Coinheritance of non-deletional hemoglobin H disease with sickle cell trait. [PDF]
Komninaka V, Ntelaki EE.
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Variability in Notification of Positive Newborn Screening Results for Sickle Cell Trait Across the United States. [PDF]
Scott JL +4 more
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Myopericarditis and Pericardial Effusion as the Initial Presentation of Systemic Lupus Erythematosus in a Patient with Sickle Cell Trait: A Case Report. [PDF]
Rojas-Cadena M +5 more
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The Performance of Three Systems of Glycated Hemoglobin Measurements Among Patients With Sickle Cell Trait in Basrah, Iraq. [PDF]
Al-Naseri RF +3 more
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A Scoping Review on Sex and Gender Differences in the Adverse Health Outcomes of Individuals with Sickle Cell Trait. [PDF]
Phillips AK +5 more
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Haemoglobin Ottawa, sickle cell trait and vaso-occlusive crises. [PDF]
Bobillier C +3 more
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Ancestry-independent risk of venous thromboembolism in individuals with sickle cell trait vs factor V Leiden. [PDF]
Lin KH +4 more
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PARACENTRAL ACUTE MIDDLE MACULOPATHY WITH SICKLE CELL TRAIT. [PDF]
Baker M, Neuhouser A, Nazari H.
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Sickle-cell trait and sickle-cell anaemia
Transactions of the Royal Society of Tropical Medicine and Hygiene, 1951Abstract (1) If sickle-cell trait is regarded as a heterozygous condition (Ss) and sickle-cell anaemia as a homozygous state (SS), then sickle-cell anaemia can only arise as a result of the mating of two heterozygous individuals (Ss x Ss), or the mating of a heterozygous and a homozygous (Ss x SS) or of two homozygous (SS x SS). 1.
H, FOY, A, KONDI, C, ALEXANDRIDES
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The nephropathy of sickle cell trait and sickle cell disease
Nature Reviews Nephrology, 2022Sickle cell syndromes, including sickle cell disease (SCD) and sickle cell trait, are associated with multiple kidney abnormalities. Young patients with SCD have elevated effective renal plasma flow and glomerular filtration rates, which decrease to normal ranges in young adulthood and subnormal levels with advancing age.
Kenneth I. Ataga +2 more
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