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1998, Hematology/oncology clinics of North America, Volume 12, no. 6., x, p. 1141-1371
Book
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 135, Issue 2, pp. AB121 - AB121
  Results Despite reactions consistent with IgE-mediated hypersensitivity, each patient had negative skin testing to vWF products, Factor VIII, and polysorbate... 
Allergy and Immunology | Medical tests | Skin | Von Willebrand factor | Patients | Medical treatment | Allergies
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 3784 - 3784
Abstract Introduction Early detection of joint problems and musculoskeletal (MSK) abnormities is a priority in hemophilia care worldwide; however, there is no... 
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 10/2016, Volume 63, Issue 10, pp. 1822 - 1828
Journal Article
Blood, ISSN 0006-4971, 11/2013, Volume 122, Issue 21, pp. 563 - 563
Abstract Background Patients (pts) with thalassemia major (TM) require regular red blood cell transfusions. Adequate iron chelation prevents morbidity and... 
Journal Article
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program, ISSN 1520-4391, 2010, Volume 2010, Issue 1, pp. 451 - 455
Over the past four decades, there have been dramatic improvements in survival for patients with thalassemia major due in large measure to improved iron... 
HEMATOLOGY | EDUCATION, SCIENTIFIC DISCIPLINES | Iron Chelating Agents - therapeutic use | Iron Overload - drug therapy | Humans | Thalassemia - drug therapy | Thalassemia - economics | Clinical Trials as Topic | Drug Therapy, Combination | Iron Chelating Agents - economics
Journal Article
Blood, ISSN 0006-4971, 11/2012, Volume 120, Issue 21, pp. 3368 - 3368
Abstract Abstract 3368 Background: The role of pharmacokinetic (PK) assessment of factor VIII (fVIII) plasma levels in hemophilia A patients (pts) is evolving.... 
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 08/2010, Volume 1202, Issue 1, pp. ix - x
Journal Article
Blood, ISSN 0006-4971, 11/2011, Volume 118, Issue 21, pp. 3314 - 3314
Abstract Abstract 3314 BACKGROUND: For congenital hemophilia patients who develop inhibitors to factors VIII or IX, the management of bleeding episodes can be... 
Journal Article
Blood, ISSN 0006-4971, 11/2011, Volume 118, Issue 21, pp. 2066 - 2066
Abstract Abstract 2066 Background: Most newborns with HS have a family history of disease since the most common inheritance pattern is autosomal dominant.... 
Journal Article
Blood, ISSN 0006-4971, 11/2011, Volume 118, Issue 21, pp. 1088 - 1088
Abstract Abstract 1088 Introduction: MRI estimates are gradually replacing liver biopsy for liver iron concentration (LIC) measurements in clinical trials and... 
Journal Article
American Journal of Hematology, ISSN 0361-8609, 07/2014, Volume 89, Issue 7, pp. 684 - 688
Journal Article
Blood, ISSN 0006-4971, 11/2010, Volume 116, Issue 21, pp. 4279 - 4279
Abstract Abstract 4279 Background: A fraction of patients (up to 30%) with transfusional iron overload on deferasirox (DFX, Exjade®) have less-than-adequate... 
Journal Article
Blood, ISSN 0006-4971, 01/2008, Volume 111, Issue 2, pp. 479 - 479
Quinn and colleagues evaluate 3 early severity predictors defined from the Cooperative Study of Sickle Cell Disease in an independent prospective newborn... 
HEMATOLOGY | CELL-ANEMIA | CHILDREN
Journal Article
Blood, ISSN 0006-4971, 11/2011, Volume 118, Issue 21, pp. 5296 - 5296
Abstract Abstract 5296 Introduction: MRI assessment of LIC concentration is increasing utilized as the primary outcome variable of clinical trials for iron... 
Journal Article
Journal Article
Blood, ISSN 0006-4971, 11/2010, Volume 116, Issue 21, pp. 3675 - 3675
Abstract Abstract 3675 Background: The FDA-approved label for recombinant FVIIa (rFVIIa), for treatment of bleeding episodes and prevention of bleeding in... 
Journal Article
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