Physician
Pediatric Hematology & Oncology
Dr. Kathleen T. McKie, MD
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Kathleen T. McKie, MD practices Pediatric Hematology & Oncology. She studied medicine at Medical University of South Carolina College of Medicine. Kathleen T. McKie is also published. She has 23 publications published. The lastest publication: "Long-term stroke risk in children with sickle cell disease screened with transcranial Doppler.'
Publications
- Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury.
- Risk factors for microalbuminuria in children with sickle cell anemia.
- Diagnostic complication and molecular characteristics of Hb SC-Chicago disease with alpha-thal-2 (-alpha3.7 deletion): effects of multiple variant on patient''s phenot...
- The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on s...
- Alpha thalassemia and stroke risk in sickle cell anemia.
- Long-term stroke risk in children with sickle cell disease screened with transcranial Doppler.
- Spleen in sickle cell anemia: comparative studies of Nigerian and U.S. patients.
- The use of transcranial ultrasonography to predict stroke in sickle cell disease.
- Cerebral vessel stenosis in sickle cell disease: criteria for detection by transcranial Doppler.
- Molecular characterization of Hb S(C) beta-thalassemia in American blacks.
- Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin gene.
- Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia.
- A new variant, HB Muscat [alpha 2 beta (2)32(B14)Leu----Val] observed in association with HB S in an Arabian family.
- Cerebral infarction in sickle cell anemia: mechanism based on CT and MRI.
- MR and CT investigation of cerebrovascular disease in sickle cell patients.
- Three sickle cell anemia patients each with a different alpha chain variant. Diagnostic complications.
- Sickle cell disease and tonsillectomy. Preoperative management and postoperative complications.
- Stroke in sickle cell disease.
- The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes.
- Neuropsychologic impairment in children with sickle cell anemia.
- Postnatal changes in the quantities of globin chains and hemoglobin types in two babies with Hb H disease.
- Different zeta globin gene deletions among black Americans.
Schools
Med Coll Of Ga Sch Of Med
Med College Ga
Doctors Specialties
- Pediatric Pulmonology
- Pediatric Hematology
- Oncology
Accepted Insurances
Education
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William Beaumont Army Medical Center -
Medical University of South Carolina College of Medicine
Hospital
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Georgia Regents Medical Center
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