Birth Prevalence of Sickle Cell Disease in India: A Systematic Review and Meta-Analysis. [PDF]
Rahiman EA, Anne RP, Warrier RP.
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Avoidable under-5 mortality from congenital and genetic disorders: a frontier analysis of GBD 2023 identifying intervention targets. [PDF]
Ruan J +8 more
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Sickle cell β-thalassemia diagnosed at age 40: a case report. [PDF]
Nikolaidis CG +3 more
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Burden of hemoglobinopathies and hemolytic anemias in the World Health Organization African region, 2000-2021: Findings from the Global Burden of Disease 2021 study. [PDF]
GBD 2021 Hemoglobinopathies and Hemolytic Anemias Collaborators +32 more
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Assessment of β-Thalassemia Trait Occurrence in an Outpatient Sample from Southern Chile: A Retrospective Study. [PDF]
Balcázar-Villarroel M +9 more
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Glomerular Injury Findings in Patients with Thalassemia Minor. [PDF]
Hexner-Erlichman Z +4 more
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Caught by Whole-Exome Sequencing: Hemoglobin Sun Prairie in a Patient With Unexplained Hemolytic Anemia From Nepal. [PDF]
Upadhaya P, Shrestha A.
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Acute erythroblastopenia due to Parvovirus B19 in hemoglobinopathies: a retrospective case series at Ibn Sina Hospital, Rabat, Morocco. [PDF]
Regragui I +6 more
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First Report of Co-Inheritance of Hemoglobin British Columbia (HBB:c.304G>A) and β-Thalassemia IVS-I-6 (HBB:c.92+6T>C): Clinical Characterization of an Iranian Case. [PDF]
Fathalizade K +5 more
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