Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography.
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Summary
Transfusion greatly reduces the risk of a first stroke in children with sickle cell anemia who have abnormal results on transcranial Doppler ultrasonography.
- Type
- article
- Published
- 1998-07-02
- Cited by
- 1,876
- References
- 27
- Access
- Open access
- OpenAlex
- https://openalex.org/W2314213298
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:30671263
Keywords
Medicine, Stroke (engine), Transcranial Doppler, Hematocrit, Anemia
References
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- Detection of cerebrovascular disease in patients with sickle cell disease using transcranial Doppler sonography: correlation with MRI, MRA and conventional angiography
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- High-performance liquid chromatographic separation of human haemoglobins. Simultaneous quantitation of foetal and glycated haemoglobins.
- A modified transfusion program for prevention of stroke in sickle cell disease.
- Cerebrovascular accidents in sickle cell disease: rates and risk factors.
- Long‐term stroke risk in children with sickle cell disease screened with transcranial doppler
- A validation study on the reproducibility of transcranial Doppler velocimetry.
- The natural history of stroke in sickle cell disease.
- Stroke prevention trial in sickle cell anemia.
- Sickle cell anemia and central nervous system infarction: A neuropathological study
- Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions.
- Cerebrovascular disease in symptomatic and asymptomatic patients with sickle cell anemia: screening with duplex transcranial Doppler US--correlation with MR imaging and MR angiography.
- Transcranial Doppler measurements of the middle cerebral artery. Effect of hematocrit.
- Less intensive long-term transfusion therapy for sickle cell anemia and cerebrovascular accident.
- Transcranial Doppler Correlation With Cerebral Angiography in Sickle Cell Disease
- The spectrum of brain MR abnormalities in sickle-cell disease: a report from the Cooperative Study of Sickle Cell Disease.
- Stroke With Negative Brain Magnetic Resonance Imaging
- Cerebral Vascular Accidents in Patients over the Age of 60: II. Prognosis
- Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia.
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- Etude descriptive des profils cognitifs d’un groupe d’enfants atteints de drépanocytose
- The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease
- Control de los pacientes con drepanocitosis en atención primaria
- A new look at neuropathology in sickle cell disease
- The Coagulation System
- TCD in sickle cell disease: an important and useful test
- The epidemiology of stroke in sickle cell patients in Yaounde, Cameroon.
- Optimal Management Strategies for Chronic Iron Overload
- Hypercoagulability in sickle cell disease: new approaches to an old problem.
- Evaluation of a comprehensive transcranial doppler screening program for children with sickle cell anemia
- Iron Metabolism and Iron Chelation in Sickle Cell Disease
- Sickle cell disease: new insights into pathophysiology and treatment.
- Evidence of persistent neurologic injury following thrombotic thrombocytopenic purpura
- Neuroimaging in assessment of risk of stroke in children with sickle cell disease.
- Advantages of isovolemic hemodilution‐red cell exchange therapy to prevent recurrent stroke in sickle cell anemia patients
- Frequency and distribution of asymptomatic brain lesions in patients with β-thalassemia intermedia
- Sickle Cell Disease in Childhood
- Transcranial doppler velocity and brain MRI/MRA changes in children with sickle cell anemia on chronic transfusions to prevent primary stroke
- Ferritin and LIC: Predicting Liver Injury in Children With Sickle Cell
- Management of sickle cell disease in the community
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