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Bradley Dixon, MD

Provider's Specialties

Nephrology - Pediatric
Pediatrics

Provider's location(s)

Anschutz Medical Campus, Aurora

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Patient ratings

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Why?

Department of Pediatric Nephrology

(720)777-6263

Insurance plans accepted

We participate with most major health insurance plans and national transplant networks.

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Prepare for your visit

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My care philosophy

I treat patients the way I would want my own family to be treated by a health care provider. I strive to take as much time as needed to listen to the patient's and family's concerns, and explain the condition as well as testing and treatment options.

Get to know Bradley Dixon, MD

Departments and Programs

Conditions Treated

Proteinuria Nephrotic Syndrome
Polycystic Kidney Disease
IgA Nephropathy
Kidney Disease

Experience and background

My research interests are primarily focused on diseases of the kidney caused by abnormalities in the complement system, specifically atypical hemolytic uremic syndrome (aHUS), C3 Glomerulopathy (C3G), and Membranoproliferative Glomerulonephritis (MPGN). These interests are focused on development and improvement of blood tests that are used to diagnose these diseases, as well as clinical trials in new medications being developed to treat these diseases. I also have a clinical research interest in the wide variety of kidney diseases that have a genetic cause, especially cystic kidney diseases but also tubular diseases like Bartter syndrome and Gitelman syndrome, and glomerular diseases like Alport syndrome.

Undergraduate 1995

The College of Wooster (OH)

Medical Education 1999

University of Tennessee Health Science Center College of Medicine

Residency 2003

Cincinnati Children's Hospital Medical Center Program

Fellowship 2006

Cincinnati Children's Hospital Medical Center Program

For Patients:
My research interests are primarily focused on diseases of the kidney caused by abnormalities in the complement system, specifically atypical hemolytic uremic syndrome (aHUS), C3 Glomerulopathy (C3G), and Membranoproliferative Glomerulonephritis (MPGN). These interests are focused on development and improvement of blood tests that are used to diagnose these diseases, as well as clinical trials in new medications being developed to treat these diseases. I also have a clinical research interest in the wide variety of kidney diseases that have a genetic cause, especially cystic kidney diseases but also tubular diseases like Bartter syndrome and Gitelman syndrome, and glomerular diseases like Alport syndrome.

For Referring Providers:
•Complement-mediated Renal Diseases including aHUS and C3 Glomerulopathy •Functional Roles of Primary Cilia in Renal Cystic Diseases