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Endocarditis caused by Stenotrophomonas maltophilia-A rare presentation of an emerging opportunistic pathogen.

Serum Iron Levels and Copper-to-Zinc Ratio in Sickle Cell Disease.

Screening for neuropathic pain in patients with sickle cell disease

Barriers to Pediatric Sickle Cell Disease Guideline Recommendations.

Hemoglobin level and macular thinning in sickle cell disease.

Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa

Preliminary evidence that hydroxyurea is associated with attenuated peripheral sensitization in adults with sickle cell disease.

Lymphoma and hematological conditions

Lung Function Abnormalities in Sickle Cell Anaemia

Interventions for preventing high altitude illness

IgM antibodies against phosphorylcholine measured early after acute ST-elevation myocardial infarction in relation to atherosclerotic disease burden and long-term clinical outcome.

Negative affectivity and social inhibition are associated with increased cardiac readmission in patients with heart failure

Plasma NT-proBNP levels associated with cardiac structural abnormalities in asymptomatic health examinees with preserved ejection fraction

Number of blood pressure measurements needed to estimate long-term visit-to-visit systolic blood pressure variability for predicting cardiovascular risk

BR2054-01-10.pdf

Historical and Current Adenosine Receptor Agonists in Preclinical and Clinical Development

The 9-Item Physician Documentation Quality Instrument (PDQI-9) score is not useful in evaluating EMR (scribe) note quality in Emergency Medicine.

Impact of scribes on emergency medicine doctors' productivity and patient throughput

Biochemical effects and safety of Gum arabic (Acacia Senegal) supplementation in patients with sickle cell anemia.

Microcytosis in children and adolescents with the sickle cell trait in Basra, Iraq

Sickle cell disease and fetal hemoglobin

A Glycoengineered Interferon-β Mutein (R27T) Generates Prolonged Signaling by an Altered Receptor-Binding Kinetics.

Polarity Specific Effects of Cross-Hemispheric tDCS Coupled With Approach-Avoidance Training on Chocolate Craving.01500

Automated Generation of Radiologic Descriptions on Brain Volume Changes From T1-Weighted MR Images

Plasma Calcitonin Gene-Related Peptide

Do Th17 Lymphocytes and IL-17 Contribute to Parkinson's Disease? A Systematic Review of Available Evidence.

Is There a Future for Non-invasive Brain Stimulation as a Therapeutic Tool?

Characteristics of Moyamoya Syndrome in Sickle-Cell Disease by Magnetic Resonance Angiography

Targeted HIV testing for male partners of HIV-positive pregnant women in a high prevalence setting in Nigeria

The Characteristics and Outcomes of Abernethy Syndrome in Korean Children

Perioperative Endocarditis Management in a Patient with Homozygous Sickle Cell Disease.

Risk factors for recurrent severe anemia among previously transfused children in Uganda

Isolated Propriospinal Myoclonus as a Presentation of Cervical Myelopathy.

Salmonella enterica serovar Typhi osteomyelitis in a young adult with sickle cell and thalassemia traits

Vaso Occlusive Crisis in Sickle Cell Disease Current paradigm on pain management.

Effective sickle hemoglobin reduction by automated red cell exchange using Spectra Optia in three Emirati patients with sickle cell disease before allogeneic hematopoietic stem cell transplantation.-04-14

Sickle Cell Disease

Blessing in disguise; a case of Hereditary Persistence of Fetal Hemoglobin.

Sickle cell disease

Prevalence and risk factors of preconception anemia

The spatial epidemiology of sickle-cell anaemia in India.

Safety and effectiveness of antimalarial therapy in sickle cell disease

Philadelphia chromosome positive AML arising from JAK2-positive myelofibrosis.

An Implantable Sensorized Lead for Continuous Monitoring of Cardiac Apex Rotation.

Type 1 cardiorenal syndrome in a patient with an acute infection caused by Trypanosoma cruzi in the Brazilian Amazon region - a case report.

HbS-Sicilian (δβ)0-Thalassemia

Shape oscillations of single blood drops

Emergency treatment of sickle cell diseases in the Blood Diseases Department at the Koutoukou Maga National Teaching Hospital, Cotonou, Benin

A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania.