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Blood Diseases

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What's New

Last Posted: Jul 12, 2018

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• Adapting medical guidelines to be patient-centered using a patient-driven process for individuals with sickle cell disease and their caregivers.  
  Cronin Robert Michael et al. BMC hematology 2018 1812
• Sickle SCAN™ (BioMedomics) fulfills analytical conditions for neonatal screening of sickle cell disease.  
  Nguyen-Khoa Thao et al. Annales de biologie clinique 2018 Jul
• Clinical Utility of Quantitative PCR for Chimerism and Engraftment Monitoring after Allogeneic Stem Cell Transplantation for Hematologic Malignancies.  
  Ahci Müberra et al. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2017 Oct 23(10) 1658-1668
• Factor VII Deficiency: From Basics to Clinical Laboratory Diagnosis and Patient Management.  
  Sevenet Pierre-Olivier et al. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2017 Oct 23(7) 703-710
• Hemochromatosis: pathophysiology, evaluation and management of hepatic iron overload with a focus on MRI.  
  Golfeyz Shmuel et al. Expert review of gastroenterology & hepatology 2018 Jul
• MANAGEMENT OF PATIENTS WITH SICKLE CELL DISEASE IN ORAL SURGERY: Literature Review and Update.  
  Prevost Raphaelle et al. Journal of stomatology, oral and maxillofacial surgery 2018 Jun
• People who have a family history of thyroid disease are more likely to have hyperthyroidism.  
  NIDDK, 2018
• Specifying sickle cell disease interventions: a study protocol of the Sickle Cell Disease Implementation Consortium (SCDIC).  
  Baumann Ana A et al. BMC health services research 2018 Jun 18(1) 500
• Are Payers Ready To Address The Financial Challenges Associated With Gene Therapy?  
  Health Affairs Blog, June 28, 2018
• Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.  
  Raffield Laura M et al. PLoS genetics 2018 14(3) e1007293
• Genetic Risk Factors and Inhibitor Development in Hemophilia: What Is Known and Searching for the Unknown.  
  Margaglione Maurizio et al. Seminars in thrombosis and hemostasis 2018 Jun
• Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran.  
  Nourizadeh Maryam et al. Scandinavian journal of immunology 2018 Jun e12699
• Screening to Prevent Osteoporotic Fractures: Updated Evidence Report and Systematic Review for the US Preventive Services Task Force.  
  Viswanathan Meera et al. JAMA 2018 Jun 319(24) 2532-2551
• [Awareness and attitudes of 50 congolese families affected by sickle cell disease: a local survey].  
  Mukinayi Benoît Mbiya et al. The Pan African medical journal 2018 2924
• Community Counts 
  Explore health issues, medical complications, and causes of death that affect people with bleeding disorders who receive care at U.S. Hemophilia Treatment Centers