The 20 Best Hereditary Hyperekplexia Doctors Near Me in Maryland, US

Find the Top Hereditary Hyperekplexia Experts and Specialists

The 20 Best Hereditary Hyperekplexia Doctors in Maryland, US

Last Updated: 02/22/2026

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MediFind found 12 doctor with experience in Hereditary Hyperekplexia near Maryland, US. Of these, 9 are Experienced, 2 are Advanced and 1 are Distinguished.

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12 providers found
    Scott Newsome
    Distinguished in Hereditary Hyperekplexia
    Distinguished in Hereditary Hyperekplexia

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English
    Offers Telehealth

    Neurologist Scott Newsome specializes in the care of patients with neuroimmunological and neuroinflammatory disorders of the central nervous system. He works within the Division of Neuroimmunology and Neurological Infections at The Johns Hopkins Hospital, and has special interest in evaluating and treating patients with multiple sclerosis, transverse myelitis, neuromyelitis optica and stiff person syndrome. After completing fellowship training, Dr. Newsome joined the Johns Hopkins Multiple Sclerosis and Transverse Myelitis Centers, and he is the director of the Johns Hopkins Neurosciences Consultation and Infusion Center and the Stiff Person Syndrome Center. He is also director of the Johns Hopkins Neuroimmunology and Neurological Infectious Disease Fellowship Program and co-director of the Multiple Sclerosis Experimental Therapeutics Program. Dr. Newsome received his medical degree from the New York College of Osteopathic Medicine, with honors. During his neurology residency, he was awarded the Golden Apple Outstanding Resident Teaching Award, and later was chosen to be chief resident. He subsequently completed a fellowship in neuroimmunology at The Johns Hopkins Hospital with the support of a Sylvia Lawry Physician Fellowship Award from the National Multiple Sclerosis Society. Identifying and testing novel therapies and therapeutic strategies for multiple sclerosis and other neuroimmunological disorders is Dr. Newsome’s main research focus. Other research endeavors include validating the use of new quantitative clinical outcome measures and imaging techniques in multiple sclerosis and identifying risk factors of disease onset and severity, response to treatment and long-term outcomes in neuroimmunological disorders. An adviser for the National Multiple Sclerosis Society and a member of the Miller-Coulson Academy of Clinical Excellence, Dr. Newsome has also served as president of the Consortium of Multiple Sclerosis Centers. Dr. Newsome is rated as a Distinguished provider by MediFind in the treatment of Hereditary Hyperekplexia. His top areas of expertise are Stiff Person Syndrome, Multiple Sclerosis (MS), Transverse Myelitis, and Relapsing Multiple Sclerosis (RMS).

    Daniel Gold
    Advanced in Hereditary Hyperekplexia
    Neurology
    Advanced in Hereditary Hyperekplexia
    Neurology

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English
    Offers Telehealth

    With fellowship training in neuro-ophthalmology and additional training in neuro-vestibular disorders, Dr. Daniel Gold sees patients with neuro-ophthalmic disorders (affecting vision, eyelids, pupils, or causing nystagmus or double vision) in addition to oto-neurologic disorders (causing dizziness and vertigo). Videos 2018 Best Consulting Physician Award Tele-(Dizzy) Medicine. Dr. Gold is rated as an Advanced provider by MediFind in the treatment of Hereditary Hyperekplexia. His top areas of expertise are Vertigo, Benign Paroxysmal Positional Vertigo, Brown Syndrome, and Stiff Person Syndrome.

    Ahmet Hoke
    Experienced in Hereditary Hyperekplexia
    Neurology
    Experienced in Hereditary Hyperekplexia
    Neurology

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English, Turkish

    Dr. Ahmet Hoke is Professor of Neurology and Neuroscience, W. W. Smith Charitable Trust Professor of Neuroimmunology at Johns Hopkins School of Medicine, Director of the Daniel B. Drachman Division of Neuromuscular Diseases and Director of the Merkin Peripheral Neuropathy and Nerve Regeneration Center at Johns Hopkins University School of Medicine. He completed his medical training at Hacettepe University School of Medicine in Ankara, Turkey followed by his PhD studies in developmental neuroscience at Case Western Reserve University in Cleveland, Ohio, and neurology residency at Johns Hopkins Hospital. After completing his neuromuscular training at University of Calgary, Canada, he returned to Johns Hopkins University as faculty and rose through the ranks. He is the recipient of several awards including Derek Denny Brown Young Neurological Scholar Award (2005) and Wolfe Neuropathy Research prize (2018) given by the American Neurological Association, Myung Memorial Lecture Award (2017) by the Korean Neurological Association, Nejat Eczacibasi Medical Scientist Award (2019) by the Eczacibasi Foundation, Turkey, and Alan J. Gebhart Prize in Excellence in Neuropathy Research (2022) by the Peripheral Nerve Society. He is an Ex-Officio member of the Board of Directors of the American Neurological Association, and Vice-President of the Toxic Neuropathy Consortium. He serves on several editorial boards and is the Editor-in-Chief of Annals of Clinical and Translational Neurology. Dr. Hoke is rated as an Experienced provider by MediFind in the treatment of Hereditary Hyperekplexia. His top areas of expertise are Wallerian Degeneration, Peripheral Neuropathy, Tomaculous Neuropathy, Spinal Muscular Atrophy with Arthrogryposis, and Prostatectomy.

