ALLMedicine™ Hemoglobin C Disease Center
Research & Reviews 51 results
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298816
American Journal of Hematology; Steele C, Sinski A et. al.
Oct 5th, 2018 - Sickle cell disease (SCD) is a common, life-threatening genetic disorder that is best managed when diagnosed early by newborn screening. However, SCD is most prevalent in low-resource regions of the world where newborn screening is rare and diagno...
https://clinicaltrials.gov/ct2/show/NCT03619798
Aug 7th, 2018 - Sickle cell disease is a life-threatening genetic disorder that can be effectively treated following early diagnosis via newborn screening. However, sickle cell disease is most prevalent in low-resource regions of the world, where newborn screenin...
https://doi.org/10.3233/CH-180412
Clinical Hemorheology and Microcirculation; Beral L, Lemonne N et. al.
Jun 5th, 2018 - Our study investigated the prevalence of retinopathy and maculopathy in sickle cell patients and tested the association between these two conditions. In addition, we tested whether hematological and hemorheological parameters, as well as genotype,...
https://doi.org/10.1016/j.bcmd.2017.03.015
Blood Cells, Molecules & Diseases; Charlot K, Antoine-Jonville S et. al.
Apr 15th, 2017 - The present study investigated cerebral and muscle hemoglobin oxygen saturation (tissue oxygen index, TOI) in children with sickle cell anemia (SS), sickle cell hemoglobin C disease (SC) and healthy children (AA). TOI was measured by near-infrared...
https://emedicine.medscape.com/article/200853-overview
Jan 18th, 2017 - Overview Hemoglobin C (Hb C) is one of the most common structural hemoglobin variants in the human population. Persons with hemoglobin C trait (Hb AC) are phenotypically normal, with no clinically evident limitations or symptoms, while those with ...
Clinicaltrials.gov 51 results
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298816
American Journal of Hematology; Steele C, Sinski A et. al.
Oct 5th, 2018 - Sickle cell disease (SCD) is a common, life-threatening genetic disorder that is best managed when diagnosed early by newborn screening. However, SCD is most prevalent in low-resource regions of the world where newborn screening is rare and diagno...
https://clinicaltrials.gov/ct2/show/NCT03619798
Aug 7th, 2018 - Sickle cell disease is a life-threatening genetic disorder that can be effectively treated following early diagnosis via newborn screening. However, sickle cell disease is most prevalent in low-resource regions of the world, where newborn screenin...
https://doi.org/10.3233/CH-180412
Clinical Hemorheology and Microcirculation; Beral L, Lemonne N et. al.
Jun 5th, 2018 - Our study investigated the prevalence of retinopathy and maculopathy in sickle cell patients and tested the association between these two conditions. In addition, we tested whether hematological and hemorheological parameters, as well as genotype,...
https://doi.org/10.1016/j.bcmd.2017.03.015
Blood Cells, Molecules & Diseases; Charlot K, Antoine-Jonville S et. al.
Apr 15th, 2017 - The present study investigated cerebral and muscle hemoglobin oxygen saturation (tissue oxygen index, TOI) in children with sickle cell anemia (SS), sickle cell hemoglobin C disease (SC) and healthy children (AA). TOI was measured by near-infrared...
https://emedicine.medscape.com/article/200853-overview
Jan 18th, 2017 - Overview Hemoglobin C (Hb C) is one of the most common structural hemoglobin variants in the human population. Persons with hemoglobin C trait (Hb AC) are phenotypically normal, with no clinically evident limitations or symptoms, while those with ...
