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Office
4650 W Sunset Blvd
Los Angeles, CA 90027Phone+1 323-361-2121Fax+1 323-660-7128
Education & Training
- Indiana University School of MedicineFellowship, Pediatric Hematology/Oncology, 1978 - 1982
- Indiana University School of MedicineResidency, Pediatrics, 1975 - 1978
- University of Michigan Medical SchoolClass of 1975
Certifications & Licensure
- CA State Medical License 1985 - 2025
- IN State Medical License 1977 - 2003
- American Board of Pediatrics Pediatrics
- American Board of Pediatrics Pediatric Hematology-Oncology
Awards, Honors, & Recognition
- Super Doctor SuperDoctors.com
- Whos Who in Medicine and Healthcare Marquis Whos Who
Clinical Trials
- Cardiac T2* in Beta-thalassemia Patients on Deferasirox Treatment Start of enrollment: 2006 Feb 01
- Assessment of Pain in People With Thalassemia Who Are Treated With Regular Blood Transfusions Start of enrollment: 2009 Jul 01
- Clinical Importance of Treating Iron Overload in Sickle Cell Disease Start of enrollment: 2009 Apr 01
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Publications & Presentations
PubMed
- 28 citationsIron overload in transfusion-dependent patientsThomas D. Coates
Hematology. American Society of Hematology. Education Program. 2019-12-06 - 801 citationsMRI R2 and R2* mapping accurately estimates hepatic iron concentration in transfusion-dependent thalassemia and sickle cell disease patientsJohn C. Wood, Cathleen Enriquez, Nilesh R. Ghugre, J. Michael Tyzka, Susan Carson
Blood. 2005-08-15 - 176 citationsLongitudinal analysis of heart and liver iron in thalassemia majorLeila Noetzli, Susan Carson, Anne Nord, Thomas D. Coates, John C. Wood
Blood. 2008-10-01
Journal Articles
- Increased Brain Iron Deposition in Patients with Sickle Cell Disease: An MRI Quantitative Susceptibility Mapping StudyThomas D Coates, John C Wood, Benita Tamrazi, Blood
- A Novel Cross-Correlation Methodology for Assessing Biophysical Responses Associated with PainLonnie K Zeltzer, Roberta M Kato, Jon Detterich, Thomas D Coates, John Sunwoo, John C Wood, Journal of Pain Research
Abstracts/Posters
- Role of Exosomes in Hepcidin Regulation in _-ThalassemiaThomas Coates, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/7/2019
- Lower Oxygen Saturation in the Internal Cerebral Vein of Patients with Sickle Cell Disease Revealed By Qsm-MRIThomas Coates, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/7/2019
- Evaluating Luspatercept Responders in the Phase 3, Randomized, Double-Blind, Placebo-Controlled BELIEVE Trial of Luspatercept in Adult Beta-Thalassemia Patients (Pts) ...Thomas Coates, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/9/2019
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Lectures
- IRON: How to Manage When There is Too Much or Too Little of It61st Annual American Society of Hematology Meeting - Orlando, FL - 12/7/2019
- Hemolysis and Tricuspid Regurgitation Jet Velocity Predict Mortality in Patients with Sickle Cell Disease2018 ASH Annual Meeting - San Diego, CA - 12/1/2018
- The Believe Trial: Results of a Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Luspatercept in Adult Beta-Thalassemia Patients Who Require Regular Red ...2018 ASH Annual Meeting - San Diego, CA - 12/1/2018
Other
- Introduction to a Review Series on Iron Metabolism and Its DisordersThomas Coates, MD, Blood
https://www.doximity.com/articles/96240f18-92a9-4256-8c87-d9707f5074e9
UpToDate, Wolters Kluwer Health - 2012-08-21 - Introduction to a How I Treat Series on Sickle Cell Disease and ThalassemiaThomas Coates, MD, Blood
https://www.doximity.com/articles/871a92cf-5f2a-47cb-b191-4e7d07f93840
UpToDate, Wolters Kluwer Health - 2012-03-22 - Introduction to a How I Treat Series on Sickle Cell Disease and ThalassemiaThomas Coates, MD, Blood
https://www.doximity.com/articles/871a92cf-5f2a-47cb-b191-4e7d07f93840
UpToDate, Wolters Kluwer Health - 2012-11-19 - Join now to see all
Press Mentions
- Researchers at Children’s Hospital Los Angeles Are Unraveling the Biological Mechanism That Triggers Pain in People with Sickle Cell Disease—and Confirming What Mothers Have Been Saying All AlongJanuary 10th, 2022
- Here Are the Best and Worse Case Scenarios for Omicron. Both Are BadDecember 27th, 2021
- Overview of Beta ThalassemiaJanuary 31st, 2020
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Grant Support
- Southern California Blood Safety Surveillance Program In Hematological DisorfersCenters For Disease Control And Prevention2012
- Basic And Translational Research ProgramNational Heart, Lung, And Blood Institute2009–2011
- Sickle Cell Scholar ComponentNational Heart, Lung, And Blood Institute2008–2011
- Impact Of Blood Viscosity On Oxygen Delivery In Humans With Sickle Cell AnemiaNational Heart, Lung, And Blood Institute2008–2011
- Administration CoreNational Heart, Lung, And Blood Institute2008–2011
- Research Initiatives For The Preventions Of Complications Of ThalassemiaCenters For Disease Control And Prevention2007–2011
- Human Models Of Sickle Cell Vascular DamageNational Center For Research Resources2006–2009
- Comprehensive Sickle Cell CenterNational Heart, Lung, And Blood Institute2008
- Human Models Of Sickle Cell Vascular Damage: (AIM2) Response Of Plasma MarkersNational Center For Research Resources2006
- Human Models Of Sickle Cell Vascular DamageNational Heart, Lung, And Blood Institute2003–2006
- Modeling Of Neutrophil MotilityNational Center For Research Resources1999–2002
- Leukocyte Activation And Rheology In Sickle Cell Disease--Vascular OcclusionNational Heart, Lung, And Blood Institute1998–2002
- Granules And Organelles And Leukocyte ActivationNational Institute Of Allergy And Infectious Diseases1995–1998
- Neutrophil Activation And Rheology In Sickle Cell Disease--Vascular OcclusionNational Heart, Lung, And Blood Institute1996–1997
- Core--Data CoordinatingNational Heart, Lung, And Blood Institute1996–1997
- Role Of Granules &Organelles In Leukocyte ActivationNational Institute Of Allergy And Infectious Diseases1988–1992
- Role Of Granules And Organelles In Leukocyte ActivationNational Institute Of Allergy And Infectious Diseases1985–1986
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