Total: 3 |
|
PMID (PMCID) | ||
---|---|---|
21461009 |
MIXED_SAMPLE | Child |
[Co-inheritance of autosomal dominant polycystic kidney disease and sickle cell trait in African Americans]. | ||
Peces R, Peces C, Cuesta-Lopez E, Vega-Cabrera C, Azorin S, Perez-Duenas V, Selgas R. Nefrologia. 2011;31(2):162-8. |
||
Metabolic or environmental changes such as hypoxia, acidosis, dehydration, hyperosmolality or hyperthermia may transform silent sickle-cell trait into a syndrome resembling sickle-cell disease with vaso-occlusive crisis due to an accumulation of low deformable red blood cells in the microcirculation originating haematuria from papilar necrosis. | ||
9881989 |
MIXED_SAMPLE | Adult |
Acute nonoliguric renal failure in children associated with nonsteroidal antiinflammatory agents. | ||
Schaller S, Kaplan BS. Pediatr Emerg Care. 1998;14(6):416-8. |
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None of the patients had features of hemolytic uremic syndrome, systemic lupus, dehydration, obstructive uropathy or sickle cell disease. | ||
7074213 |
MALE | Adult |
Exercise-induced hemolysis in sickle cell anemia: shear sensitivity and erythrocyte dehydration. | ||
Platt OS. Blood. 1982;59(5):1055-60. |
||
Exercise-induced hemolysis in sickle cell anemia: shear sensitivity and erythrocyte dehydration. |