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HAEMOPHILIA
Rivista
Codice:
E073850
ISSN:
1351-8216
Dati Generali
Dati Generali
Pubblicazioni (55)
Pulisci
Ordina Pubblicazioni:
crescente
decrescente
3 apps in 1: MyCBDR, myWAPPS and myPROBE
Abstract
A new genetic mechanism for congenital afibrinogenemia: maternal uniparental isodisomy for chromosome 4 containing a 15-kb deletion in fibrinogen Aalpha-chain gene
Abstract
Ageing successfully with haemophilia : A multidisciplinary programme
Articolo
Arteriovenous fistula as stable venous access in children with severe haemophilia
Articolo
Befovacimab, an anti‐tissue factor pathway inhibitor antibody: Early termination of the multiple‐dose, dose‐escalating Phase 2 study due to thrombosis
Articolo
Bleeding events in people with congenital haemophilia A without factor VIII inhibitors receiving prophylactic factor VIII treatment: A systematic literature review
Recensione
CANADIAN CLINICAL EXPERIENCE ON SWITCHING FROM OCTOCOG ALFA TO EXTENDED-HALF-LIFE FVIII DAMOCTOCOG ALFA PEGOL IN PATIENTS WITH SEVERE HAEMOPHILIA A
Abstract
Canadian clinical experience on switching from standard half-life recombinant factor VIII (rFVIII), octocog alfa, to extended half-life rFVIII, damoctocog alfa pegol, in persons with haemophilia A ≥ 12 years followed in a Comprehensive Hemophilia Care Program in Canada
Articolo
Characterization of the genetic basis of FXI deficiency in two Turkish patients
Articolo
Clinical trials and haemophilia : does the Bayesian approach make the ideal and desirable good friends?
Articolo
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations
Articolo
DEVELOPMENT AND TESTING OF THE ONLINE PROBE SURVEY AND THE MYPROBE APP AND INTEGRATION WITH THE CANADIAN BLEEDING DISORDER REGISTRY
Articolo
Dental surgery in inherited bleeding disorders with minimal factor support: commentary
Articolo
Evaluation of an automated chromogenic assay for Factor VIII clotting activity measurement in patients affected by haemophilia A
Articolo
Evaluation of the sexual health in people living with hemophilia
Articolo
F8 haplotype and inhibitor risk: results from the Hemophilia Inhibitor Genetics Study (HIGS) Combined Cohort
Articolo
F8 mRNA studies in haemophilia A patients with different splice site mutations
Articolo
Feasibility of Administering the Patient Reported Outcomes, Burdens and Experiences (PROBE) Questionnaire Through the Canadian Bleeding Disorders Registry (CBDR) and Comparison of Data From the Two Sources
Articolo
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency
Articolo
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women.
Articolo
Genetic defects in congenital afibrinogenemia
Abstract
Genetic diagnosis of haemophilia and other inherited bleeding disorders
Articolo
Haemophilia care in children - benefits of early prophylaxis for inhibitor prevention
Articolo
Health‐related quality of life and caregiver burden of emicizumab in children with haemophilia A and factor VIII inhibitors—Results from the HAVEN 2 study
Articolo
High adherence to prophylaxis regimens in haemophilia B patients receiving rIX‐FP: Evidence from clinical trials and real‐world practice
Articolo
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay.
Articolo
Identification of the first missense mutation in the fibrinogen Aalpha-chain gene in a case of afibrinogenemia
Abstract
Identification of two novel missense mutations causing factor XI deficiency
Abstract
Integrated postural analysis in children with haemophilia
Articolo
Involvement of the IgE-basophil system and mild complement activation in haemophilia B with anti-factor IX neutralizing antibodies and anaphylaxis
Articolo
Low thrombin generation during major orthopaedic surgery fails to predict the bleeding risk in inhibitor patients treated with bypassing agents
Articolo
Molecular characterization of three novel splicing mutations causing severe factor V deficiency
Abstract
Molecular investigation of 41 patients affected by coagulation factor XI deficiency
Articolo
Mortality and causes of death in Italian persons with haemophilia, 1990-2007
Articolo
Muscle function deterioration in patients with haemophilia: Prospective experience from Costa Rica
Articolo
Non-severe haemophilia: Is it benign? - Insights from the PROBE study
Articolo
Orthopaedic management of haemophilia arthropathy of the ankle
Articolo
Outcomes for studies assessing the efficacy of hemostatic therapies in persons with congenital bleeding disorders
Articolo
PROTECT VIII kids extension study: Long‐term safety and efficacy of BAY 94‐9027 (damoctocog alfa pegol) in children with severe haemophilia A
Articolo
Patient data meta-analysis of Post-Authorization Safety Surveillance (PASS) studies of haemophilia A patients treated with rAHF-PFM
Articolo
Performing Large‐Scale Genetic Analysis in the Bleeding Disorders Community
Articolo
Polypharmacy in older adults with severe haemophilia
Articolo
Prevention of arthropathy in haemophilia: prophylaxis
Articolo
Rare coagulation deficiencies
Articolo
Relationship of EQ-5D Pain Domain and Bleeds - Insights from the PROBE Study
Abstract
Results from a large multinational clinical trial (guardian (TM) 1) using prophylactic treatment with turoctocog alfa in adolescent and adult patients with severe haemophilia A: safety and efficacy
Articolo
Sequential combined bypassing therapy is safe and effective in the treatment of unresponsive bleeding in adults and children with haemophilia and inhibitors
Articolo
State of the art of rare bleeding disorders database (RBDD)
Abstract
Synoviorthesis in haemophilia patients with inhibitors
Articolo
Synovitis and joint health in patients with haemophilia: Statements from a European e‐Delphi consensus study
Articolo
Test-retest reliability of a mobile application of the patient reported outcomes burdens and experiences (PROBE) study
Articolo
The spectrum of FXI deficiency in Italy
Articolo
The thrombin generation assay distinguishes inhibitor from non‐inhibitor patients with severe haemophilia A
Articolo
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients
Abstract
Venous access in haemophilic children: choice and management
Articolo
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