109 results on '"McKie, K."'
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2. 598 Evaluating Georgia’s cystic fibrosis newborn screening algorithm to inform recommendations for improving quality and equity
3. 267 Skeletal muscle oxygenation extraction is lower in women than men with cystic fibrosis
4. Constructing Gendered Bodies
5. INFLAMMATION AND OXIDATIVE STRESS DURING EXERCISE IN PATIENTS WITH CYSTIC FIBROSIS: 403★
6. STOPPING THE SPREAD OF MRSA: EFFECTIVE USE OF INFECTION CONTROL MEASURES IN A PEDIATRIC CF CENTER: 284
7. INTERACTION AMONG LUNG FUNCTION, VASCULAR FUNCTION, AND EXERCISE CAPACITY IN PATIENTS WITH CYSTIC FIBROSIS: 339★
8. EFFICACY OF AN ERADICATION PROTOCOL TO REDUCE MRSA COLONIZATION IN PEDIATRIC CF PATIENTS: 258★
9. IMPLEMENTATION OF AN ERADICATION PROTOCOL TO REDUCE MRSA RATES IN PEDIATRIC PATIENTS WITH CYSTIC FIBROSIS: 437
10. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, βS-globin gene haplotype, co-inherited α-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia
11. Regulation of primary Strongyloides ratti infections in mice: a role for interleukin-5
12. P3.16-45 The Rates and Survival of Surgically-Resected Second Primary Lung Cancers in Patients Undergoing Resection of an Initial Primary Lung Cancer.
13. MA23.05 Post-Operative Radiation Improves Overall Survival in Patients with Node-Positive Non-Small Cell Lung Cancer Undergoing Sublobar Resections
14. Adjuvant Chemotherapy and Radiation Options and Their Associated Outcomes in Surgically Resected Non-Small Cell Carcinoma
15. Different ζ globin gene deletions among Black Americans
16. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, betaS-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia
17. Serial transcranial Doppler ultrasonography in a child with sickle cell anemia and stroke
18. Long-term stroke risk in children with sickle cell disease screened with transcranial doppler
19. Sickle Cell Disease and Tonsillectomy: Preoperative Management and Postoperative Complications
20. Spleen in sickle cell anemia: Comparative studies of Nigerian and U.S. patients
21. Three Sickle Cell Anemia Patients Each with a Different α Chain Variant. Diagnostic Complications
22. Postnatal changes in the quantities of globin chains and hemoglobin types in two babies with Hb H disease
23. A new Variant, Hb Muscat [α2β232(B14)Leu→val] Observed in Association With Hb S in an Arabian Family
24. Sensory impairment in adults with intellectual disabilities---an exploration of the awareness and practices of social care providers.
25. Molecular characterization of Hb S(C) β‐thalassemia in American blacks
26. Arterial stenosis in sickle cell disease
27. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, βS-globin gene haplotype, co-inherited α-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
28. Cerebral infarction in sickle cell anemia.
29. A new Variant, Hb Muscat [α2β232(B14)Leu→val] Observed in Association With Hb S in an Arabian Family.
30. Severe Hb S-β°-thalassaemia with a T → C substitution in the donor splice site of the first intron of the β-globin gene.
31. Effects of α-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from georgia.
32. The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes
33. The Rare α-Thalassemia-1 of Blacks is a ζ-Thalassemia-1 Associated with Deletion of All α- and ζ-Globin Genes
34. Erythrocyte Membrane Protein Kinase C in Sickle Cell Disease.
35. Hemorheologic Parameters in Children with Homozygous Sickle Cell Anemia Receiving Chronic Red Cell Transfusions for Large Cerebral Vessel Vasculopathy.
36. Different ? globin gene deletions among Black Americans
37. α‐thalassemia among Pediatric Hemoglobin S Homozygotes
38. 747 Improving timeliness of sweat chloride scheduling for infants in Georgia with abnormal CF newborn screen.
39. 741 Expanded use of remote objective monitoring during telehealth visits for people with CF experiencing acute symptoms: the EUROPA Study.
40. Inspirational student will make a wonderful nurse.
41. Real-World Vein Mapping Practice Patterns Before Endovascular Treatment of Limb Ischemia.
42. Inherent Ethyl Acetate Selectivity in a Trianglimine Molecular Solid.
43. Impact of Nutritional Deficiencies on Children and Young Adults with Crohn's Disease Undergoing Intraabdominal Surgery.
44. Risk Factors for Venous Thromboembolism in Children and Young Adults With Inflammatory Bowel Disease.
45. The Role of Race and Economic Characteristics in the Presentation and Survival of Patients With Surgically Resected Non-Small Cell Lung Cancer.
46. Population-based differences in the outcome and presentation of lung cancer patients based upon racial, histologic, and economic factors in all lung patients and those with metastatic disease.
47. Diagnostic complication and molecular characteristics of Hb SC-Chicago disease with alpha-thal-2 (-alpha3.7 deletion): effects of multiple variant on patient's phenotype.
48. The dimensions of public health law research.
49. Sickle cell disease and tonsillectomy. Preoperative management and postoperative complications.
50. Inhibition of nitric oxide: effects on interleukin-1 beta-enhanced ovulation rate, steroid hormones, and ovarian leukocyte distribution at ovulation in the rat.
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