Overview
Dr. Hilary E. Gwynn is an instructor on the medical staff at Kennedy Krieger Institute in the Division of Neurology and Developmental Medicine. She teaches medical trainees and provides patient care at the Center for Development and Learning and on the Pediatric Rehabilitation Unit. She is also the site coordinator for the Johns Hopkins pediatric resident developmental disabilities rotation at the Kennedy Krieger Institute. Dr. Gwynn earned her medical degree at the University of Maryland School of Medicine in Baltimore, Maryland in 2000 and completed her pediatrics residency there in 2003. She subsequently joined the Kennedy Krieger Institute in 2003 to attend the fellowship in neurodevelopmental disabilities through the Kennedy Krieger Institute and Johns Hopkins University School of Medicine. Since graduation from the fellowship program in 2007, she has been an active member of the medical staff at Kennedy Krieger Institute. She teaches medical trainees and provides patient care at the Center for Development and Learning and on the Pediatric Rehabilitation Unit. She is also a member of the clinical staff of the Department of Pediatrics at Johns Hopkins School of Medicine. Contact for Research Inquiries 801 N. Broadway Baltimore, MD 21205 Phone: (443) 923-3246 Research Summary Dr. Gwynn's clinical and research interests include diagnosis and treatment of the child with developmental disability. She is also investigating medical training methodology as it applies to resident and fellow training in the practice of developmental medicine and child neurology.
Dr. Gwynn is rated as an Experienced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Cerebral Palsy, Focal Dystonia, Spastic Diplegia Infantile Type, and Moebius Syndrome.
Her clinical research consists of co-authoring 3 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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Locations
707 N Broadway, Baltimore, MD 21205
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.
Kennedy Krieger Institute
Dr. Jaqueline Weissman is an assistant professor in the Department of Neurology, Kennedy Krieger Institute, Department of Pediatrics Johns Hopkins Hospital and Institute of Genomic Medicine at Johns Hopkins Hospital. She is also director of the Center for Tuberous Sclerosis and Related Disorder at Kennedy Krieger Institute. She focuses on genetic and epigenetic causes of neurodevelopmental disorders - particularly intellectual disability - and how specific genetic and epigenetic changes lead to specific neuroanatomic, neurophysiologic and cognitive phenotypes. She is also interested in developing specific cognitive profiles in genetic syndromes as potential outcome measures for trials and to help localize deficits. Currently most of her research is centered around Kabuki Syndrome. Dr. Weissman received her B.A. with. Dr. Harris is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Odontotrichomelic Syndrome, Kabuki Syndrome, 3MC Syndrome, and Coffin-Lowry Syndrome.
Kennedy Krieger Associates
Amena Fine is a Pediatrics provider in Baltimore, Maryland. Dr. Fine is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Adrenoleukodystrophy (ALD), CACH Syndrome, HNRNPH2-Related Disorder, and Alexander Disease.
Johns Hopkins Outpatient Center
Dr. Barañano earned her M.D. and Ph.D. degrees from the Johns Hopkins University School of Medicine, where she also completed residencies in pediatrics and neurology, along with a fellowship in neurogenetics at the Kennedy Krieger Institute. Dr. Barañano is an Associate Professor of Clinical Neurology. She specializes in the diagnosis and management of rare neurogenetic disorders. She has a particular interest in the genetic control and function of the cerebellum and expertise in childhood-onset and inherited ataxias. She is a member of the multidisciplinary Fetal Management group and is available for prenatal consultations. Dr. Barañano's research includes collaborative efforts with the Johns Hopkins Department of Genetic Medicine and the Division of Neurogenetics at the Kennedy Krieger Institute. Dr. Baranano is rated as a Distinguished provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Hypotonia, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Focal or Multifocal Malformations in Neuronal Migration, and Hereditary Ataxia.
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
- Cerebral PalsyDr. Gwynn isAdvanced. Learn about Cerebral Palsy.
- DysarthriaDr. Gwynn isAdvanced. Learn about Dysarthria.
- Focal DystoniaDr. Gwynn isAdvanced. Learn about Focal Dystonia.
- Hereditary Spastic ParaparesisDr. Gwynn isAdvanced. Learn about Hereditary Spastic Paraparesis.
- L1 SyndromeDr. Gwynn isAdvanced. Learn about L1 Syndrome.
- Moebius SyndromeDr. Gwynn isAdvanced. Learn about Moebius Syndrome.
- Experienced
- 2q37 Deletion SyndromeDr. Gwynn isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Gwynn isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Gwynn isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Gwynn isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Accessory Deep Peroneal NerveDr. Gwynn isExperienced. Learn about Accessory Deep Peroneal Nerve.
- Acrodermatitis EnteropathicaDr. Gwynn isExperienced. Learn about Acrodermatitis Enteropathica.