Nocturnal enuresis and K+ transport in red blood cells from patients with sickle cell anemia
Autor: | Sanjay Tewari, Halima Al Balushi, Oluwabukola T. Gbotosho, David C. Rees, Anke Hannemann, John S. Gibson |
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Přispěvatelé: | Hannemann, Anke [0000-0002-2925-1124], Gibson, John [0000-0001-6145-9139], Apollo - University of Cambridge Repository |
Jazyk: | angličtina |
Rok vydání: | 2016 |
Předmět: |
Adult
Pediatrics medicine.medical_specialty Cell Membrane Permeability Erythrocytes Adolescent 030232 urology & nephrology macromolecular substances Anemia Sickle Cell Sickle cell nephropathy 03 medical and health sciences Young Adult 0302 clinical medicine Enuresis Medicine Humans Online Only Articles Child Ion Transport business.industry Renal damage Hematology Potassium transport medicine.disease Intermediate-Conductance Calcium-Activated Potassium Channels Sickle cell anemia nervous system Child Preschool Potassium medicine.symptom business 030215 immunology Nocturnal Enuresis |
Zdroj: | Tewari, S, Rees, D C, Hannemann, A, Gbotosho, O T, Al Balushi, H W M & Gibson, J S 2016, ' Nocturnal enuresis and K+ transport in red blood cells from patients with sickle cell anemia ', Haematologica, vol. 101, no. 12, pp. e469-e472 . https://doi.org/10.3324/haematol.2016.149500 |
DOI: | 10.17863/cam.5980 |
Popis: | Sickle cell anemia (SCA) is one of the commonest severe inherited disorders affecting millions worldwide. Complications are extensive although severity varies markedly. Renal damage [or sickle cell nephropathy (SCN)] occurs in approximately one-third of SCA children1,2 and a significant number develop renal failure as adults.3 It is not yet possible to predict which children will develop SCN and would, therefore, benefit from earlier, more aggressive management |
Databáze: | OpenAIRE |
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