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A significant proportion of children of African descent with HbSβ<sup>0</sup> thalassaemia are inaccurately diagnosed based on phenotypic analyses alone.
- Published in:
- Angewandte Chemie, 2019, v. 131, n. 15, p. 153, doi. 10.1111/bjh.15400
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- Article
Effect of allogeneic hematopoietic stem cell transplantation on sickle cell disease‐related organ complications: A systematic review and meta‐analysis.
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- American Journal of Hematology, 2024, v. 99, n. 6, p. 1129, doi. 10.1002/ajh.27297
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- Article
Transcranial doppler velocity in iron‐deficient Nigerian children with sickle cell anemia.
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- American Journal of Hematology, 2024, v. 99, n. 4, p. 797, doi. 10.1002/ajh.27230
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- Article
Low FEV<sub>1</sub> is associated with fetal death in pregnant women with sickle cell disease.
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- American Journal of Hematology, 2021, v. 96, n. 8, p. E303, doi. 10.1002/ajh.26236
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- Article
Nocturnal peripheral vasoconstriction predicts the frequency of severe acute pain episodes in children with sickle cell disease.
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- American Journal of Hematology, 2021, v. 96, n. 1, p. 60, doi. 10.1002/ajh.26014
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- Article
Reduction in transcranial doppler ultrasound (TCD) velocity after regular blood transfusion therapy is associated with a change in hemoglobin S fraction in sickle cell anemia.
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- American Journal of Hematology, 2020, v. 95, n. 11, p. E308, doi. 10.1002/ajh.25954
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- Article
Evidence of transfusion‐induced reductions in cerebral capillary shunting in sickle cell disease.
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- American Journal of Hematology, 2020, v. 95, n. 9, p. E228, doi. 10.1002/ajh.25863
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- Article
Haptoglobin genotype predicts severe acute vasoocclusive pain episodes in children with sickle cell anemia.
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- American Journal of Hematology, 2020, v. 95, n. 4, p. E92, doi. 10.1002/ajh.25728
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- Article
Cerebral hemodynamics and metabolism are similar in sickle cell disease patients with hemoglobin SS and Sβ<sup>0</sup> thalassemia phenotypes.
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- American Journal of Hematology, 2020, v. 95, n. 3, p. E66, doi. 10.1002/ajh.25698
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- Article
Third trimester and early postpartum period of pregnancy have the greatest risk for ACS in women with SCD.
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- American Journal of Hematology, 2019, v. 94, n. 12, p. E328, doi. 10.1002/ajh.25643
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- Article
Approximately 40 000 children with sickle cell anemia require screening with TCD and treating with hydroxyurea for stroke prevention in three states in northern Nigeria.
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- American Journal of Hematology, 2019, v. 94, n. 11, p. E305, doi. 10.1002/ajh.25616
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- Article
Haploidentical bone marrow transplantation improves cerebral hemodynamics in adults with sickle cell disease.
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- American Journal of Hematology, 2019, v. 94, n. 6, p. E155, doi. 10.1002/ajh.25455
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- Article
BMI percentile is an independent predictor of increase in lung function in children with sickle cell anemia.
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- American Journal of Hematology, 2019, v. 94, n. 5, p. E136, doi. 10.1002/ajh.25433
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- Article
Multidisciplinary care results in similar maternal and perinatal mortality rates for women with and without SCD in a low‐resource setting.
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- American Journal of Hematology, 2019, v. 94, n. 2, p. 223, doi. 10.1002/ajh.25356
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- Publication type:
- Article
Progressive loss of brain volume in children with sickle cell anemia and silent cerebral infarct: A report from the silent cerebral infarct transfusion trial.
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- American Journal of Hematology, 2018, v. 93, n. 12, p. E406, doi. 10.1002/ajh.25297
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- Article
Clustering of end‐organ disease and earlier mortality in adults with sickle cell disease: A retrospective‐prospective cohort study.
