241 results on '"Piomelli, Sergio"'
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2. The Mechanism of Enzyme Decline in the Red Blood Cell During the 'In Vivo' Aging Process
3. Separation of Younger Red Cells with Improved Survival in vivo: An Approach to Chronic Transfusion Therapy
4. Isozymes of Human Phosphofructokinase: Identification and Subunit Structural Characterization of a New System
5. Threshold for Lead Damage to Heme Synthesis in Urban Children
6. Chemical Toxicity of Red Cells
7. Childhood Lead Poisoning in the '90s.
8. Workshop Summaries: The Splenectomy Controversy
9. Separation of Normoblasts from Whole Blood by Ultracentrifugation on Arabino-Galactane Discontinuous Gradients: A Tool for Prenatal Diagnosis
10. Blood Lead Concentrations in a Remote Himalayan Population
11. Pulmonary embolism developing in patients with sickle cell disease on hypertransfusion and IV deferoxamine chelation therapy
12. Piomelli and Schoenbrod re Needleman
13. Erythropoietic Protoporphyria: Four Novel Frameshift Mutations in the Ferrochelatase Gene
14. Effects of Total Hemoglobin and Hemoglobin S Concentration on Cerebral Blood Flow During Transfusion Therapy to Prevent Stroke in Sickle Cell Disease
15. Hydroxyurea In Congenital Erythropoietic Porphyria
16. Childhood Lead Poisoning in the '90s.
17. Use of Penicillamine in Children with Small Lead Burdens
18. Hereditary Hemolytic Anemia Due to Enzyme Defects of Glycolysis
19. G6PD-RELATED NEONATAL JAUNDICE The work of the author referred to in this article was supported by NIH Grant #AM26793-06.
20. THE EFFECT OF ANDROGENS ON SOME ASPECTS OF BODY COMPOSITION AND ERYTHROPOISIS IN OCTOGENARIAN MALES*
21. ERYTHROCYTES AS A TOOL IN STUDIES ON RABBIT RADIATION CHIMERAS AND SECONDARY DISEASE *
22. Acute Chest Syndrome Is Strongly Associated Parvo Virus B19 Seroconversion in Patients with Hemoglobin SC Disease.
23. Childhood lead poisoning
24. Rapid prenatal diagnosis of sickle cell diseases using oligonucleotide ligation assay coupled with laser-induced capillary fluorescence detection
25. CHILDHOOD LEAD POISONING PREVENTION
26. Human HKR Isozyme: Organization of the Hexokinase I Gene, the Erythroid-Specific Promoter, and Transcription Initiation Site
27. Serum transferrin receptor as a marker of erythropoiesis suppression in patients on chronic transfusion
28. Assessment of Erythropoiesis Suppression in Patients on Chronic Blood Transfusions: Value of Serum Transferrin Receptor, Erythropoietin and Reticulocytes † 803
29. The Molecular Basis of Different Hexokinase (HK) Defects; Two Isozymes (HKr and HK1) Produced from a Single Gene by Alternate Promoters ♦ 787
30. In Sickle Cell Disease Patients Coagulation Abnormalities Are Not A Major Predisposing Factor To Stroke † 768
31. Identification of the cDNA for Human Red Blood Cell–Specific Hexokinase Isozyme
32. Haplotypes of the human β-like globin gene cluster: Analyzing the 3′ Hpa I polymorphic site by long distance PCR
33. Systematic screening for RNA with skipped exons - splicing mutations of the ferrochelatase gene
34. Recent advances in the management of thalassemia
35. A novel splicing mutation in the ferrochelatase gene responsible for erythropoietic protoporphyria
36. Experience with 500 prenatal diagnoses of sickle cell diseases: The effect of gestational age on affected pregnancy outcome
37. Screening for ferrochelatase mutations: molecular heterogeneity of erythropoietic protoporphyria
38. 10 Management of Cooley's anaemia
39. Mechanism of red blood cell aging: Relationship of cell density and cell age
40. Neonatal screening for glucose-6-phosphate dehydrogenase deficiency
41. Prevention of carryover contamination in the detection of βS and βC genes by polymerase chain reaction
42. Expression of myeloid differentiation antigens in acute nonlymphocytic leukemia: Increased concentration of CD33 antigen predicts poor outcome—A report from the childrens cancer study group
43. Decay of mammalian hexokinase: characterization of the specific proteolytic activity
44. Management of Thalassemia Major (Cooley’s Anemia)
45. Oral Iron Chelators for the Clinical Management of Iron Overload.
46. Cystic Fibrosis in a Black Child with Hemoglobin S-D Disease
47. Planning an Exchange Transfusion in Patients with Sickle Cell Syndromes
48. Chelation Therapy and Cardiac Status in Older Patients with Thalassemia Major
49. Childhood Lead Poisoning Prevention.
50. Rapid Diagnosis of Iron Deficiency by Measurement of Free Erythrocyte Porphyrins and Hemoglobin: The FEP/Hemoglobin Ratio.
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