23. 2006..After a description of the structure and physiology of VWF, all these aspects are discussed in the present review...
Thyroid-associated autoimmune coagulation disordersMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
J Thromb Thrombolysis 29:87-91. 2010..Finally, we conclude that the prompt recognition of possible concomitant autoimmune coagulation disorders is important for the correct management of these patients...
Adverse reactions in blood and apheresis donors: experience from two Italian transfusion centresIsabella Crocco
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Blood Transfus 7:35-8. 2009....
Efficacy of Haemate-P as prophylaxis of recurrent bleeding in a patient with type 2B von Willebrand's diseaseMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Blood Coagul Fibrinolysis 16:571-2. 2005..Prophylaxis with Haemate-P was shown to be safe and effective in this patient, thus enabling completion of radiochemotherapy...
The antiphospholipid syndrome: an updateMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Clin Lab 52:11-7. 2006..The most important advances in the pathophysiology, diagnosis and treatment of this condition are discussed in this review...
Inherited thrombophilia: an updateMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Clin Lab 51:357-65. 2005..Finally, we discuss the synergism between genetic and acquired prothrombotic risk factors in some conditions such as pregnancy and cardiovascular diseases...
Interpatient phenotypic inconsistency in severe congenital hemophilia: a systematic review of the role of inherited thrombophiliaMassimo Franchini
Department of Pathology and Laboratory Medicine, Immunohematology and Transfusion Center, University Hospital of Parma, Italy
Semin Thromb Hemost 35:307-12. 2009..Further trials on a large population of patients are needed to establish the role of genetic thrombophilia in the phenotypic expression of severe hemophilia...
Iron and thrombosisMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Verona, Italy
Ann Hematol 87:167-73. 2008..The results of the literature on the effect of iron deficiency and overload on vascular health are critically reviewed in this study from a pathogenic and clinical point of view...
Advances in the diagnosis and management of von Willebrand diseaseMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Hematology 11:219-25. 2006..In this review, the present knowledge regarding the diagnosis and the management of VWD is briefly analyzed...
Prophylaxis in von Willebrand diseaseMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Verona, Italy
Ann Hematol 86:699-704. 2007....
The role of von Willebrand factor in hemorrhagic and thrombotic disordersMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Crit Rev Clin Lab Sci 44:115-49. 2007..The role of VWF in normal and pathological hemostasis is discussed in this review, and important advances in the pathophysiology, diagnosis, and treatment of VWF-associated disorders are also described...
Inhibitors in mild/moderate haemophilia A: two case reports and a literature reviewAnna Chiara Giuffrida
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Italy
Blood Transfus 6:163-8. 2008
Moderate red wine consumption and cardiovascular disease risk: beyond the "French paradox"Giuseppe Lippi
U O Diagnostica Ematochimica, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Semin Thromb Hemost 36:59-70. 2010....
Rituximab in the treatment of adult acquired hemophilia A: a systematic reviewMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Ospedale Policlinico, Piazzale Ludovico Scuro, Azienda Ospedaliera di Verona, 37134 Verona, Italy
Crit Rev Oncol Hematol 63:47-52. 2007..However, large, prospective, randomized trials are needed to confirm these positive preliminary results...
Co-morbidities and quality of life in elderly persons with haemophiliaMassimo Franchini
Immunohaematology and Transfusion Centre, Department of Pathology and Laboratory Medicine, University Hospital of Parma, Italy
Br J Haematol 148:522-33. 2010..This review focuses on co-morbidities in the ageing haemophilia patients, their impact on quality of life and their complex management...
The use of desmopressin in congenital factor XI deficiency: a systematic reviewMassimo Franchini
Servizio di Immunoematologia e Medicina Trasfusionale, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Ann Hematol 88:931-5. 2009..However, these findings need to be supported by further trials on large population of patients...
Acquired hemophilia AMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Verona, Italy
Hematology 11:119-25. 2006..Moreover, new therapeutic strategies (anti-CD20 monoclonal antibody and immune tolerance protocols) are very promising and may further improve the prognosis of acquired hemophilia A...
Advantages and limits of ADAMTS13 testing in thrombotic thrombocytopenic purpuraMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Italy
Blood Transfus 6:127-35. 2008
The bidirectional relationship of cancer and hemostasis and the potential role of anticoagulant therapy in moderating thrombosis and cancer spreadMassimo Franchini
Immunohematology and Transfusion Center, Department of Pathology and Laboratory Medicine, University Hospital of Parma, Parma, Italy
Semin Thromb Hemost 35:644-53. 2009..The main biological and clinical evidence on the relationship between cancer and hemostasis are briefly summarized in this review, as is the potential benefits of anticoagulant therapy in this setting...
The platelet-function analyzer (PFA-100) for evaluating primary hemostasisMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, Verona, Italy
Hematology 10:177-81. 2005..Given its high sensitivity, speed and simplicity of use, we conclude that the PFA-100 could replace the in vivo bleeding time as a screening test for primary hemostasis in routine clinical practice...
Thrombotic microangiopathies: an updateMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona, Verona, Italy
Hematology 11:139-46. 2006..In this review, we focus on the epidemiologic and diagnostic criteria as well as on the most recent insights into the pathophysiology and treatment of these two conditions...
Vaccination, squalene and anti-squalene antibodies: facts or fiction?Giuseppe Lippi
U O Diagnostica Ematochimica, Dipartimento di Patologia e Medicina di Laboratorio, Azienda Ospedaliero Universitaria di Parma, Parma, Italy
Eur J Intern Med 21:70-3. 2010..This review summarizes the current scientific evidence about the relationship between squalene, anti-squalene antibodies and vaccination...
Recent acquisitions in acquired and congenital von Willebrand disordersMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera Policlinico, Piazzale L Scuro, and Istituto di Chimica e Microscopia Clinica, Dipartimento di Scienze Biomediche e Morfologiche, Universita di Verona, Italy
Clin Chim Acta 377:62-9. 2007..Its deficiency is associated with a bleeding tendency. The progresses in the pathophysiology, diagnosis and management of inherited von Willebrand disease and acquired von Willebrand syndrome will be discussed in this review...
Iron overload and hematologic malignanciesMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Centro Emofilia, Azienda Ospedaliera di Verona, 37134 Verona, Italy
Hematol J 5:381-3. 2004..In this review, we briefly report the present knowledge regarding the association between iron overload and hematologic malignancies...
