Overview
William Gahl is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Gahl and is rated as an Advanced provider by MediFind in the treatment of Gangliosidosis. His top areas of expertise are Oculocutaneous Albinism Type 2, Oculocutaneous Albinism, Oculocutaneous Albinism Type 1, and Hermansky-Pudlak Syndrome.
His clinical research consists of co-authoring 369 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 3 articles in the study of Gangliosidosis.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
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.
2 Clinical Trials
Cynthia Tifft is a Medical Genetics provider in Washington, Washington, D.c.. Dr. Tifft and is rated as an Elite provider by MediFind in the treatment of Gangliosidosis. Her top areas of expertise are Sandhoff Disease, Gangliosidosis, GM1 Gangliosidosis, and Tay-Sachs Disease.
David Adams is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Adams and is rated as an Elite provider by MediFind in the treatment of Gangliosidosis. His top areas of expertise are Oculocutaneous Albinism, Oculocutaneous Albinism Type 1, Hermansky-Pudlak Syndrome, and Oculocutaneous Albinism Type 2.
Iskren Menkovic is a Medical Genetics provider in Washington, Washington, D.c.. Dr. Menkovic and is rated as an Experienced provider by MediFind in the treatment of Gangliosidosis. His top areas of expertise are GM1 Gangliosidosis, Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), Gangliosidosis, and Brachydactyly Mononen Type.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- Achalasia Microcephaly Syndrome
- Alkaptonuria
- Cortical Dysplasia
- Microcephaly
- Piebaldism
- Smith-Magenis Syndrome
- Advanced
- Aminoaciduria
- Cardiomyopathy Hypogonadism Metabolic Anomalies
- Cerebellar Hypoplasia
- Focal or Multifocal Malformations in Neuronal Migration
- Gangliosidosis
- GM1 Gangliosidosis
- Experienced
- ALG1-CDG
- Alternating Hemiplegia of Childhood
- Aspartylglucosaminuria
- Autism Spectrum Disorder
- Batten Disease
- Brachydactyly Mononen Type