Physician

Pediatric Hematology & Oncology

Dr. Kathleen M. McKie, MD

Kathleen McKie practices Pediatric Hematology & Oncology. She graduated from Medical University of South Carolina College of Medicine. Dr. Kathleen M. McKie is a published MD. She has 23 publications published. The most current 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 Univ Of Sc Coll Of Med

Doctors Specialties

Adolescent Medicine
Pediatric Hematology
Oncology

Accepted Insurances

Education

William Beaumont Army Medical Center
Medical University of South Carolina College of Medicine

Hospital

Georgia Regents Medical Center

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