scholarly article | Q13442814 |
P50 | author | Betty S Pace | Q41839522 |
P2093 | author name string | Steven R Goodman | |
P2860 | cites work | Minireview: Clinical severity in sickle cell disease: the challenges of definition and prognostication | Q36913577 |
Original Research: Generation of non-deletional hereditary persistence of fetal hemoglobin β-globin locus yeast artificial chromosome transgenic mouse models: -175 Black HPFH and -195 Brazilian HPFH | Q36913598 | ||
Original Research: Sickle cell anemia and pediatric strokes: Computational fluid dynamics analysis in the middle cerebral artery | Q37107179 | ||
Original Research: Stable expression of miR-34a mediates fetal hemoglobin induction in K562 cells | Q37107187 | ||
Original Research: Use of hydroxyurea and phlebotomy in pediatric patients with hemoglobin SC disease | Q37107190 | ||
Minireview: Multiomic candidate biomarkers for clinical manifestations of sickle cell severity: Early steps to precision medicine | Q37107194 | ||
Original Research: Diametric effects of hypoxia on pathophysiology of sickle cell disease in a murine model. | Q37107198 | ||
Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease | Q37107201 | ||
Minireview: Prognostic factors and the response to hydroxurea treatment in sickle cell disease | Q37107206 | ||
Minireview: Genetic basis of heterogeneity and severity in sickle cell disease | Q38758451 | ||
Original Research: Parvovirus B19 infection in children with sickle cell disease in the hydroxyurea era. | Q38760008 | ||
Original Research: Acute chest syndrome in sickle cell disease: Effect of genotype and asthma | Q41946514 | ||
P433 | issue | 7 | |
P921 | main subject | sickle-cell disease | Q185034 |
P304 | page(s) | 677-678 | |
P577 | publication date | 2016-04-01 | |
P1433 | published in | Experimental Biology and Medicine | Q15716535 |
P1476 | title | Sickle cell disease severity: an introduction | |
P478 | volume | 241 |
Q90115143 | Serum Potassium, Sodium, and Chloride Levels in Sickle Cell Disease Patients and Healthy Controls: A Case-Control Study at Korle-Bu Teaching Hospital, Accra | cites work | P2860 |
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