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4. Book reviews.

6. Variant chronic granulomatous disease: modulation of the neutrophil defect by severe infection

7. Exercise-induced hemolysis in sickle cell anemia: shear sensitivity and erythrocyte dehydration

8. Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort.

9. Age- and gender-dependent obesity in individuals with 16p11.2 deletion.

10. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

11. Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathy.

12. Pulmonary hypertension and nitric oxide depletion in sickle cell disease.

13. Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.

14. SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss.

15. Protective effects of phosphodiesterase-4 (PDE-4) inhibition in the early phase of pulmonary arterial hypertension in transgenic sickle cell mice.

16. Hydroxyurea for the treatment of sickle cell anemia.

17. Association between microdeletion and microduplication at 16p11.2 and autism.

18. Quantitative trait loci for peripheral blood cell counts: a study in baboons.

19. Quantitative trait loci for baseline erythroid traits.

20. Prevention and management of stroke in sickle cell anemia.

21. Quantitative trait loci for baseline white blood cell count, platelet count, and mean platelet volume.

22. Genetic influences on peripheral blood cell counts: a study in baboons.

23. Acquisition of mutans streptococci and caries prevalence in pediatric sickle cell anemia patients receiving long-term antibiotic therapy.

24. Sickle cell anemia as an inflammatory disease.

25. The acute chest syndrome of sickle cell disease.

26. Transposing sequences between fetal and adult hemoglobins indicates which subunits and regulatory molecule interfaces are functionally related.

27. Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group.

28. Silent cerebral infarcts in sickle cell anemia: a risk factor analysis. The Cooperative Study of Sickle Cell Disease.

31. Therapy with oral clotrimazole induces inhibition of the Gardos channel and reduction of erythrocyte dehydration in patients with sickle cell disease.

32. Sickle cell paths converge on hydroxyurea.

33. Mortality in sickle cell disease. Life expectancy and risk factors for early death.

35. A highly conserved region of human erythrocyte ankyrin contains the capacity to bind spectrin.

36. Pain in sickle cell disease. Rates and risk factors.

37. Reliability of Tanner stage assessments in a multi-center study.

38. Hydroxyurea enhances fetal hemoglobin production in sickle cell anemia.

39. Isobutyl nitrite toxicity by ingestion.

40. Glycosylation of variant hemoglobins in normal and diabetic subjects.

41. Influence of sickle hemoglobinopathies on growth and development.

42. Exercise-induced hemolysis in xerocytosis. Erythrocyte dehydration and shear sensitivity.

43. Newborn bleeding disorders: a practical approach.

44. Hydroxyurea increases fetal hemoglobin production in sickle cell anemia.

45. Cation depletion by the sodium pump in red cells with pathologic cation leaks. Sickle cells and xerocytes.

46. Pathology of membrane proteins in sickle erythrocytes.

48. Chemotherapy to increase fetal hemoglobin in patients with sickle cell anemia.

49. Lung function in children with sickle cell anemia.

50. Energy reserve and cation composition of irreversibly sickled cells in vivo.

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