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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
- Proteinuria Nephrotic Syndrome
- Polycystic Kidney Disease
- IgA Nephropathy
- Kidney Disease
One of my primary clinical interests focuses on the ways in which the complement system, a series of proteins within the immune system, can cause kidney diseases in children and adults. I also have a strong clinical interest in the large number of kidney conditions that have a genetic cause.
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.
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
•Complement-mediated Renal Diseases including aHUS and C3 Glomerulopathy •Functional Roles of Primary Cilia in Renal Cystic Diseases
Susan Apkon, MD
Pediatric Physical Medicine & Rehabilitation, Pediatrics, Physical Medicine & Rehabilitation
Austin Larson, MD
Clinical Genetics and Genomics - General, Medical Biochemical Genetics, Pediatrics
Kathryn Chatfield, MD
Clinical Genetics and Genomics - General, Cardiology - Pediatric, Pediatrics
Vivian Shih, MD
Nephrology - Pediatric, Pediatrics