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    Ankur Butala
    Experienced in Hereditary Hyperekplexia
    Experienced in Hereditary Hyperekplexia

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English, Spanish
    Offers Telehealth

    Dr. Ankur Butala specializes in the care of persons with complex neuropsychiatric conditions, including persons with advanced Parkinson Disease or other movement or neurodegenerative disorders. Upon graduating from a selective Physician-Scientist program at Albany Medical College, he joined the University of Massachusetts in an uncommon residency in both Neurology and Psychiatry. Dual-trained neuropsychiatrists such as Dr. Butala have experience with: Parkinson Disease and atypical Parkinsonism, Huntington Disease, Ataxia, Dystonia, early-onset dementia, traumatic brain injury and chronic traumatic encephalopathy, autism spectrum disorders, medication refractory mood and psychotic disorders, epilepsy and functional neurological disorders. In residency, he developed an interest in circuit models of brain function and how non-pharmacological approaches such as Neuromodulation and brain stimulation may be used to address treatment-resistant conditions. Consequently, he joined Johns Hopkins University School of Medicine as a Clinical and Research Fellow from 2015 to 2018, where he developed a skill set including deep brain stimulation, non-invasive brain stimulation (tDCS), and measurement of eye movements. Currently, Dr. Butala's clinical and research interests are in diagnosing and managing persons with advanced Parkinson's Disease, movement disorders, and neuropsychiatric conditions using neuromodulation, cannabinoids, and entheogens. He has ongoing multidisciplinary collaborations with colleagues at the Whiting School of Engineering - Center of Speech & Language Processing in using Machine-Learning Models and Artificial Intelligence to improve the detection and diagnosis of Movement and Neuropsychiatric disorders. LinkedIn https://www.linkedin.com/in/ankurbutalamd Videos Neurology: Junior Faculty Spotlight. Dr. Butala is rated as an Experienced provider by MediFind in the treatment of Hereditary Hyperekplexia. His top areas of expertise are Parkinson's Disease, Corticobasal Degeneration, Movement Disorders, Drug Induced Dyskinesia, and Deep Brain Stimulation.

    Lisa R. Sun
    Experienced in Hereditary Hyperekplexia
    Neurology | Pediatric Neurology
    Experienced in Hereditary Hyperekplexia
    Neurology | Pediatric Neurology

    Johns Hopkins Outpatient Center

    Baltimore, MD 
    Languages Spoken:
    English

    Dr. Sun is an expert in both pediatric neurology and cerebrovascular neurology, with a special interest in pediatric and young adult stroke. She focuses on both acute care of stroke as well as longitudinal management of an array of neurologic conditions that affect children and young adults. Dr. Sun’s research focuses broadly on pediatric and young adult stroke, with emphasis on discovering the causes, treatments, and prevention of stroke in the young. More specifically, Dr. Sun is investigating novel monitoring and stroke prevention techniques in children with moyamoya disease, which is a rare disease that places affected children and young adults at high risk of stroke. The goal of Dr. Sun's research is to improve outcomes and quality of life of individuals affected by stroke and moyamoya disease. In addition to her clinical and research interests, Dr. Sun is the associate program director of the Child Neurology residency program at Johns Hopkins. After completing medical school at the Johns Hopkins University School of Medicine, Dr. Sun completed her pediatrics and neurology residency training at Johns Hopkins, and subsequently she completed a fellowship in Vascular Neurology/Stroke. Dr. Sun is rated as an Experienced provider by MediFind in the treatment of Hereditary Hyperekplexia. Her top areas of expertise are Moyamoya Disease, Stroke, Stiff Person Syndrome, Thrombectomy, and Cerebral Artery Bypass Surgery.