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- American Journal of Hematology, 2018, v. 93, n. 9, p. 1153, doi. 10.1002/ajh.25202
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- Article
A case series describing causes of death in pregnant women with sickle cell disease in a low‐resource setting.
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- American Journal of Hematology, 2018, v. 93, n. 7, p. E167, doi. 10.1002/ajh.25115
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- Article
Children with sickle cell anemia with normal transcranial Doppler ultrasounds and without silent infarcts have a low incidence of new strokes.
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- American Journal of Hematology, 2018, v. 93, n. 6, p. 760, doi. 10.1002/ajh.25085
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- Article
Inhaled corticosteroid use to prevent severe vaso‐occlusive episode recurrence in children between 1 and 4 years of age with sickle cell disease: a multicenter feasibility trial.
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- American Journal of Hematology, 2018, v. 93, n. 4, p. E101, doi. 10.1002/ajh.25033
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- Article
Sleep disordered breathing does not predict acute severe pain episodes in children with sickle cell anemia.
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- American Journal of Hematology, 2018, v. 93, n. 4, p. 478, doi. 10.1002/ajh.25013
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- Article
Feasibility trial for primary stroke prevention in children with sickle cell anemia in Nigeria (SPIN trial).
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- American Journal of Hematology, 2018, v. 93, n. 3, p. E83, doi. 10.1002/ajh.25012
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- Article
Age is a predictor of a small decrease in lung function in children with sickle cell anemia.
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- American Journal of Hematology, 2018, v. 93, n. 3, p. 408, doi. 10.1002/ajh.25003
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- Publication type:
- Article
Implementation of multidisciplinary care reduces maternal mortality in women with sickle cell disease living in low-resource setting.
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- American Journal of Hematology, 2017, v. 92, n. 9, p. 872, doi. 10.1002/ajh.24790
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- Article
Feasibility trial for primary stroke prevention in children with sickle cell anemia in Nigeria (SPIN trial).
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- American Journal of Hematology, 2017, v. 92, n. 8, p. 780, doi. 10.1002/ajh.24770
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- Article
Elevated tricuspid regurgitant jet velocity, reduced forced expiratory volume in 1 second, and mortality in adults with sickle cell disease.
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- American Journal of Hematology, 2017, v. 92, n. 2, p. 125, doi. 10.1002/ajh.24598
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- Article
Rapidly progressive acute chest syndrome in individuals with sickle cell anemia: a distinct acute chest syndrome phenotype.
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- American Journal of Hematology, 2016, v. 91, n. 12, p. 1185, doi. 10.1002/ajh.24539
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- Article
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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- American Journal of Hematology, 2016, v. 91, n. 1, p. 5, doi. 10.1002/ajh.24235
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- Article
Increased risk of severe vaso-occlusive episodes after initial acute chest syndrome in children with sickle cell anemia less than 4 years old: Sleep and asthma cohort.
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- American Journal of Hematology, 2015, v. 90, n. 5, p. 371, doi. 10.1002/ajh.23959
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- Article
Health-related quality of life in children with sickle cell anemia: Impact of blood transfusion therapy.
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- American Journal of Hematology, 2015, v. 90, n. 2, p. 139, doi. 10.1002/ajh.23877
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- Article
Factors associated with growth and blood pressure patterns in children with sickle cell anemia: Silent Cerebral Infarct Multi-Center Clinical Trial cohort.
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- American Journal of Hematology, 2015, v. 90, n. 1, p. 2, doi. 10.1002/ajh.23854
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- Article
Factors predicting future ACS episodes in children with sickle cell anemia.
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- American Journal of Hematology, 2014, v. 89, n. 11, p. E212, doi. 10.1002/ajh.23819
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- Article
Females with FVIII and FIX deficiency have reduced joint range of motion.
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- American Journal of Hematology, 2014, v. 89, n. 8, p. 831, doi. 10.1002/ajh.23754
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- Article
Parent education and biologic factors influence on cognition in sickle cell anemia.
