
Overview
Constantine Stratakis is a Medical Genetics specialist and a Gastroenterologist in Bethesda, Maryland. Dr. Stratakis has been practicing medicine for over 30 years and is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. His top areas of expertise are Cushing's disease, Neuroendocrine Tumor, Gastrointestinal Stromal Tumor, Orchiectomy, and Hormone Replacement Therapy (HRT).
His clinical research consists of co-authoring 531 peer reviewed articles and participating in 5 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 2 articles in the study of Beckwith-Wiedemann 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.
5 Clinical Trials
Leslie Biesecker is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Biesecker and is rated as an Elite provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. His top areas of expertise are Proteus Syndrome, Proteus-Like Syndrome, Acromicric Dysplasia, and Lenz Microphthalmia Syndrome.
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
- Acromegaloid Facial Appearance Syndrome
- Gastrointestinal Stromal Tumor
- Hypertrichosis-Acromegaloid Facial Appearance Syndrome
- Intersex
- Peutz-Jeghers Syndrome
- Advanced
- Li-Fraumeni Syndrome
- Mosaicism
- Neurofibromatosis
- Neurofibromatosis Type 1 (NF1)
- Obesity
- Ornithine Transcarbamylase Deficiency
- Experienced
- Anemia
- Aplasia Cutis Congenita
- Beckwith-Wiedemann Syndrome
- Clouston Syndrome
- Congenital Aplastic Anemia
- Cortical Dysplasia