Dr. Gerald Raymond is a clinical geneticist and neurologist at Johns Hopkins where he is also a professor of genetic medicine and neurology. He obtained his MD at the University of Connecticut and was trained in Pediatrics at Johns Hopkins Hospital and Neurology at the Mass. General Hospital. He received additional training in developmental neuropathology at the Universite Catholique de Louvain in Belgium and clinical genetics at the Harvard Program. Dr. Raymond’s research has been at the overlap of genetics and neurology with specific focus on peroxisomal disorders including adrenoleukodystrophy. He has been actively involved in newborn screening for ALD and in developing clinical follow-up programs. He has extensive experience in clinical management of neurogenetic issues including peroxisomal and lysosomal disorders. He presently serves as the Director of the Lysosomal Storage Disease program in the department of Genetic Medicine. Dr. Raymond is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are Adrenoleukodystrophy (ALD), CACH Syndrome, Zellweger Syndrome, and Leukodystrophy.

Dr. Charlotte Sumner is a Professor of Neurology and Neuroscience at Johns Hopkins University School of Medicine. Dr. Sumner cares for patients with genetically-mediated neuromuscular diseases. Her practice is notable for a focus on individuals with inherited neuromuscular disorders of peripheral nerves and motor neurons, including spinal muscular atrophy (SMA) and Charcot-Marie-Tooth (CMT) disease. She co-directs the Johns Hopkins Muscular Dystrophy Association Care Center, the Spinal Muscular Atrophy (SMA), and the Charcot-Marie-Tooth (CMT) clinics, which deliver multidisciplinary clinical care, engage in international natural history studies, and provide cutting edge therapeutics. Dr. Sumner’s research focuses on developing treatments for degenerative disorders of motor neurons and peripheral nerves. Her laboratory uses human tissues and induced pluripotent cell lines, mouse models and cultured cells to characterize disease mechanisms and develop treatments. Dr. Charlotte Sumner received her medical degree from the University of Pennsylvania School of Medicine following undergraduate studies at Princeton University. She completed internal medicine internship and neurology residency at the University of California San Francisco, after which she returned to the east coast for a neuromuscular fellowship at Johns Hopkins and a neurogenetics fellowship in the Neurogenetics Branch at the National Institute of Neurological Disorders and Stroke. She joined the neurology faculty at Johns Hopkins in 2006. Dr. Sumner is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. Her top areas of expertise are Spinal Muscular Atrophy (SMA), Charcot-Marie-Tooth Disease, Primary Lateral Sclerosis, Spinal Muscular Atrophy Type 2, and Gastrostomy.

Dr. Ricardo Roda earned a combined MD/PhD degree from University of Rochester and completed an adult neurology residency, followed by a clinical neuromuscular fellowship at Johns Hopkins University School of Medicine. During residency, Dr. Roda developed a special interest in both auto-immune disorders and genetic disorders. Following residency, he spent three years in neurogenetics branch of National Institute of Neurological Disorders and Stroke (NINDS) working with Dr. Craig Blackstone, focusing on the use of the newer DNA sequencing techniques in genetic diagnosis, and in establishing genotype/phenotype correlations neuromuscular disorders. His current clinical interests include developing testing strategies for undiagnosed genetic disorders and myasthenia gravis. Dr. Roda is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are Spastic Paraplegia Type 7, Hereditary Spastic Paraparesis, Myasthenia Gravis, and Spastic Paraplegia Type 2.

