Overview
Barbara Pober is a Pediatrics specialist and a Medical Genetics provider in Boston, Massachusetts. Dr. Pober is rated as an Elite provider by MediFind in the treatment of Williams Syndrome. Her top areas of expertise are Williams Syndrome, Chromosome 7p Deletion, Vici Syndrome, and Townes-Brocks Syndrome. Dr. Pober is currently accepting new patients.
Her clinical research consists of co-authoring 40 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 30 articles and participated in 1 clinical trial in the study of Williams Syndrome.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
Locations
55 Fruit St, Boston, MA 02114
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
2 Clinical Trials
The General Hospital Corporation
Takara Stanley is a Pediatrics specialist and an Endocrinologist in Boston, Massachusetts. Dr. Stanley is rated as an Advanced provider by MediFind in the treatment of Williams Syndrome. Her top areas of expertise are Williams Syndrome, Obesity, HIV/AIDS, Adrenoleukodystrophy (ALD), and Gastric Bypass. Dr. Stanley is currently accepting new patients.
Department Of Cardiology
Daniel Castellanos is a Pediatrics provider in Boston, Massachusetts. Dr. Castellanos is rated as a Distinguished provider by MediFind in the treatment of Williams Syndrome. His top areas of expertise are Aberrant Subclavian Artery, Congenital Heart Disease (CHD), Tetralogy of Fallot, and Double Aortic Arch.
The General Hospital Corporation
Nina Gold is a Pediatrics specialist and a Medical Genetics provider in Boston, Massachusetts. Dr. Gold is rated as an Experienced provider by MediFind in the treatment of Williams Syndrome. Her top areas of expertise are Maple Syrup Urine Disease, Inborn Amino Acid Metabolism Disorder, Retinopathy Pigmentary Mental Retardation, and Williams Syndrome. Dr. Gold is currently accepting new patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Elite
- Williams SyndromeDr. Pober isElite. Learn about Williams Syndrome.
- Advanced
- Chromosome 7p DeletionDr. Pober isAdvanced. Learn about Chromosome 7p Deletion.
- Experienced
- 2q37 Deletion SyndromeDr. Pober isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Pober isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Pober isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Pober isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acrodermatitis EnteropathicaDr. Pober isExperienced. Learn about Acrodermatitis Enteropathica.
- Acrorenal Mandibular SyndromeDr. Pober isExperienced. Learn about Acrorenal Mandibular Syndrome.