Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia. (Q37178468)

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scientific article published on 07 September 2012

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English	Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia.	scientific article published on 07 September 2012

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12 February 2020

Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia (English)

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sickle-cell disease

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Christopher Bean

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Mathula Thangarajh

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Genyan Yang

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Dana Fuchs

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Maria R Ponisio

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Robert C McKinstry

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Alok Jaju

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Michael J Noetzel

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James F Casella

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Emily Barron-Casella

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W Craig Hooper

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Sheree L Boulet

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Meredith E Pyle

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Amanda B Payne

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Jennifer Driggers

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Heidi A Trau

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Bruce A Vendt

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Mark Rodeghier

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Michael R DeBaun

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7 September 2012

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352-359

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12 February 2020

Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure

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Novel therapies targeting the endothelium in sickle cell disease

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Genetic predictors for stroke in children with sickle cell anemia

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Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease

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Comparison of real-time microvascular abnormalities in pediatric and adult sickle cell anemia patients

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Acute silent cerebral infarction in children with sickle cell anemia

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6 September 2017

Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directions

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Silent Cerebral Infarct Transfusion (SIT) trial imaging core: application of novel imaging information technology for rapid and central review of MRI of the brain

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Glucose-6-phosphate dehydrogenase deficiency

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Cognitive functioning and brain magnetic resonance imaging in children with sickle Cell disease. Neuropsychology Committee of the Cooperative Study of Sickle Cell Disease

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10.1111/BJH.12034

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12 February 2020

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