Sickle-cell anaemia is the name of a specific form ... include sickle-haemoglobin C disease (HbSC), sickle beta-plus-thalassaemia (HbS/β+) and sickle beta-zero-thalassaemia (HbS/β0).

The prevalence of thalassemia and sickle cell anaemia—both inherited blood disorders affecting haemoglobin—is significantly higher among Tharu tribals on the Indo-Nepal border compared to the ...

Sickle cell ... or beta-thalassaemia. Symptoms: Those with SCT usually show no symptoms except under extreme conditions, whereas individuals with SCD often suffer chronic pain, anaemia, fatigue ...

Sickle-cell anaemia is the name of a specific form ... include sickle-haemoglobin C disease (HbSC), sickle beta-plus-thalassaemia (HbS/β+) and sickle beta-zero-thalassaemia (HbS/β0).

Sickle cell experts say the future of a critical data collection program is in flux after staff at the CDC's Division of ...

Thalassemia and Sickle Cell Anaemia are common genetic disorders, with options for treatment and prevention available.

I was recently at the American Red Cross to donate blood and was given interesting material on the need for Black blood ...

Groundbreaking gene-editing treatment exa-cel is now available for NHS patients with sickle cell disease, offering a ...

Vertex and CRISPR Therapeutics have won the backing of NICE for their gene-editing therapy Casgevy as a treatment for the blood disorder beta thalassaemia ... it down for sickle cell disease.

Sebastien Beauzile became the first person in NY to be made symptom-free after undergoing a new type of gene therapy.

Meet the low-cost standard for hypoxic and physioxic environment cell culture that enabled HIF-1α Nobel Prize-winning research. Lab safety rules dictate that one must tie back long hair. Rosemarie ...