Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease
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Interventions for preventing silent cerebral infarcts in people with sickle cell diseaseInterventions for preventing silent cerebral infarcts in people with sickle cell diseaseBlood transfusion for preventing primary and secondary stroke in people with sickle cell diseaseSilent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemiaStroke in patients with sickle cell disease.Magnetic resonance imaging/angiography and transcranial Doppler velocities in sickle cell anemia: results from the SWiTCH trial.How I manage cerebral vasculopathy in children with sickle cell disease.Hemoglobin and mean platelet volume predicts diffuse T1-MRI white matter volume decrease in sickle cell disease patients.Frequent red cell transfusions reduced vascular endothelial activation and thrombogenicity in children with sickle cell anemia and high stroke riskDiscontinuing prophylactic transfusions increases the risk of silent brain infarction in children with sickle cell disease: data from STOP II.Understanding sickle cell brain drain.Health-related quality of life in children with sickle cell anemia: impact of blood transfusion therapy.Allogeneic hematopoietic stem cell transplantation for sickle cell disease: the time is now.Peripheral vasoconstriction and abnormal parasympathetic response to sighs and transient hypoxia in sickle cell disease.Effects of chronic transfusions on abdominal sonographic abnormalities in children with sickle cell anemiaHow I treat and manage strokes in sickle cell disease.Effect of Chronic Blood Transfusion on Biomarkers of Coagulation Activation and Thrombin Generation in Sickle Cell Patients at Risk for Stroke.Stroke With Transfusions Changing to Hydroxyurea (SWiTCH).Examination of Reticulocytosis among Chronically Transfused Children with Sickle Cell Anemia.Hematopoietic Stem Cell Transplantation in Adult Sickle Cell Disease: Problems and Solutions.Prospects for primary stroke prevention in children with sickle cell anaemiaCerebral hemodynamic assessment and neuroimaging across the lifespan in sickle cell disease.HLA-haploidentical bone marrow transplantation with posttransplant cyclophosphamide expands the donor pool for patients with sickle cell disease.Low-shear red blood cell oxygen transport effectiveness is adversely affected by transfusion and further worsened by deoxygenation in sickle cell disease patients on chronic transfusion therapy.Acute silent cerebral ischemic events in children with sickle cell anemia.Applicability of the SMART Model of Transition Readiness for Sickle-Cell DiseaseCurrent management of sickle cell anemia.Patent foramen ovale in patients with sickle cell disease and stroke: case presentations and review of the literature.Hematopoietic stem-cell transplantation for sickle cell disease: current evidence and opinions.Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia.Non-invasive imaging of oxygen extraction fraction in adults with sickle cell anaemiaPRIMARY STROKE PREVENTION IN CHILDREN WITH SICKLE CELL ANEMIA LIVING IN AFRICA: THE FALSE CHOICE BETWEEN PATIENT-ORIENTED RESEARCH AND HUMANITARIAN SERVICE.Cerebral infarction in children with sickle cell disease: a concise overview.The epidemiology, evaluation and treatment of stroke in adults with sickle cell disease.Indications and complications of transfusions in sickle cell disease.Advances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia.The case for and against initiating either hydroxyurea therapy, blood transfusion therapy or hematopoietic stem cell transplant in asymptomatic children with sickle cell disease.Blood and marrow transplantation for sickle cell disease: is less more?Current concepts in pediatric stroke.Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years.
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P2860
Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease
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2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Silent cerebral infarcts occur ...... ldren with sickle cell disease
@ast
Silent cerebral infarcts occur ...... ldren with sickle cell disease
@en
Silent cerebral infarcts occur ...... ldren with sickle cell disease
@nl
type
label
Silent cerebral infarcts occur ...... ldren with sickle cell disease
@ast
Silent cerebral infarcts occur ...... ldren with sickle cell disease
@en
Silent cerebral infarcts occur ...... ldren with sickle cell disease
@nl
prefLabel
Silent cerebral infarcts occur ...... ldren with sickle cell disease
@ast
Silent cerebral infarcts occur ...... ldren with sickle cell disease
@en
Silent cerebral infarcts occur ...... ldren with sickle cell disease
@nl
P2093
P2860
P50
P1433
P1476
Silent cerebral infarcts occur ...... ldren with sickle cell disease
@en
P2093
Alexis A Thompson
Gerald M Woods
James F Casella
JoAnne L Lacey
Jonathan E Mullin
Julie A Panepinto
Kofi A Anie
Mark Rodeghier
Michael Noetzel
P2860
P304
P356
10.1182/BLOOD-2010-01-261123
P407
P577
2010-10-12T00:00:00Z