Sickle Cell Disease
Author:
Affiliation:
1. Director, Hematology Program, Children's Hospital at Montefiore, Bronx, NY
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology and Child Health
Link
https://publications.aap.org/pediatricsinreview/article-pdf/28/7/259/998004/zpx00707000259.pdf
Reference12 articles.
1. Adams RJ, McKie VC, Hsu L, et al. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography. N Engl J Med. 1998;339:5–11
2. Ashley-Koch A, Yang Q, Olney RS. Sickle hemoglobin allele and sickle cell disease: A HuGE Review. Am J Epidemiol. 2000;151:839–845
3. Gladwin MT, Sachdev V, Jison ML, et al. Pulmonary hypertension as a risk factor for death in patients with sickle cell disease. N Engl J Med. 2004;350:886–895
4. Machado RF, Anthi A, Steinberg MH, et al. N-terminal pro-brain natriuretic peptide levels and risk of death in sickle cell disease. JAMA. 2006;296:310–318
5. Miller ST, Sleeper LA, Pegelow CH. Prediction of adverse outcomes in children with sickle cell anemia. N Engl J Med. 2000;342:83–89
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1. Fatigue, Stress Appraisal, and Emotional Functioning Among Youth With Sickle Cell Disease: A Daily Diary Study;Journal of Pediatric Psychology;2023-05-11
2. Caregivers’ Perspective on the Psychological Burden of Living with Children Affected by Sickle Cell Disease in Kinshasa, the Democratic Republic of Congo;Children;2023-01-31
3. Clinical management of the acute complications of sickle cell anemia: 11 years of experience in a tertiary hospital;Anales de Pediatría (English Edition);2022-07
4. The distinct longitudinal impact of pain catastrophizing on pain interference among youth living with sickle cell disease and chronic pain;Journal of Behavioral Medicine;2022-02-16
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