    Experienced in Hereditary Hyperekplexia
    Experienced in Hereditary Hyperekplexia

    Johns Hopkins University

    600 N Wolf St, 
    Baltimore, MD 
    Languages Spoken:
    English

    Peter Calabresi is a Neurologist in Baltimore, Maryland. Dr. Calabresi is rated as an Experienced provider by MediFind in the treatment of Hereditary Hyperekplexia. His top areas of expertise are Multiple Sclerosis (MS), Optic Neuritis, Relapsing Multiple Sclerosis (RMS), and CACH Syndrome.

    Experienced in Hereditary Hyperekplexia
    Experienced in Hereditary Hyperekplexia

    Pacific Neuromonitoring Associates Inc

    10275 Little Patuxent Pkwy Ste 300, 
    Columbia, MD 
    Languages Spoken:
    English

    Evgeny Tsimerinov is a Neurologist in Columbia, Maryland. Dr. Tsimerinov is rated as an Experienced provider by MediFind in the treatment of Hereditary Hyperekplexia. His top areas of expertise are Cervical Myelopathy, Dysembryoplastic Neuroepithelial Tumors (DNET), Invertebral Disc Disease, and Brain Stem Cancer.

    Advanced in Hereditary Hyperekplexia
    Advanced in Hereditary Hyperekplexia

    Johns Hopkins Hospital

    600 N Wolfe St, 
    Baltimore, MD 
    Languages Spoken:
    English

    Olwen Murphy is a Neurologist in Baltimore, Maryland. Dr. Murphy is rated as an Advanced provider by MediFind in the treatment of Hereditary Hyperekplexia. Her top areas of expertise are Multiple Sclerosis (MS), Stiff Person Syndrome, Acute Flaccid Myelitis (AFM), and Cramp-Fasciculation Syndrome.

    Experienced in Hereditary Hyperekplexia
    Medical Genetics | Oncology
    Experienced in Hereditary Hyperekplexia
    Medical Genetics | Oncology

    Kennedy Krieger Associates

    707 N Broadway, 
    Baltimore, MD 
    Languages Spoken:
    English

    Jeffrey Ehmsen is a Medical Genetics specialist and an Oncologist in Baltimore, Maryland. Dr. Ehmsen is rated as an Experienced provider by MediFind in the treatment of Hereditary Hyperekplexia. His top areas of expertise are Hereditary Hyperekplexia, Inborn Amino Acid Metabolism Disorder, and Homocystinuria.

    Experienced in Hereditary Hyperekplexia
    Experienced in Hereditary Hyperekplexia

    9000 Franklin Square Dr. 2ND Floor

    9000 Franklin Square Dr # 2, 
    Baltimore, MD 
    Languages Spoken:
    English
    Offers Telehealth

    Noushin Jazebi is a Neurologist in Baltimore, Maryland. Dr. Jazebi is rated as an Experienced provider by MediFind in the treatment of Hereditary Hyperekplexia. Her top areas of expertise are Cramp-Fasciculation Syndrome, Spinal and Bulbar Muscular Atrophy, Spinal Muscular Atrophy Type 3, and Stiff Person Syndrome.

    Experienced in Hereditary Hyperekplexia
    Neurology
    Experienced in Hereditary Hyperekplexia
    Neurology

    Johns Hopkins Hospital

    600 N Wolfe St, 
    Baltimore, MD 
    Languages Spoken:
    English
    Offers Telehealth

    Shiv Saidha is a Neurologist in Baltimore, Maryland. Dr. Saidha is rated as an Experienced provider by MediFind in the treatment of Hereditary Hyperekplexia. His top areas of expertise are Multiple Sclerosis (MS), Optic Neuritis, Relapsing Multiple Sclerosis (RMS), and Stiff Person Syndrome.

    Experienced in Hereditary Hyperekplexia
    Neurology
    Experienced in Hereditary Hyperekplexia
    Neurology

    Office

    733 N Broadway Ste 731, 
    Baltimore, MD 
    Languages Spoken:
    English

    Ted Dawson is a Neurologist in Baltimore, Maryland. Dr. Dawson is rated as an Experienced provider by MediFind in the treatment of Hereditary Hyperekplexia. His top areas of expertise are Parkinson's Disease, Movement Disorders, Dementia, Lewy Body Dementia (LBD), and Vagotomy.

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    Last Updated: 02/22/2026

    What is the definition of Hereditary Hyperekplexia?

    Hereditary hyperekplexia is a condition in which affected infants have increased muscle tone (hypertonia) and an exaggerated startle reaction to unexpected stimuli, especially loud noises. Following the startle reaction, infants experience a brief period in which they are very rigid and unable to move. During these rigid periods, some infants stop breathing, which, if prolonged, can be fatal. Infants with hereditary hyperekplexia have hypertonia at all times, except when they are sleeping.

