Description of the Bayesian hierarchical model used to create the phenotype in the CSSCD cohort. Supplementary Figure 1 contains information on the LD structure of the UGT1A region in the CSCCD cohort

NIAID Data Ecosystem50

LGALS3 +191 and +292 with vaso-occlusive crisis and respiratory tract infection in children with sickle cell anemia attended in Hemope Foundation—Recife/Brazil.

镰状细胞贫血并发症

遗传标记与疾病关联

LGALS3 +191 and +292 with vaso-occlusive crisis and respiratory tract infection in children with sickle cell anemia attended in Hemope Foundation—Recife/Brazil.

NIAID Data Ecosystem40

Multivariate analysis of associations between gene polymorphisms and laboratory biomarkers in SCA and HbSC patients with a previous history of priapism.

医学遗传学

镰状细胞贫血并发症

Multivariate analysis of associations between gene polymorphisms and laboratory biomarkers in SCA and HbSC patients with a previous history of priapism.

Figshare2021-02-04 更新50

DATA FOR SCA AND CONTROLS

镰状细胞贫血并发症

儿童肾病临床指标

The research focused on persistent proteinuria among a cohort of Nigerian children with sickle cell anaemia and apparently healthy age- and sex-matched haemoglobin AA controls. Persistent proteinuria

Figshare2026-03-19 更新40

ECHOCARDIOGRAPHIC EVALUATION IN CHILDREN WITH SICKLE CELL ANEMIA: CONTRIBUTION OF 2D STRAIN

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