Cargando…
Prevalence of Vitamin D Deficiency Varies Widely by Season in Canadian Children and Adolescents with Sickle Cell Disease
Sickle cell disease (SCD) is an inherited disorder caused by a variant (rs334) in the β-globin gene encoding hemoglobin. Individuals with SCD are thought to be at risk of vitamin D deficiency. Our aim was to assess serum 25-hydroxyvitamin D (25OHD) concentrations, estimate deficiency prevalence, and...
Autores principales: | Samson, Kaitlyn L. I., McCartney, Heather, Vercauteren, Suzanne M., Wu, John K., Karakochuk, Crystal D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852430/ https://www.ncbi.nlm.nih.gov/pubmed/29385701 http://dx.doi.org/10.3390/jcm7020014 |
Ejemplares similares
-
Detectable Unmetabolized Folic Acid and Elevated Folate Concentrations in Folic Acid-Supplemented Canadian Children With Sickle Cell Disease
por: Williams, Brock A., et al.
Publicado: (2021) -
P-082: VITAMIN B-6 STATUS AND DIETARY INTAKE AMONG CANADIAN CHILDREN WITH SICKLE CELL DISEASE
por: B., WILLIAMS, et al.
Publicado: (2022) -
Folic acid supplementation in children with sickle cell disease: study protocol for a double-blind randomized cross-over trial
por: Williams, Brock A., et al.
Publicado: (2020) -
Perspective: Weekly Iron and Folic Acid Supplementation (WIFAS): A Critical Review and Rationale for Inclusion in the Essential Medicines List to Accelerate Anemia and Neural Tube Defects Reduction
por: Roche, Marion L, et al.
Publicado: (2021) -
Comparison of a New Multiplex Immunoassay for Measurement of Ferritin, Soluble Transferrin Receptor, Retinol-Binding Protein, C-Reactive Protein and α(1)-Acid-glycoprotein Concentrations against a Widely-Used s-ELISA Method
por: Karakochuk, Crystal D., et al.
Publicado: (2018)