The 20 Best Hereditary Ataxia Doctors Near Me in Jamaica Plain, MA

Jeremy Schmahmann is a Neurologist in Boston, Massachusetts. Dr. Schmahmann is rated as an Elite provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Spinocerebellar Ataxia, Acute Cerebellar Ataxia, Olivopontocerebellar Atrophy, Drug Induced Dyskinesia, and Gastrostomy.

Christopher Stephen is a Neurologist in Boston, Massachusetts. Dr. Stephen is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Drug Induced Dyskinesia, Spinocerebellar Ataxia Type 27, Movement Disorders, and Tay-Sachs Disease.

Patricia Greenstein is a Neurologist in Boston, Massachusetts. Dr. Greenstein is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Spinocerebellar Ataxia, Cervical Myelopathy, Harding Ataxia, and Infantile-Onset Spinocerebellar Ataxia (IOSCA).

Elizabeth Raynor is a Neurologist in Boston, Massachusetts. Dr. Raynor is rated as an Advanced provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Peripheral Neuropathy, Post Polio Syndrome, Primary Lateral Sclerosis, and Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease).

David Simon is a Neurologist in Boston, Massachusetts. Dr. Simon is rated as an Advanced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Parkinson's Disease, Movement Disorders, Serotonin Syndrome, Hereditary Ataxia, and Deep Brain Stimulation.

Nathaniel Robbins is a Neurologist in Jamaica Plain, Massachusetts. Dr. Robbins is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Distal Median Nerve Dysfunction, Peripheral Neuropathy, Hyperkalemic Periodic Paralysis, and Thyrotoxic Periodic Paralysis.

Arvind Pandey is a Cardiologist in Jamaica Plain, Massachusetts. Dr. Pandey is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Hypertension, Venous Thromboembolism (VTE), Shwartzman Phenomenon, and Heart Failure.

Vikram Khurana is a Neurologist in Boston, Massachusetts. Dr. Khurana is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Movement Disorders, Parkinson's Disease, Multiple System Atrophy, and Hereditary Ataxia.

Nutan Sharma received an AB from Stanford University, and her MD and PHD from the State University of New York at Stony Brook. She competed a Neurology residency at Yale University, and a fellowship in movement disorders with Brad Hyman at MGH. She became an instructor in Neurology at Harvard medical School in 2001, attaining the rank of Associate Professor in 2011.  In 2001, Dr. Sharma established the first Dystonia Clinic for comprehensive care of patients with dystonia at the Massachusetts General Hospital and Brigham and Women’s Hospital.  In 2005, the International Movement Disorders Society honored Dr. Sharma for Excellence in Basic Science. She is also director of the Collaborative Center for the study of X-linked Dystonia-Parkinsonism (XDP), which funds research and medical care for those with XDP. Dr. Sharma is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Drug Induced Dyskinesia, Focal Dystonia, Movement Disorders, Dopa-Responsive Dystonia, and Deep Brain Stimulation.

Allan H. Ropper, MD, is Professor of Neurology at Harvard Medical School. Dr. Ropper is an associate editor of the New England Journal of Medicine and a fellow of the Royal College of Physicians and the American College of Physicians. He has over 150 publications and is an author of the most widely consulted textbook of neurology, Principles of Neurology, which is currently in its ninth edition. He is a longtime contributor to several major textbooks of medicine, including Harrison’s Principles of Internal Medicine. Dr. Ropper is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Transient Global Amnesia, Neurosyphilis, Lewy Body Dementia (LBD), Stiff Person Syndrome, and Thymectomy.

Dr. Calum Archibald MacRae is Vice Chair for Scientific Innovation in the Department of Medicine at Brigham and Women’s Hospital (BWH), a Professor of Medicine at Harvard Medical School, and an expert member of BWH’s Cardiovascular Genetics Program, which comprehensively evaluates, diagnoses and manages care for inherited cardiac disorder patients. In addition, he is a leading investigator at the BWH Genomics Center and an associate professor of medicine at Harvard Medical School.He received his medical degree from University of Edinburgh College of Medicine. He completed two internal medicine residency programs: one at Wellcome Trust Centre for Neuroimaging in London and the other at BWH. He then completed a fellowship in cardiovascular disease at Massachusetts General Hospital. Dr. MacRae is board certified in internal medicine and cardiovascular disease.Dr. MacRae is a cardiologist and geneticist whose clinical interests include investigating new phenotypes and how research findings—including genomics discoveries—can be systematically implemented into clinical care. His research focuses on the biology and genomics of cardiovascular disease, specifically the biological basis of different arrhythmia susceptibilities. He holds five patents, has authored over 160 peer-reviewed publications and received research funding from the National Institutes of Health’s National Human Genome Research Institute. Dr. Macrae is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Cardiomyopathy, Familial Hypertrophic Cardiomyopathy, Hypertrophic Cardiomyopathy (HCM), Dilated Cardiomyopathy (DCM), and Cardiac Ablation.

