Overview
Hind Alsharhan is a Medical Genetics 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).
Her clinical research consists of co-authoring 20 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
- HMO
- POS
- PPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- INSURANCE PLAN
- MEDICARE PDP
- PPO
- HMO
- POS
- PPO
- 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
600 North Wolfe Street, Blalock 1008 Medical Genetics, Blalock 1008 Medical Genetics, Baltimore, MD 21287
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.
Rubenstein Child Health Building
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 Maple Syrup Urine Disease.
Rubenstein Child Health Building
Dr. Hilary Vernon is a Professor of Genetic Medicine and pediatrics at the Johns Hopkins University School of Medicine. She is also an attending physician at Kennedy Krieger Institute. Hilary Vernon has expertise in treating inborn errors of metabolism and mitochondrial disorders. She is the director of the Mitochondrial Care Center at The Johns Hopkins Hospital and the Barth Syndrome Interdisciplinary Clinic at the Kennedy Krieger Institute. Her research interests include understanding intermediary metabolism in Barth syndrome and in disorders of branch chain amino acid metabolism. Dr. Vernon also co-directs the Department of Genetic Medicine Clinical Trials Unit, and is the principal investigator on multiple clinical trials for rare diseases. Dr. Vernon received her medical degree and doctorate from Rutgers University, New Brunswick, New Jersey. She completed residencies in genetics and pediatrics at The Johns Hopkins University, and a fellowship in clinical laboratory biochemical genetics at The Johns Hopkins University. Dr. Vernon was recognized with the 2010 Francis F. Schwentker Award for Excellence in Research at Johns Hopkins University and the 2011 James B. Sidbury Jr. Fellowship in Biochemical Genetics at Johns Hopkins University. Dr. Vernon is rated as a Distinguished provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Infantile Neutropenia, Progressive External Ophthalmoplegia, and Gastrostomy.
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.
- Crouzon SyndromeDr. Alsharhan isExperienced. Learn about Crouzon Syndrome.
- Farber LipogranulomatosisDr. Alsharhan isExperienced. Learn about Farber Lipogranulomatosis.
- Gaucher DiseaseDr. Alsharhan isExperienced. Learn about Gaucher Disease.