Physiology and Pathophysiology of Iron in Hemoglobin-Associated Diseases

Por Coates, Thomas D
Publicado no Free Radic Biol Med (2014)

Iron overload in transfusion-dependent patients

Por Coates, Thomas D.
Publicado no Hematology Am Soc Hematol Educ Program (2019)

HOW WE MANAGE IRON OVERLOAD IN SICKLE CELL PATIENTS

Por Coates, Thomas D., Wood, John C.
Publicado no Br J Haematol (2017)

Spleen R2 and R2* in Iron-Overloaded Patients With Sickle Cell Disease and Thalassemia Major

Por Brewer, Casey J., Coates, Thomas D., Wood, John C.
Publicado em 2009

Diminished Cerebral Oxygen Extraction and Metabolic Rate in Sickle Cell Disease using T2 Relaxation Under Spin Tagging MRI

Por Bush, Adam M, Coates, Thomas D, Wood, John C
Publicado no Magn Reson Med (2017)

Early Cardiac Iron Overload in a Child on Treatment of Acute Lymphoblastic Leukemia

Por Reitman, Aaron J., Coates, Thomas D., Freyer, David R.
Publicado no Pediatrics (2015)

MAGNETIC RESONANCE DETECTION OF KIDNEY IRON DEPOSITION IN SICKLE CELL DISEASE: A MARKER OF CHRONIC HEMOLYSIS

Por Schein, Aaron, Enriquez, Cathleen, Coates, Thomas D., Wood, John C.
Publicado em 2008

Pancreatic iron loading predicts cardiac iron loading in thalassemia major

Por Noetzli, Leila J., Papudesi, Jhansi, Coates, Thomas D., Wood, John C.
Publicado em 2009

Prediabetes, elevated iron and all-cause mortality: a cohort study

Por Mainous, Arch G, Tanner, Rebecca J, Coates, Thomas D, Baker, Richard
Publicado no BMJ Open (2014)

Analgesic Response to Morphine in Children with Sickle Cell Disease: A Pilot Study

Por Jacob, Eufemia, Hockenberry, Marilyn, Mueller, Brigitta U., Coates, Thomas D., Zeltzer, Lonnie
Publicado em 2008

Mechanisms of Tissue–Iron Relaxivity: Nuclear Magnetic Resonance Studies of Human Liver Biopsy Specimens

Por Ghugre, Nilesh R., Coates, Thomas D., Nelson, Marvin D., Wood, John C.
Publicado em 2005

Sickle Cell Disease in California: A Population-Based Description of Emergency Department Utilization

Por Wolfson, Julie A., Schrager, Sheree M., Coates, Thomas D., Kipke, Michele D.
Publicado em 2010

Graph Lasso-Based Test for Evaluating Functional Brain Connectivity in Sickle Cell Disease

Por Coloigner, Julie, Phlypo, Ronald, Coates, Thomas D., Lepore, Natasha, Wood, John C.
Publicado no Brain Connect (2017)

Longitudinal analysis of heart and liver iron in thalassemia major

Por Noetzli, Leila J., Carson, Susan M., Nord, Anne S., Coates, Thomas D., Wood, John C.
Publicado em 2008

Onset of cardiac iron loading in pediatric patients with thalassemia major

Por Wood, John C., Origa, Raffaella, Agus, Annalisa, Matta, Gildo, Coates, Thomas D., Galanello, Renzo
Publicado em 2008

Sickle Cell Disease in California: Sociodemographic Predictors of Emergency Department Utilization

Por Wolfson, Julie A., Schrager, Sheree M., Khanna, Rachna, Coates, Thomas D., Kipke, Michele D.
Publicado em 2011

The impact of chelation therapy on survival in transfusional iron overload: a meta-analysis of myelodysplastic syndrome

Por Mainous, Arch G., Tanner, Rebecca J., Hulihan, Mary M., Amaya, Mirna, Coates, Thomas D.
Publicado no Br J Haematol (2014)

Improved R2* Measurements in Myocardial Iron Overload

Por Ghugre, Nilesh R., Enriquez, Cathleen M., Coates, Thomas D., Nelson, Marvin D., Wood, John C.
Publicado em 2006

A significant proportion of thalassemia major patients have adrenal insufficiency detectable on provocative testing

Por Huang, Karen E., Mittelman, Steven D., Coates, Thomas D., Geffner, Mitchell E., Wood, John C.
Publicado no J Pediatr Hematol Oncol (2015)

Biventricular dimensions and function in pediatric sickle-cell disease and thalassemia major patients without cardiac iron

Por Meloni, Antonella, Detterich, Jon, Berdoukas, Vasili, Pepe, Alessia, Lombardi, Massimo, Coates, Thomas D, Wood, John C
Publicado em 2013