Dr. Thomas M. Michel is a cardiovascular medicine specialist at Brigham and Women’s Hospital (BWH). In addition, he is a professor of medicine (Biochemistry) at Harvard Medical School (HMS) and the associate director of the Harvard/Massachusetts Institute of Technology MD-PhD Program.After graduating from Harvard College, he received his MD and PhD degrees from Duke University School of Medicine. He completed an internal medicine residency, a clinical cardiology fellowship and a genetics research fellowship at BWH. He is board certified in internal medicine and cardiovascular disease.Dr. Michel’s clinical interests include general cardiology and ischemic heart disease. The author of over 160 peer-reviewed publications, Dr. Michel’s research uses biochemical and cell biological approaches to understand signal transduction pathways in the cardiovascular system. His laboratory has studied endothelial nitric oxide synthase (eNOS), a signaling enzyme involved in the control of vascular tone, myocardial contractibility and platelet aggregation. An active educator, he served as the dean for education at Harvard Medical School. For the past two decades, the National Institutes of Health has provided continuous funding for his research endeavors. Dr. Michel is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Heart Failure, Dilated Cardiomyopathy (DCM), Familial Ventricular Tachycardia, Cardiac Ablation, and Pacemaker Implantation.

Dr. Spyropoulos is an Attending neonatologist in the Newborn Intensive Care Unit (NICU)and an Instructor in Pediatrics at Harvard Medical School. Dr. Spyropoulos performs basic and translational research in hemodynamics and cardiac metabolism as relates to cardiopulmonary diseases of prematurity. His research focuses on elucidating the mechanisms of cardiac metabolic dysregulation in heart failure and identifying novel therapies for prevention and treatment of this devastating disease. Dr. Spyropoulos is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are High Blood Pressure in Infants, Cerebral Hypoxia, Pulmonary Hypertension, and Premature Infant.

Pushpa Narayanaswami is a Neurologist in Boston, Massachusetts. Dr. Narayanaswami is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Myasthenia Gravis, Limb-Girdle Muscular Dystrophy, Polymyositis, Wyburn-Mason Syndrome, and Thymectomy.

Marc Fisher is a Neurologist in Boston, Massachusetts. Dr. Fisher is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Stroke, Transient Ischemic Attack (TIA), Peripheral Neuropathy, Spastic Paraplegia-Epilepsy-Intellectual Disability Syndrome, and Thrombectomy.

Robert Thomas is an Internal Medicine provider in Boston, Massachusetts. Dr. Thomas is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Central Sleep Apnea, Obstructive Sleep Apnea, Idiopathic Hypersomnia, and Irregular Sleep-Wake Syndrome.

Ludy Shih is a Neurologist in Boston, Massachusetts. Dr. Shih is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Movement Disorders, Parkinson's Disease, Essential Tremor, Drug Induced Dyskinesia, and Deep Brain Stimulation.

Lan Luo is a Neurologist in Boston, Massachusetts. Dr. Luo is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Movement Disorders, Parkinson's Disease, Striatonigral Degeneration Infantile, and Dopa-Responsive Dystonia.

Samuel Frank is a Neurologist in Boston, Massachusetts. Dr. Frank is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Progressive Hemifacial Atrophy, Huntington Disease, Mcleod Neuroacanthocytosis Syndrome, and Drug Induced Dyskinesia.

Anoopum Gupta is a Neurologist in Boston, Massachusetts. Dr. Gupta is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Hereditary Ataxia, Spinocerebellar Ataxia Type 27, Drug Induced Dyskinesia, and Acute Cerebellar Ataxia.