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Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue 22, pp. 2331 - 2338
Sickle cell trait (SCT) is unique among the carrier states that are identified during newborn screening. Unlike other heterozygous states for rare recessive... 
KIDNEY-DISEASE | DIAGNOSIS | UNITED-KINGDOM | VENOUS THROMBOEMBOLISM | RENAL MEDULLARY CARCINOMA | SUDDEN-DEATH | ALPHA-THALASSEMIA | RISK | BETA-THALASSEMIA | HEMATOLOGY | ASSOCIATION | Review
Journal Article
Blood, ISSN 0006-4971, 11/2019, Volume 134, Issue Supplement_1, pp. 3392 - 3392
BACKGROUND: The American Board of Internal Medicine (ABIM) offers separate board examinations for adult hematology and medical oncology, yet the vast majority... 
Journal Article
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program, 2012, Volume 2012, pp. 208 - 214
Journal Article
Blood, ISSN 0006-4971, 02/2017, Volume 129, Issue 6, pp. 661 - 662
In this issue of Blood, 2 important studies by Liem et al and Bello et al take advantage of robust phenotypic and genotypic data from well-established cohorts... 
DEATH | HEMATOLOGY | ASSOCIATION | CARRIERS | CELL TRAIT
Journal Article
Hematology. American Society of Hematology. Education Program, ISSN 1520-4391, 11/2018, Volume 2018, Issue 1, pp. 474 - 481
Sickle cell trait (SCT) is unique among the carrier states that are identified during newborn screening. Unlike other heterozygous states for rare recessive... 
KIDNEY-DISEASE | DIAGNOSIS | UNITED-KINGDOM | VENOUS THROMBOEMBOLISM | RENAL MEDULLARY CARCINOMA | SUDDEN-DEATH | ALPHA-THALASSEMIA | RISK | BETA-THALASSEMIA | HEMATOLOGY | ASSOCIATION | EDUCATION, SCIENTIFIC DISCIPLINES | Sickle Cell Disease | New Frontiers
Journal Article
The American Journal of Medicine, ISSN 0002-9343, 10/2013, Volume 126, Issue 10, pp. e15 - e15
Journal Article
American Journal of Medicine, ISSN 0002-9343, 10/2013, Volume 126, Issue 10, p. e15
Journal Article
The American Journal of Medicine, ISSN 0002-9343, 10/2013, Volume 126, Issue 10, p. e15
Journal Article
Blood, ISSN 0006-4971, 11/2013, Volume 122, Issue 21, pp. 2214 - 2214
Abstract Background An increased risk of venous thromboembolism (VTE) among individuals with sickle cell disease (SCD) has only recently been recognized.... 
Journal Article
Thrombosis Research, ISSN 0049-3848, 05/2016, Volume 141, p. 35
Venous thromboembolism (VTE) is common in sickle cell disease (SCD); however, the risk factors associated with VTE in patients with sickle variant syndromes... 
Sickle cell anemia | Hemoglobin | Thalassemia | Genotype | Genetic aspects | Adults | Thromboembolism | Risk factors | Medical research | Glycosylated hemoglobin | Medicine, Experimental
Journal Article
American Journal of Medicine, The, ISSN 0002-9343, 2013, Volume 126, Issue 10, pp. e15 - e15
Journal Article
Blood, ISSN 0006-4971, 11/2012, Volume 120, Issue 21, pp. 3243 - 3243
Abstract Abstract 3243 Background: Sickle cell disease (SCD) is a hypercoagulable state, leading to increased rates of thrombotic complications such as stroke... 
Journal Article
American Journal of Medicine, ISSN 0002-9343, 05/2013, Volume 126, Issue 5, pp. 443 - 449
Background: Sickle cell disease is recognized as a hypercoagulable state; however, the frequency and characteristics of venous thromboembolism in sickle cell... 
Journal Article
The American Journal of Medicine, ISSN 0002-9343, 05/2013, Volume 126, Issue 5, p. 443
  Naik et al establish the prevalence and risk factors for venous thromboembolism in a large cohort of patients with sickle cell disease and determine the... 
Mortality | Medical treatment | Sickle cell disease | Thrombosis | Patients | Risk factors
Journal Article
JAMA, ISSN 0098-7484, 11/2014, Volume 312, Issue 20, pp. 2115 - 2125
Journal Article
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