E. Leila JeromeClayMD, MCTS

Journal Articles

• Stroke in a child with hemoglobin SC disease: a case report describing use of hydroxyurea after transfusion therapy  
  Diana Fridlyand, Caroline Wilder, E. Leila Jerome Clay, Bruce Gilbert, Betty S. Pace, Pediatric Reports, 1/1/2017
• A survey of Pneumococcal Prophylaxis Practices among Sickle Cell Providers  
  Clay, ELJ, Hsu G, Jordan L. Xu H and Pace BS, J Pediatr and Child Health Care, 1/1/2016
• The Polymorphisms in the Vitamin D Receptor Gene and Disease Severity in Sickle Cell Disease  
  Clay ELJ, Motsinger-Reif A, Hoskins J, Veit L, Calikoglu A and Redding-Lallinger R, Advances in Biological Chemistry, 1/1/2015
• Immunogenicity of pneumococcal vaccination in a patient with sickle hemoglobinopathy: a case report  
  Clay ELJ, Burrell T, Belhorn T, Redding-Lallinger R, Clinical Case Reports, 1/1/2015
• Go Girl  
  Clay EL, 1/1/2015
• Fetal Hemoglobin Induction to Treat b-Hemoglobinopathies: From Bench to Bedside  
  Makala L, Torres C, Clay EL, Neunert C, Pace B, J Hematol Transfus, 1/1/2014
• A 19-year- old man with sickle cell disease presenting with spinal infarction: a case report  
  Edwards A, Clay EL, Jewells V, Adams S, Crawford RD, Redding-Lallinger R, J Med Case Rep, 1/1/2013
• Sickle Cell Disease Transition Assessment and Readiness: A Baseline Analysis  
  Wilder C, George N, Xu H, Clay ELJ, Journal of Sickle Cell Disease and Hemoglobinopathy, 1/15/2016
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Abstracts/Posters

