Results 71 to 80 of about 5,240,823 (173)

Neuroimaging Biomarkers in Paediatric Sickle Cell Disease [PDF]

, 2015
Sickle Cell Disease (SCD) is a collection of genetic haemoglobinopathies, the most common and severe being homozygous sickle cell anaemia. In the UK, it has been estimated that 1 in 2000 children are born with SCD. The disease is characterised by chronic
Kawadler, JM
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A Multicenter, Open‐Label, Phase 2 Trial Comparing Crizanlizumab Combined With Standard Therapy to Standard Therapy Alone on Renal Function in Patients With Sickle Cell Nephropathy (STEADFAST)

American Journal of Hematology, Volume 101, Issue 10, Page 2666-2671, October 2026.
Kenneth I. Ataga, Pablo Bartolucci, Santosh L. Saraf, Vimal K. Derebail, Adlette Inati, Jeffrey D. Lebensburger, Laurie DeBonnett, Rodolfo D. Cancado, Claire C. Sharpe   +8 more
wiley   +1 more source

Antisickling effects of hydroethanolic extract of Oxytenanthera abyssinica leaves

National Journal of Physiology, Pharmacy and Pharmacology
Background: Sickle cell disease is a hereditary hemoglobinopathy. It is characterized by the presence of abnormal hemoglobin S (HbS) levels at high concentrations in red blood cells.
Sène Mbaye, Diouf Ibrahima, Ba Awa, Ba Fatoumata, Fall Cheikhouna Khadim, Diaw Absatou, Kane Modou Oumy, Sarr Mamadou   +7 more
doaj   +1 more source

Fatal sickling-associated microvascular occlusive crisis in a young with sickle cell trait

Autopsy and Case Reports, 2021
Sickle cell trait (SCT), a heterozygous state characterized by hemoglobin AS, occurs commonly in sub-Saharan Africa, South America, Central America, India, and the Mediterranean countries.
Deepti Mutreja, Benjith Paul K, Tilak TVSVGK   +2 more
doaj  

Get screened to know your sickle cell status [PDF]

To find out whether you or your loved one has sickle cell disease (SCD) or sickle cell trait (SCT), blood tests must be done to screen for these conditions.

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Haemoglobinopathies and health disparities: findings of a large-scale sample survey among indigenous populations in Odisha, India

BMJ Open
Objectives To estimate the prevalence of sickle cell trait, sickle cell disease, beta-thalassaemia minor and beta-thalassaemia major among Odisha’s indigenous populations and to examine associated haematological profiles and survival outcomes based on ...
Sanghamitra Pati, Jaya Singh Kshatri, Debdutta Bhattacharya, Sneha Singh, Haimanti Bhattacharya, Rachita Pradhan, A K Kavitha   +6 more
doaj   +1 more source

Sickle Cell Trait Causing Splanchnic Venous Thrombosis

Case Reports in Hepatology, 2015
Sickle cell trait is considered as a benign condition as these individuals carry only one defective gene and typically have their life span similar to the normal population without any health problems related to sickle cell. Only under extreme conditions,
Priyanka Saxena, Pratibha Dhiman, Chhagan Bihari, Archana Rastogi   +3 more
doaj   +1 more source

Avascular necrosis of the femoral head among children and adolescents with sickle cell disease in Greece

Haematologica, 2002
Hemoglobinopathies are very common in Greece, the incidence of beta-thalassemia trait being 8% and that of sickle cell trait ranging from 1 to 32% in various districts.
M Athanassiou-Metaxa, J Kirkos, A Koussi, E Hatzipantelis, I Tsatra, M Economou   +5 more
doaj  

Sickle cell trait and damage to the spleen: get the facts! [French]

Sickle cell trait and damage to the spleen: get the facts! [French]Les personnes porteuses du trait dr\ue9panocytaire (SCT) sont g\ue9n\ue9ralement en bonne sant\ue9 et souffrent rarement de probl\ue8mes de la rate.

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Sickle Cell Data Collection Program Brief : Hospital Encounters Among Adults Living With Sickle Cell Disease in Georgia 2012-2016 [PDF]

The Georgia Sickle Cell Data Collection Program (SCDC) identified 5,405 adults living with sickle cell disease in Georgia from 2012 through 2016. Adults with sickle cell disease live in almost every county throughout Georgia.Nearly nine in 10 (88%) of ...

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