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  1. 221
    Comparative analysis of oral health and treatment necessities in hemophilia individuals of Davangere population — A case control study
    “... for individuals with congenital blood disorder (CBD) to maintain oral health-related quality of life in Davangere...”
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    Article
  2. 222
    Comparison of deferasirox and deferoxamine effect on liver enzyme activities and ferritin level in patients with beta-thalassemia
    “..., which is a genetic blood disorder of hemoglobin synthesis that causes severe anemia. This study aimed...”
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    Article
  3. 223
    Assessing the role of family well-being on the quality of life of Indian children with thalassemia
    “... established. As thalassemia is chronic blood disorder with burdensome treatment procedures, patients...”
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    Article
  4. 224
    The therapeutic potential of genome editing for β-thalassemia [version 1; referees: 2 approved]
    by Astrid Glaser, Bradley McColl, Jim Vadolas
    Published 2015-12-01
    “... of this technology for the therapy of β-thalassemia. This blood disorder is caused by mutations in the gene encoding...”
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    Article
  5. 225
    Prevalence of Alpha(α)-Thalassemia in Southeast Asia (2010–2020): A Meta-Analysis Involving 83,674 Subjects
    “...Alpha(α)-thalassemia is a blood disorder caused by many types of inheritable α-globin gene...”
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    Article
  6. 226
    Specifying sickle cell disease interventions: a study protocol of the Sickle Cell Disease Implementation Consortium (SCDIC)
    “...Abstract Background Sickle cell disease (SCD) is an inherited blood disorder that results in a...”
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    Article
  7. 227
    The impact of missense mutation in PIGA associated to paroxysmal nocturnal hemoglobinuria and multiple congenital anomalies-hypotonia-seizures syndrome 2: A computational study
    “...Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal blood disorder that manifests...”
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    Article
  8. 228
    Automated in situ chromatin profiling efficiently resolves cell types and gene regulatory programs
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    Article
  9. 229
    Evaluation of health-related quality of life and muscular strength in children with beta thalassemia major
    “...Background: Thalassemia is an inherited blood disorder that requires repeated blood transfusions...”
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    Article
  10. 230
    An unusual ultrasound appearance of renal hemosiderosis in acute sickle cell nephropathy
    “...Sickle cell disease is the most common inherited blood disorder in the United States. The primary...”
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    Article
  11. 231
    A Comparison of Quality of Life between Adolescences with Beta Thalassemia Major and their Healthy Peers
    “...Background The chronic genetic blood disorder, thalassemia, affects Quality of life (QOL...”
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    Article
  12. 232
    Ocular manifestations of sickle cell disease and genetic susceptibility for refractive errors
    “...Purpose: Sickle cell disease (SCD) is the most common and serious form of an inherited blood...”
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    Article
  13. 233
    Quantitative sensory testing is feasible and is well-tolerated in patients with sickle cell disease following a vaso-occlusive episode
    by Bakshi N, Lukombo I, Belfer I, Krishnamurti L
    Published 2018-02-01
    “..., PA, USA Introduction: Sickle cell disease (SCD) is an inherited blood disorder characterized...”
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    Article
  14. 234
    Dietary intakes and nutritional status of children with sickle cell disease at the Princess Marie Louise Hospital, Accra – a survey
    by Isaac Boadu, Agartha Ohemeng, Lorna Awo Renner
    Published 2018-08-01
    “...Abstract Background Sickle cell disease (SCD) is a chronic genetic blood disorder common among...”
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    Article
  15. 235
    An Investigation of the Antioxidant Capacity in Extracts from Moringa oleifera Plants Grown in Jamaica
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    Article
  16. 236
    Proponent or collaborative: Physician perspectives and approaches to disease modifying therapies in sickle cell disease.
    “...Sickle cell disease (SCD) is an inherited blood disorder that primarily affects African-American...”
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    Article
  17. 237
    Capillary electrophoresis improving clinical measurement of clozapine
    by Hsu, Pei-Chun (Lisa)
    Published 2009
    “... the development of agranulocytosis, a possible lethal blood disorder. Therefore, constant therapeutic drug...”
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  18. 238
    Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation
    by Awojoodu, Anthony O.
    Published 2016
    “...Sickle cell disease is a hereditary blood disorder caused by a point mutation in the gene encoding...”
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  19. 239
    Tripartite collaboration of blood‐derived endothelial cells, next generation RNA sequencing and bioengineered vessel‐chip may distinguish vasculopathy and thrombosis among sickle cell disease patients
    “...Abstract Sickle cell disease (SCD) is the most prevalent inherited blood disorder in the world...”
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    Article
  20. 240
    Incidence, Survival Rate and Complications in Patients with Beta-Thalassemia Major in Taiwan: Nationwide Survey from 2007-2011.
    by Yin-Chen Chang, 張盈甄
    Published 2015
    “... blood disorder and patients withβ-Thalassemia major needed to treat with transfusion and deferoxamine...”
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