MS
Highly rated in
10
conditions
Highly rated in
10
conditions
Check Dr. Michele J. Spencer-Manzon's experience treating your condition:
About Dr. Michele J. Spencer-Manzon

Michele Spencer-Manzon is a Medical Genetics expert in New Haven, Connecticut. Spencer-Manzon has been practicing medicine for over 18 years and is highly rated in 10 conditions, according to our data. Her top areas of expertise are Beta-Ketothiolase Deficiency, Tyrosinemia Type 2, Tyrosinemia Type 3, and Tyrosinemia Type 1. She is licensed to treat patients in North Carolina. Spencer-Manzon is currently accepting new patients.

Her clinical research consists of co-authoring 14 peer reviewed articles and participating in 1 clinical trial in the past 15 years.

Insurance

MediFind strives to display the most accurate insurance information for every doctor. If you do not see your insurance listed for Dr. Michele J. Spencer-Manzon it is best to call her office and ask if your insurance is accepted.

Accepts Medicare

Dr. Michele J. Spencer-Manzon accepts the following insurance:

  •  Ambetter
  •  Bright Health

Call to see if your plan is accepted.
Locations
1 Long Wharf Dr, New Haven, CT 06511
Background & Education
Graduate Institution
University Of Massachusetts Medical School, 2004
Specialties
Medical Genetics
Licenses
Internal Medicine in NC
Hospital Affiliations
Bridgeport Hospital
Yale New Haven Hospital
Yale New Haven Childrens Hospital
Languages Spoken
English
Gender
Female
Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Doctors 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.


1 Clinical Trials

Efficacy and Safety Study of Vatiquinone for the Treatment of Mitochondrial Disease Subjects With Refractory Epilepsy
14 Total Publications

A retrospective cohort analysis of the Yale pediatric genomics discovery program.


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