Overview
Nancy Braverman is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Braverman is rated as an Experienced provider by MediFind in the treatment of Lowe Syndrome. Her top areas of expertise are Zellweger Syndrome, Chondrodysplasia Punctata Syndrome, X-Linked Chondrodysplasia Punctata 2, and Acromesomelic Dysplasia.
Her clinical research consists of co-authoring 88 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Lowe Syndrome.
Insurance
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Locations
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.
1 Clinical Trials
Children's Hospital
Natasha Shur is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Shur is rated as an Advanced provider by MediFind in the treatment of Lowe Syndrome. Her top areas of expertise are Pyruvate Carboxylase Deficiency, Phenylketonuria (PKU), Ehlers-Danlos Syndrome (EDS), and Lowe Syndrome.
William Gahl is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Gahl is rated as an Elite provider by MediFind in the treatment of Lowe Syndrome. His top areas of expertise are Oculocutaneous Albinism Type 2, Hermansky-Pudlak Syndrome, Oculocutaneous Albinism Type 1, Oculocutaneous Albinism, and Deep Brain Stimulation.
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
- AchondrogenesisDr. Braverman isElite. Learn about Achondrogenesis.
- Acromesomelic DysplasiaDr. Braverman isElite. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Chondrodysplasia Punctata Syndrome
- Distinguished
- Congenital CataractDr. Braverman isDistinguished. Learn about Congenital Cataract.
- HypotoniaDr. Braverman isDistinguished. Learn about Hypotonia.
- Advanced
- Dubowitz SyndromeDr. Braverman isAdvanced. Learn about Dubowitz Syndrome.
- Malonyl-CoA Decarboxylase DeficiencyDr. Braverman isAdvanced. Learn about Malonyl-CoA Decarboxylase Deficiency.
- Experienced
- Aase SyndromeDr. Braverman isExperienced. Learn about Aase Syndrome.
- Adrenoleukodystrophy (ALD)Dr. Braverman isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Argininosuccinic AciduriaDr. Braverman isExperienced. Learn about Argininosuccinic Aciduria.
- Bietti Crystalline Dystrophy (BCD)Dr. Braverman isExperienced. Learn about Bietti Crystalline Dystrophy (BCD).
- HypermethioninemiaDr. Braverman isExperienced. Learn about Hypermethioninemia.
- Infantile Refsum DiseaseDr. Braverman isExperienced. Learn about Infantile Refsum Disease.