• Chronic Kidney Disease Is Under-Screened in SCD and Mild Albuminuria Is Associated with a Drop in Hemoglobin: A Report from the Grndad Sickle Cell Registry
  E. Leila Jerome Clay, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/8/2019
• Vitamin D Repletion Mitigates Oxidative Stress Induce Pulmonary Artery Remodeling in Sickle Cell Disease
  Julia Brittain, E. Leila Jerome Clay, Ryan Harris, Itia Lee, Abdullah Kutlar and Sanjiv Kumar, Blood, 1/1/2017
• Evolution of Chronic Pain in Sickle Cell Disease
  Michael Pope, Camila Albo, Kyle Michael Kidwell, Hongyan Xu, Latanya Bowman, Leigh Wells, Nadine Barrett, Sabine Fields, Pritam Bora, E. Leila Jerome Clay, Niren Patel..., Blood, ASH Annual Meeting, 1/1/2016
• Sickle Cell Disease and Vitamin D
  Clay EL, Georgia Regents University, Medical College of Georgia Department of Internal Medicine Grand Rounds, Georgia Regents University, GA, 1/1/2015
• Hydroxyurea Delivery: A survey of primary care providers
  Nadirah El Amin, Robert Gibson, E. Leila Jerome Clay, Cindy Neunert, Foundation of Sickle Cell Disease Research, 1/1/2015
• High dose vitamin D repletion improves vascular endothelial function in patients with Sickle Cell Disease.
  E. Leila Jerome Clay, Benjamin Sookhoo, Latanya Bowman, Hongyan Xu, Abdullah Kutlar, Ryan A. Harris, Foundation of Sickle Cell Disease Research, 1/1/2015
• A Pilot Study of Vitamin D Repletion Shows Improvement in Pain and Vascular Endothelial Function in Adult Patients with Sickle Cell Disease
  Mary K Lintel, Latanya Bowman, Xu Hongyan, Abdullah Kutlar, Ryan A Harris, E. Leila Jerome Clay, Blood, 1/1/2015
• Demographic Features of a Mixed Urban/Rural Adult Sickle Cell Population: Opportunities and Challenges for Improving Health Care
  Amauri Bowman, Sydney Taylor, Pritam Bora, Hongyan Xu, Leigh Wells, Latanya Bowman, Nadine Barrett, Richard Lottenberg, E. Leila Jerome Clay, Betty Pace, Matthew Lyon,..., Blood, 1/1/2015
• Are There True Non- Responders to Hydroxyurea in Sickle Cell Disease? a Multiparameter Analysis
  Arati Rani Chand, Hongyan Xu, Leigh G Wells, Betsy Clair, Cindy Neunert, Alison E Spellman, Leila Jerome Clay, Kavita Natrajan, Abdullah Kutlar, Blood, 1/1/2014
• Hydroxyurea in Sickle Cell Disease: Lack of Response or Non-Compliance?
  Arati Chand, MBBS, Hongyan Xu, PhD, Betsy Clair, Leila Clay, MD, Leigh Wells, RN, FNP, Kavita Natarajan, MBBS, Abdullah Kutlar, MD, Foundation of Sickle Cell Disease Research, 1/1/2014
• Hydroxyurea in Sickle Cell Disease: Lack of Response or Non-Compliance?
  Chand A, Hongyan X, Clair B, Clay ELJ, Wells L, Natarajan K, Kutlar A, Foundation of Sickle Cell Disease Research/American Society of Hematology, 1/1/2014
• The Impact of High Dose Vitamin D repletion in Vitamin D-Deficient Patients with Sickle Cell Disease
  Sookhoo B, Bowman L, Wells L, Bora P, Harris R, Britain J, Kutlar A, Clay ELJ, Georgia Regents University, 6th Annual Medical Scholars Research Day, 1/1/2014
• The Role of Vitamin D and receptor in Sickle Cell Disease Severity
  Clay EL, UNC Benign Hematology Conference/UNC Pediatric Hematology Oncology Conference, University of North Carolina, NC, 2012; Georgia Regents University, Cancer Center, 2013, 1/1/2013
• Vitamin D supplementation, its effect and outcome in Sickle Cell Disease
  Clay EL, Program to Increase Diversity among Individual Engaged in Health-Related Research (PRIDE)' Functional and Applied Genomics of Blood Disorders Cohort III presentations, Georgia Regents University, GA, 1/1/2013
• What with the D in SCD?
  Clay EL, Georgia Regents University, Medical College of Georgia Department of Pediatric Grand Rounds, Georgia Regents University, GA, 1/1/2013
• Spinal Infarction in Sickle Cell Disease, a rare and Unexplained Complication
  April Edwards, MD, E. Leila Jerome Clay, Valerie Jewells, Regina Crawford, Rupa Redding- Lallinger, AJH (Foundation of Sickle Cell Disease Research), 1/1/2013
• A review of vitamin D deficiency, treatment and patient knowledge among patients with sickle cell disease and Parents
  E. Leila Jerome Clay, Elizabeth Robinson, Rupa Redding- Lallinger, AJH (Foundation of Sickle Cell Disease Research), 1/1/2013
• A review of vitamin D deficiency, treatment and patient knowledge among patients with sickle cell disease and Parents
  Clay ELJ, Robinson E, Redding-Lallinger R, Foundation of Sickle Cell Disease Research, 1/1/2013
• Spinal Infarction in Sickle Cell Disease, a rare and Unexplained Complication
  Edwards A, Clay ELJ, Jewells V, Crawford R, Redding-Lallinger R, Foundation of Sickle Cell Disease Research, 1/1/2013
• Vitamin D Deficiency, CD40L and VEGF in a young population with sickle cell disease
  E. Leila Jerome Clay, MD, Julia Brittain, PhD, Rupa Redding-Lallinger, MD, Blood, 1/1/2012
• The Vitamin D Receptor Gene and Disease Severity in Sickle Cell Anemia
  Clay ELJ, Hoskins J, Motsinger-Reif A, Veit L, Barrow D, Calikoglu A, Redding-Lallinger R, Evening of Scholarship, University of North Carolina at Chapel Hill, NC, 1/1/2012
• High Grade Rhabdomyosarcoma
  Clay EL, Tumor Board Pediatric Hematology Oncology, UNC - Cancer Hospital, University of North Carolina, NC, 1/1/2011
• Follicular Lymphoma
  Clay EL, Tumor Board Pediatric Hematology Oncology, UNC - Cancer Hospital, University of North Carolina, NC, 1/1/2011
• Pheochromocytoma in the Pediatric Patient
  Clay EL, Tumor Board Pediatric Hematology Oncology, UNC - Cancer Hospital, University of North Carolina, NC, 1/1/2011
• Brain Stem Tumors
  Clay EL, Tumor Board Pediatric Hematology Oncology, UNC - Cancer Hospital, University of North Carolina, NC, 1/1/2011
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Lectures

• Preventing Long-Term Complications in Sickle Cell Disease 
  60th American Society of Hematology Annual Meeting - 11/30/2018
• Sickle Cell Disease Transition Assessment and Readiness: Baseline vs. Post-Intervention Analysis 
  Ft. Lauderdale, FL - 1/1/2017
• Platelet Disorders 
  VA Hospital, University of Medicine and Dentistry of New Jersey - 1/1/2010
• Transition Matters 
  1/10/2016
• A model of Transition of Care, the Augusta Story 
  Atlanta, GA - 1/25/2017
• A model of Transition for Sickle Cell Patients 
  Asheville, NC, 2015; New York, NY, 2016
• Transition of Care for Sickle Cell Disease 
  Cote De Arcadins, Haiti - 1/24/2017
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Other

• The Growing Concern about Vitamin D Deficiency 
  Clay EL, The Magazine of Metropolitan Augusta
  1/1/2014