Overview
Natasha Shur is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Shur is rated as an Experienced provider by MediFind in the treatment of Osteogenesis Imperfecta. Her top areas of expertise are Pyruvate Carboxylase Deficiency, Phenylketonuria (PKU), Ehlers-Danlos Syndrome (EDS), and Lowe Syndrome.
Her clinical research consists of co-authoring 55 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Osteogenesis Imperfecta.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- HMO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE ASSISTANCE PROGRAM
- MEDICARE MAPD
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- PPO
Locations
111 Michigan Ave Nw, Washington, DC 20010
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.
Joan Marini is a Medical Genetics provider in Bethesda, Maryland. Dr. Marini is rated as a Distinguished provider by MediFind in the treatment of Osteogenesis Imperfecta. Her top areas of expertise are Osteogenesis Imperfecta, Kyphomelic Dysplasia, Congenital Bowing of Long Bones, and Brachydactyly Mononen Type.
Children's Hospital
Laura Tosi is a Pediatric Orthopedics specialist and an Orthopedics provider in Washington, Washington, D.c.. Dr. Tosi is rated as a Distinguished provider by MediFind in the treatment of Osteogenesis Imperfecta. Her top areas of expertise are Osteogenesis Imperfecta, Macrodactyly of the Foot, Osteoporosis, and Acromicric Dysplasia.
The Johns Hopkins Hospital
Dr. David Valle is a professor of pediatrics and ophthalmology at the Johns Hopkins School of Medicine and former director of the Johns Hopkins Department of Genetic Medicine. He also serves as a geneticist for the Johns Hopkins Children’s Center. Dr. Valle holds a bachelor’s degree and medical degree from Duke University. He completed a pediatric residency at Johns Hopkins University before joining the Johns Hopkins faculty. He is interested in the genetic contributions to health and disease. He is the founding director of the Johns Hopkins Center for Inherited Disease Research. Over the years, his laboratory has discovered the genetic causation for more than 20 diseases, including those responsible for inborn errors of metabolism, inherited retinal degeneration, disorders of cellular organelle biogenesis and genetic variations that contribute risk for common disorders such as schizophrenia. Dr. Valle also serves as director of the Predoctoral Training Program in Human Genetics, as well as co-director of the Genes to Society program. He was a 2014 recipient of the annual Victor A. McKusick Leadership Award from the American Society of Human Genetics, which recognizes individuals whose professional achievements have fostered and enriched the development of human genetics as well as its assimilation into the broader context of science, medicine and health. Dr. Valle is rated as an Advanced provider by MediFind in the treatment of Osteogenesis Imperfecta. His top areas of expertise are Spondyloepimetaphyseal Dysplasia Strudwick Type, Micrognathia, Urea Cycle Disorders (UCD), and Spondyloepiphyseal Dysplasia Congenita.
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
- Distinguished
- Ehlers-Danlos Syndrome (EDS)Dr. Shur isDistinguished. Learn about Ehlers-Danlos Syndrome (EDS).
- Phenylketonuria (PKU)Dr. Shur isDistinguished. Learn about Phenylketonuria (PKU).
- Pyruvate Carboxylase DeficiencyDr. Shur isDistinguished. Learn about Pyruvate Carboxylase Deficiency.
- Advanced
- HypotoniaDr. Shur isAdvanced. Learn about Hypotonia.
- Krabbe DiseaseDr. Shur isAdvanced. Learn about Krabbe Disease.
- Lowe SyndromeDr. Shur isAdvanced. Learn about Lowe Syndrome.
- Pierre Robin SequenceDr. Shur isAdvanced. Learn about Pierre Robin Sequence.
- Experienced
- 2q37 Deletion SyndromeDr. Shur isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Shur isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Shur isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Shur isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acrodermatitis EnteropathicaDr. Shur isExperienced. Learn about Acrodermatitis Enteropathica.
- Acrorenal Mandibular SyndromeDr. Shur isExperienced. Learn about Acrorenal Mandibular Syndrome.