Morris, C.R. (2005) Dysregulated Arginine Metabolism, Hemolysis-Associated Pulmonary Hypertension, and Mortality in Sickle Cell Disease. JAMA, 294, 81-90.
https://doi.org/10.1001/jama.294.1.81

has been cited by the following article:

• TITLE: Asthma Attack Revealing Sickle Cell Disease

  AUTHORS: Khaoula Achir, Ilham Tadmori, Moustapha Hida

  KEYWORDS: Sickle Cell Disease, Asthma, Morbidity

  JOURNAL NAME: Open Journal of Pediatrics, Vol.14 No.5, September 10, 2024

  ABSTRACT: Sickle cell disease is a genetic disorder characterized by the presence of hemoglobin S (HbS) and a significant reduction in normal hemoglobin A (HbA) in red blood cells. In deoxygenated conditions, HbS molecules polymerize, causing vascular occlusions and hemolysis. Pulmonary complications associated with this disease result from vascular occlusion, ischemia-reperfusion, and inflammation. Literature reports that asthma is observed in 30% to 70% of patients with sickle cell disease. We present the case of a boy whose sickle cell disease diagnosis was established following an asthma attack.