Overview
Hind Alsharhan is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Alsharhan is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are ALG3-CDG, Ornithine Transcarbamylase Deficiency, Coenzyme Q Cytochrome C Reductase Deficiency, and Phenylketonuria (PKU). Dr. Alsharhan is currently accepting new patients.
Her clinical research consists of co-authoring 17 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Homocystinuria.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- POS
- PPO
- HMO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
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.
Charles Venditti is a Medical Genetics provider in Bethesda, Maryland. Dr. Venditti is rated as a Distinguished provider by MediFind in the treatment of Homocystinuria. His top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Homocystinuria, and Niemann-Pick Disease.
Meral Gunay-Aygun is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Gunay-Aygun is rated as an Advanced provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are Phenylketonuria (PKU), Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, and Argininosuccinic Aciduria. Dr. Gunay-Aygun is currently accepting new patients.
Johns Hopkins University
Shira Ziegler is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Ziegler is rated as an Advanced provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are Hypercementosis, Inborn Amino Acid Metabolism Disorder, Homocystinuria, and Chediak-Higashi Syndrome. Dr. Ziegler is currently accepting new patients.
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
- Advanced
- ALG3-CDGDr. Alsharhan isAdvanced. Learn about ALG3-CDG.
- Ornithine Transcarbamylase DeficiencyDr. Alsharhan isAdvanced. Learn about Ornithine Transcarbamylase Deficiency.
- Experienced
- Achalasia Microcephaly SyndromeDr. Alsharhan isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Coenzyme Q Cytochrome C Reductase DeficiencyDr. Alsharhan isExperienced. Learn about Coenzyme Q Cytochrome C Reductase Deficiency.
- Cortical DysplasiaDr. Alsharhan isExperienced. Learn about Cortical Dysplasia.
- Farber LipogranulomatosisDr. Alsharhan isExperienced. Learn about Farber Lipogranulomatosis.
- Gaucher DiseaseDr. Alsharhan isExperienced. Learn about Gaucher Disease.
- HomocystinuriaDr. Alsharhan isExperienced. Learn about Homocystinuria.