Dr. Tom Crawford has been a member of the Department of Neurology since 1987. He is co-director of the MDA clinic for Neuromuscular Disorders and Neurologist for the Ataxia Telangiectasia Clinical Center at Johns Hopkins. His practice involves general child neurology with a principal interest in caring for children with neuromuscular, neuromotor, and ataxic disorders. Primary research interests involve the basic science and clinical characterization of two important neurologic disorders that affect children: Spinal Muscular Atrophy and Ataxia Telangiectasia. He is also actively involved in the Biology of neurofilaments by characterization of transgenic animal models. He is on the Medical and Scientific Advisory Boards of Families of Spinal Muscular Atrophy, and the Medical Advisory Committee for the Muscular Dystrophy Association. He is the Neurologist for the Ataxia Telangiectasia Clinical Center at Johns Hopkins, which has evaluated almost half of the known patients with this disorder in the United States. Additional specific clinical interests include evaluation and treatment of children with brachial plexus palsies. Dr. Crawford received his medical degree from the University of Southern California. He completed a pediatric internship and residency at the Pediatric Pavilion of the Los Angeles County / University of Southern California Medical Center, followed by a pediatric chief residency. He completed his training in Neurology with Special Qualification in Child Neurology at the Los Angeles Childrens Hospital. He then traveled east to the laboratory of Dr John Griffin at Johns Hopkins for a fellowship in Neuromuscular Disorders. Prior to medical training and Neurology residency, he majored in Psychology and Religion at Yale College. Dr. Crawford has published extensively and presented nationally and internationally. He has an active role in teaching medical students and residents in neurology. In addition, Dr. Crawford has special interest and experience in EMG studies of children and adults. Dr. Crawford is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are Primary Lateral Sclerosis, Spinal Muscular Atrophy (SMA), Ataxia-Telangiectasia, and Spinal Muscular Atrophy Type 2.

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

Vinay Chaudhry is a Neurologist in Baltimore, Maryland. Dr. Chaudhry is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease), Myasthenia Gravis, Spinal and Bulbar Muscular Atrophy, Spinal Muscular Atrophy Type 3, and Advanced Bronchoscopy.

Robert Clark is a primary care provider, practicing in Internal Medicine in Bethesda,, Maryland. Dr. Clark is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are Postmenopausal Osteoporosis, Osteoporosis, Richter Syndrome, Colonoscopy, and Endoscopy.

Christopher Grunseich is a Neurologist in Columbia, Maryland. Dr. Grunseich is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are Spinal and Bulbar Muscular Atrophy, Spinal Muscular Atrophy (SMA), Primary Lateral Sclerosis, and Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease).

Kenneth Fischbeck is a Neurologist in Bethesda, Maryland. Dr. Fischbeck is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are Spinal and Bulbar Muscular Atrophy, Spinal Muscular Atrophy (SMA), Primary Lateral Sclerosis, and Progressive Myoclonic Epilepsy.

Ami Mankodi is a Neurologist in Baltimore, Maryland. Dr. Mankodi is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. Her top areas of expertise are Paramyotonia Congenita, Cytoplasmic Body Myopathy, Myotonic Dystrophy, and Myotonic Dystrophy Type 2.

Thomas Byrne is a primary care provider, practicing in Internal Medicine in Hebron, Maryland. Dr. Byrne is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are Dementia, Togaviridae Disease, Vascular Dementia, and Alzheimer's Disease.

Muhammad Naeem is a primary care provider, practicing in Internal Medicine in Glen Burnie, Maryland. Dr. Naeem is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are Anemia, Hypothyroidism, Hypertension, and Glucocorticoid-Remediable Aldosteronism. Dr. Naeem is currently accepting new patients.

John Abel is a primary care provider, practicing in Internal Medicine in Westminster, Maryland. Dr. Abel is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are High Cholesterol, Familial Hypertension, Hypertension, and Glucocorticoid-Remediable Aldosteronism. Dr. Abel is currently accepting new patients.

Kamrudin Mithani is a primary care provider, practicing in Family Medicine in Havre De Grace, Maryland. Dr. Mithani is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are High Cholesterol, Maturity Onset Diabetes of the Young, Sengers Syndrome, and Chronic Cough.

Jennifer Riedinger is a primary care provider, practicing in Internal Medicine in Millersville, Maryland. Dr. Riedinger is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. Her top areas of expertise are Anemia, Dementia, Glucocorticoid-Remediable Aldosteronism, and Hypertension.

Kavita Tripathi is a primary care provider, practicing in Family Medicine in Leonardtown, Maryland. Dr. Tripathi is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. Her top areas of expertise are Type 2 Diabetes (T2D), Hypertension, Glucocorticoid-Remediable Aldosteronism, and Familial Hypertension. Dr. Tripathi is currently accepting new patients.

Leonard Raucher is a primary care provider, practicing in Family Medicine in Owings Mills, Maryland. Dr. Raucher is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. His top areas of expertise are Type 2 Diabetes (T2D), Vitamin D Deficiency, Glucocorticoid-Remediable Aldosteronism, and Familial Hypertension. Dr. Raucher is currently accepting new patients.