The 20 Best GM1 Gangliosidosis Doctors Near Me

Cynthia Tifft is a Medical Genetics provider in Washington, Washington, D.c.. Dr. Tifft is rated as an Elite provider by MediFind in the treatment of GM1 Gangliosidosis. Her top areas of expertise are Sandhoff Disease, Gangliosidosis, GM1 Gangliosidosis, and Tay-Sachs Disease.

Maria Acosta is a Pediatric Neurologist in Silver Spring, Maryland. Dr. Acosta is rated as an Elite provider by MediFind in the treatment of GM1 Gangliosidosis. Her top areas of expertise are GM1 Gangliosidosis, Neurofibromatosis, Sandhoff Disease, and Autism Spectrum Disorder.

Chester Whitley is a Pediatrics specialist and a Medical Genetics provider in Minneapolis, Minnesota. Dr. Whitley is rated as an Elite provider by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), and Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A). Dr. Whitley is currently accepting new patients.

Raymond Wang is a Medical Genetics provider in Orange, California. Dr. Wang is rated as a Distinguished provider by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Pompe Disease, and Adenoidectomy.

. Dr. Givens is rated as an Experienced provider by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are Glucocorticoid-Remediable Aldosteronism, Familial Hypertension, Hypertension, and Lung Metastases.

Dr. Adam Hartman is an Adjunct Associate Professor of Neurology and Pediatrics at Johns Hopkins School of Medicine. He focuses on treating children with epilepsy, with an emphasis on those whose seizures have not been adequately controlled with medication. He evaluates and manages patients in his clinic who may be candidates for epilepsy surgery, including those with Rasmussen syndrome, brain malformations, and perinatal strokes. Patients who may not be surgery candidates due to inborn errors of metabolism (particularly mitochondrial disorders) also are a special interest for Dr. Hartman. Dr. Hartman is currently a Physician at NINDS/NIH, serving as a Program Director in the Division of Clinical Research. Previously, Dr. Hartman was the Associate Program Director for the Pediatric Neurology Residency at Johns Hopkins Hospital. He also was the Co-Director of the Neurology Intensive Care Nursery and an Attending Physician on the Pediatric Neurology Inpatient Service at Johns Hopkins Hospital. Dr. Hartman’s prior laboratory work was funded by National Institute of Neurological Disorders and Stroke (NIH), Technology Development Corporation (State of Maryland), a Johns Hopkins University School of Medicine Clinician Scientist Award, the Pakula Family, and the Becker Family. Dr. Hartman received his medical degree from Northwestern University Medical School. After completing his residency in Pediatrics in the National Capital Uniformed Services Pediatric Residency Program (National Naval Medical Center, Walter Reed Army Medical Center), he served as a general pediatrician in the US Navy for five years (the last as division head of general pediatrics at Naval Medical Center San Diego). He completed his residency in pediatric neurology and a fellowship in clinical neurophysiology/pediatric epilepsy, both at Johns Hopkins. Dr. Hartman is rated as an Advanced provider by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are Hemimegalencephaly, Seizures, Epilepsy, and Increased Head Circumference.

Rebecca Kuenzler is a Neuromusculoskeletal Medicine provider in Cleveland, Ohio. Dr. Kuenzler has been practicing medicine for over 32 years and is rated as an Advanced provider by MediFind in the treatment of GM1 Gangliosidosis. Her top areas of expertise are Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease), Spinal Muscular Atrophy Type 3, Spinal Muscular Atrophy (SMA), and Spinal and Bulbar Muscular Atrophy.

Poorwa Kenkre is a primary care provider, practicing in Pediatrics and Internal Medicine in Wilmington, Delaware. Dr. Kenkre is rated as an Advanced provider by MediFind in the treatment of GM1 Gangliosidosis. Her top areas of expertise are Infant Hyperglycemia, GM1 Gangliosidosis, High Cholesterol, and Type 2 Diabetes (T2D).

Scott Shaffer, MD, is Director of Child and Adolescent Psychiatry Consult-Liaison Service and Deputy Director of Training, Child and Adolescent Psychiatry. He is also an Assistant Professor at our Albert Einstein College of Medicine. Dr. Shaffer is rated as an Advanced provider by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are Postpartum Depression, GM1 Gangliosidosis, Dementia, and Conversion Disorder.

Yoshiyuki Suzuki practices in Tokyo, Japan. Mr. Suzuki is rated as a Distinguished expert by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are GM1 Gangliosidosis, Gangliosidosis, Fabry Disease, and Gaucher Disease.

Roberto Giugliani practices in Porto Alegre, Brazil. Mr. Giugliani is rated as a Distinguished expert by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Acid Sphingomyelinase Deficiency (ASMD), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), and Bone Marrow Transplant.

Martin Thonhofer practices in Graz, Austria. Mr. Thonhofer is rated as a Distinguished expert by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are GM1 Gangliosidosis, Gangliosidosis, Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), and Brachydactyly Mononen Type.

William Gahl is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Gahl is rated as a Distinguished provider by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are Oculocutaneous Albinism Type 2, Hermansky-Pudlak Syndrome, Oculocutaneous Albinism Type 1, Oculocutaneous Albinism, and Deep Brain Stimulation.

Debra Regier is a Pediatrics provider in Washington, Washington, D.c.. Dr. Regier is rated as a Distinguished provider by MediFind in the treatment of GM1 Gangliosidosis. Her top areas of expertise are Gangliosidosis, GM1 Gangliosidosis, Cantu Syndrome, and Maple Syrup Urine Disease.

Amelia Morrone practices in Florence, Italy. Ms. Morrone is rated as a Distinguished expert by MediFind in the treatment of GM1 Gangliosidosis. Her top areas of expertise are Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), Brachydactyly Mononen Type, Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A), and PMM2-Congenital Disorder of Glycosylation.

Arnold Stutz practices in Graz, Austria. Mr. Stutz is rated as a Distinguished expert by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are GM1 Gangliosidosis, Gangliosidosis, Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), and Brachydactyly Mononen Type.

Katsumi Higaki practices in Yonago, Japan. Mr. Higaki is rated as a Distinguished expert by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are Niemann-Pick Disease, GM1 Gangliosidosis, Non-Langerhans-Cell Histiocytosis, and Gangliosidosis.

Osamu Yamato practices in Kagoshima, Japan. Mr. Yamato is rated as a Distinguished expert by MediFind in the treatment of GM1 Gangliosidosis. His top areas of expertise are Gangliosidosis, Tay-Sachs Disease, GM1 Gangliosidosis, and Sandhoff Disease.

Anna Caciotti practices in Florence, Italy. Ms. Caciotti is rated as a Distinguished expert by MediFind in the treatment of GM1 Gangliosidosis. Her top areas of expertise are GM1 Gangliosidosis, Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), Gangliosidosis, and Brachydactyly Mononen Type.

Akira Yabuki practices in Kagoshima, Japan. Yabuki is rated as a Distinguished expert by MediFind in the treatment of GM1 Gangliosidosis. Their top areas of expertise are Gangliosidosis, GM1 Gangliosidosis, Tay-Sachs Disease, and Sandhoff Disease.