    When should I see a Hereditary Hyperekplexia doctor in Maryland, US?

    There are various reasons why you may want to see a specialist, such as: 

    • Your primary care provider recommends it. 
    • Your condition requires expert knowledge and specialized care. 
    • Your symptoms persist or worsen despite treatment. 
    • You need specialized testing or procedures. 
    • You want a second opinion.  

    What should I consider when choosing a Hereditary Hyperekplexia doctor in Maryland, US?

    It’s important to see a provider with expertise in your specific condition. Each provider profile in MediFind’s doctor database includes information on which conditions they treat, years of experience, research contributions, languages spoken, insurance plans accepted, and more.  

    How does MediFind rank Hereditary Hyperekplexia doctors in Maryland, US?

    MediFind’s rankings are based on a variety of data sources, such as the number of articles a doctor has published in medical journals, participation in clinical trials and industry conferences, as well as the number of patients that provider sees for a given condition. Note that MediFind’s provider database is not based on user reviews, and providers do not pay to be included in the database. 

    What types of insurance are accepted by Hereditary Hyperekplexia doctors in Maryland, US?

    Most profiles in MediFind’s doctor database include a list of insurance plans accepted by that provider. However, it’s a good idea to contact the provider’s office to make sure they still accept your insurance, then doublecheck by contacting your insurance plan to confirm they’re in network. 

    How can I book an appointment online with a Hereditary Hyperekplexia doctor in Maryland, US?

    MediFind offers direct scheduling for certain providers using the “Request Appointment” button on that provider’s profile. If the schedule option is not available for a provider, tap the red “Show Phone Number” button on their profile to get their contact information. If you prefer to find providers who offer online scheduling, select “Schedules online” under the “Availability” category of the filter feature on the left side of the Hereditary Hyperekplexia doctor search results page. 

    Why is it important to get a second opinion from a different Hereditary Hyperekplexia doctor?

    Second opinions are an opportunity to confirm a diagnosis and its root cause, learn about alternative treatment options, or simply gain peace of mind. Many people, especially those with serious diagnoses, get second opinions so they can understand all their options and make informed decisions, so don’t hesitate to get one if you have any doubts or need more information or clarification regarding your care. Note that some insurance plans require second opinions, while others don’t cover second opinions, so be sure to confirm with your insurance provider first.   

    How can I prepare for my appointment with a Hereditary Hyperekplexia doctor in Maryland, US?

    Prepare for your appointment by gathering the following items: 

    • Copies of medical records (dating back at least one year) 
    • Your medical history, including illnesses, medical conditions, surgeries, and other doctors you see 
    • Family history of disease 
    • List of current prescription drugs, over-the-counter medicines, vitamins, and herbal remedies or supplements including names and doses 
    • Allergies to medications, food, latex, insects, etc.  
    • List of questions and concerns 
    • Your insurance card 

    You might also contact the provider’s office to see if they offer transportation or childcare services or if you’re allowed to bring a loved one for support or to take notes during your visit. 

    What questions should I ask my Hereditary Hyperekplexia doctor?

    Here are some sample questions: 

    • Can you explain in simple terms what this condition is and how it’s treated? 
    • What symptoms or side effects should I watch for? 
    • What tests will be involved, and when can I expect results? 
    • Are there other specialists I need to see? 
    • What’s the best way to reach you if I have follow-up questions? 

    How can I learn about the latest clinical trials and research advances my Hereditary Hyperekplexia doctor may know about?

    MediFind’s Clinical Trials tool asks you a series of questions to help you narrow down your search by health condition, age, gender, location, how far you’re willing to travel, and more. Each question you answer filters down the number of trials until you find the ones that are most relevant to you. 

    MediFind’s Latest Advances tool features summaries of recent articles published in medical journals. We use cutting-edge technology to scour medical publication databases for the latest research advancements on any given condition, then we simplify this information in a way that’s useful and easy to understand. 

    Can I filter my search to show male or female Hereditary Hyperekplexia doctors in Maryland, US?

    Look for the filter feature on the left side of the Hereditary Hyperekplexia doctor search results page. Select “Female” or “Male” under the “Gender” category to search for female or male providers exclusively. If the “Any” option is selected, it will pull results for both male and female providers. 

    Can I filter my search to find a Hereditary Hyperekplexia doctor that offers video calls?

    Look for the filter feature on the left-side of the Hereditary Hyperekplexia doctor search results page. Select “Offers telehealth visits” under the Availability category to search for providers who offer virtual appointments (video calls). 

    Reviewed on: 11/11/24  

    By: MediFind Medical Staff 

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