Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemia - Wikidata - wikimedia - TriplyDB

Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemia

Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemia

http://www.wikidata.org/entity/Q27026479

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Interventions for preventing silent cerebral infarcts in people with sickle cell disease Interventions for preventing silent cerebral infarcts in people with sickle cell disease Novel insights in the management of sickle cell disease in childhood Hematopoietic stem cell transplantation in sickle cell disease: patient selection and special considerations Neuroimaging findings in sickle cell disease Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients A biopsychosocial model for the management of patients with sickle-cell disease transitioning to adult medical care Proteomic and biomarker studies and neurological complications of pediatric sickle cell disease Implementation of a Process for Initial Transcranial Doppler Ultrasonography in Children With Sickle Cell Anemia.Stroke in patients with sickle cell disease.Transitioning Adolescents and Young Adults With Sickle Cell Disease From Pediatric to Adult Health Care: Provider Perspectives.How I manage cerebral vasculopathy in children with sickle cell disease.Magnetic resonance imaging in pediatric sickle cell anemia.Development and feasibility of a home-based education model for families of children with sickle cell disease Sickle cell detection using a smartphone.Social skills and executive function among youth with sickle cell disease: a preliminary investigation Hemoglobin and mean platelet volume predicts diffuse T1-MRI white matter volume decrease in sickle cell disease patients.Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.Reproducibility of detecting silent cerebral infarcts in pediatric sickle cell anemia.Sickle cell disease: a neglected chronic disease of increasing global health importance Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease Parent education and biologic factors influence on cognition in sickle cell anemia Management of sickle cell disease: a review for physician education in Nigeria (sub-saharan Africa).Coagulation activation in children with sickle cell disease is associated with cerebral small vessel vasculopathy.Cognition and the Default Mode Network in Children with Sickle Cell Disease: A Resting State Functional MRI Study.Interventions for preventing silent cerebral infarcts in people with sickle cell disease.Predictors of cerebral blood flow in patients with and without anemia.Intellectual function evaluation of first generation immigrant children with sickle cell disease: the role of language and sociodemographic factors Coagulation abnormalities of sickle cell disease: Relationship with clinical outcomes and the effect of disease modifying therapies.Extent of silent cerebral infarcts in adult sickle-cell disease patients on magnetic resonance imaging: is there a correlation with the clinical severity of disease?Current management of sickle cell anemia.Original Research: Sickle cell anemia and pediatric strokes: Computational fluid dynamics analysis in the middle cerebral artery.School Performance and Disease Interference in Adolescents with Sickle Cell Disease.Psychometric Properties of the Psychosocial Assessment Tool-General in Adolescents and Young Adults With Sickle Cell Disease.Effects of dietary nitrates on systemic and cerebrovascular hemodynamics.Advances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia.Sickle cell disease: time for a closer look at treatment options?Transition from paediatric to adult care for patients with sickle cell disease.Management of sickle cell disease in the community.Nocturnal enuresis in sickle cell disease.

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P2860

Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemia

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P2860

Diffusion-weighted MR imaging in acute stroke: theoretic considerations and clinical applications.

Cerebral venous sinus thrombosis in children: risk factors, presentation, diagnosis and outcome.

Physiological correlates of intellectual function in children with sickle cell disease: hypoxaemia, hyperaemia and brain infarction.

Etiology of strokes in children with sickle cell anemia.

Acute silent cerebral infarction in children with sickle cell anemia

Silent brain infarcts: a review of MRI diagnostic criteria.

Multicenter prospective study of children with sickle cell disease: radiographic and psychometric correlation.

Discontinuing prophylactic transfusions increases the risk of silent brain infarction in children with sickle cell disease: data from STOP II.

Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia.

Left ventricular hypertrophy and diastolic dysfunction in children with sickle cell disease are related to asleep and waking oxygen desaturation.

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