Dr. Thomas Coates, MD

• Pediatric Hematology & Oncology

• Pediatrics

*Healthgrades does not verify qualifications for medical specialties. Please verify your provider's specialty and qualifications directly with your provider and applicable medical board.

• University Of Michigan / Medical Center

  Medical School, 1975

• English

• Armenian

• French

• White matter has impaired resting oxygen delivery in sickle cell patients, 2019-02-21

• Concordance with comprehensive iron assessment, hepatitis A vaccination, and hepatitis B vaccination recommendations among patients with sickle cell disease and thalassaemia receiving chronic transfusions: an analysis from the Centers for Disease Control haemoglobinopathy blood safety project, 2021-08-24

• Patterns of hepatic iron distribution in patients with chronically transfused thalassemia and sickle cell disease, 2010-06-03

• Sickle Cell Disease in California: A Population-Based Description of Emergency Department Utilization, 2010-11-24

• Early Cardiac Iron Overload in a Child on Treatment of Acute Lymphoblastic Leukemia, 2015-08-17

• Comparison of biventricular dimensions and function between pediatric sickle-cell disease and thalassemia major patients without cardiac iron, 2013-02-06

• Biventricular dimensions and function in pediatric sickle-cell disease and thalassemia major patients without cardiac iron, 2013-01-30

• Hemoglobin H-constant spring in North America: an alpha Thalassemia with frequent complications, 2014-11-26

• Contrasting resting-state fMRI abnormalities from sickle and non-sickle anemia, 2017-10-05

• Vasoconstriction Response to Mental Stress in Sickle Cell Disease: The Role of the Cardiac and Vascular Baroreflexes, 2021-11-04

• Erythrocyte and plasma oxidative stress appears to be compensated in patients with sickle cell disease during a period of relative health, despite the presence of known oxidative agents, 2019-07-03

• Pulmonary function in thalassaemia major and its correlation with body iron stores, 2011-08-02

• DESIGN OF THE SILENT CEREBRAL INFARCT TRANSFUSION (SIT) TRIAL, 2017-07-14

• Nutritional deficiencies in iron overloaded patients with hemoglobinopathies, 2010-06-03

• Individuals with sickle cell disease have a significantly greater vasoconstriction response to thermal pain than controls and have significant vasoconstriction in response to anticipation of pain, 2017-08-17

• DETERMINANTS OF RESTING CEREBRAL BLOOD FLOW IN SICKLE CELL DISEASE, 2016-07-04

• Autonomically-mediated decrease in microvascular blood flow due to mental stress and pain in sickle cell disease: A target for neuromodulatory interventions, 2020-02-15

• Patients with sickle cell anemia on simple chronic transfusion protocol show gender differences for hemodynamic and hematologic responses to transfusion, 2012-11-26

• The Role of Carbon Monoxide and Heme Oxygenase in the Prevention of Sickle Cell Disease Vaso-Occlusive Crises, 2017-04-29

• Nocturnal peripheral vasoconstriction predicts the frequency of severe acute pain episodes in children with sickle cell disease, 2020-10-23

• Functional near-infrared spectroscopy-based prefrontal cortex oxygenation during working memory tasks in sickle cell disease, 2023-10-17

• MAGNETIC RESONANCE DETECTION OF KIDNEY IRON DEPOSITION IN SICKLE CELL DISEASE: A MARKER OF CHRONIC HEMOLYSIS, 2008-08-07

• Sickle Cell Disease Subjects Have a Distinct Abnormal Autonomic Phenotype Characterized by Peripheral Vasoconstriction With Blunted Cardiac Response to Head-Up Tilt, 2019-04-11

• Kidney iron deposition by R2* is associated with hemolysis and urinary iron, 2020-11-20

• Biophysical markers of the peripheral vasoconstriction response to pain in sickle cell disease, 2017-05-24

• Reduced global cerebral oxygen metabolic rate in sickle cell disease and chronic anemias, 2021-05-12

• Sickle Cell Disease in California: Sociodemographic Predictors of Emergency Department Utilization, 2011-02-25

• Tricuspid regurgitant jet velocity and myocardial tissue doppler parameters predict mortality in a cohort of patients with sickle cell disease spanning from pediatric to adult age groups - revisiting this controversial concept after sixteen years of additional evidence., 2020-10-12

• Spleen R2 and R2* in Iron-Overloaded Patients With Sickle Cell Disease and Thalassemia Major, 2010-06-03

• Vaso-Occlusion in Sickle Cell Disease: Is Autonomic Dysregulation of the Microvasculature the Trigger?, 2019-10-15

• Anemia predicts lower white matter volume and cognitive performance in sickle and non-sickle cell anemia syndrome, 2019-07-23

• Identifying Elevated Risk for Future Pain Crises in Sickle-Cell Disease Using Photoplethysmogram Patterns Measured During Sleep: A Machine Learning Approach, 2021-07-26

• Autonomic responses to cold face stimulation in sickle cell disease: a time-varying model analysis, 2015-07-14

• Aura and mental stress are associated with reports of pain in sickle cell disease-a pilot study using a mobile application, 2020-02-05

• Diminished Cerebral Oxygen Extraction and Metabolic Rate in Sickle Cell Disease using T2 Relaxation Under Spin Tagging MRI, 2017-12-01

• Human T-cell lymphotropic virus type 1 infection among U.S. Thalassemia patients, 2014-01-07

• Sickle Cell Microvascular Paradox - oxygen supply-demand mismatch, 2019-04-19

• Emergency department utilization by Californians with sickle cell disease, 2005-2014, 2016-12-21

• Transient Hypoxia Model Revealed Cerebrovascular Impairment in Anemia Using BOLD MRI and Near-Infrared Spectroscopy, 2020-07-09

• A significant proportion of thalassemia major patients have adrenal insufficiency detectable on provocative testing, 2014-06-10

• Calibration of T2oximetry MRI for subjects with sickle cell disease, 2021-03-14

• Physiology and Pathophysiology of Iron in Hemoglobin-Associated Diseases, 2014-04-12