Overview
Katherine Peeler is an Intensive Care Medicine specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Peeler is rated as an Experienced provider by MediFind in the treatment of Beta-Ketothiolase Deficiency. Her top areas of expertise are Acid Sphingomyelinase Deficiency (ASMD), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B), and Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A).
Her clinical research consists of co-authoring 20 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
Locations
300 Longwood Ave, Boston, MA 02115
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.
Children's Hospital Pediatric Associates, Inc
Stephanie Sacharow is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Sacharow is rated as a Distinguished provider by MediFind in the treatment of Beta-Ketothiolase Deficiency. Her top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Cat Eye Syndrome, and Dihydropteridine Reductase Deficiency. Dr. Sacharow is currently accepting new patients.
Anne O'donnell-Luria is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. O'donnell-Luria is rated as an Advanced provider by MediFind in the treatment of Beta-Ketothiolase Deficiency. Her top areas of expertise are Chromosome 11 Uniparental Disomy, Mosaic Variegated Aneuploidy Syndrome, Chromosome 2 Uniparental Disomy, and Tetrasomy 9p. Dr. O'donnell-Luria is currently accepting new patients.
William Brucker is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Brucker is rated as an Advanced provider by MediFind in the treatment of Beta-Ketothiolase Deficiency. His top areas of expertise are Lysosomal Acid Lipase Deficiency, Cholesteryl Ester Storage Disease, Wolman Disease, and Fetal Thalidomide Syndrome.
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
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)Dr. Peeler isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Acute PancreatitisDr. Peeler isExperienced. Learn about Acute Pancreatitis.
- Agyria Pachygyria PolymicrogyriaDr. Peeler isExperienced. Learn about Agyria Pachygyria Polymicrogyria.
- Asthma in ChildrenDr. Peeler isExperienced. Learn about Asthma in Children.
- Beta-Ketothiolase DeficiencyDr. Peeler isExperienced. Learn about Beta-Ketothiolase Deficiency.
- Bilateral Perisylvian PolymicrogyriaDr. Peeler isExperienced. Learn about Bilateral Perisylvian Polymicrogyria.