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- American Journal of Hematology, 2014, v. 89, n. 2, p. 162, doi. 10.1002/ajh.23604
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- Article
Recurrent, severe wheezing is associated with morbidity and mortality in adults with sickle cell disease.
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- American Journal of Hematology, 2011, v. 86, n. 9, p. 756, doi. 10.1002/ajh.22098
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- Article
Plasma glial fibrillary acidic protein levels in children with sickle cell disease.
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- American Journal of Hematology, 2011, v. 86, n. 5, p. 427, doi. 10.1002/ajh.21995
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- Article
Finally, a consensus statement on sickle cell disease manifestations: A critical step in improving the medical care and research agenda for individuals with sickle cell disease.
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- American Journal of Hematology, 2010, v. 85, n. 1, p. 1, doi. 10.1002/ajh.21583
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- Article
Urinary cysteinyl leukotriene E<sub>4</sub> significantly increases during pain in children and adults with sickle cell disease.
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- American Journal of Hematology, 2009, v. 84, n. 4, p. 231, doi. 10.1002/ajh.21370
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- Article
Urinary cysteinyl leukotriene E<sub>4</sub> is associated with increased risk for pain and acute chest syndrome in adults with sickle cell disease.
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- American Journal of Hematology, 2009, v. 84, n. 3, p. 158, doi. 10.1002/ajh.21348
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- Article
Sibling history of asthma is a risk factor for pain in children with sickle cell anemia.
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- American Journal of Hematology, 2008, v. 83, n. 11, p. 855, doi. 10.1002/ajh.21275
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- Article
Elevated urinary leukotriene E<sub>4</sub> levels are associated with hospitalization for pain in children with sickle cell disease.
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- American Journal of Hematology, 2008, v. 83, n. 8, p. 640, doi. 10.1002/ajh.21199
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- Publication type:
- Article
Longitudinal analysis of pulmonary function in adults with sickle cell disease.
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- American Journal of Hematology, 2008, v. 83, n. 7, p. 574, doi. 10.1002/ajh.21176
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- Article
Barriers and motivators to blood and cord blood donations in young African-American women.
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- American Journal of Hematology, 2005, v. 78, n. 3, p. 198, doi. 10.1002/ajh.20308
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- Publication type:
- Article
Higher prevalence of wheezing and lower FEV1 and FVC percent predicted in adults with sickle cell anaemia: A cross-sectional study.
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- Respirology, 2017, v. 22, n. 2, p. 284, doi. 10.1111/resp.12895
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- Article
Effect of Blood Transfusion on Cerebral Hemodynamics and Vascular Topology Described by Computational Fluid Dynamics in Sickle Cell Disease Patients.
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- Brain Sciences (2076-3425), 2022, v. 12, n. 10, p. 1402, doi. 10.3390/brainsci12101402
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- Article
Discordance between Self-Report and Genetic Confirmation of Sickle Cell Disease Status in African-American Adults.
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- Public Health Genomics, 2014, v. 17, n. 3, p. 169, doi. 10.1159/000360260
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- Article
Effects of Experimental Asthma on Inflammation and Lung Mechanics in Sickle Cell Mice.
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- American Journal of Respiratory Cell & Molecular Biology, 2012, v. 46, n. 3, p. 389, doi. 10.1165/rcmb.2011-0097OC
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- Article
Chronic transfusion therapy for stroke in sickle cell disease.
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- Journal of Clinical Apheresis, 2017, v. 32, n. 5, p. 368, doi. 10.1002/jca.21523
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- Article
Differential cerebral hemometabolic responses to blood transfusions in adults and children with sickle cell anemia.
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- 2019
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- Publication type:
- journal article
Reply: Decline of Lung Function in Children with Sickle Cell Disease Is Not Associated with Restrictive Defects.
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- 2017
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- Publication type:
- letter
Decline of Lung Function in Children with Sickle Cell Disease Is Not Associated with Restrictive Defects.
- Published in:
- 2017
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- Publication type:
- letter